What Manufacturing Jobs are in Bellmead?
Showing 488 Manufacturing jobs in Bellmead
Job Description
Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Responsible for overall quality of AbbVie products including small molecule pharmaceuticals and/or biologics, combination products, and medical devices-complying with delivery time objectives; local, divisional, and corporate policies; and ext. agency regulations worldwide. Scope of responsibility can also include business processes supporting new product introduction, product monitoring, or post-market quality systems. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), produced by AbbVie or third-party manufacturer Intermediates/Drug Products. Acts as the principle, quality, global supply chain rep. with external manufacturing businesses. Builds and maintains relationships with TPM Operations, TPM Business Alliance, Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, R&D, and S&T to align strategic initiatives. Develop regulatory strategies for brands with Regulatory Affairs. Grade depe
Responsibilities
Develop and lead a quality professional team responsible for assigned products' transfer activities and end-to-end product quality-conforming to worldwide standards/regulations throughout the NPI supply chain & departmental budget. Lead Product Quality Assurance Transfer Mngr.s to develop strong relationships with Third Party Manufacturers, AbbVie plants, affiliates, & other functional groups. Help them understand each project's quality, compliance, & org. resource needs; & align roles and res
+ Ensure delivery of all quality elements needed to facilitate new product launches including Third Party Manufacturer's that provide products directly to distribution centers, or to AbbVie domestic and International plants for further manufacturing, packaging and/or testing.
+ Core team member or strategic programs lead; including Pipeline Teams, New Product Introductions, Governance Process, CMC Leadership Team, Product Transfers, Specification Approval Team, Regulatory Starting Material Core Team, Global Strategic Sourcing, Due Diligence, and Site Selection. Make primary decisions on product quality, compliance and regulatory conformance issues for sterile, biological, liquid, solids, and/or device products and elevates medium and high risk events to AbbVie mngmnt.
+ Develop and implement a global Product Quality Assurance strategy to support quality systems or product requirements associated with pharmaceuticals, biologics, devices and combination products manufactured at AbbVie plants or third party manufacturing (TPM) facilities. Provide a Quality Assurance perspective during new product development and address resolution of quality and compliance issues.
+ Support development of the legal supply agreements, contracts and letters of intent to ensure the appropriate quality, compliance, and regulatory aspects are met for the products and services covered. Manage and approve organizations actions-like Quality and Technical agreements- as a representative of AbbVie, within the legal boundaries of these documents. Approves negotiated quality and technical agreement as a representative of AbbVie.
+ Key decision maker on product quality, compliance, and regulatory conformance issues for sterile, biological, liquid, solids and/or device products. Complete management reviews with assigned TPMs that identify and address quality, operational, and organizational issues. Interface with Quality Assurance audit team to develop audit plans, due diligence plans, and inspection readiness plans, review audit observations and responses, and maintain corrective action timetable.
+ Provide support for quality audits, initial site approvals and due diligence activities. Direct and manage pre-approval inspection readiness as related to the third party manufacturers to ensure regulatory approvals are obtained, with no delays to market entries. Actively participates and interfaces directly/indirectly with the FDA, EMA, MHRA, ANVISA, MoH, etc. for pre-approval inspections.
+ Function as main Quality liaison between Third Party Manufacturers (TPMs) and AbbVie Operations in support of commercial operations, new product introductions, and product transfers. Negotiates with external companies' upper management to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide AbbVie with the agreed service.
+ Establish and maintain relationships and open communication with Third Party Manufacturers (TPMs), AbbVie plants, affiliates and other functional groups (R&D, Regulatory, Purchasing, etc.) to define roles and responsibilities and identify potential projects and issues. Obtain an in-depth understanding of the quality, compliance, and resource needs at each transfer site. Provide quality oversight and guidance for successful validations (processes, test methods, etc.) and qualifications.
+ Communicate and negotiate with the TPM's quality organization to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide AbbVie with the agreed service. Prioritize programs, initiatives, and problem solving with consideration for impact to timelines, resources and conflicting priorities.
Qualifications
+ Bachelor's Degree in relevant Life Science, Pharmacy, or Engineering is required. Graduate degree preferred.
+ Technical or Analytical background required for problem resolution with technical, quality, product and or engineering related issues.
+ Total combined years of experience 15+ years. In the pharmaceutical, biologics, device, or chemical industry-a minimum of 5 years of experience in Manufacturing and 4 years of experience in QA, R&D, and/or S&T. Minimum of 6 years Management and Supervision experience.
+ Minimum of 5 years' experience in a direct Plant pharmaceutical setting role. Required regulatory inspection experience with direct interaction with regulatory inspectors.
+ Expert knowledge and a comprehensive understanding of biological and/or pharmaceutical technologies (sterile, biological, liquid, ointments, devices, solid tablets and caplets, suspensions, granulations, soft elastic capsules, gel caps, extended release products, coating solutions, and/or active pharmaceutical ingredients).
+ Possesses knowledge and a skill set to operate within an environment that requires a high degree of urgency, positive interpersonal skills, ability to manage multiple complex tasks simultaneously.
+ Capable of analyzing data facts and informed opinion to direct the development of effective action plans as well as the ability to problem solve without the benefit of precedent.
+ The incumbent must be capable of understanding and overcoming differing cultural and language obstacles to provide solutions that satisfy Corporate, Divisional, regional, and local objectives to effectively manage the action plans that will resolve the issues.
+ Strong leadership skills required to manage professional staff and effectively interface with senior leaders both internally as well as with external organizations. Capacity to perform as a leader, team member, and individual.
+ Experience with the requirements for third party external manufacturing.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$160,500
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Responsible for overall quality of AbbVie products including small molecule pharmaceuticals and/or biologics, combination products, and medical devices-complying with delivery time objectives; local, divisional, and corporate policies; and ext. agency regulations worldwide. Scope of responsibility can also include business processes supporting new product introduction, product monitoring, or post-market quality systems. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), produced by AbbVie or third-party manufacturer Intermediates/Drug Products. Acts as the principle, quality, global supply chain rep. with external manufacturing businesses. Builds and maintains relationships with TPM Operations, TPM Business Alliance, Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs, R&D, and S&T to align strategic initiatives. Develop regulatory strategies for brands with Regulatory Affairs. Grade depe
Responsibilities
Develop and lead a quality professional team responsible for assigned products' transfer activities and end-to-end product quality-conforming to worldwide standards/regulations throughout the NPI supply chain & departmental budget. Lead Product Quality Assurance Transfer Mngr.s to develop strong relationships with Third Party Manufacturers, AbbVie plants, affiliates, & other functional groups. Help them understand each project's quality, compliance, & org. resource needs; & align roles and res
+ Ensure delivery of all quality elements needed to facilitate new product launches including Third Party Manufacturer's that provide products directly to distribution centers, or to AbbVie domestic and International plants for further manufacturing, packaging and/or testing.
+ Core team member or strategic programs lead; including Pipeline Teams, New Product Introductions, Governance Process, CMC Leadership Team, Product Transfers, Specification Approval Team, Regulatory Starting Material Core Team, Global Strategic Sourcing, Due Diligence, and Site Selection. Make primary decisions on product quality, compliance and regulatory conformance issues for sterile, biological, liquid, solids, and/or device products and elevates medium and high risk events to AbbVie mngmnt.
+ Develop and implement a global Product Quality Assurance strategy to support quality systems or product requirements associated with pharmaceuticals, biologics, devices and combination products manufactured at AbbVie plants or third party manufacturing (TPM) facilities. Provide a Quality Assurance perspective during new product development and address resolution of quality and compliance issues.
+ Support development of the legal supply agreements, contracts and letters of intent to ensure the appropriate quality, compliance, and regulatory aspects are met for the products and services covered. Manage and approve organizations actions-like Quality and Technical agreements- as a representative of AbbVie, within the legal boundaries of these documents. Approves negotiated quality and technical agreement as a representative of AbbVie.
+ Key decision maker on product quality, compliance, and regulatory conformance issues for sterile, biological, liquid, solids and/or device products. Complete management reviews with assigned TPMs that identify and address quality, operational, and organizational issues. Interface with Quality Assurance audit team to develop audit plans, due diligence plans, and inspection readiness plans, review audit observations and responses, and maintain corrective action timetable.
+ Provide support for quality audits, initial site approvals and due diligence activities. Direct and manage pre-approval inspection readiness as related to the third party manufacturers to ensure regulatory approvals are obtained, with no delays to market entries. Actively participates and interfaces directly/indirectly with the FDA, EMA, MHRA, ANVISA, MoH, etc. for pre-approval inspections.
+ Function as main Quality liaison between Third Party Manufacturers (TPMs) and AbbVie Operations in support of commercial operations, new product introductions, and product transfers. Negotiates with external companies' upper management to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide AbbVie with the agreed service.
+ Establish and maintain relationships and open communication with Third Party Manufacturers (TPMs), AbbVie plants, affiliates and other functional groups (R&D, Regulatory, Purchasing, etc.) to define roles and responsibilities and identify potential projects and issues. Obtain an in-depth understanding of the quality, compliance, and resource needs at each transfer site. Provide quality oversight and guidance for successful validations (processes, test methods, etc.) and qualifications.
+ Communicate and negotiate with the TPM's quality organization to maintain a consistent level of quality and a level of expectation that will minimize compliance risks but also balance the cost of operating to provide AbbVie with the agreed service. Prioritize programs, initiatives, and problem solving with consideration for impact to timelines, resources and conflicting priorities.
Qualifications
+ Bachelor's Degree in relevant Life Science, Pharmacy, or Engineering is required. Graduate degree preferred.
+ Technical or Analytical background required for problem resolution with technical, quality, product and or engineering related issues.
+ Total combined years of experience 15+ years. In the pharmaceutical, biologics, device, or chemical industry-a minimum of 5 years of experience in Manufacturing and 4 years of experience in QA, R&D, and/or S&T. Minimum of 6 years Management and Supervision experience.
+ Minimum of 5 years' experience in a direct Plant pharmaceutical setting role. Required regulatory inspection experience with direct interaction with regulatory inspectors.
+ Expert knowledge and a comprehensive understanding of biological and/or pharmaceutical technologies (sterile, biological, liquid, ointments, devices, solid tablets and caplets, suspensions, granulations, soft elastic capsules, gel caps, extended release products, coating solutions, and/or active pharmaceutical ingredients).
+ Possesses knowledge and a skill set to operate within an environment that requires a high degree of urgency, positive interpersonal skills, ability to manage multiple complex tasks simultaneously.
+ Capable of analyzing data facts and informed opinion to direct the development of effective action plans as well as the ability to problem solve without the benefit of precedent.
+ The incumbent must be capable of understanding and overcoming differing cultural and language obstacles to provide solutions that satisfy Corporate, Divisional, regional, and local objectives to effectively manage the action plans that will resolve the issues.
+ Strong leadership skills required to manage professional staff and effectively interface with senior leaders both internally as well as with external organizations. Capacity to perform as a leader, team member, and individual.
+ Experience with the requirements for third party external manufacturing.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our long-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$160,500
Is this job a match or a miss?
Apply Now
0
Job Description
Company Description
Please note that you are applying to our Compounding A1 Shift: 6am-6:30pm Sunday - Tuesday & every other Wednesday
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please note that you are applying to our Compounding A1 Shift: 6am-6:30pm Sunday - Tuesday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials
+ Maintaining inventory levels
+ Sampling of in process and raw materials
+ Running glass washer / autoclave
+ Buffer / media preparation
+ Equipment preparation (CIP/SIP)
+ Cell culture (from vial thaw to production scale)
+ Column chromatography
+ Tangential flow filtration
Qualifications
+ Associates degree in science, or equivalent experience with 2+ years relevant experience. BS, with 1+ years relevant experience. BS in Engineering, with 0+ year relevant experience.
+ Applies acquired job skills and company policies and procedures to complete assigned tasks.
+ Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
+ Normally follows established procedures on routine work, requires instructions only on new assignments.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$21
Please note that you are applying to our Compounding A1 Shift: 6am-6:30pm Sunday - Tuesday & every other Wednesday
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please note that you are applying to our Compounding A1 Shift: 6am-6:30pm Sunday - Tuesday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials
+ Maintaining inventory levels
+ Sampling of in process and raw materials
+ Running glass washer / autoclave
+ Buffer / media preparation
+ Equipment preparation (CIP/SIP)
+ Cell culture (from vial thaw to production scale)
+ Column chromatography
+ Tangential flow filtration
Qualifications
+ Associates degree in science, or equivalent experience with 2+ years relevant experience. BS, with 1+ years relevant experience. BS in Engineering, with 0+ year relevant experience.
+ Applies acquired job skills and company policies and procedures to complete assigned tasks.
+ Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
+ Normally follows established procedures on routine work, requires instructions only on new assignments.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$21
Is this job a match or a miss?
Apply Now
1
Manufacturing Technician I, MD Fill, A2 Shift - (6pm-6:30am Sunday-Tuesday & every other Saturday)
76702 Waco
AbbVie
Posted 2 days ago
Job Viewed
Job Description
Company Description
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday-Tuesday & every other Saturday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday/Monday/Tuesday & every other Saturday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration
+ Wear an aseptic gown during an 8 hr shift. This gown covers the full body.
+ Willing to complete a lot cleaning sanitation during the work shift
+ Follow all clean room entry and exit procedures
+ Wear the required aseptic gowning and PPE correctly at all times
+ Perform hand hygiene and sanitization before entering the clean room
+ Maintain aseptic technique to prevent contamination of materials and products
+ Sanitize work surfaces, tools, and equipment on a frequent and consistent basis
+ Minimize movement, talking, and unnecessary activity in the clean room
+ Inspect gowning and PPE for proper fit and integrity before use
+ Report any contamination concerns, spills, or equipment issues immediately
+ Handle sterile materials only in approved areas and in a controlled manner
+ Follow all environmental monitoring and cleaning requirements
+ Dispose of waste and contaminated materials according to procedure
+ Complete all required documentation accurately and on time. Good hand writing will be a huge plus.
Qualifications
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday-Tuesday & every other Saturday
Qualifications
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday-Tuesday & every other Saturday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday/Monday/Tuesday & every other Saturday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration
+ Wear an aseptic gown during an 8 hr shift. This gown covers the full body.
+ Willing to complete a lot cleaning sanitation during the work shift
+ Follow all clean room entry and exit procedures
+ Wear the required aseptic gowning and PPE correctly at all times
+ Perform hand hygiene and sanitization before entering the clean room
+ Maintain aseptic technique to prevent contamination of materials and products
+ Sanitize work surfaces, tools, and equipment on a frequent and consistent basis
+ Minimize movement, talking, and unnecessary activity in the clean room
+ Inspect gowning and PPE for proper fit and integrity before use
+ Report any contamination concerns, spills, or equipment issues immediately
+ Handle sterile materials only in approved areas and in a controlled manner
+ Follow all environmental monitoring and cleaning requirements
+ Dispose of waste and contaminated materials according to procedure
+ Complete all required documentation accurately and on time. Good hand writing will be a huge plus.
Qualifications
This is a MD Fill - Aseptic Gown - A2 Shift: 6pm-6:30am Sunday-Tuesday & every other Saturday
Qualifications
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
Is this job a match or a miss?
Apply Now
2
Production Manager II - East Texas Region
76673 Mount Calm
NextEra Energy
Posted 1 day ago
Job Viewed
Job Description
**Production Manager II - East Texas Region**
**Date:** Jul 23, 2026
**Location(s):** Mt Calm, TX, US, 76673
**Company:** NextEra Energy
**Requisition ID:** 96266
NextEra Energy Resources is one of America's largest wholesale electricity generators, harnessing diverse energy sources to power progress. We deliver tailored energy solutions that fuel economic growth, strengthen communities, and help customers achieve their energy goals. Ready to make a lasting impact? Take the next step in your career with us!
**Position Specific Description**
NextEra Energy is seeking a technically skilled leader to manage a portfolio of new and developing solar and storage assets associated with our ROI fleet **across the East Texas Region of the United States** . The individual will lead a team of technicians in the daily operations and maintenance of solar and storage assets varying in size and scale. The ideal candidate will live in the region to support the travel schedule.
The manager will be responsible for the safety of all personnel and environmental compliance with all required regulatory permits. The individual will be responsible for delivering on key performance indicators including availability, production, and cost.
**Leaders are expected to:**
+ Collaborate with peers, stakeholders, central organization support teams, vendors, and OEMs to advance organizational goals
+ Ensure all safety, environmental, performance, and budget targets are met
+ Develop and grow the team and business
+ Oversee and approve procurement activities of the sites
+ Perform other job-related duties as assigned
**Strongly Preferred:**
+ Engineering Degree- Electrical preferred
+ Demonstrated strong leadership and management skills
+ Solid technical background and field services experience with strong problem-solving skills
+ Ability to successfully handle multiple projects simultaneously, set priorities, and meet deadlines in a fast-paced environment
+ Superior organizational, time management, and interpersonal skills
+ Ability to manage multiple complex tasks and achieve flawless execution
+ Strong project management skills
+ Strong business process management skills
+ Six Sigma skills or equivalent quality experience
**Additional Information:**
+ Travel Required: 50%
**Job Overview**
This job leads a team involved in operating a power plant. Under general direction, leaders in this role manage all aspects of site business and operations, achieving all production and business targets while maintaining an injury-free work site.
**Job Duties & Responsibilities**
- Ensures all business activities are conducted following corporate policies and are in compliance with all applicable local, state, and federal permits, codes, standards, and regulations
- Develops multi-year Operations and Maintenance budgets
- Ensures all budget targets are met
- Oversees and approves procurement activities of the site
- Performs other job-related duties as assigned
**Required Qualifications**
- High School Grad / GED
- Bachelor's or Equivalent Experience
- Experience: 5+ years
- Supervisor/Management Experience: 2+ years
**Preferred Qualifications**
- Bachelor's Degree
NextEra Energy offers a wide range of benefits to support our employees and their eligible family members. Clickto learn more.
**Employee Group:** Exempt
**Employee Type:** Full Time
**Job Category:** Operations
**Organization:** NextEra Energy Operating Services, LLC
**Relocation Provided:** Yes, if applicable
NextEra Energy is an Equal Opportunity Employer. Qualified applicants are considered for employment without regard to race, color, age, national origin, religion, marital status, sex, sexual orientation, gender identity, gender expression, genetics, disability, protected veteran status or any other basis prohibited by law.
NextEra Energy provides reasonable accommodation in its application and selection process for qualified individuals, including accommodations related to compliance with conditional job offer requirements, consistent with federal, state, and local laws. Supporting medical or religious documentation will be required where applicable and permitted by applicable law. To request a reasonable accommodation, please send an e-mail to, providing your name, telephone number and the best time for us to reach you.
NextEra Energy will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
NextEra Energy **does not** accept any unsolicited resumes or referrals from **any third-party recruiting firms or agencies** . Please see ourfor more information.
**Date:** Jul 23, 2026
**Location(s):** Mt Calm, TX, US, 76673
**Company:** NextEra Energy
**Requisition ID:** 96266
NextEra Energy Resources is one of America's largest wholesale electricity generators, harnessing diverse energy sources to power progress. We deliver tailored energy solutions that fuel economic growth, strengthen communities, and help customers achieve their energy goals. Ready to make a lasting impact? Take the next step in your career with us!
**Position Specific Description**
NextEra Energy is seeking a technically skilled leader to manage a portfolio of new and developing solar and storage assets associated with our ROI fleet **across the East Texas Region of the United States** . The individual will lead a team of technicians in the daily operations and maintenance of solar and storage assets varying in size and scale. The ideal candidate will live in the region to support the travel schedule.
The manager will be responsible for the safety of all personnel and environmental compliance with all required regulatory permits. The individual will be responsible for delivering on key performance indicators including availability, production, and cost.
**Leaders are expected to:**
+ Collaborate with peers, stakeholders, central organization support teams, vendors, and OEMs to advance organizational goals
+ Ensure all safety, environmental, performance, and budget targets are met
+ Develop and grow the team and business
+ Oversee and approve procurement activities of the sites
+ Perform other job-related duties as assigned
**Strongly Preferred:**
+ Engineering Degree- Electrical preferred
+ Demonstrated strong leadership and management skills
+ Solid technical background and field services experience with strong problem-solving skills
+ Ability to successfully handle multiple projects simultaneously, set priorities, and meet deadlines in a fast-paced environment
+ Superior organizational, time management, and interpersonal skills
+ Ability to manage multiple complex tasks and achieve flawless execution
+ Strong project management skills
+ Strong business process management skills
+ Six Sigma skills or equivalent quality experience
**Additional Information:**
+ Travel Required: 50%
**Job Overview**
This job leads a team involved in operating a power plant. Under general direction, leaders in this role manage all aspects of site business and operations, achieving all production and business targets while maintaining an injury-free work site.
**Job Duties & Responsibilities**
- Ensures all business activities are conducted following corporate policies and are in compliance with all applicable local, state, and federal permits, codes, standards, and regulations
- Develops multi-year Operations and Maintenance budgets
- Ensures all budget targets are met
- Oversees and approves procurement activities of the site
- Performs other job-related duties as assigned
**Required Qualifications**
- High School Grad / GED
- Bachelor's or Equivalent Experience
- Experience: 5+ years
- Supervisor/Management Experience: 2+ years
**Preferred Qualifications**
- Bachelor's Degree
NextEra Energy offers a wide range of benefits to support our employees and their eligible family members. Clickto learn more.
**Employee Group:** Exempt
**Employee Type:** Full Time
**Job Category:** Operations
**Organization:** NextEra Energy Operating Services, LLC
**Relocation Provided:** Yes, if applicable
NextEra Energy is an Equal Opportunity Employer. Qualified applicants are considered for employment without regard to race, color, age, national origin, religion, marital status, sex, sexual orientation, gender identity, gender expression, genetics, disability, protected veteran status or any other basis prohibited by law.
NextEra Energy provides reasonable accommodation in its application and selection process for qualified individuals, including accommodations related to compliance with conditional job offer requirements, consistent with federal, state, and local laws. Supporting medical or religious documentation will be required where applicable and permitted by applicable law. To request a reasonable accommodation, please send an e-mail to, providing your name, telephone number and the best time for us to reach you.
NextEra Energy will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
NextEra Energy **does not** accept any unsolicited resumes or referrals from **any third-party recruiting firms or agencies** . Please see ourfor more information.
Is this job a match or a miss?
Apply Now
3
Job Description
Company Description
About AbbVie
Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration.
Qualifications
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
About AbbVie
Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please not this is our B1 Shift: 6am-6:30pm Thursday/Friday/Saturday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration.
Qualifications
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
Is this job a match or a miss?
Apply Now
4
Job Description
Company Description
Please note you are applying to an A1 Shift: 6am-6:30pm Sunday-Tuesday & every other Wednesday
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please note you are applying to an A1 Shift: 6am-6:30pm Sunday-Tuesday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
Shipping finished materials
+ Maintaining inventory levels
+ Sampling of in process and raw materials
+ Running glass washer / autoclave
+ Buffer / media preparation
+ Equipment preparation (CIP/SIP)
+ Cell culture (from vial thaw to production scale)
+ Column chromatography
+ Tangential flow filtration
Qualifications
+ Associates degree in science (or equivalent experience), with 2+ years relevant experience. BS, with 1+ years relevant experience.BS in Engineering, with 0+ year relevant experience.
+ Applies acquired job skills and company policies and procedures to complete assigned tasks.
+ Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
+ Normally follows established procedures on routine work, requires instructions only on new assignments.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount isearned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits thatare allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole andabsolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$21
Please note you are applying to an A1 Shift: 6am-6:30pm Sunday-Tuesday & every other Wednesday
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on LinkedIn, ( Facebook, Instagram ( , X ( and YouTube. ( Description
Please note you are applying to an A1 Shift: 6am-6:30pm Sunday-Tuesday & every other Wednesday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
Shipping finished materials
+ Maintaining inventory levels
+ Sampling of in process and raw materials
+ Running glass washer / autoclave
+ Buffer / media preparation
+ Equipment preparation (CIP/SIP)
+ Cell culture (from vial thaw to production scale)
+ Column chromatography
+ Tangential flow filtration
Qualifications
+ Associates degree in science (or equivalent experience), with 2+ years relevant experience. BS, with 1+ years relevant experience.BS in Engineering, with 0+ year relevant experience.
+ Applies acquired job skills and company policies and procedures to complete assigned tasks.
+ Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from accepted practice.
+ Normally follows established procedures on routine work, requires instructions only on new assignments.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this roleat the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on manyfactors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount isearned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits thatare allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole andabsolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$21
Is this job a match or a miss?
Apply Now
5
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Aseptic Manufacturing Training Lead is responsible for designing, delivering, and implementing training programs for the assigned department members. The Aseptic Manufacturing Training Lead also has responsibility for maintaining employee training profiles in training system, filing training records, investigating late training events, and providing review of training related document updates. Ensures consistent compliance with external and internal AbbVie policies/procedures impacting the training program for the assigned department. Works with cross-functional team to assure consistent training practices throughout the operations. Leads continuous improvement projects to enhance training delivery and effectiveness and evaluate use of new technologies to enhance the training experience.
Responsibilities
+ Ensure AbbVie Training Policy, process and procedures and regulatory training requirements are implemented at the site.
+ Train new and existing employees on appropriate cleanroom behavior and best practices including but not limited to activities such as equipment intervention and sampling.
+ Supports implementation of global Aseptic Best Practices related to aseptic processes and training
+ Identify areas of improvement with current aseptic processes at the site and manage continued improvement projects, as needed.
+ Observe employees aseptic gowning technique and provide coaching.
+ Gowning Training (initial and recertification)
+ Partner with Microbiology and Operations for Environmental Monitoring and Sanitization Training
+ Monthly shift touchpoints focused on a pre-established rolling Aseptic refresher (target 15-20 min 10 topics, conducted when semi-annual refresher training is not performed)
+ Monthly Gemba walks with Aseptic MQA / site leadership
+ 20% of time dedicated to Aseptic Auditing
+ Work with global Aseptic Trainers to develop, then deliver targeted aseptic trainings based on site needs
+ This position will support the entire site for aseptic training. It will be working with the global staff to identify and help roll out additional training if required. Gemba walks and on the floor training reinforcement.
+ Work with department/area supervisors and SMEs to schedule training on more complex methods/techniques.
+ Maintain training profiles for all trainees and enter completed and verified training into the training system and file training records as needed.
+ Complete periodic review and updates of training related documents as needed.
+ May also need to provide hands-on training for basic to more complex skills/techniques.
Qualifications
+ Bachelor's degree required. Degree program or professional certification in Education, Communication, Training, or a related field is beneficial.
+ Knowledge of regulations and standards for Aseptic manufacturing and application to training.
+ At least 3 years of Aseptic Operations/Quality/Training, combined experience is required.
+ Essential experience should include knowledge of GMPs, aseptic manufacturing, and training processes.
+ Knowledge of regulations and standards for pharmaceutical testing operations and application to training.
+ Strong organizational skills and the ability to work in a team environment.
+ Excellent presentation skills required. Proven ability to lead and conduct critical training classes.
+ Essential experience will include knowledge of GMP and training process.
+ Ability to problem solve, initiate, and manage projects.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$96,500
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
The Aseptic Manufacturing Training Lead is responsible for designing, delivering, and implementing training programs for the assigned department members. The Aseptic Manufacturing Training Lead also has responsibility for maintaining employee training profiles in training system, filing training records, investigating late training events, and providing review of training related document updates. Ensures consistent compliance with external and internal AbbVie policies/procedures impacting the training program for the assigned department. Works with cross-functional team to assure consistent training practices throughout the operations. Leads continuous improvement projects to enhance training delivery and effectiveness and evaluate use of new technologies to enhance the training experience.
Responsibilities
+ Ensure AbbVie Training Policy, process and procedures and regulatory training requirements are implemented at the site.
+ Train new and existing employees on appropriate cleanroom behavior and best practices including but not limited to activities such as equipment intervention and sampling.
+ Supports implementation of global Aseptic Best Practices related to aseptic processes and training
+ Identify areas of improvement with current aseptic processes at the site and manage continued improvement projects, as needed.
+ Observe employees aseptic gowning technique and provide coaching.
+ Gowning Training (initial and recertification)
+ Partner with Microbiology and Operations for Environmental Monitoring and Sanitization Training
+ Monthly shift touchpoints focused on a pre-established rolling Aseptic refresher (target 15-20 min 10 topics, conducted when semi-annual refresher training is not performed)
+ Monthly Gemba walks with Aseptic MQA / site leadership
+ 20% of time dedicated to Aseptic Auditing
+ Work with global Aseptic Trainers to develop, then deliver targeted aseptic trainings based on site needs
+ This position will support the entire site for aseptic training. It will be working with the global staff to identify and help roll out additional training if required. Gemba walks and on the floor training reinforcement.
+ Work with department/area supervisors and SMEs to schedule training on more complex methods/techniques.
+ Maintain training profiles for all trainees and enter completed and verified training into the training system and file training records as needed.
+ Complete periodic review and updates of training related documents as needed.
+ May also need to provide hands-on training for basic to more complex skills/techniques.
Qualifications
+ Bachelor's degree required. Degree program or professional certification in Education, Communication, Training, or a related field is beneficial.
+ Knowledge of regulations and standards for Aseptic manufacturing and application to training.
+ At least 3 years of Aseptic Operations/Quality/Training, combined experience is required.
+ Essential experience should include knowledge of GMPs, aseptic manufacturing, and training processes.
+ Knowledge of regulations and standards for pharmaceutical testing operations and application to training.
+ Strong organizational skills and the ability to work in a team environment.
+ Excellent presentation skills required. Proven ability to lead and conduct critical training classes.
+ Essential experience will include knowledge of GMP and training process.
+ Ability to problem solve, initiate, and manage projects.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$96,500
Is this job a match or a miss?
Apply Now
6
Manufacturing Technician I, MD Fill, B2 Shift (6pm-6:30am Wednesday-Friday & every other Saturday)
76702 Waco
AbbVie
Posted 7 days ago
Job Viewed
Job Description
Company Description
This is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
This is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration
+ Wear an aseptic gown during an 8 hr shift. This gown covers the full body.
+ Willing to complete a lot cleaning sanitation during the work shift
+ Follow all clean room entry and exit procedures
+ Wear the required aseptic gowning and PPE correctly at all times
+ Perform hand hygiene and sanitization before entering the clean room
+ Maintain aseptic technique to prevent contamination of materials and products
+ Sanitize work surfaces, tools, and equipment on a frequent and consistent basis
+ Minimize movement, talking, and unnecessary activity in the clean room
+ Inspect gowning and PPE for proper fit and integrity before use
+ Report any contamination concerns, spills, or equipment issues immediately
+ Handle sterile materials only in approved areas and in a controlled manner
+ Follow all environmental monitoring and cleaning requirements
+ Dispose of waste and contaminated materials according to procedure
+ Complete all required documentation accurately and on time. Good hand writing will be a huge plus.
Please note that the YouTube video is not owned, produced, or sponsored by AbbVie and does not accurately depict AbbVie's aseptic processes and procedures. The video is provided solely as an example of the aseptic gowning process.
is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Aseptic experience (Preferred)
+ Aseptic PPE Experience (Preferred)
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
This is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
This is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials. Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process.
Responsibilities
+ Shipping finished materials.
+ Maintaining inventory levels.
+ Sampling of in process and raw materials.
+ Running glass washer / autoclave.
+ Buffer / media preparation.
+ Equipment preparation (CIP / SIP).
+ Cell culture (from vial thaw to production scale).
+ Column chromatography.
+ Tangential flow filtration
+ Wear an aseptic gown during an 8 hr shift. This gown covers the full body.
+ Willing to complete a lot cleaning sanitation during the work shift
+ Follow all clean room entry and exit procedures
+ Wear the required aseptic gowning and PPE correctly at all times
+ Perform hand hygiene and sanitization before entering the clean room
+ Maintain aseptic technique to prevent contamination of materials and products
+ Sanitize work surfaces, tools, and equipment on a frequent and consistent basis
+ Minimize movement, talking, and unnecessary activity in the clean room
+ Inspect gowning and PPE for proper fit and integrity before use
+ Report any contamination concerns, spills, or equipment issues immediately
+ Handle sterile materials only in approved areas and in a controlled manner
+ Follow all environmental monitoring and cleaning requirements
+ Dispose of waste and contaminated materials according to procedure
+ Complete all required documentation accurately and on time. Good hand writing will be a huge plus.
Please note that the YouTube video is not owned, produced, or sponsored by AbbVie and does not accurately depict AbbVie's aseptic processes and procedures. The video is provided solely as an example of the aseptic gowning process.
is our MD Fill - Aseptic Gown - B2 night shift: 6pm-6:30am Wednesday - Friday & every other Saturday
+ High School diploma (or equivalent experience), with 2+ years experience. Associates degree in science, with 1+ years relevant experience. Bachelor's Degree with 0+ year relevant experience.
+ Aseptic experience (Preferred)
+ Aseptic PPE Experience (Preferred)
+ Acquires job skills and learns company policies and procedures to complete routine tasks.
+ Works on assignments that are routine in nature, requiring limited judgment.
+ Has the ability to recognize when accepted practices are deviated from.
+ Normally receives detailed instructions on all work.
+ Works under close supervision.
Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
+ The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
+ We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
+ This job is eligible to participate in our short-term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
$18.6
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7
CDL-A Local Driver / Forklift Operator, Part-time
76702 Waco
ABF Freight
Posted 3 days ago
Job Viewed
Job Description
Job Description
Pickup and delivery of cargo to and from various destinations usually within proximity of the consolidation/distribution center. The loading and unloading of trailers utilizing the same techniques, technology and procedures as a dock worker. Actual duties and schedule may vary depending on terminal location.
Responsibilities
* Pickup and delivery of cargo to and from various destinations usually within proximity of the consolidation/distribution center.
* Loading and unloading of trailers utilizing the same techniques, technology and procedures as a dock worker.
* Actual duties and schedule may vary depending on terminal location.
Requirements
Experience:
* 1 year of verifiable tractor/trailer experience (Candidates with less than 1 year experience may be eligible for training).
Certifications:
* Class-A CDL with doubles/triples, tanker and hazardous materials endorsements and no automatic restriction
Additional Requirements:
* Minimum 21 years of age.
* Good stable work record.
* Safe driving record (from MVR and previous employment).
* Be able to pass DOT pre-employment drug screen and meet DOT medical requirements.
* Shift days and hours required for this position vary by location and may include days, nights, and/or weekends. Being able to work the required hours at this location will be considered a minimum requirement.
Other Details
Work Hours:
* Schedule may vary depending on Service Center location.
Travel Requirements:
* Minimal
Compensation:
* This is a hourly position paid weekly.
About Us
ABF Freight®, an ArcBest® company, is one of the nation's largest, most trusted less-than-truckload carriers. With over a century of experience, 240 service centers spanning North America, and an unwavering commitment to quality, safety and customer service, ABF offers best-in-class LTL transportation for companies of all sizes and industries. We're driven for excellence.
An Equal Opportunity Employer including Vet/Disability
Pickup and delivery of cargo to and from various destinations usually within proximity of the consolidation/distribution center. The loading and unloading of trailers utilizing the same techniques, technology and procedures as a dock worker. Actual duties and schedule may vary depending on terminal location.
Responsibilities
* Pickup and delivery of cargo to and from various destinations usually within proximity of the consolidation/distribution center.
* Loading and unloading of trailers utilizing the same techniques, technology and procedures as a dock worker.
* Actual duties and schedule may vary depending on terminal location.
Requirements
Experience:
* 1 year of verifiable tractor/trailer experience (Candidates with less than 1 year experience may be eligible for training).
Certifications:
* Class-A CDL with doubles/triples, tanker and hazardous materials endorsements and no automatic restriction
Additional Requirements:
* Minimum 21 years of age.
* Good stable work record.
* Safe driving record (from MVR and previous employment).
* Be able to pass DOT pre-employment drug screen and meet DOT medical requirements.
* Shift days and hours required for this position vary by location and may include days, nights, and/or weekends. Being able to work the required hours at this location will be considered a minimum requirement.
Other Details
Work Hours:
* Schedule may vary depending on Service Center location.
Travel Requirements:
* Minimal
Compensation:
* This is a hourly position paid weekly.
About Us
ABF Freight®, an ArcBest® company, is one of the nation's largest, most trusted less-than-truckload carriers. With over a century of experience, 240 service centers spanning North America, and an unwavering commitment to quality, safety and customer service, ABF offers best-in-class LTL transportation for companies of all sizes and industries. We're driven for excellence.
An Equal Opportunity Employer including Vet/Disability
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Apply Now
8
Director of Manufacturing Project Delivery
76796 Waco
States Manufacturing Corporation
Posted 5 days ago
Job Viewed
Job Description
States Manufacturing Corporation is seeking a Director of Project Management to lead the order lifecycle from acknowledgment to final delivery in a custom manufacturing environment. This leadership role involves managing a team of Project Managers while building effective systems for timely and accurate order execution.
The ideal candidate will have over 8 years of project management experience, strong communication skills, and proficiency in ERP systems. Opportunities for periodic travel to manufacturing sites are included in the position.
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Note: If you’re asked to pay for a job, avoid the role and report the job to us immediately.
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9