127 Manufacturing jobs in Pittsboro
Senior Manager Manufacturing - Manufacturing Support Manufacturing Systems
Posted 10 days ago
Job Viewed
Job Description
At Amgen, if you feel like you're part of something bigger, it's because you are. Our shared mission-to serve patients living with serious illnesses-drives all that we do.
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease- we reach millions of patients each year. As a member of the Amgen team, you'll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you'll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Be part of Amgen's newest and most advanced drug substance manufacturing plant. When completed, the Amgen FleX batch facility will combine the latest in single use technologies with traditional stainless steel equipment to allow for maximum flexibility in operations. The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.
**Senior Manager Manufacturing - Manufacturing Support Manufacturing Systems**
**What you will do**
Let's do this. Let's change the world. In this vital role you will provide leadership and oversight for a team responsible for New Product Introduction (NPI), Process Ownership (PO), Single-Use Systems (SUS), and Cleaning Validation within the site's manufacturing operations. You are accountable for the performance, goals, and management of these functions, ensuring operational readiness, compliance, and successful introduction of new products to the Amgen North Carolina Drug Substance manufacturing facility.
+ New Product Introduction (NPI): Lead site activities to introduce new products and process changes; conduct facility fit assessments; own change controls, documentation, project management, and cross-functional alignment to achieve operational readiness.
+ Program & Governance Leadership: Lead the NPI core team meetings to drive scope, schedule, risks, and decisions; present at Tech Transfer Steering Committee (TTSC) meetings with high-level summaries and project coordination to enable timely governance decisions.
+ Process Owners: Oversee process ownership teams accountable for lifecycle management, continuous improvement, and compliance of core manufacturing processes, including process change controls, CAPAs, and SOPs.
+ Single-Use Systems: Provide leadership for the design, implementation, change management, and ongoing support of SUS used in manufacturing operations, including the leak and defect management program.
+ Cleaning Validation: Direct validation programs and activities related to equipment cleaning validation (CIP/COP), sterilization (SIP/Autoclaves), and controlled temperature chambers.
+ Team Leadership: Build, mentor, and develop a high-performing team with clear goals, accountability, and results across all managed functions.
+ Cross-functional Leadership: Act as a key liaison with Manufacturing, Quality, Process Development, Supply Chain, Facilities & Engineering, and Finance to align priorities and execution.
+ Compliance & Continuous Improvement: Drive operational excellence, ensure regulatory compliance, and foster a culture of safety, Lean Manufacturing, and continuous improvement.
**What we expect of you**
We are all different, yet we all use our unique contributions to serve patients. The manufacturing professional we seek is a leader with these qualifications.
**Basic Qualifications:**
+ High school diploma / GED & 12 years Quality and/or Manufacturing experience OR
+ Associate's degree & 10 years of Quality and/or Manufacturing experience OR
+ Bachelor's degree & 8 years of Quality and/or Manufacturing experience OR
+ Master's degree & 6 years of Quality and/or Manufacturing experience OR
+ Doctorate degree & 2 years of Quality and/or Manufacturing experience
**Preferred Qualifications:**
+ Current leadership role in a GMP manufacturing facility.
+ Experience in biologics manufacturing operations for licensed commercial products.
+ Proven track record in NPI/tech transfer and project governance.
+ Depth in process validation lifecycle (process design, PPQ, CPV).
+ Expertise in SUS management and cleaning validation programs.
+ Excellent communication and executive-level presentation skills.
+ Experience operating in matrixed, cross-site, or global networks.
+ Demonstrated application of Lean/Operational Excellence in drug substance manufacturing.
**What you can expect of us**
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way.
In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.
**Apply now and make a lasting impact with the Amgen team!**
**careers.amgen.com**
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Manufacturing Technician
Posted 1 day ago
Job Viewed
Job Description
Description
Purpose Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to GMP guidelines Function Setup, operate, monitor & control equipment, systems & processes • Clean & sanitize manufacturing, filling & packaging rooms & equipment per SOPs • Execute production schedule to achieve production goals • Handle labeling & components correctly; transferring, counting, FIFO, returns, etc • Participate actively in & support event response • Review & author SOPs & other documents as required • Identify, report & resolve quality issues • Execute &/or assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance • Train fellow employees in areas of expertise & aggressively learn systems & equipment outside of own expertise (with the appropriate experience & skill level) • Record/review production data in BPR & associated forms • Follow all safety & environmental requirements in the performance of duties • Other accountabilities, as assigned
Skills
Production, Cgmp, Sop
Top Skills Details
Production,Cgmp
Additional Skills & Qualifications
GMP Manufacturing
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $23.50 - $23.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Durham,NC.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Manufacturing Technician
Posted 11 days ago
Job Viewed
Job Description
Duration: 12+ Months with poss. of ext.
Timing: 7P-7:30A rotation shift. One week you will work four days Monday - Thursday and the next three days Monday - Wednesday.
Pay Rate: $16.50/hr + 15% Shift Differential = $18.98/hr Overtime availability once fully trained.
Job Description:
The Manufacturing Technician position is responsible for the operation of high speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner.
The position may perform or assist in the setup, inspection, preventive maintenance, troubleshooting and cleaning of equipment used throughout the BacT/ALERT Manufacturing and Packaging processes.
Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated tasks
AQL inspections, reworks and Material reconciliation that goes along with the batch.
Main Accountabilities:
- Production Manufacturing & Packaging: Operate high speed manufacturing equipment, in some cases highly automated, using HMI/SCADA interfaces
- Filling: chemical weighing and reagent formulation
- Execute production activities per approved Manufacturing Directions while maintaining compliance with all job related SOPs
- Quality Ensure that all batch paperwork is completed in an accurate, thorough, and timely manner
- Perform and document all processes and procedures in a timely manner, while maintaining compliance with all company and regulatory agency regulations
- Provide assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product.
- Assist with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns
- Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements
- SafetyComply with all safety policies and procedures at all times
- Appropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties.
- Other DutiesGenerate reports, charts and KPI's and interpret the data to identify problems, and proceed with proper decision making
- Assist with executing validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state
- Perform computer applications
- Perform other duties as assigned by Management
- Experience Minimum of 0-1 years in a regulated production/operations environment
- Skills Certification in Bioworks Program preferred
- For Manufacturing and Packaging Demonstrated proficiency in the operation of high speed, highly automated, production equipment preferred.
- For Filling Background in Bulking and/or compounding in food, supplement, cosmetic, medical device, or pharmaceutical chemical formulation is desired.
- Familiarity with measurement scales, mixing, blending, chemical mills and other formulation manufacturing equipment strongly desired.
- Knowledge of and experience in following OSHA regulations (LOTO, electrical safety, etc.) preferred.
- Knowledge of FDA and/or GMP regulations preferred.
- Mechanical background preferred.
- Ability to rapidly learn new procedures and reduce them to practice.
- Must be able to learn, comprehend and demonstrate competency in operating new equipment within a 75-day period of working with a trainer.
- Performs all job functions and responsibilities in a safe and responsible manner.
- Ability to regularly climb stairs to perform work.
- Ability to routinely lift 20-40 lbs.
- Ability to stand for extended periods of time on shifts that could range from 8-12 hours.
- Ability to operate motorized pallet jacks.
- May be exposed to and require the handling of chemicals, antibiotics and/or hazardous materials.
- May be exposed to strong odors incurred during media production or other operations.
- Lab work is performed wearing various types of PPE which include but is not limited to a hairnet, beard cover, safety glasses, safety shoes, hearing protection, gloves, PAPRs, face mask and lab coats. Make-up and jewelry are prohibited in certain areas of Manufacturing.
- Ability to maintain reliable and punctual attendance
- Ability to work overtime as required to support a 24/7 production operation
Manufacturing Tech
Posted 11 days ago
Job Viewed
Job Description
Title: Manufacturing Tech
Location: 100 Rodolphe Street Durham NC 27712 (Onsite)
Duration: 18+ months
Shift: Friday-Sunday 7:00pm-7:30am,.
Pay Rate: $17.83/hr on W2
Client : Biomerieux
Req ID- BIO
Job Description
Working hours will be Hours: Friday-Sunday 7:00pm-7:30am,
Pay Rate: $5.50/hour + 15% Shift Differential = 17.83
Position Summary:
The Manufacturing Technician position is responsible for the operation of high speed equipment used in the production and packaging of BacT/ALERT bottles and/or preparing and formulating the liquid reagents that fill the finished BacT/ALERT bottle in a cGMP compliant manner.
The position may perform or assist in the setup, inspection, preventive maintenance, troubleshooting and cleaning of equipment used throughout the BacT/ALERT Manufacturing and Packaging processes.
Additionally, this individual will be responsible for completing production batches and corresponding documentation for the associated tasks
AQL inspections, reworks and Material reconciliation that goes along with the batch.
Main Accountabilities:
• Production Manufacturing & Packaging: Operate high speed manufacturing equipment, in some cases highly automated, using HMI/SCADA interfaces
• Filling: chemical weighing and reagent formulation
• Execute production activities per approved Manufacturing Directions while maintaining compliance with all job related SOPs
• Quality ensure that all batch paperwork is completed in an accurate, thorough, and timely manner.
• Perform and document all processes and procedures in a timely manner, while maintaining compliance with all company and regulatory agency regulations
• Provide assistance with the review and revision of Manufacturing Directions and SOPs necessary for the manufacture and packaging of product.
• ssist with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns.
• Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements.
• Safety comply with all safety policies and procedures at all times
• ppropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties.
• Other Duties Generate reports, charts and KPI's and interpret the data to identify problems, and proceed with proper decision making
• ssist with executing validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state
• Perform computer applications.
• Perform other duties as assigned by Management.
Studies, Experience, Skills and Qualifications:
• Experience: Minimum of 0-1 years in a regulated production/operations environment
• Skills Certification in Bioworks Program preferred.
• For Manufacturing and Packaging Demonstrated proficiency in the operation of high
• Knowledge of and experience in following OSHA regulations (LOTO, electrical safety, etc.) preferred.
• Knowledge of FDA and/or GMP regulations preferred.
• Mechanical background preferred.
• bility to rapidly learn new procedures and reduce them to practice.
• Must be able to learn, comprehend and demonstrate competency in operating new equipment within a 75-day period of working with a trainer.
Additional Information:
• Performs all job functions and responsibilities in a safe and responsible manner.
• bility to regularly climb stairs to perform work.
• bility to routinely lift 20-40 lbs.
• bility to stand for extended periods of time on shifts that could range from 8-12 hours.
• bility to operate motorized pallet jacks.
• May be exposed to and require the handling of chemicals, antibiotics and/or hazardous materials.
• May be exposed to strong odors incurred during media production or other operations.
• Lab work is performed wearing various types of PPE which include but is not limited to a hairnet, beard cover, safety glasses, safety shoes, hearing protection, gloves, PAPRs, face mask and lab coats. Make-up and jewelry are prohibited in certain areas of Manufacturing.
• bility to maintain reliable and punctual attendance.
• bility to work overtime as required to support a 24/7 production operation
Manufacturing Technician
Posted 13 days ago
Job Viewed
Job Description
Purpose Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to GMP guidelines Function Setup, operate, monitor & control equipment, systems & processes - Clean & sanitize manufacturing, filling & packaging rooms & equipment per SOPs - Execute production schedule to achieve production goals - Handle labeling & components correctly; transferring, counting, FIFO, returns, etc - Participate actively in & support event response - Review & author SOPs & other documents as required - Identify, report & resolve quality issues - Execute &/or assist during equipment maintenance, including restoration of lost function, predictive & preventative maintenance - Train fellow employees in areas of expertise & aggressively learn systems & equipment outside of own expertise (with the appropriate experience & skill level) - Record/review production data in BPR & associated forms - Follow all safety & environmental requirements in the performance of duties - Other accountabilities, as assigned
Skills
Production, Cgmp, Sop
Top Skills Details
Production,Cgmp
Additional Skills & Qualifications
GMP Manufacturing
Experience Level
Entry Level
Pay and Benefits
The pay range for this position is $23.50 - $23.50/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Durham,NC.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.
Manufacturing Associate
Posted 14 days ago
Job Viewed
Job Description
Manufacturing
Holly Springs, NC, US
Pay Rate Low: 18.00 | Pay Rate High: 20.00
+ Added - 25/09/2025
Apply for Job
Our client, a renowned leader in biotechnology, is revolutionizing the use of living cells to create groundbreaking biologic medicines. As a guiding force in the biotech industry, they set the bar for innovation and advancement.
We are seeking a Manufacturing Associate to join our dynamic team and support GMP drug substance manufacturing and validation activities. This individual will play a crucial role in manufacturing operations, ensuring compliance with industry standards while contributing to process optimization and data analysis.
Location: Raleigh/Apex, NC
Contract to Hire
Pay: 18-20/hr.
**Key Responsibilities**
+ Execute manufacturing operations and support activities on the production floor.
+ Perform GMP and non-GMP production runs (small- and large-scale).
+ Handle material preparation, equipment setup, and cleaning validation in compliance with GMP guidelines.
+ Assist in process validation and technical support for manufacturing activities.
+ Collect and analyze data related to manufacturing performance and validation.
+ Support documentation processes, including batch records and deviation reports.
+ Collaborate with cross-functional teams (Engineering, Process Development, and Quality Assurance) to optimize manufacturing workflows.
+ Contribute to continuous improvement efforts and best practices in drug substance manufacturing.
**Education & Experience Options:**
+ High School Diploma/GED + 4 years of relevant work experience
+ Associate's Degree + 2 years of relevant work experience
+ Bachelor's Degree + 6 months of relevant work experience
**Required Skills:**
+ Hands-on experience in GMP technical support, validation, engineering, or process development.
+ Knowledge of drug substance manufacturing processes.
+ Exposure to project management and process improvement initiatives.
**Preferred Skills:**
+ Experience with equipment and cleaning validation.
+ Proficiency in data analysis and visualization tools.
+ Strong technical writing skills for documenting manufacturing processes and validation reports.
**Why Join Us?**
Opportunity to work on cutting-edge drug manufacturing processes.
Hands-on experience in a regulated GMP environment.
Collaborative, growth-focused team with opportunities for career advancement.
If you are detail-oriented, eager to contribute to high-quality manufacturing processes, and excited about making an impact in the pharmaceutical industry, we encourage you to apply!
** **_This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you**_**
#LI-DNP
INDBH
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Industrial Electrician (Manufacturing)
Posted 7 days ago
Job Viewed
Job Description
Industrial Electrician (Manufacturing)
Mebane, NC (
Job Type
Full-time
Description
Our mission is to be the best in the world at what we do and have fun doing it. This means using to the fullest extent the talents of all Revere people working as a team in a safe, environmentally sound and ethical manner to achieve absolute customer satisfaction through superior quality and reliability.
At Revere we look for people who will show up as themselves because we value diversity and involvement. If you think you align with our values and culture come check out our company page and become a member of the Revere family!
Requirements
Summary:
Member of the Operations Team. Responsible for electrical machine preventative maintenance, maintenance planning and break-down repair. Duties are assigned based on operational need and will include safety. Participate in a team-based environment of roles and responsibilities. Help improve maintenance processes. Build relationships with co-workers. Contribute best efforts to continuously improve maintenance safety, quality, productivity and efficiency.
Duties and Responsibilities:
Safety
Participate in safety activities to identify risks and hazards. Share thoughts and ideas with the team regarding reduction of risks and hazards. Evaluate work area for risks and hazards. Determine safe work method before starting work. Pause and step back to consider safe work method when something unexpected occurs. Report any concerns.
Electrical Maintenance
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Perform maintenance repair. Conduct preventative maintenance.
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Create maintenance planning and scheduling, troubleshoot, construct and install electrical components for machinery and equipment.
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Work on temperature control instruments and recording devises.
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Program programmable controllers, VFD's.
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Install/Build control panels to basic circuit design
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NEC understanding, Example) Run motor circuit with proper sizing
Communication and Relationships
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Actively communicate thoughts, ideas, needs and issues related to the successful performance of assigned duties.
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Share all relevant information regarding day-to-day experience in safety and equipment status.
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work hand in hand with engineering to lead others in execution of work and projects
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Execute trouble shooting, repairs, and installs.
Equipment Reliability
Follow Reliability and Maintenance roles and responsibilities. Assist Operators with learning and understanding Operator Basic Care.
Special Demands:
Actively apply appropriate prevention techniques to reduce risks and hazards in the manufacturing environment.
Qualifications:
Minimum:
- Journeyman level skilled trade
Preferred:
-
3-5 years of Industrial Electrician or Maintenance Technician experience with a strong background in PLCs, automation, motor control and industrial equipment
-
Industrial Electrical or Maintenance Technician diploma/degree considered an asset
-
Strong analytical and troubleshooting skills
-
Strong interpersonal and communication skills
-
Ability to work in a safe and efficient manner
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Ability to work independently and in a team environment
-
Solid background in heavy industry and construction
Education / Training:
Minimum:High School/GED.
Desirable:Post High School or vocational education.
Preferred:Bachelor Arts or Science.
Job Type: Full-time
Benefits:
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401(k) matching
-
Dental insurance
-
Health insurance
-
Life insurance
-
Retirement plan
-
Vision insurance
Schedule:
-
8 hour shift M-F 7am-3:30pm
-
On call
-
Overtime
-
Weekend availability
Salary Description
$30.25 - $35.00
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Manufacturing Lead (Dayshift)
Posted today
Job Viewed
Job Description
The Manufacturing Lead (Upstream) oversees and performs Current Good Manufacturing Practice (CGMP) manufacturing operations for manufactured biopharmaceutical products. This role ensures the effective use of material, equipment, and personnel while making products at high-quality levels. Additionally, this role is recognized as a subject matter lead regarding manufacturing processes and leads more junior members of the shift through manufacturing processes.
**Job Description**
Responsibilities:
+ As a highly skilled specialist, contributes to the development of concepts and techniques.
+ Completes complex tasks in creative and effective ways.
+ Acts independently to determine methods and procedures on new assignments. Often acts as a facilitator and team leader.
+ Consistently works on complex assignments requiring independent action and a high degree of initiative to resolve issues. Makes recommendations for new procedures.
+ Assists the Production manager with developing team members through continuous coaching and training.
+ Ensures team activities, equipment, facilities, and personnel are operated and maintained in a state of compliance with appropriate requirements.
+ Ensures effective manufacturing delivery upon production supply schedule.
+ Mentors technicians with the goal of achieving employee empowerment.
+ Assists the team with the development of objectives and ensures alignment with site and department goals.
+ Provides ongoing feedback to managers on technician performance, development, and training needs.
+ Provides real-time coaching and feedback to team members and assists with training, as needed.
+ Serves as the senior technical lead over floor activities and manufacturing processes.
+ Helps troubleshoot equipment problems, and identifies the need for new equipment or modifications to existing equipment to optimize throughput.
+ Provides feedback to support teams for troubleshooting and continuous improvement purposes.
+ Observes all critical operations to ensure deviation-free / right-first-time performance and building skills with technicians.
+ Meets daily shift goals and provides team assignments to meet those goals.
+ Ensures room and equipment are in a ready state (e.g., cleaning, logbook, and equipment staged for a project) prior to the start of a shift or daily activities.
+ Leads the tier 1 meetings to ensure detailed turnover of information to the oncoming shift.
+ Attends departmental and team meetings focused on equipment or process improvement to provide SME feedback.
+ Serves as liaison between shifts, teams, and other departments to give updates, as required.
+ Provides escalation to management when process issues arise, or daily goals will be delayed, as needed.
+ Ensures GMP documents are completed accurately and timely (provides a daily review of batch records and logbooks).
+ Ensures completion of real-time documentation of observations or execution events and initiates any necessary investigations or deviations.
+ Initiates safety incidents and supports corrective and preventative actions.
+ Ensures technicians are qualified to perform tasks prior to execution.
+ Ensures the execution and closure of SFOs in Pas-X prior to records being removed from the floor.
+ Performs other duties, as assigned.
Requirements:
+ High School Diploma/GED with 8 years of experience in a related technical field
+ Demonstrated leadership, interpersonal, technical aptitude, and problem-solving skills
+ Strong teambuilding skills, including the ability to coach/develop teams, provide training, motivate and empower others, and conflict resolution
+ Goal-oriented and able to manage risks
+ Ability to be flexible and manage multiple priorities
+ Strong computer skills with proficiency in using Microsoft Office (Word, Excel, PowerPoint, etc.) for data gathering, entry, and reporting
+ Good communication, both written and verbal
+ Must be able to work shift, including weekends or nights, per assigned shift schedule
Preferred Requirements:
+ Bachelor's degree in Life Science, Engineering or another technical field
+ Experience leading and coaching others
To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.
*#LI-Onsite
**Job Locations** _US-NC-Research Triangle Park_
**Posted Date** _11 hours ago_ _(10/9/2025 3:11 PM)_
**_Requisition ID_** _ _
**_Category_** _Manufacturing_
**_Company (Portal Searching)_** _FUJIFILM Biotechnologies_
Manufacturing Support Specialist
Posted 3 days ago
Job Viewed
Job Description
**Monday-Friday 8am-5pm**
**Contract role**
**$30-$40/hour**
**Must have electronic batch record experience required.**
**About the Job**
This role involves supporting manufacturing operations to ensure compliant, efficient, and reliable production processes. As the facility operates 24/7, flexibility with working hours may be required.
**Job Description**
**What You'll Do:**
+ Lead operational readiness efforts and support commissioning and qualification activities during the project phase
+ Troubleshoot issues within assigned process areas
+ Recommend and execute documentation updates
+ Coordinate non-batch activities, including documentation for tech transfer, equipment changeovers, preventive maintenance plans, and column packing
+ Create and manage records for change control, investigations, CAPAs (Corrective and Preventive Actions), and continuous improvement initiatives
+ Drive and implement improvement projects within drug substance manufacturing
+ Collaborate with cross-functional teams to support equipment startup and transition to GMP operations
+ Use documentation to configure electronic batch records for specific products and processes
+ Work with stakeholders to define process steps, parameters, and sample requirements for electronic batch records
+ Support inspections and audits by preparing and providing necessary documentation
+ Perform other duties as assigned
**Basic Requirements:**
+ High School Diploma or GED with 6 years of relevant experience **OR**
+ Associate degree with 4 years of direct experience **OR**
+ Bachelor's degree with 2 years of direct experience **OR**
+ Equivalent military training/experience
**Preferred Qualifications:**
+ Associate or Bachelor's degree in life sciences or engineering
+ Experience with Manufacturing Execution Systems (MES), preferably Syncade
+ Experience with Electronic Document Management Systems (EDMS), ideally Veeva
+ Completion of BioWorks or BTEC Capstone cGMP coursework is a plus
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
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Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
Manufacturing Engineering Technician
Posted 3 days ago
Job Viewed
Job Description
+ Perform electrical troubleshooting, emergency repairs, and preventive maintenance on production equipment
+ Assist in the installation and inspection of complex systems and machinery
+ Conduct quality tests and inspections using independent judgment
+ Analyze routine technical issues and apply effective solutions
+ Follow operational procedures and ensure compliance with internal policies and regulatory codes
+ Apply safe work practices and use personal protective equipment as required
+ Organize daily work schedule based on shifting priorities
+ Support internal communications and contribute to small-scale change initiatives
+ Participate in training and development activities to build technical capabilities
**What You Bring**
+ Post-secondary technical education or equivalent
+ 7-12 months of experience in industrial electrical maintenance or mechatronics
+ Strong verbal communication and organizational skills
+ Ability to interpret and apply policies, procedures, and safety regulations
+ Familiarity with equipment utilization and service interactions
+ Customer-oriented mindset and technical support capabilities
+ Willingness to learn and grow through formal and informal development channels
**Our Values in Action**
At GKN, we value:
+ **Ingenuity** : Managing complexity, making smart decisions, and driving improvement
+ **Collaboration** : Navigating organizational dynamics and building strong relationships
+ **Principled Leadership** : Accountability, effective communication, and safety-first mindset
+ **Drive** : Prioritizing effectively, taking action, and embracing new challenges
Ready to power up your career in a fast-paced, high-tech manufacturing environment?
GKN Driveline provides equal employment and affirmative action opportunities to applicants and employees without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, age, genetic information, pregnancy, or disability.