53 Manufacturing Technicians jobs in Grayslake
Quality Control Technician

Posted 1 day ago
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Job Description
**Location:** Des Plaines IL (100% Onsite)
**Duration:** 12 Months
**Shift Time :** 2pm to 10:30pm
**Pay Range :** $22 hr to $24/hr (On W2)
We are looking for a **"Quality Control Technician"** to join one of our Fortune 500 clients.
**Job Summary:**
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Understand the manufacturing processes of Company products and ability to recognize deviations from approved documented procedures.
**Top Skills:**
+ Perform a wide variety of activities to support the Quality Management System.
+ Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP).
+ Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence
**Job Responsibilities:**
+ Conduct product testing, including testing to support complaint investigations and stability verification
+ Generate product testing results reports
+ Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
+ Review finished goods batch records.
+ Report all deviations in these records and assures these have been addressed and resolved prior to issuing approval.
+ Conduct spot-check inspections/audits of production operations
+ Participate in the internal audit program
+ Write, review and approve Standard Operating Procedures (SOPs) as necessary
+ May assist in supporting the Document Control program, record retention areas, and sample retention areas
+ May support returned instrument processing
+ Log returned instruments from the field.
+ Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
+ Inspect returned instruments for damage, and performing basic investigation and documenting results prior to second level processing.
+ As necessary, process instrument documentation for return to repair facility, and pack instruments as required.
**Education and/or Experience:**
+ Bachelor's degree in a scientific or technical area or equivalent combination of experience and education.
+ At least one year in quality assurance role in medical device industry is preferred.
**Other Skills and Abilities:**
+ Ability to follow procedures and accurately document results.
+ Ability to use bleach for cleaning purposes is required.
+ To perform this job successfully, an individual should have knowledge of Database software; Internet software; Inventory software; Spreadsheet software and Word Processing software.
+ While performing the duties of this Job, the employee is regularly required to sit and stand. The employee is occasionally required to walk.
**We are looking for the candidate who are eligible to work with any employers without sponsorship** .
If you're interested, please click **"Apply"** button
ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.
Quality Control Laboratory Technician

Posted 1 day ago
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Job Description
The Quality Control Technician is responsible for analyzing raw and production materials to ensure compliance with specifications. This role requires the ability to solve quality non-conformance issues, run product testing, and apply critical thinking skills. The position involves more than routine quality testing, demanding a tech-savvy individual who is good at researching and resolving issues.
Responsibilities
+ Approve raw materials and finished goods for use.
+ Determine physical values of materials and ensure chromatographic compliance as per Quality Control procedural manual.
+ Conduct tests such as pH, specific gravity, refractory, titrations, GC, and micro plating.
+ Report discrepancies to the Quality Control Manager and assist in determining their origin.
+ Calibrate instrumentation and perform preventive maintenance according to technical manuals.
+ Adhere to safety guidelines within the workplace.
Requirements
+ 1-3 years of quality control laboratory experience in the food industry.
+ Understanding of chemistry and mixing of chemicals.
+ Strong organizational skills.
+ Problem-solving and creative thinking abilities.
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
Diversity, Equity & Inclusion
At Actalent, Diversity And Inclusion Are a Bridge Towards The Equity And Success Of Our People. DE&I Are Embedded Into Our Culture Through:
+ Hiring diverse talent
+ Maintaining an inclusive environment through persistent self-reflection
+ Building a culture of care, engagement, and recognition with clear outcomes
+ Ensuring growth opportunities for our people
Pay and Benefits
The pay range for this position is $23.00 - $25.00/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 Northbrook,IL.
Application Deadline
This position is anticipated to close on Oct 14, 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.
Inspector Quality Control - 3rd Shift

Posted 1 day ago
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At Nestlé USA, we're all working towards the same goal - to delight and deliver for our consumers. With a rich portfolio of beloved brands, including DiGiorno, Toll House, and Coffee mate, in 97% of U.S. households, we have a unique opportunity - and responsibility - to be there for every moment in our consumers' lives.
Joining Nestlé means becoming part of an inclusive workplace that inspires innovation, encourages strategic thinking and creativity, and celebrates your achievements. No matter where you work within the organization, you are empowered to challenge the status quo, embrace risk-taking, and pioneer new ideas. Our supportive and collaborative environment encourages bold ambitions and continuous learning so that everyone can grow and thrive.
_This position is not eligible for Visa Sponsorship._
**Quality Control Inspector - Nestlé Schaumburg, IL**
Join Nestlé at Schaumburg, IL - Where Quality Meets Opportunity
Nestlé's Schaumburg facility is a dynamic and fast-paced environment focused on delivering high-quality products. As part of a global leader in nutrition, health, and wellness, you'll be joining a team that values safety, quality, and continuous improvement. If you're looking for stability, growth, and a place where your contributions matter-this is it.
**Schedule That Works for You**
Enjoy the consistency and structure of a **3rd shift role** perfect for night owls or those seeking daytime flexibility.
Schedule: **10pm to 6:30am, Sunday to Saturday, 6 days/week**
**Training Breakdown**
Training may occur on a different shift to ensure proper onboarding and hands-on learning. You'll be supported by experienced team members and supervisors to help you succeed from day one.
**Overtime Opportunities**
Overtime is available and encouraged-giving you the chance to boost your earnings while supporting production goals. It's a great way to maximize your paycheck and demonstrate your reliability.
**What's In It For You**
Pay: **$20.68/hr + $.25 shift differential**
Benefits: Comprehensive Nestlé benefits after 30 days of employment, including health, dental, vision, and more
**What You'll Accomplish**
- Conduct daily pre-operational and changeover checks
- Perform Lock Out Tag Out procedures
- Sanitize QA equipment and document sanitation checks
- Prepare daily Bill of Materials (BOMs)
- Monitor production personnel for GMP compliance
- Communicate safety, sanitation, or product issues to supervisors
- Participate in product evaluations to ensure top quality
**What You Will Bring**
- 1-2 years in Quality Control
- High School Diploma/GED preferred
- Willingness to work overtime, irregular hours, or rotating shifts
- Ability to lift up to 50 lbs frequently
**You're a Great Fit If You.**
- Are detail-oriented and committed to quality
- Can follow safety rules and operating procedures
- Have basic math skills and can use a calculator
- Can read and interpret documents such as manuals and safety instructions
- Are comfortable performing basic lab tasks
- Speak, write, and understand English (Spanish/English bilingual is a plus)
- Have previous food manufacturing and/or sanitation experience (6+ months preferred)
The approximate hourly pay for this position is $ 0.68. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position.
Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at Nestle in the US Benefits | Nestle in the US Benefits | Nestlé Careers (nestlejobs.com) ( is our business imperative to remain a very inclusive workplace.
To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home.
The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at or please dial 711 and provide this number to the operator: .
This position is not eligible for Visa Sponsorship.
Review our applicant privacy notice before applying at Requisition:
Quality Control Inspector - 3rd Shift

Posted 1 day ago
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**Summary:**
Actively participate and effectively execute all the duties and responsibilities of a quality inspector per the outline below performing audits, inspections, and testing that ensures our customer's product meets or exceeds their specifications and requirements.
**Duties & Responsibilities**
+ Audit and monitor quality requirements in accordance with company quality assurance policies, documents, and customer specifications.
+ Conduct inspections at First Article, In-Process, Incoming and completes Final Inspections per inspection plans.
+ Perform routine visual/functional/dimensional testing per required specifications and procedures for the Quality and Assembly departments
+ Identify nonconforming material and initiate nonconforming reports per established procedures.
+ Communicate effectively with management, operators, process technicians and other inspectors about quality related concerns required.
+ Utilize inspection tools such as calipers, micrometers, smart scope, scales, fixtures, gages, and microscopes to measure or inspect parts for compliance.
+ Read and interpret blueprints and specifications, Process Flow Diagrams, Potential Failure Mode and Effects Analysis and Process Control Plans.
+ Provide input on inspection methods related to continuous improvement initiatives related to the job.
+ Conduct Layered Process Audits.
+ Conduct Process Control Plan Audits
+ Assist quality, engineering and production personnel with investigations of part defects or any quality related issues.
+ Complete accurate and legible reports on the in-process inspection plans.
+ Organize work and storage areas for efficient workflow.
+ Perform basic mathematical operations and perform measured conversions.
+ Understand and comply with the company's quality management system based on ISO 13485.
+ Understand and comply with the company's environmental management system based on ISO 14001.
+ Understand and comply with the company's safety policies and procedures.
+ Perform additional duties to comply with departmental objectives as required
+ Complete appropriate documentation, including release/hold paperwork/ databases
**Qualifications and Skills**
+ High school diploma or equivalent
+ 1 or more years of job-related experience
+ Injection Molding experience (desired)
+ Basic math skills to use scales and measure weights
+ Basic knowledge of Microsoft Office
+ Good verbal and written communication skills
+ Ability to read and write English
+ Attention to detail, organization, and strong multitasking abilities
+ Ability to work in a team setting
+ Excellent decision making and time management skills
+ Ability to read and interpret blueprints and specifications
+ Knowledge or ability to understand and use various test methods
+ Commitment to continuous improvement
+ Good Manufacturing practice
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily, follow work instructions and job training requirements. Individual must be able to stand for full manufacturing shift, have ability to complete hand assembly process. Ability to reach with arms extended and/or overhead, excellent hand dexterity, ability to bend, stoop, stretch and similar activities and able to lift up to 35-50 pounds frequently.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job.
This job description should not be construed to contain every function/responsibility that may be required to be performed by an incumbent in this position. Incumbents are required to perform other related functions as assigned
**Compensation Information:**
**Pay Range** **:** $18.00 - $23.00 an hour
This compensation range is provided as a reasonable estimate of the current salary range for this role. Compensation depends on relevant experience and/or education, specific skills, market level, other job-related factors, geographic location, and other factors as applicable by law. As applicable this role will also receive overtime compensation and may be eligible for shift premium compensation.
**Benefits:**
Benefits for this role can be seen by clicking on the following link: ITW Benefits for Life Your Way . In addition, employees can qualify for vacation, sick, and holiday compensation benefits.
+ Vacation - up to 80 hours within first year
+ Sick - up to 40 hours within first year
+ Floating Holiday - up to 8 hours within first year
+ Holiday - 10 paid holidays per year, these holidays are selected by the Division
Manager, Quality Assurance & Quality Control

Posted 1 day ago
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Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System ( which makes everything possible.
The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.
This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.
In this role, you will have the opportunity to:
+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.
The essential requirements of the job include:
+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
+ Track record of collaborating with technical groups to identify product improvement opportunities
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Travel requirements <5% of the time, domestic and international
+ Overnight travel may be required
+ Be able to occasionally lift and/or move up to 40 pounds.
+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times
It would be a plus if you also possess previous experience in:
+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
+ Experience and/or knowledge of NCRs
The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
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, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
#LI-GC1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .
Supervisor, Food Safety and Quality Control
Posted 1 day ago
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Manufacturing Production Technician I
Posted 4 days ago
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Job Description
We are immediately hiring a Manufacturing Production Technician I to join our dynamic team.
Why Mobile Air? Here are some of the perks & rewards:
- Full-time positions with overtime and weekend opportunities
- Competitive hourly pay with quarterly bonus opportunities
- Health, Vision, and Dental Insurance
- Life Insurance
- 401k with company match
- Paid time off (vacation, sick days, holidays)
- Career development and advancement potential
- Employee discount programs
Under the direction of the Manufacturing Production Supervisor, the Manufacturing Production Technician I performs a variety of tasks to support the remanufacturing process, including receiving, assembly, material handling, shipping, and general shop operations.
Key Responsibilities:
- Perform a range of shop floor activities including receiving, disassembly, assembly, materials handling, shipping, and scrapping.
- Accurately complete all required documentation related to work performed.
- Identify and communicate opportunities for process improvements to enhance efficiency and/or safety.
- Support other production operations and assist team members as needed.
- Set up and ensure proper use of safety equipment and personal protective equipment (PPE) in compliance with company safety policies.
- Maintain a clean and organized work area, including cleaning of equipment, hand tools, and workstations.
Qualifications:
- High school diploma or equivalent required.
- Previous experience in a manufacturing or warehouse environment preferred; experience in shipping and receiving is a plus.
- Valid driver's license with a satisfactory motor vehicle report (MVR).
- Candidates must be willing to undergo a background check and 10-panel drug screen prior to employment
- Ability to lift/move up to 50 lbs. using safe lifting practices.
- A willingness to learn and develop within the company.
- Basic proficiency with computer systems, including Microsoft Office Suite, email, and internet use is a plus.
- Forklift and overhead crane experience is a plus; training and certification will be provided on site.
- Strong work ethic, good attendance, and the ability to work effectively in a team environment are essential.
Work Schedule:
This position is full-time, first shift, with a minimum of 40 hours per week. Overtime, evenings, and weekend work may be required. Overtime and double-time pay rates apply for applicable hours worked.
Join our team of dedicated professionals and contribute to the success of our HVAC operations while advancing your career in a fast-paced environment!
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Production Technician
Posted 3 days ago
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Spherion - JobID: (Production Operator / Assembly Line Worker) As a Production Technician at Spherion, you'll: Operate machinery to assemble products; Inspect finished goods for quality control; Maintain equipment by performing routine maintenance; Follow safety protocols to ensure a safe work environment; Collaborate with team members to meet production goals; Document production data for reporting purposes.Hiring Immediately >>
Production Technician l
Posted 4 days ago
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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
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
The Production Technician I executes manufacturing processes in formulation, encapsulation, primary and secondary packaging with oversight by Supervision. Sets up equipment for routine processes. Identify and resolve performance related equipment issues in a timely and efficient manner while adhering to GMP guidelines and procedures to meet or exceed target OEE. Execute assigned jobs and maintains operating conditions within the desired range. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Displays AbbVie behaviors.
Responsibilities
- Proficient in Team Member responsibilities or equivalent. Knowledgeable of basic jobs in assigned area of responsibility and Good Manufacturing Practice (GMP) policies. Demonstrates compliance to local and industry quality and safety standards.
- Work directly on the line while executing scheduling priorities, daily assignment, and production expectations for the day. Ability to proficiently operate multiple unit operations across the business. Monitor manufacturing process and communicate any issues that arise with appropriate resources.
- Directly responsible for setting up, running, blowing, cleaning, and clearing equipment according to the BOP/Master batch record.
- Minor troubleshooting on equipment and process related issues and performs repairs. Perform all in process quality checks accurately.
- Trains colleagues on equipment and process for which they are a qualified trainer.
- Demonstrates AbbVie behaviors good attendance, teamwork, respectful communications, positive attitude.
- Follow all Environmental Health and Safety procedures and guideline policies and participate in safety initiatives.
- Complete batch record steps following ALCOA and GMP processes as needed. Maintain audit ready production area and adhere to all regulations and company policies.
- High school diploma or GED required.
- Technical certificate or degree preferred. Previous general manufacturing experience required, preferably 2-3 years cGMP manufacturing (i.e. food, chemical, petrochemical, consumer products)
- Strong technical aptitude. The ability to troubleshoot and communicate issues to the appropriate operations engineer and mechanical teams.
- Basic computer skills and ability to learn new programs and applications required.
- A demonstrated understanding of the importance of maintaining the highest level of quality and ensuring compliance to site level policies and procedures.
- Demonstrated understanding of HMI controls, vision inspection systems, and product serialization systems.
- Ability to train fellow technicians preferred.
- Understanding and experience with systems such as POMs, SAP, and MAXIMO.
- Requires standing up to 8-12hrs per day and lifting up to 25 pounds.
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:
- The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location,andwemay ultimatelypay more or less than the posted range. This range may be modified in thefuture.
- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.
- This job is eligible to participate in our short-term incentiveprograms.
- This job is eligible to participate in our long-term incentiveprograms
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
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
Company
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at . Follow @abbvie on Twitter , Facebook , Instagram , and YouTube .
Stock Symbol: ABBV
Stock Exchange: NYSE
Company info
Website Phone Location 1 North Waukegan Road
North Chicago
Illinois
60064
United States
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Production Technician l

Posted 1 day ago
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Job 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
Purpose
Describe the primary goals, objectives or functions or outputs of this position.
The Production Technician I executes manufacturing processes in formulation, encapsulation, primary and secondary packaging with oversight by Supervision. Sets up equipment for routine processes. Identify and resolve performance related equipment issues in a timely and efficient manner while adhering to GMP guidelines and procedures to meet or exceed target OEE. Execute assigned jobs and maintains operating conditions within the desired range. Communicates all operational events and issues with appropriate individuals. Identifies opportunities for improvement throughout the operations and assists in the implementation of changes both in physical operations and written documents. Displays AbbVie behaviors.
Responsibilities
+ Proficient in Team Member responsibilities or equivalent. Knowledgeable of basic jobs in assigned area of responsibility and Good Manufacturing Practice (GMP) policies. Demonstrates compliance to local and industry quality and safety standards.
+ Work directly on the line while executing scheduling priorities, daily assignment, and production expectations for the day. Ability to proficiently operate multiple unit operations across the business. Monitor manufacturing process and communicate any issues that arise with appropriate resources.
+ Directly responsible for setting up, running, blowing, cleaning, and clearing equipment according to the BOP/Master batch record.
+ Minor troubleshooting on equipment and process related issues and performs repairs. Perform all in process quality checks accurately.
+ Trains colleagues on equipment and process for which they are a qualified trainer.
+ Demonstrates AbbVie behaviors - good attendance, teamwork, respectful communications, positive attitude.
+ Follow all Environmental Health and Safety procedures and guideline policies and participate in safety initiatives.
+ Complete batch record steps following ALCOA and GMP processes as needed. Maintain audit ready production area and adhere to all regulations and company policies.
Qualifications
+ High school diploma or GED required.
+ Technical certificate or degree preferred. Previous general manufacturing experience required, preferably 2-3 years cGMP manufacturing (i.e. food, chemical, petrochemical, consumer products)
+ Strong technical aptitude. The ability to troubleshoot and communicate issues to the appropriate operations engineer and mechanical teams.
+ Basic computer skills and ability to learn new programs and applications required.
+ A demonstrated understanding of the importance of maintaining the highest level of quality and ensuring compliance to site level policies and procedures.
+ Demonstrated understanding of HMI controls, vision inspection systems, and product serialization systems.
+ Ability to train fellow technicians preferred.
+ Understanding and experience with systems such as POMs, SAP, and MAXIMO.
+ Requires standing up to 8-12hrs per day and lifting up to 25 pounds.
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 ofthis 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.
+ 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 anybonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's soleand 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 - $32.1