Technician, Manufacturing II (Sunday to Wednesday, 6:00am - 4:30pm)
AbbVie
July 02, 2026
On-site
Worcester, MA
$21 - $37.80 USD yearly
Operations
Job Description:
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, and performing rework and quality testing related to parts, components, and final materials. Uses programs such as LIMS, SAP, and automated control systems to collect and evaluate operating data for 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:
- Associate degree in science (or equivalent experience) with 2+ years relevant experience; or BS with 1+ years relevant experience; or BS in Engineering with 0+ years relevant experience.
- Applies acquired job skills and company policies/procedures to complete assigned tasks.
- Semi-routine assignments; recognizes need for occasional deviation from accepted practice.
- Normally follows established procedures; requires instructions only on new assignments.
Benefits (as stated):
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k) to eligible employees
- Eligible for short-term incentive programs
Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, and performing rework and quality testing related to parts, components, and final materials. Uses programs such as LIMS, SAP, and automated control systems to collect and evaluate operating data for 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:
- Associate degree in science (or equivalent experience) with 2+ years relevant experience; or BS with 1+ years relevant experience; or BS in Engineering with 0+ years relevant experience.
- Applies acquired job skills and company policies/procedures to complete assigned tasks.
- Semi-routine assignments; recognizes need for occasional deviation from accepted practice.
- Normally follows established procedures; requires instructions only on new assignments.
Benefits (as stated):
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k) to eligible employees
- Eligible for short-term incentive programs