Technician, Manufacturing II (Wednesday to Saturday 4:00pm - 2:30am)
About the Role
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
- Associate’s degree in science (or equivalent experience), with 2+ years relevant experience
- BS, with 1+ years relevant experience
- BS in Engineering, with 0+ years 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.
Benefits
- Paid time off (vacation, holidays, sick)
- Medical/dental/vision insurance
- 401(k) retirement plan
- Eligibility to participate in short-term incentive programs