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Unless specifically stated otherwise this role isOn-Site at the location detailed in the job post.
Job Description
Purpose
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
Associates degree in science (or equivalent experience) with 2 years relevant experience. BS with 1 years relevant 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.