Live opening · Posted 7 hours ago
At a glance
The key details from the original listing.
About the role
Description supplied by the original job listing.
This our UD Fill - A1 Shift: 7am-7:30pm Sunday/Monday/Tuesday & every other Wednesday
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.
Bachelor's Degree (or equivalent experience), with 4+ years area specific relevant experience.
Must have the ability to become Aseptic Certified
As a skilled specialist, completes tasks in resourceful and effective ways.
Works on assignments requiring considerable judgment and initiative.
Understands implications of work and makes recommendations for solutions
Employment type
Full-time
Work arrangement
No
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