Job Description

• Maintains and supports the production schedule.
• Investigates problem areas and areas of desirable improvement.
• Undertakes new procedures and observes proper safety precautions.
• Responsible for in-process QC testing of manufacturing material as it relates to qualifications, quality inspections and titration.
• Maintains quality systems and proper GMP/GLP.
• Creates and follows protocols designed around product improvement.
• Responsible for making critical and non-critical bioreagents for use in product and manufacturing processes using Standard Operating Procedures (SOPs).
• Works in a team setting and coordinates manufacturing efforts based upon a set production schedule and maintaining the raw bioreagent supply as needed to support this schedule.

• Bachelor's Degree in a Chemistry, Life Sciences, or related field or equivalent combination of education and experience.
• Prior Experience in the following areas.
• Pipette.
• Spectrophotometry.
• HPLC.
• pH meters.
• Gel Electrophoresis o SDS Page.
• ELISA assays.

• bility to work successfully as a member of a team and independently with moderate supervision.
• Skill in using computer applications including spreadsheet, database, manufacturing, and word processing software.

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