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.
Basic Qualifications | Education:
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
Competencies
Ability 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.
Seniority level
Entry level
Employment type
Contract
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
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