Job Description:

Responsibilities: 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.
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.

Cynet Systems