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.

QUALIFICATION:

• 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, 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.

PAY RANGE:

$25 TO $30