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:

o Pipette

o Spectrophotometry

o HPLC

o pH meters

o Gel Electrophoresis o SDS Page

o ELISA assays