Quality Assurance Scientist III Opportunity in SoCal – GMP Manufacturing Environment

We are currently working on a QA Specialist III position in the Southern California region (relo assistance offered) focused on performing internal and external GMP audits, GMP system improvements and technical writing/review of GMP documentation and reports.  Our client is a technology-based, biochemicals company providing full service to the pharma and biotech industry.  They are an employee focused organization that values continued education, training and advancement.  They offer their customers a high-class combination of products and technical services.

Desired Experience:

–          B.S. in Chemistry, Biology, Biological Science.
–          At least 3 years’ experience within Quality Assurance in the Pharma/Biopharma market with experience in Intermediates, APIs and Pharmaceutical products.
–          Experience in working in a GMP environment, preparing for audits and technical review in a QA setting.
–          Experience in writing SOPs, speficications and technical reports.  Experience in validation/qualification.
–          Must be located in CA area or open to relocation to the area.

If you are interested in learning more about this opportunity, please email an updated copy of your resume to DML@TeamBailiwick.com or apply on our web site!