Quality Specialist II/Validation (GMP/GLP) #319

Across the globe, pharmaceutical and biopharmaceutical companies rely on BioReliance, a leading provider of GLP and cGMP compliant laboratory services for more than 60 years. Our testing services include analytical analysis; safety testing of bulk and final product; the manufacture and characterization of cell banks; clearance validation; and toxicology studies.

 

As one of the world’s largest specialists in the growing biologics and drug development sectors, we seek a variety of professionals to support our mission of ensuring the safety of our customers’ products.

 

Quality Specialist II/Validation (GMP/GLP) #319

 

Oversee Quality System compliance issues.  Review assay data, protocols, reports, technical specifications, and RIRs.  Review batch records and other documents for auditing requirements. Conduct facility and in-process inspections.  Train other QA auditors as a Qualified Trainer. Audits custom assays; review SOPs/other documents for compliance requirements; review validation protocols and reports; work with Operations Groups to implement procedures to improve data accuracy; and  demonstrate verifiable turnaround times. Take independent ownership of specific quality system aspects.  May be relied upon to provide regulatory guidance in specific areas.  Has regulatory knowledge in defined areas. BS degree in a life sciences is preferred. 2+ years experience in Quality Assurance in a GMP or GLP environment is required.

 

Apply Online: http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=BIORELIANCE&cws=1&rid=319

 

Please visit www.BioReliance.com and explore our current opportunities.

Equal Opportunity Employer