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Associate Scientist II, Microbiology Product Testing #339
| Details |
Country: USA
Location: Maryland-Montgomery County Rockville, MD 20850
Total applied: 50 Job Category:Biotech/R&D/Science
Relevant Work Experience:5+ to 7 Years
Education Level:Bachelor's Degree
Location:Rockville, MD 20850
Status:Full Time, Employee
Occupations:General/Other: R&D/Science
Career Level:Student (High School)
Relevant Work Experience:5+ to 7 Years
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Associate Scientist II, Microbiology Product Testing #339
Advance Research. Improve Life.
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.
Associate Scientist II, Microbiology Product Testing #339
Execute microbiological assays, review and optimize batch records, deviation investigation, CAPA, micro certifications, SOP, EM assessment, change control, and validation review and approval. Work with data and metric management, project management, audits, and technical and regulatory assessments. Participate with investigations within the microbiology division (mycoplasma, sterility and bacteriology) and assist with audits, regulatory assessments, and product complaint investigations/product impact analysis. Apply BioReliance's Quality Management Systems to operations while supporting the testing of biological product. Requires 5- 7 years of quality control/assurance, manufacturing experience, or related role performing or supporting GMP operations; basic project management skills; knowledge of process equipment and aseptic processes; the ability to interpret and apply cGMP and other regulations in non-routine cases; ability to evaluate documentation and operations according to company and regulatory guidelines (such as FDA or EMEA). Bachelor's Degree in Microbiology or Life Sciences and experience with Investigations/Non-conformances, CAPA, EM programs, Validation, and Change Control is preferred.
Apply Online
http://tbe.taleo.net/NA7/ats/careers/requisition.jsp?org=BIORELIANCE&cws=1&rid=339
Please visit www.BioReliance.com and explore our current opportunities.
Equal Opportunity Employer
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