BioPharma Consulting JAD
Join a growing QA Validation group at a leading biotechnology company in Boston, Massachusetts, providing QA oversight for commissioning, qualification, and validation within a cGMP cell and gene therapy manufacturing facility and its QC laboratories. The role involves reviewing and approving validation protocols, supporting change controls, risk assessments, and audits, and authoring SOPs in Veeva. This position offers a contract opportunity with potential extension, starting immediately.
Headquarters
Cambridge, Massachusetts, United States
BioPharma Consulting JAD Group (BPC-JAD) is a consulting firm founded in 2010 that provides engineering, validation, quality, regulatory compliance, and project management services to the FDA-regulated biopharmaceutical industry. The company offers specialized services including commissioning and qualification, system validation and automation, and laboratory quality operations. With business locations in Massachusetts, Texas, California, Florida, and Puerto Rico, BPC-JAD serves major industry clients such as Pfizer, Moderna, Amgen, and Bristol Myers Squibb.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
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