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© All Rights Reserved. ApplyBlast.com
Afton Scientific
A Quality Assurance Manager at Afton Scientific ensures compliance with FDA regulations, EU GMP, and Annex 1 requirements for sterile pharmaceutical manufacturing. The role involves batch record review, lot release, deviation investigations, CAPA management, and collaboration with cross-functional teams to maintain product sterility and regulatory compliance.
Headquarters
Charlottesville, Virginia, United States
Company Size
51-200 employees
Founded
1991
Afton Scientific Sterile Manufacturing is a contract sterile drug‑product manufacturer that provides GMP fill‑finish and sterile processing services for pharmaceutical and biotechnology customers. Their capabilities include aseptic filling for vials, syringes and ampoules, sterile formulation and packaging, plus analytical testing and regulatory support to help move products from clinical development to commercial supply. The company emphasizes regulatory compliance, quality systems, and flexible capacity to serve small‑batch and commercial production needs for complex injectable and ophthalmic products.
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
View leadership team, funding history,
and employee contacts for Afton Scientific.
Afton Scientific didn’t post a salary, so this is our estimate from similar listings.
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