Centrient Pharmaceuticals
A Quality Assurance Associate in the pharmaceutical industry ensures that products meet customer specifications and applicable regulatory standards (cGMP/GLP/ICH/USFDA/ISO). The role supports quality governance across manufacturing operations, maintaining documentation and records to demonstrate compliance. It also contributes to safety and environmental health practices to ensure a safe workplace.
Headquarters
Rotterdam, South Holland, Netherlands
Company Size
1001-5000 employees
Founded
1869
Centrient Pharmaceuticals is a sustainable leader in the production of antibiotics, statins, and antifungals. The company focuses on delivering high-quality healthcare solutions while prioritizing environmental sustainability and social responsibility. Centrient is committed to addressing pressing health challenges such as antimicrobial resistance through innovation and collaboration, ensuring that medicines reach those who need them most. With a strong emphasis on corporate governance and sustainability initiatives, Centrient fosters a responsible approach to pharmaceutical manufacturing.
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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Centrient Pharmaceuticals didn’t post a salary, so this is our estimate from similar listings.