Simtra BioPharma Solutions
The Quality Supervisor supports the Quality Assurance Leadership Team by overseeing Quality Operations and Manufacturing to ensure finished products meet specifications and regulatory standards. This role involves supervising QALO personnel, driving quality-first decision-making, and leading process improvement initiatives. The position requires strong leadership, technical expertise, and effective communication across cross-functional teams.
Headquarters
Parsippany, New Jersey, United States
Company Size
1001-5000 employees
Simtra BioPharma Solutions is a contract development and manufacturing organization (CDMO) focused on sterile injectable products. They offer end-to-end services — from formulation and analytical development through aseptic fill/finish, packaging, quality and regulatory support — to advance programs from clinical stages to commercial supply. Simtra emphasizes flexible product delivery options and a compliance-driven approach to meet biopharma partners’ timelines and manufacturing requirements.
Simtra BioPharma Solutions expands global manufacturing footprint to advance the future of sterile injectables
Oct 27, 2025
Simtra BioPharma Solutions expands to bring commercial ADC drug product manufacturing to US
Jul 25, 2025
Simtra BioPharma Expands Global Footprint
Oct 29, 2025
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 Simtra BioPharma Solutions.
Simtra BioPharma Solutions didn’t post a salary, so this is our estimate from similar listings.
Simtra BioPharma Solutions’ $241M investment expansion in Monroe County moves forward
Aug 27, 2025
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