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© All Rights Reserved. ApplyBlast.com
Intas Pharmaceuticals
This role involves conducting parenteral qualification and regulatory summary submissions within a pharmaceutical setting. The incumbent prepares validation protocols and reports, coordinates with production and external agencies, and reviews technical documents for accuracy. Key duties include managing annual re-qualification schedules and identifying deviations during the qualification process.
Intas Pharmaceuticals is a leading multinational pharmaceutical formulation development, manufacturing, and marketing company present in more than 85 countries worldwide. The company offers a wide range of products including generics, oncology, parenterals, biosimilars, and plasma-derived therapies, supported by a strong R&D team of 550+ scientists. Headquartered in Ahmedabad, India, Intas serves highly regulated markets including the EU and US, with approximately 70% of revenues coming from international markets.
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 Intas Pharmaceuticals.
48% below the average for this role
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