Quality Alert Expert
ZentivaGujarat, India
Posted September 26, 2025
Full Time
About the Company
Zentiva is a pharmaceutical company with a strong focus on quality and regulatory affairs.
Job Description
Quality Alert Expert role involves coordinating quality alert issues/investigation, managing quality alerts in the Zentiva QMS system, and providing regular reporting. The position requires 10-12 years of experience in Quality or Regulatory Affairs, with a strong background in pharmaceutical manufacturing and GxP know-how.
Requirements
- Graduated/Post-graduate in Pharmacy/Medicine or Chemistry
- 10 to 12 years minimum experience in Quality or Regulatory Affairs
- Experience obtained in pharmaceutical manufacturing sites (+5 years)
- Skilled in the usage of IT tools (for example: Trackwise, Share/DrugTrack, eDMS)
- English speaker
- Good organizational skills, stress resistance, and flexibility
- Good Team player and good at decision-making
- Experience in the pharmaceutical industry with a good level of GxP know-how is a strong plus