Zentiva is hiring for multiple Quality Control positions in Ankleshwar. Explore pharma jobs, QA jobs, QC jobs, and pharmaceutical careers in India with a leading European pharmaceutical company. Apply for Executive, Assistant Manager, and Manager roles in QC Pharma.
About the Company
Zentiva is a leading European pharmaceutical company dedicated to providing high-quality, affordable medicines. Part of the Sanofi group, Zentiva focuses on innovation, regulatory compliance, and patient-centric solutions.
The company operates modern manufacturing facilities in India and Europe, serving patients across multiple markets. With a strong commitment to quality, sustainability, and growth, Zentiva offers a dynamic environment where professionals can contribute to healthcare while advancing their careers in a global organization.
Job Details
- Company Name: Zentiva
- Experience: 2-15 years (varies by role)
- Qualification: M.Sc, B.Pharm, M.Pharm, B.Sc
- Location: Ankleshwar, Gujarat
- Work Type: On-site
Job Description
Zentiva is expanding its Quality Control team in Ankleshwar. The roles involve analytical testing, method development, and ensuring compliance with cGMP standards for formulation and API products.
Executive QC Pharma (2 Positions)
- Department: Quality Control
- Role: Executive QC Pharma
- Experience: 3-5 years
- Education/Qualification: Post-Graduate in Science or Pharmacy
Executive QC Pharma (LCMS)
- Department: Quality Control
- Role: Executive QC Pharma (LCMS)
- Experience: 2-5 years
- Education/Qualification: M.Sc (Organic / Analytical Chemistry)
Assistant Manager – QC Pharma
- Department: Quality Control
- Role: Assistant Manager QC Pharma
- Experience: 8-10 years
- Education/Qualification: M.Sc (Organic/Analytical Chem) or B.Pharm/M.Pharm
Manager QC Pharma
- Department: Quality Control
- Role: Manager QC Pharma
- Experience: 12-15 years
- Education/Qualification: M.Sc in Analytical/Organic/Applied/Pharma Chemistry
Skills/Qualifications
- Hands-on experience in chemical and instrumental testing
- Proficiency in HPLC, UPLC, GC, and other analytical instruments
- Strong knowledge of cGMP, GLP, and data integrity
- Experience in method validation and stability studies
- Excellent documentation and review skills
- Ability to work in a regulated environment
Key Responsibilities
- Perform chemical and instrumental analysis
- Conduct method validation and transfer activities
- Review analytical data and ensure compliance
- Support stability and in-process testing
- Maintain laboratory instruments and records
- Participate in audits and inspections
- Ensure timely release of materials and products
Benefits/Perks
- Career growth in quality control
- Learning opportunities with advanced analytics
- Competitive salary and benefits
- Professional work culture with global standards
- Exposure to European pharma practices
How to Apply
Apply online using the Workday links provided or email your CV to [email protected], mentioning the Position Code in the subject line. For more pharma jobs, visit Pharma Recruiter.
Strong CTA: Join Zentiva and advance your QC career. Apply today for these exciting opportunities in Ankleshwar!
Walk-in Interview Details
Not applicable. Apply online or via email.
Why You Should Join
Zentiva offers a dynamic, quality-focused culture with opportunities for professional development. Employees benefit from long-term career stability, recognition for expertise, and continuous learning in a compliant environment. Join a European pharmaceutical leader committed to innovation and patient well-being while building a rewarding career in quality control.
FAQs
1. What qualifications are required for QC roles at Zentiva?
M.Sc, B.Pharm, M.Pharm, or B.Sc with relevant experience.
2. What is the experience range?
Experience ranges from 2-15 years depending on the position.
3. Where is the job location?
4. What growth opportunities does Zentiva offer?
Strong career progression in quality control with European standards.
