QA Specialist Position at Zentiva Ankleshwar
A rare chance has emerged for experienced Quality Assurance professionals at Zentiva in Ankleshwar, Gujarat. The Zentiva QA Specialist role requires a minimum of five years of relevant experience and offers an opportunity to contribute significantly to quality management in the pharmaceutical sector.
About Zentiva
Zentiva Private Limited is a producer of high-quality, affordable medicines serving patients in Europe and beyond. With a dedicated team of more than 4,700 people and a network of production sites—including flagship sites in Prague, Bucharest, and Ankleshwar—Zentiva strives to be a champion of branded and generic medicines in Europe to better support people’s daily healthcare needs. The organization is committed to ensuring that healthcare is a right and not a privilege.
Company: Zentiva Private Limited
Location: Ankleshwar, Gujarat
Experience: Minimum 5 years relevant experience in Quality Assurance
Qualification: University degree in Pharmacy, Chemistry, Biology, or relevant Life Science
Posted on: 25 September 2026
Application Deadline: Not specified
Req ID: zentiva-qa-specialist-R2469647
Zentiva QA Specialist Job Description
The ESO Quality QA Specialist is responsible for the quality lifecycle management of an assigned subcontracted product portfolio and independent Quality Assurance oversight of assigned products and suppliers. In this Zentiva QA Specialist position, the role ensures compliance with applicable Quality Management System, GMP, GDP, and regulatory requirements and supports audits, product lifecycle activities, and quality decision-making.
Key Responsibilities
- Operational quality management of an assigned product portfolio.
- Independently manage routine deviations, complaints, and related CAPAs.
- Conduct Root Cause Analysis and follow up on agreed corrective and preventive actions.
- Review and assess change controls and their Quality impact.
- Review GMP manufacturing documentation, analytical data, CoAs/CoCs, and relevant batch documentation.
- Support batch release decisions through review of Quality documentation.
- Conduct routine Quality Risk Assessments.
- Prepare and maintain Quality Agreements with third parties and subcontractors.
Zentiva QA Specialist Eligibility Criteria
- University degree in Pharmacy, Chemistry, Biology, or relevant Life Science.
- Knowledge of pharmaceutical GxP regulations and Quality system.
- Strong understanding of GDP principles (EU GDP Guidelines).
- Experience in pharmaceutical quality systems or supply chain compliance.
- Strong documentation, organizational, and communication skills.
- Ability to manage competing priorities with a sense of urgency.
- Good Microsoft applications knowledge and computer skills.
- Advanced knowledge of English.
How to Apply
Interested candidates should apply via the official Workday link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Additional Information
The position emphasizes adherence to GxP principles and internal Quality standards, ensuring compliance with applicable regulatory requirements. Candidates are expected to report any suspicion of adverse events related to medicinal products or medical devices in line with relevant internal regulations.
Why Join Zentiva
Zentiva is dedicated to creating an environment where healthcare is accessible to all. By joining the team, candidates will be part of a mission-driven organization that values quality, innovation, and collaboration. The company fosters professional growth and provides opportunities to make a meaningful impact in the healthcare sector.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
This Zentiva QA Specialist opportunity is ideal for qualified candidates looking to advance their careers in Quality Assurance. Interested individuals are encouraged to apply at the earliest.
