Quality Assurance Job at Zentiva
A rare chance has emerged for aspiring Quality Assurance Specialists at Zentiva in Ankleshwar, Gujarat. Additionally, this Zentiva QA job offers an opportunity to support Dutch WDA and GDP QA processes, ensuring compliance and quality in a dynamic pharmaceutical environment. Candidates with relevant qualifications are encouraged to apply before the deadline.
About Zentiva
Zentiva is a leading pharmaceutical company operating in the healthcare sector, focused on providing high-quality medicines and healthcare solutions. With a commitment to innovation and quality, Zentiva aims to improve patient outcomes and enhance the quality of life for people around the world. The company is headquartered in the Czech Republic and has a significant presence in various international markets, including India.
Job Details:
- Position: Quality Assurance Specialist
- Location: Ankleshwar, Gujarat, India
- Posted On: 28 August 2026
Zentiva QA Job Description
In this Zentiva QA job, the Quality Assurance Specialist will support the maintenance of the Dutch WDA license and ensure compliance with GDP regulations. The role involves coordinating documentation, managing complaints and deviations, and ensuring adherence to quality standards. This position requires a proactive approach to compliance and collaboration with internal and external stakeholders.
Key Responsibilities
- Support maintenance of the Dutch WDA license in collaboration with the external RP service provider.
- Ensure all documentation required for WDA compliance is complete, current, and accessible.
- Coordinate internal inputs required for initial and ongoing WDA obligations.
- Act as the primary internal contact for the external RP/WDA service provider.
- Manage end-to-end complaints and deviation processes, ensuring accurate recording in Quality Forward.
- Coordinate review and routing of GDP-relevant documents requiring RP approval.
- Support implementation and maintenance of GDP-related SOPs.
- Maintain oversight of WDA-related KPIs and compliance status.
Eligibility Criteria
- University degree in Pharmacy, Chemistry, Biology, or relevant Life Science.
- Knowledge of pharmaceutical GxP regulations and Quality systems.
- Strong understanding of GDP principles (EU GDP Guidelines).
- Experience in pharmaceutical quality systems or supply chain compliance.
- Very good communication skills and a customer-oriented approach.
- Flexibility and ability to manage competing priorities.
- Advanced knowledge of English.
Required Skills
- Strong documentation, organizational, and communication skills.
- Ability to coordinate external service providers and internal stakeholders.
- Collaborative and team-oriented mindset.
- Proven hands-on attitude, flexible and adaptable.
- Good knowledge of Microsoft applications and computer skills.
Documents Required
- Updated resume/CV.
- Educational certificates.
- Any relevant certifications.
Why Join Zentiva
For candidates considering this Zentiva QA job, Zentiva is dedicated to fostering a culture of quality and compliance, ensuring that its employees are equipped to meet the challenges of the pharmaceutical industry. Furthermore, the organization values collaboration, innovation, and a commitment to excellence, making it an ideal workplace for professionals seeking to make a meaningful impact in healthcare.
Therefore, qualified candidates are encouraged to seize this opportunity at Zentiva and apply before the deadline to contribute to a leading pharmaceutical organization focused on quality and compliance.
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