Zentiva Hiring Executive-Quality Assurance Role | Pharma Graduates Apply
Looking for Quality Assurance Jobs in the pharmaceutical industry? Zentiva Careers is hiring for the position of Executive I – Quality Assurance in Ankleshwar. This excellent opportunity is open to B.Pharm, M.Pharm, Pharmaceutical Sciences, and Life Sciences graduates with 1–5 years of Quality Assurance experience. If you have expertise in cGMP, GDP, validation, documentation, and regulatory compliance, explore these Quality Assurance Jobs through Zentiva Careers and take the next step in your pharmaceutical career.
- Job Position: Executive-Quality Assurance
- Location: Ankleshwar, India
- Job Requisition ID: R2469337
About the Company
Zentiva is a pharmaceutical company focused on providing high-quality generic medicines. Operating in the pharmaceutical sector, Zentiva is committed to ensuring the highest standards of quality and compliance in its operations. The company is known for its dedication to improving patient access to essential medications and operates globally, with a significant presence in various markets.
Job Description
The Executive in Quality Assurance at Zentiva will be responsible for ensuring compliance with quality standards and regulatory requirements. This role involves overseeing quality management processes, conducting in-process checks, and maintaining documentation control to assure product quality. Candidates should possess strong analytical and organizational skills to effectively contribute to the quality assurance team.
Key Responsibilities
- Conduct line clearance and shop floor compliance checks.
- Carry out in-process checks and calibration of IPQC instruments.
- Manage documentation control and review of Batch Manufacturing & Packing Records.
- Assist in complaint investigation and qualification/validation systems.
- Prepare and review the Annual Product Quality Review.
- Ensure adherence to company quality standards and local regulations.
- Develop training modules and coordinate GMP training activities.
- Review maintenance and calibration programs.
Eligibility Criteria
- Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences or a related discipline.
- 1–5 years of relevant experience in Pharma Quality Assurance/Documentation.
Required Skills
- Strong knowledge of cGMP, GDP, and Quality Systems.
- Hands-on experience with batch documentation and document control systems.
- Good understanding of APQR preparation and regulatory expectations.
- Strong analytical, organizational, and coordination skills.
- Effective communication and cross-functional collaboration abilities.
- Attention to detail and commitment to data integrity.
Why Join Zentiva?
Zentiva is dedicated to fostering a culture of quality and compliance, making it an ideal workplace for professionals in the pharmaceutical sector. Employees benefit from a collaborative environment where they can enhance their skills and contribute to meaningful projects that improve patient health outcomes. Joining Zentiva means being part of a team that values integrity, innovation, and excellence in quality assurance.
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