Zentiva Life Sciences QA Job Opening – Apply Online
Join Zentiva, a global leader in pharmaceuticals, as an ESO QA Specialist in Ankleshwar, India. This role focuses on quality lifecycle management, GMP compliance, and auditing for subcontracted product portfolios. If you have a degree in Pharmacy, Chemistry, or Life Sciences with 5+ years of GMP-related experience, apply now to contribute to high-quality pharmaceutical standards.
Company Overview:
Zentiva is a leading pharmaceutical company dedicated to ensuring the quality and safety of its product portfolio. As an organization committed to excellence, Zentiva is seeking qualified individuals who share our vision for maintaining high operational standards and regulatory compliance.
- Job Title: ESO QA Specialist
- Locations: India / Ankleshwar
- Job Requisition ID: R2467677
Mission Statement:
To ensure the quality lifecycle management for dedicated, subcontracted product portfolio. Qualified auditor.
ESO QA Specialist Zentiva Main Accountabilities and Duties:
- Quality management of deviation and complaint records and their related CAPAs
- Assessment and management of change controls
- Edition of Quality Assurance Agreements with Zentiva third parties and subcontractors
- Collection and evaluation of PQRs and stability data
- Compliance evaluation of Third Parties and products
- Maintenance of product database
- Collection and review of CoA/CoC
- Quality Assurance support of product launches and transfers
- GMP, GDP, MDR, HACCP, Food Supplements and Cosmetics regulations and legislations
ESO QA Specialist Zentiva Required Qualifications, Experience & Skills:
- University degree in Pharmacy, Chemistry, Biology, or relevant Life Science
- Minimum of 5 years in a similar role or equivalent GMP-related experience
- Thorough knowledge of GMP requirements and pharmaceutical regulatory standards
- Proven project management skills, and strong communication and negotiation abilities
- Proactive, problem-solving, and collaborative
- Knowledge of IT tools, advanced level of English language proficiency
Why Join Zentiva?
- Be part of a globally recognized pharmaceutical company
- Contribute to high-quality drug manufacturing & compliance
- Opportunities for professional growth in Quality Management
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