Zentiva Careers: Executive I Pharma QA Job | B Pharm/ M Pharm Graduates | Apply Now
Looking for a promising Pharma QA Job in the pharmaceutical industry? Zentiva is hiring for the position of Executive I – Quality Assurance in Ankleshwar, India. This exciting opportunity under Zentiva Careers is ideal for professionals with experience in pharmaceutical quality systems, documentation, cGMP compliance, validation, and regulatory operations who want to grow their careers in Quality Assurance.
- Position Title: Executive I – Quality Assurance, Pharma
- locations: India / Ankleshwar
- Job requisition ID: R2469154
About the Company
Zentiva is a leading pharmaceutical company committed to delivering high-quality and affordable medicines globally. Through Zentiva Careers, professionals get opportunities to work in advanced pharmaceutical manufacturing, quality assurance, compliance, and regulatory operations.
Key Responsibilities
1. Quality Management/Continuous Improvement
- Line Clearance and shop floor compliance
- Carry out in-process checks and calibration of IPQC instruments.
- Handle the tools i.e., SAP Hana, LIMS, eDMS, Track Wise system.
- Assisting in the Complaint Investigation system at the site
- Assisting in the qualification and validation system, the change control system, and deviations
- Preparing & review the Annual Product Quality Review
- Review of Batch Manufacturing & Packing Records
- Coordination of cGMP Training activity.
2. Compliance
- Ensure adherence to company Quality Standards, Local FDA, and MHRA regulations, by
- Understanding the requirements
- Performing the Gap analysis to find out the gaps in the existing system
- Preparing a compliance plan for the closure of gaps
- Execution of compliance plans
- Review of completion for compliance activity
3. Validations & Qualifications:
- Ensure the validated status of all equipment, manufacturing processes, and cleaning processes
- Review of protocols for qualification and validation of facility/equipment/product/process
- Review of validation reports after execution of validation of facility /equipment/product/process
4. Documentation Control:
- Preparation and Review of SOPs
- Controlled distribution and archival of documents & record
- Control of master documents
5. Assuring the quality of products by
- Ensuring SOP compliance
- Review of Batch Manufacturing & Packing Records
- Ensuring implementation of Corrective actions/Preventive actions proposed in Deviations and Customer complaints
- Ensuring the effectiveness review of the implemented CAPA
6. cGMP Training
- To prepare training modules and organize training in GMP
- Execute the training program in coordination with all concerned departments
7. Other
- Review of maintenance and calibration program.
Qualifications & Experience
Educational Qualification
- Bachelor’s or master’s degree in pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline.
Experience
- 1–5 years of relevant experience in Pharma Quality Assurance / Documentation
Skills & Competencies
- 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
