Executive – Quality Assurance, Pharma
A rare chance emerged for aspiring professionals in the pharmaceutical sector when Zentiva listed the Executive – Quality Assurance position in Ankleshwar, India. This Zentiva Quality Assurance Job requires a background in pharmacy or related fields, with a focus on quality assurance practices. Candidates should verify the vacancy’s current status before applying.
About the Company
Zentiva is a leading pharmaceutical company operating in the healthcare sector. The organization is committed to providing high-quality medicines and health solutions to improve patient outcomes. With a strong presence in various markets, Zentiva focuses on innovation and excellence in pharmaceutical manufacturing and quality assurance.
Job Details:
- Company: Zentiva
- Location: India / Ankleshwar
- Job Type: Full-time
- Posted On: 12 October 2023
- Job Requisition ID: R2469645
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.
The Zentiva Quality Assurance Job involves documentation control, GMP compliance, validation support, and coordination across manufacturing and quality teams.
Key Responsibilities for the Zentiva Quality Assurance Job
- Quality Management/Continuous Improvement:
- Line Clearance and shop floor compliance.
- Carry out in-process checks and calibration of IPQC instruments.
- Handle tools such as SAP HANA, LIMS, eDMS, and the TrackWise system.
- Assisting in the complaint investigation system at site.
- Assisting in the qualification and validation system, change control system, and deviations.
- Preparing & review the Annual Product Quality Review.
- Review of Batch Manufacturing & Packing Records.
- Coordination of cGMP training activities.
- Compliance:
- Ensure adherence to company Quality Standards, Local FDA MHRA regulations by understanding the requirements.
- Performing the Gap analysis to find out the gaps in the existing system.
- Preparing a compliance plan for closure of gaps.
- Execution of compliance plans.
- Review of completion for compliance activity.
- Validations & Qualifications:
- Ensure 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.
- Documentation Control:
- Preparation and Review of SOPs.
- Controlled distribution and archival of documents & records.
- Control of master documents.
- Assuring 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.
- cGMP Training:
- To prepare training modules and organize training in GMP.
- Execute the training program in coordination with all concerned departments.
- Other:
- Review of maintenance and calibration program.
How to Apply
Interested candidates can apply for the position by following this link.
The Zentiva Quality Assurance Job outlined quality and compliance responsibilities that are important in pharmaceutical manufacturing. As this listing dates from 2023, interested individuals should confirm availability through the official Zentiva careers page before applying.
CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
