Executive – Quality Assurance, Pharma at Zentiva

A Quality Assurance Job at Zentiva is available for aspiring professionals in the pharmaceutical sector in Ankleshwar, India. This full-time position requires candidates with a background in pharmacy or the life sciences and relevant experience in quality assurance.

About Zentiva

Zentiva is a leading pharmaceutical company dedicated to providing high-quality medicines and healthcare solutions. Operating in the pharmaceutical sector, Zentiva focuses on developing, manufacturing, and distributing a wide range of pharmaceutical products. The company is committed to maintaining the highest standards of quality and compliance in its operations.

Job Details:

Company: Zentiva

Location: India / Ankleshwar

Job Type: Full time

Posted On: 13 Days Ago

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:

• This Quality Assurance Job requires 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.

Quality Assurance Job Responsibilities

• Quality Management/Continuous Improvement:

  • Line Clearance and shop floor compliance.

  • Carry out in-process checks and calibration of IPQC instruments.

  • Handle e-tools i.e. SAP Hana, LIMS, eDMS, Track Wise system.

  • Assisting in Complaint Investigation system at site.

  • Assisting in Qualification and validation system, change control system, deviations.

  • Preparing & review the Annual Product Quality Review.

  • Review of Batch Manufacturing & Packing Records.

  • Coordination of cGMP Training activity.

• Compliance:

  • In this Quality Assurance Job, ensure adherence to company Quality Standards, Local FDA MHRA regulations.

  • Understanding the requirements.

  • Performing the Gap analysis to find out the gaps in 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’s, 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:

  • 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

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

Conclusion

This Quality Assurance Job at Zentiva is ideal for qualified candidates looking to advance their careers in the pharmaceutical industry. Interested individuals are encouraged to apply at the earliest to seize this chance.