Quality Assurance Job at Zentiva | Apply Now for the Executive Role
Zentiva is hiring an Executive – Quality Assurance (Pharma) for its Ankleshwar, India facility. The Quality Assurance Job is ideal for professionals with a background in B.Pharm or M.Pharm and 3–5 years of experience in a regulatory-approved oral solid dosage (OSD) manufacturing unit. Join one of the world’s most respected pharmaceutical companies to ensure quality, compliance, and continuous improvement in every batch produced.
- Job Title: Executive – Quality Assurance, Pharma
- Locations: India / Ankleshwar
- Job Requisition ID: R2468636
About the Company
At Zentiva, we are dedicated to delivering high-quality pharmaceutical products that improve the health and lives of people around the world. With a focus on innovation and compliance, our team is committed to upholding the highest standards in all our operations.
Educational Qualification
B. Pharm / M. Pharm from a reputed university
Experience
3 to 5 years of similar experience in a regulatory-approved OSD manufacturing large unit.
Quality Management/Continuous Improvement
- Line Clearance and shop floor compliance
- Assisting in the Complaint Investigation system at site
- Assisting in the Qualification and validation system, change control system, deviations
- Preparing & reviewing the Annual Product Quality Review
- Review of Batch Manufacturing & Packing Records
- Coordination of cGMP Training activity
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 the 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 & record
- 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
Application Link:
