Pharma QA Executive Job at Zentiva, Apply Now!
Zentiva is hiring an Executive – Quality Assurance for its state-of-the-art pharmaceutical manufacturing facility in Ankleshwar, India. If you have 3–5 years of experience in OSD manufacturing and are passionate about quality systems, regulatory compliance, and continuous improvement, this is your opportunity to advance your pharma career.
About the Company:
Welcome to Zentiva! We are a pharmaceutical company dedicated to improving the health and well-being of people worldwide. Our focus is on providing high-quality pharmaceutical products that make a positive impact on the lives of patients.
Job Position: Executive – Quality Assurance, Pharma
Location: Ankleshwar, India
Job Requisition ID: R2467986
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 Complaint Investigation System at Site
- Assisting in Qualification and Validation System, Change Control System, Deviations
- Preparing & Review of 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 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 & record
- 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
- Review of maintenance and calibration program
Keywords: Zentiva, Pharma Job, Quality Assurance Executive, Ankleshwar, India, OSD Manufacturing, CAPA, Validation, cGMP, BMR Review, Pharma QA Jobs
