Officer - QA - Ankleshwar, India - Zentiva Group, a.s.
Description
Education:
- Graduate / Post Graduate in Pharmacy
- Experience:
- requirements
- 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 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 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
- 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
- Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations
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