Executive Quality Assurance Job – at Zentiva, Apply Now!
Looking to grow your career in pharmaceutical quality assurance? Zentiva is hiring an Executive – Quality Assurance, Pharma at its Ankleshwar facility. This role offers the opportunity to work in a regulatory-approved OSD manufacturing unit, ensuring cGMP compliance, process validation, and continuous improvement. If you have a B. Pharm or M. Pharm degree and 1–4 years of QA experience, this could be your next big move!
About Company:
Zentiva is a leading pharmaceutical company dedicated to improving the health and quality of life of individuals around the world. We are currently looking for a motivated Executive in Quality Assurance to join our team. If you are passionate about ensuring high quality in pharmaceutical products and have the necessary qualifications and experience, we invite you to apply for this exciting opportunity.
Job Details
Title: Executive – Quality Assurance, Pharma
Job Requisition ID: R2468224
Locations: India / Ankleshwar
Job Description
Educational Qualification: B. Pharm / M. Pharm from a reputed university
Experience: 1 to 4 years of similar experience in a regulatory-approved OSD manufacturing large unit
Quality Management / Continuous Improvement
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Line clearance and shop floor compliance
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Assisting in complaint investigation system at site for Quality Assurance
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Assisting in qualification and validation system, change control system, deviations
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Preparing & reviewing the annual product quality review
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Review of batch manufacturing & packing records
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Coordination of cGMP training activity
Compliance
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Ensure adherence to company quality standards, local FDA, MHRA regulations for Quality Assurance
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Perform gap analysis to identify gaps in existing system
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Prepare compliance plan for closure of gaps
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Execute compliance plans
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Review completion of compliance activity
Validations & Qualifications
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Ensure validated status of all equipment, manufacturing processes, and cleaning processes for Quality Assurance
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Review of protocols for qualification and validation of facility, equipment, product, process
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Review of validation reports after execution
Documentation Control
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Preparation and review of SOPs
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Controlled distribution and archival of documents and records for Quality Assurance
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Control of master documents
Assuring Quality of Products By:
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Ensuring SOP compliance
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Review of batch manufacturing & packing records
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Ensuring implementation of corrective actions/preventive actions proposed in deviations and customer complaints
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Ensuring effectiveness review of implemented CAPA
cGMP Training
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Prepare training modules and organize training in GMP for Quality Assurance
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Execute training program in coordination with all concerned departments
Other
- Review of maintenance and calibration program
Keywords: Executive, Quality Assurance, Pharma, Zentiva, Job, Ankleshwar, India
