Zentiva Pharma QA Job as an Executive – Apply Now!
Zentiva Pharma is actively hiring for the role of Executive – Quality Assurance at its Ankleshwar facility. If you have 1 to 4 years of experience in a regulatory-approved pharmaceutical manufacturing unit and a background in B.Pharm or M.Pharm, this is your chance to join a leading pharma company focused on quality, compliance, and continuous improvement.
About the company:
Zentiva is a multinational pharmaceutical company headquartered in Prague, Czech Republic, specializing in the development, manufacturing, and marketing of high-quality, affordable generic and over-the-counter (OTC) medicines. With origins dating back over 530 years to the Black Eagle Pharmacy in Prague, Zentiva has evolved into a significant player in the European pharmaceutical market. The company operates four manufacturing sites located in Prague, Bucharest, and Ankleshwar, India, producing more than 70% of its product supply.
Job Description:
We are a pharmaceutical company looking for a dedicated individual to join our team as an Executive – Quality Assurance. Below are the details of the job position:
- Job Posting: Executive – Quality Assurance, Pharma
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- locations: India / Ankleshwar
- Posted on: Today
- time type: Full time
- Job requisition id: R2467985
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:
- 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
- Validations & Qualifications
Documentation Control:
- Preparation and Review of SOPs
- Controlled distribution and archival of documents & record
- Control of master documents
Assuring quality of products by:
- Review of maintenance and calibration program
Other Responsibilities
cGMP Training:
- To prepare training modules and organize training in GMP
- Execute the training program in coordination with all concerned departments
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