Zentiva is hiring for the position of Executive I – Quality Assurance, Pharma at its pharmaceutical operations in Ankleshwar, Gujarat. The role is suitable for professionals with 1–5 years of experience in pharmaceutical Quality Assurance or documentation.
Candidates with a Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or a related discipline can apply. The position involves pharmaceutical quality systems, cGMP compliance, batch documentation, APQR, validation, CAPA, SOPs and regulatory compliance.
The vacancy is a full-time, on-site opportunity with Zentiva in Ankleshwar. The official listing identifies the position as Executive I – Quality Assurance, Pharma, requisition R2469645.
Zentiva Executive Quality Assurance Job Details
| Particular | Details |
|---|---|
| Company | Zentiva |
| Position | Executive I – Quality Assurance, Pharma |
| Department | Quality Assurance |
| Job Location | Ankleshwar, Gujarat |
| Experience | 1–5 Years |
| Qualification | Bachelor’s/Master’s in Pharmacy, Pharmaceutical Sciences, Life Sciences or related discipline |
| Job Type | Full-time |
| Industry | Pharmaceutical |
| Job Requisition ID | R2469645 |
| Salary | Approximately ₹4.1–5.8 LPA* |
*The employer’s current listing does not state a salary. A third-party listing for this Zentiva role reports ₹4.1–5.8 LPA, while another job-market source gives a lower estimate; therefore, applicants should treat the figure as an indicative range rather than confirmed compensation.
Zentiva Executive Quality Assurance Responsibilities
Selected candidates will be responsible for activities across pharmaceutical Quality Assurance, quality systems, compliance and documentation, including:
Quality Management and Continuous Improvement
- Perform line clearance and monitor shop-floor compliance.
- Carry out in-process checks and calibration of IPQC instruments.
- Work with electronic quality systems including SAP HANA, LIMS, eDMS and TrackWise.
- Assist with site complaint investigations.
- Support qualification, validation, change control and deviation systems.
- Prepare and review Annual Product Quality Reviews (APQR).
- Review Batch Manufacturing Records and Batch Packing Records.
- Coordinate cGMP training activities.
Compliance
The Executive will support compliance with company quality standards and applicable regulatory requirements, including FDA and MHRA requirements.
Key activities include:
- Understanding applicable regulatory requirements.
- Performing gap assessments.
- Preparing compliance plans.
- Supporting execution of compliance actions.
- Reviewing completion of compliance activities.
Validation and Qualification
The role involves supporting the validated status of:
- Manufacturing equipment
- Facilities
- Manufacturing processes
- Cleaning processes
The Executive will also review qualification and validation protocols and reports covering facilities, equipment, products and processes.
Documentation Control
Responsibilities include:
- Preparation and review of SOPs.
- Controlled distribution and archival of documents and records.
- Maintaining and controlling master documents.
- Reviewing batch manufacturing and packing documentation.
Product Quality Assurance
The position will support product quality by:
- Ensuring SOP compliance.
- Reviewing Batch Manufacturing and Packing Records.
- Supporting implementation of CAPA arising from deviations and customer complaints.
- Reviewing CAPA effectiveness.
- Supporting quality-system activities across the manufacturing environment.
cGMP Training
The role also includes:
- Preparing GMP training modules.
- Organizing GMP training programs.
- Coordinating training with relevant departments.
- Supporting execution of the site’s cGMP training program.
Zentiva QA Executive Qualification
Applicants should have a Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences or a related discipline.
The required experience is 1–5 years in Pharmaceutical Quality Assurance or Documentation. The role specifically seeks knowledge of cGMP, GDP, quality systems, batch documentation, document control and APQR preparation.
Who Can Apply?
Relevant candidates may include professionals holding:
- B.Pharm
- M.Pharm
- Bachelor’s/Master’s degree in Pharmaceutical Sciences
- Relevant Bachelor’s/Master’s degree in Life Sciences
- Related disciplines, where the candidate has relevant pharmaceutical QA/documentation experience
Candidates should preferably have practical exposure to pharmaceutical manufacturing quality systems and documentation.
Skills Required
Applicants should have:
- Knowledge of cGMP and GDP
- Understanding of pharmaceutical quality systems
- Experience with batch documentation
- Knowledge of document control
- Understanding of APQR
- Strong analytical and organizational skills
- Good coordination and communication abilities
- Attention to detail
- Understanding of data integrity
- Ability to work cross-functionally
Experience with SAP HANA, LIMS, eDMS and TrackWise is relevant to the responsibilities described for the position.
Career Benefits and Exposure
While Zentiva’s current job advertisement does not publish a separate benefits package, this Quality Assurance position provides professional exposure to several areas of pharmaceutical manufacturing quality, including:
- cGMP and GDP systems
- Regulatory compliance
- Batch record review
- APQR
- CAPA and deviations
- Qualification and validation
- SOP and document control
- GMP training
- Electronic quality management systems
- Cross-functional pharmaceutical operations
These areas can be particularly relevant for professionals developing their careers in Pharma QA and Quality Compliance.
Salary for Zentiva Executive Quality Assurance
Zentiva has not specified compensation in the supplied official vacancy. Current third-party listings for the same or substantially matching vacancy have reported salary estimates ranging from approximately ₹3 lakh to ₹5.8 lakh per annum, depending on the source. One listing specifically reports ₹4.1–5.8 LPA for this role.
Therefore, applicants should confirm the final CTC, benefits and compensation structure directly with Zentiva during the recruitment process.