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Piramal Pharma Trainee – Quality Assurance Job in Turbhe, Navi Mumbai
Published on: November 7, 2026
Piramal Pharma Solutions has posted a Trainee – Quality Assurance opening at its Turbhe, Navi Mumbai, Maharashtra facility. The position requires a B.Sc. or M.Sc. qualification and no prior work experience, according to the official job description.
The selected candidate will support QA functions involving pharmaceutical documentation, Standard Operating Procedures (SOPs), equipment qualification, area validation and Quality Management System (QMS) activities.
Candidates preparing for QA assessments can strengthen their fundamentals with our Free Pharma Quality Assurance Mock Test – 50 MCQs with Explanations. You can also explore other opportunities through our QA/QC Jobs page.
1. Piramal Pharma QA Job Overview
| Particulars | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Position | Trainee – Quality Assurance |
| Job ID | R00004841 |
| Location | Turbhe, Navi Mumbai, Maharashtra |
| Qualification | B.Sc. / M.Sc. |
| Experience | Not required |
| Department | Quality Assurance |
| Application | Trainee – Quality Assurance – Apply Online |
Candidates interested in exploring other openings can visit the Piramal Pharma Careers Portal to Search for More Jobs
2. About Piramal Pharma Solutions
Piramal Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO) providing pharmaceutical development and manufacturing services across the drug product lifecycle.
Its operations cover areas such as API manufacturing, finished dosage forms, pharmaceutical development, clinical trial supplies, highly potent APIs and antibody-drug conjugation.
3. Qualification and Experience
The official job description specifies the following educational qualifications:
- B.Sc.
- M.Sc.
Experience: Previous work experience is not required as per the listed criteria.
Note for pharmacy graduates: B.Pharm and M.Pharm are not specifically mentioned in the qualification details provided for this vacancy. Candidates with these degrees should confirm their eligibility with the company’s recruitment team before applying.
4. Roles and Responsibilities
The position covers several areas of pharmaceutical Quality Assurance. The main responsibilities are outlined below.
4.1 Documentation and SOP Management
The trainee will support the maintenance and control of QA documentation. Activities include:
- Issuing, archiving and retrieving quality documents.
- Maintaining controlled document copies.
- Tracking and organizing QA records.
- Maintaining backups of electronic documents.
- Supporting SOP preparation, indexing and review.
Proper document control ensures that employees follow approved procedures and that records remain available for review and audits.
4.2 Equipment Qualification and Area Validation
The responsibilities include supporting qualification and validation activities at the facility, such as:
- Qualification of new and existing equipment.
- Coordination of area validation activities.
- Reviewing calibration and preventive maintenance schedules.
- Preparing and maintaining validation-related documents.
- Supporting the Validation Master Plan (VMP).
Equipment qualification establishes documented evidence that equipment is suitable for its intended purpose. Area validation provides evidence that designated areas meet the required conditions for their intended operations.
4.3 Vendor and External Service Provider Qualification
The role also involves documentation and coordination related to:
- Vendor qualification.
- Contract testing laboratories.
- External service providers.
These processes help establish that suppliers and external service providers meet the applicable quality requirements.
4.4 Quality Management System (QMS)
The trainee will support documentation and coordination for different QMS processes.
| QMS Term | Explanation |
|---|---|
| Deviation | An unexpected departure from an approved procedure or established requirement. |
| Change Control | A documented process for evaluating and approving proposed changes. |
| OOS | Out of Specification – a result outside established acceptance criteria. |
| OOT | Out of Trend – a result showing an unexpected pattern compared with historical or expected results. |
| CAPA | Corrective and Preventive Action to address problems and help prevent recurrence. |
| Product Complaints | Recording and evaluating complaints related to products. |
| Returned Goods | Documenting and handling products returned to the company. |
| Risk Assessment | Identifying and evaluating potential risks to product quality or operations. |
| Product Recall | Coordinating the quality-system process for removing affected products from the market when necessary. |
These activities form part of the quality system used to maintain compliance, investigate issues and improve pharmaceutical manufacturing processes.
5. Departments and Stakeholders
The position involves interaction with different teams to coordinate quality-related activities.
| Internal stakeholders | External stakeholders |
|---|---|
| Production – Synthesis and Pharma | Auditors |
| Quality Assurance | Suppliers |
| Quality Control | Customers |
| Engineering | External service providers |
Good coordination between these groups is important for maintaining documentation and addressing quality-related requirements.
6. Important Skills for This QA Position
Candidates interested in this opportunity should have or develop knowledge of:
- Good Manufacturing Practices (GMP).
- Pharmaceutical documentation and record management.
- SOP preparation and document control.
- Basic equipment qualification and validation concepts.
- Quality Management System procedures.
- Calibration and preventive maintenance.
- Attention to detail and communication skills.
For freshers, understanding GMP documentation, deviations, CAPA and change control can provide a useful foundation for entry-level QA responsibilities.
7. QA Interview Preparation: Topics to Revise
Based on the responsibilities mentioned in this job description, candidates should prepare the following topics:
- What is GMP, and why is it important in pharmaceutical manufacturing?
- What is an SOP?
- What is document control?
- What is the difference between equipment qualification and process validation?
- What is a deviation, and how is it documented?
- What is Change Control?
- What is the difference between OOS and OOT?
- What is CAPA?
- What is a Validation Master Plan?
- Why are equipment calibration and preventive maintenance necessary?
Candidates should focus on understanding these concepts with practical pharmaceutical examples rather than memorizing definitions alone.
8. How to Apply
Interested candidates can access the complete job description and submit their applications through Piramal Pharma Solutions’ official careers portal.
Position: Trainee – Quality Assurance
Job ID: R00004841
Location: Turbhe, Navi Mumbai, Maharashtra
Apply for Piramal Pharma Trainee – Quality Assurance
Explore Other Job Openings:
To find additional vacancies across different departments and locations, visit the Piramal Pharma Careers Portal – Search Jobs.
Check the latest vacancy status and eligibility criteria before applying.
9. Frequently Asked Questions
1. What is the qualification for Piramal Pharma Trainee – Quality Assurance?
The provided job description specifies B.Sc. or M.Sc.
2. Is this position suitable for freshers?
Yes. Previous work experience is not required according to the listed job requirements.
3. Can B.Pharm candidates apply?
B.Pharm is not specifically mentioned in the provided eligibility criteria. Candidates should confirm their eligibility with the company.
4. What are the main responsibilities of this position?
The role includes QA documentation, SOP management, equipment qualification, area validation, vendor qualification and QMS support.
5. Where is the job location?
The vacancy is listed for Turbhe, Navi Mumbai, Maharashtra.
6. What is the job ID?
The job ID is R00004841.
10. Explore More Pharmaceutical QA/QC Opportunities
Explore other Quality Assurance and Quality Control vacancies across the pharmaceutical industry through our dedicated job section.
You can also use our Free Quality Assurance Mock Test to practice pharmaceutical QA concepts.
Disclaimer: PharmaCareerUpdates.com is an independent career information platform and is not affiliated with Piramal Pharma Solutions. The information in this article is based on the provided job description. Requirements and vacancy status may change. Always refer to the official Piramal Pharma application page for the latest details.
