Piramal Pharma Solutions is hiring for the position of Executive – Quality Assurance at its Mahad, Maharashtra location. This is a full-time opportunity for professionals interested in pharmaceutical quality assurance, in-process quality control, manufacturing documentation, compliance and shop-floor quality activities.
The role primarily focuses on IPQA (In-Process Quality Assurance) activities across manufacturing, packing and dispensing operations. The selected candidate will be responsible for line clearance, in-process checks, batch record verification, sampling, deviation and CAPA monitoring, data integrity, training and QEHS-related activities.
Piramal Pharma Solutions Executive Quality Assurance Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Position | Executive – Quality Assurance |
| Job Function | Quality Assurance / IPQA |
| Location | Mahad, Maharashtra |
| Job Type | Full Time |
| Key Area | Pharmaceutical Manufacturing Quality |
| Experience | Not Specified |
| Qualification | Not Specified |
| Requisition ID | R00004091 |
| Application Deadline | October 3, 2026 |
| Salary / CTC | Not Specified |
About Piramal Pharma Solutions
Piramal Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO) providing services across the pharmaceutical product lifecycle.
Its capabilities include drug discovery, process and pharmaceutical development, clinical trial supplies, commercial supply of APIs and finished dosage forms, as well as specialized services involving highly potent APIs and antibody-drug conjugation.
The company operates through an integrated network of facilities across North America, Europe and Asia and serves innovator and generic pharmaceutical companies.
Job Description
The Executive – Quality Assurance will support quality assurance activities at the manufacturing site, with a strong focus on IPQA operations.
The position involves monitoring manufacturing, packing and dispensing activities, verifying production documentation, conducting in-process quality checks, supporting sampling and validation activities, monitoring deviations and CAPA, and maintaining compliance with applicable quality, data integrity and QEHS requirements.
Key Responsibilities
Manufacturing and Packing Quality Assurance
- Perform area and line clearance for manufacturing, packing and dispensing operations.
- Conduct in-process quality checks during manufacturing and packing activities.
- Inspect dispensing activities at appropriate stages.
- Verify equipment and area cleanliness during line clearance.
- Perform quality checks across manufacturing operations including tablet, liquid, HNH and ANH departments.
- Conduct online monitoring of manufacturing and packing processes.
- Verify production activities against approved requirements.
Equipment and Environmental Monitoring
- Verify weighing balance calibration activities on a daily basis.
- Check environmental monitoring activities in raw-material staging, manufacturing and packing areas.
- Verify cleanliness of equipment and manufacturing areas.
- Support implementation of effective sanitation practices.
- Ensure appropriate workplace conditions are maintained.
Batch Documentation and Record Review
- Verify and review online Batch Manufacturing Records.
- Review production documents and manufacturing records.
- Verify finished goods documentation and related activities.
- Maintain appropriate quality records and documentation.
- Support document archival activities.
- Ensure the quality and integrity of GxP-related data and documentation.
Sampling and Testing Support
- Perform sampling of bulk-stage materials and finished goods for analysis and control samples.
- Conduct sampling of validation materials, including:
- Process validation samples
- Packaging validation samples
- Cleaning validation samples
- Rinse samples
- Swab samples
- Support appropriate control and documentation of samples.
Deviations, CAPA and Quality Monitoring
- Record and report daily nonconformances.
- Monitor manufacturing processes for deviations.
- Support effective implementation of CAPA.
- Participate in statistical process monitoring.
- Identify quality-related issues and communicate them to relevant stakeholders.
- Support corrective actions for identified quality and compliance issues.
- Assist with market complaint review and handling while maintaining data and documentation integrity.
Training and Personnel Development
- Provide on-the-job training to new employees working in production areas.
- Conduct required training for shop-floor personnel.
- Support training related to quality, safety and applicable procedures.
- Participate in initiatives related to quality mindset and organizational learning.
Regulatory and Compliance Responsibilities
- Support requirements applicable to food and dietary supplement products for the US export market under 21 CFR Part 111.
- Maintain compliance with applicable GxP requirements.
- Help prevent data-integrity breaches within assigned areas.
- Ensure production and quality activities follow approved procedures.
- Support implementation of quality-related corporate initiatives.
QEHS Responsibilities
The role also carries responsibilities related to Quality, Environment, Health and Safety (QEHS).
Key activities include:
- Identify internal and external QEHS issues and relevant stakeholder expectations.
- Support implementation of QEHS policies and objectives.
- Encourage worker participation and consultation.
- Ensure appropriate use of PPE.
- Identify and communicate incidents and QEHS nonconformities.
- Participate in investigations and corrective actions.
- Ensure work-permit systems are followed during maintenance activities.
- Support continual-improvement projects related to QEHS.
- Ensure proper waste disposal.
- Report hazards, incidents, accidents and near-miss events.
- Support preparation of occupational health and safety performance documentation.
- Conduct training for workmen on occupational health and safety management requirements.
- Take appropriate action to prevent unsafe or improper workplace conditions.
Educational Qualification / Eligibility Criteria
The provided vacancy does not specify a particular educational qualification for the Executive – Quality Assurance position.
Candidates should therefore review the official Piramal Pharma Solutions job listing carefully for the latest qualification requirements before applying.
Experience Requirements
The provided job description does not state a specific number of years of experience.
The responsibilities indicate that the position requires familiarity with pharmaceutical manufacturing quality processes, IPQA activities, production documentation, quality systems, compliance and shop-floor operations.
Required Skills
Relevant capabilities for the position include:
- In-process quality assurance
- Manufacturing quality checks
- Packing and dispensing quality activities
- Line clearance
- Batch Manufacturing Record review
- Production documentation
- Equipment and area cleanliness verification
- Environmental monitoring
- Sampling and validation activities
- Deviation monitoring
- CAPA implementation
- Statistical process monitoring
- Data integrity
- GxP documentation
- Quality compliance
- Training and shop-floor communication
- QEHS awareness
- Problem identification and corrective action
Work Location and Job Type
Location: Mahad, Maharashtra, India
Job Type: Full Time
The provided vacancy does not specify a remote or hybrid work arrangement. The responsibilities indicate a site-based role involving manufacturing and production-area activities.
Salary / CTC
The salary or CTC has not been specified in the provided recruitment information.
Candidates should confirm compensation and other employment terms through the official Piramal Pharma Solutions recruitment process.
Selection Process
The detailed selection process has not been mentioned in the provided vacancy. Candidates should follow the official recruitment process and complete any interview or assessment stages communicated by the company.
How to Apply for Piramal Pharma Solutions Recruitment 2026
Interested candidates can apply online through the official Piramal Pharma Solutions careers portal.
- Open the official job listing.
- Review the position requirements and responsibilities.
- Prepare an updated CV highlighting relevant QA/IPQA experience.
- Submit the online application through the official careers portal.
- Complete any additional recruitment steps requested by the company.
Important Details Before Applying
- The position is Executive – Quality Assurance.
- The job is based in Mahad, Maharashtra.
- The role is focused heavily on IPQA and pharmaceutical manufacturing quality activities.
- Responsibilities include manufacturing, packing and dispensing line clearance.
- The role involves Batch Manufacturing Record and production-document review.
- Validation sampling, environmental monitoring and equipment cleanliness verification are included.
- Deviation, CAPA and nonconformance activities are part of the role.
- Data integrity and GxP documentation are important responsibilities.
- The role includes QEHS and shop-floor safety responsibilities.
- 21 CFR Part 111 requirements for food/dietary supplement export activities are mentioned.
- The vacancy does not specify salary, qualification or years of experience.
- The stated application deadline is October 3, 2026.
- Job requisition ID: R00004091.
Frequently Asked Questions
1. What position is Piramal Pharma Solutions hiring for?
The company is hiring for Executive – Quality Assurance.
2. Where is the job located?
The position is based in Mahad, Maharashtra.
3. What type of role is this?
It is a full-time Quality Assurance/IPQA role associated with pharmaceutical manufacturing operations.
4. What are the major responsibilities?
The role includes line clearance, in-process checks, production-document review, BMR verification, sampling, environmental monitoring, deviation monitoring, CAPA, data integrity and QEHS activities.
5. Does the role involve IPQA?
Yes. The job description specifically identifies the responsibilities as Executive (IPQA) activities.
6. Does the position involve Batch Manufacturing Records?
Yes. Verification and review of online Batch Manufacturing Records are part of the responsibilities.
7. Does the role involve validation activities?
Yes. The position includes sampling of process, packaging and cleaning validation samples, as well as rinse and swab samples.
8. Does the role involve CAPA?
Yes. The position includes monitoring process deviations and supporting effective CAPA implementation.
9. Is data integrity part of the job?
Yes. The role requires preventing data-integrity breaches and maintaining the quality and integrity of GxP data and documentation.
10. Is there a specific qualification requirement?
A specific educational qualification is not stated in the provided vacancy information.
11. Is prior experience required?
The vacancy does not specify a particular number of years of experience.
12. What is the salary for this position?
The salary or CTC has not been disclosed in the provided job information.
13. What is the application deadline?
The stated application deadline is October 3, 2026.
14. What is the job requisition number?
The requisition ID is R00004091.
Important Note
Job availability, qualification requirements, experience criteria, application deadlines and employment conditions may change. Candidates should verify the latest information on the official Piramal Pharma Solutions careers portal before submitting their application.
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