Piramal Pharma Solutions is hiring an Executive – Quality Assurance for its manufacturing facility in Turbhe, Maharashtra. This is a full-time, onsite opportunity for candidates with a background in Chemistry or Pharmacy and 1–3 years of relevant experience in pharmaceutical quality assurance.
The selected candidate will be responsible for supporting cGMP compliance, quality documentation, validation activities, batch documentation review, and other quality management system activities within the manufacturing environment.
Executive – Quality Assurance Job Details
| Particular | Details |
|---|---|
| Company | Piramal Pharma Solutions |
| Job Title | Executive – Quality Assurance |
| Location | Turbhe, Maharashtra |
| Job Type | Full Time |
| Work Mode | Onsite |
| Experience | 1–3 Years |
| Qualification | M.Sc Chemistry / B.Pharm / M.Pharm |
| Division | Piramal Pharma Solutions |
| Job Requisition ID | R00004310 |
| Last Date | Not specified by the company |
Roles and Responsibilities
The Executive – Quality Assurance will support quality and compliance activities across manufacturing and related functions. Key responsibilities include:
- Reviewing executed BMR, ECR and analytical raw data.
- Reviewing BMR, ECR and MMF documents in Ensur software.
- Preparing process validation protocols and reports.
- Monitoring process validation activities.
- Performing dispatch and line clearance activities.
- Preparing and reviewing SOPs.
- Preparing Annual Product Reviews (APR).
- Handling cleaning validation activities.
- Reviewing analytical data and audit trails.
- Supporting batch release activities.
- Initiating deviations and change controls whenever required.
- Issuing, archiving and retrieving documents for R&D and ADL.
- Managing quality-related activities within R&D and ADL.
- Reviewing and approving R&D and ADL documentation.
Required Qualifications
Candidates should have one of the following educational qualifications:
- M.Sc in Chemistry
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
The position requires 1–3 years of experience in a relevant pharmaceutical quality assurance environment.
Required Skills
Candidates should have good knowledge of:
- cGMP and GDP requirements
- Pharmaceutical quality systems
- BMR, ECR, MMF and analytical data review
- Quality Control analytical documentation
- Data integrity requirements
- Annual Product Review (APR/PQR)
- Documentation and quality management processes
Experience with validation, deviations, change controls, batch release and pharmaceutical documentation will be relevant to this position.
Salary and Benefits
Piramal Pharma Solutions has not specified the salary package or detailed benefits for this vacancy in the provided job posting. Compensation is expected to depend on the candidate’s qualifications, relevant experience and company policies.
Candidates should refer to the official recruitment page for any compensation or benefits information provided during the application process.
About Piramal Pharma Solutions
Piramal Pharma Solutions (PPS) is a contract development and manufacturing organization (CDMO) providing development and manufacturing services across the drug life cycle. Its capabilities include drug discovery solutions, process and pharmaceutical development, clinical trial supplies, commercial supply of APIs and finished dosage forms, and 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.