Piramal Pharma is inviting applications for the role of Trainee – Quality Assurance at Turbhe, MH. This opportunity is suitable for freshers with B.Sc or M.Sc qualifications who want to begin their career in pharmaceutical quality assurance, GMP documentation, validation support and quality systems.
Job Details
| Company | Piramal Pharma |
| Division | Piramal Pharma Solutions |
| Position | Trainee – Quality Assurance |
| Department | Quality Assurance |
| Location | Turbhe,MH |
| Employment Type | Full time |
| Reporting To | Quality Assurance Manager |
Job Description
As a Quality Assurance Trainee, the selected candidate will support Quality Assurance activities related to document control, SOP management, qualification and validation support, and compliance monitoring in line with GMP and regulatory requirements.
The role involves issuance, archival and tracking of QA documents, coordination of equipment qualification and area validation activities, review of calibration and preventive maintenance schedules, preparation of validation-related documents, and support in vendor qualifications, external service providers, deviations, change controls and related QA processes.
Key Responsibilities
- Support Quality Assurance activities related to document control, SOP management, qualification and validation support.
- Assist in compliance monitoring as per GMP and regulatory requirements.
- Handle issuance, archival, retrieval and tracking of QA documents.
- Issue control copies to the respective departments.
- Maintain backup of QA soft copies and organize QA documents and records.
- Maintain SOPs with proper indexing and support preparation and review of SOPs.
- Perform qualifications for new equipment and existing equipment.
- Coordinate area validation activities.
- Review calibration and preventive maintenance schedules.
- Prepare VMP and validation documents.
- Support vendor qualification activities.
- Handle contract testing laboratory and external service provider related activities.
- Support handling of deviations, change controls, OOS, OOT, CAPA, compliants, return goods, risk assessment and product recall as part of QMS related activities.
- Coordinate with internal stakeholders including Production (Synthesis + Pharma) Team, Quality Assurance Team, Quality Control Team and Engineering Department as per the requirement of the allocated task.
- Coordinate with auditors, suppliers and customers as per the requirement of the allocated task.
Qualification
- M.Sc.
- B.Sc.
Experience
Experience is not required. Freshers can apply.
Skills and Competencies
- Basic understanding of GMP, documentation and quality systems.
- Strong attention to detail and compliance orientation.
- Good coordination and communication skills.
- Ability to manage and organize QA documents and records.
- Willingness to learn and adapt in a regulated pharmaceutical environment.
How to Apply
Interested candidates can apply online through the official Piramal Pharma careers application link given below.
