Location: Ahmedabad, Gujarat
Department: Analytical Development, Formulation Development, QA/QC
Qualification: M.Sc/ M.Pharm
Experience: 2–7 years
Job Description
Piramal Pharma Solutions, a global leader in pharmaceutical services, is hiring Senior Research Associates (SRAs) for multiple roles in Analytical Development (AD), Quality Assurance (QA), Quality Control (QC), and Formulation Development (FD).
1. Senior Research Associate – AD-QA
Key Responsibilities:
- Monitor and close Analytical Incidents, Deviations, and Change Controls per cGMP/regulatory norms.
- Review clinical batch data, method validation, and stability studies.
- Oversee instrument calibration (IQ/OQ/PQ, CSV) and lab logbook maintenance.
- Conduct internal audits, SOP preparation, and analyst training on GLP/GMP/GDP.
- Ensure data integrity and lab automation compliance.
2. Senior Research Associate – AD-QC
Key Responsibilities:
- Perform method validation/verification for clinical/stability samples.
- Maintain GLP/GDP standards and instrument calibration schedules.
- Prepare technical documents (COA, validation protocols, audit trails).
- Manage raw material testing and non-project lab activities.
3. Senior Research Associate – AD (Method Development)
Key Responsibilities:
- Develop analytical methods for tablets, capsules, and FDC formulations.
- Operate HPLC, UPLC, UV, Dissolution Testers, etc.
- Conduct stability testing and instrument calibration.
4. Senior Research Associate – Formulation Development (FD)
Key Responsibilities:
- Develop and optimize oral solid dosage forms (OSD) using QbD principles.
- Handle formulation equipment and prepare technology transfer documents.
- Ensure compliance with regulatory guidelines for NCE/Generic projects.
About Piramal Pharma Solutions
Piramal Pharma Solutions is a trusted CDMO (Contract Development & Manufacturing Organization) offering end-to-end drug development services. Known for innovation and compliance, Piramal serves global pharmaceutical clients with cutting-edge solutions in analytical and formulation development.
Eligibility Criteria
- Education: M.Sc (Chemistry/Pharmaceutics) or M.Pharm.
- Experience: 2–7 years in pharma R&D, QA/QC, or formulation.
- Skills:
- Hands-on experience with HPLC, UPLC, dissolution apparatus.
- Knowledge of cGMP, ICH guidelines, and data integrity.
- Strong documentation and audit trail management.
How to Apply
Interested candidates must email their CV to:
- Kinjal Pal: Kinjal.pal@piramal.com
- Prathamesh Shinde: Prathamesh.shinde2@Piramal.com
Subject Line:
- For AD-QA: “Vacancy – SRA – AD-QA Role”
- For AD-QC: “Vacancy – SRA – AD-QC Role”
- For AD-Method Development: “Vacancy – SRA – AD-Method Development Role”
- For FD: “Vacancy – SRA-FD Role”
OR
Apply via the Official Piramal Application Form.
