QC / QA Pharma Jobs – Piramal Pharma Limited is conducting a walk-in interview for experienced professionals in Quality Control (FG/Stability/RM, LIMS, Lab QA) and Quality Assurance (IPQA/Process Validation/CSV) at its Pithampur, Indore plant.
This is a prime opportunity for candidates with LCMS, HPLC, GC, Dissolution, LIMS, audit trail, process validation, and CSV experience in regulated OSD/formulation environments to join a globally respected pharmaceutical organization.
Contents
About the Company
Piramal Pharma Limited is a prominent global pharmaceutical company with a strong footprint in complex hospital generics, injectables, APIs, and CDMO services.
Part of the Piramal Group, it operates state-of-the-art manufacturing facilities across India, including the Pithampur (Indore) plant in Madhya Pradesh, specializing in high-quality formulations with stringent regulatory compliance (USFDA, EU-GMP, MHRA, WHO).
The company focuses on innovation, operational excellence, patient safety, and employee development while serving markets worldwide through reliable, high-standard pharmaceutical products.
Job Details
- Company Name: Piramal Pharma Limited
- Location: Pithampur Plant, Indore, Madhya Pradesh, India
- Work Type: On-site
Job Description
Piramal Pharma Limited is hiring for key QC and QA roles to support analytical testing, data integrity, system management, and in-process quality assurance in a regulated OSD/formulation setup.
QC Executive – FG / Stability / RM
- Department: Quality Control
- Experience: Minimum 3 Years
- Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)
- Relevant Experience:
- Analysis of Finished Goods (FG), Raw Materials (RM), and Stability samples
- Hands-on with QC instruments: LCMS, HPLC, GC, Dissolution, Malvern 3000, etc.
- Exposure to LIMS preferred
QC – Deputy Manager – LIMS
- Department: Quality Control – LIMS
- Experience: Minimum 2 Years on LIMS
- Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)
- Relevant Experience:
- LIMS implementation, master data creation, and review
- Strong knowledge of LIMS workflows and data integrity
QA Executive – IPQA / Process Validation / CSV
- Department: Quality Assurance
- Experience: Minimum 3 Years in OSD unit
- Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)
- Job Profile:
- In-Process QA (IPQA) activities
- Process Validation and Technology Transfer
- Computer System Validation (CSV) activities
QC – Deputy Manager – Lab QA
- Department: Quality Control – Lab QA
- Experience: Minimum 5 Years
- Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)
- Relevant Experience:
- Analytical data review and audit trail of QC instruments
- Lab investigations (OOS, OOT, deviations)
Skills/Qualifications
- Experience in regulated pharmaceutical environment (OSD/formulation preferred)
- Proficiency in analytical instruments (HPLC, GC, LCMS, Dissolution) and data integrity tools
- Knowledge of GMP, GLP, ICH guidelines, and quality systems
- Strong documentation, investigation, and compliance skills
- Shift readiness for QC roles
Key Responsibilities
- Conduct analytical testing of RM, FG, and stability samples using advanced instruments
- Manage LIMS implementation, master data, and system review
- Perform IPQA checks, process validation, technology transfer, and CSV
- Review analytical data, audit trails, and handle lab investigations
- Ensure compliance with regulatory standards and maintain data integrity
How to Apply
Walk-in Interview – Bring photocopies of last three months’ salary slips, increment letter, updated resume, educational certificates, and experience documents.
- Date: 22nd March 2026 (Sunday)
- Time: 9:00 AM – 3:00 PM
- Venue: Sayaji Hotel, H/1, Near Meghdoot Garden, Scheme No. 54, Vijay Nagar, Indore – 452010, Madhya Pradesh
- Contact: Ashish Singh – 9644700970 / 9149695594
For more pharma jobs, QC/QA opportunities, and walk-ins in Madhya Pradesh, visit Pharma Recruiter.
Attend the walk-in and take the next step in your career with Piramal Pharma Limited!
Why You Should Join
Piramal Pharma Limited provides a world-class environment in a globally compliant facility with exposure to advanced analytical and quality systems.
Benefit from professional growth, cutting-edge instrumentation, regulatory excellence, and stability in a reputed organization committed to quality and innovation—perfect for QC/QA professionals seeking impactful roles in the pharmaceutical industry.
FAQs
What experience is required for QC Executive – FG/Stability/RM?
Minimum 3 years with hands-on experience in FG/RM/Stability analysis using LCMS, HPLC, GC, Dissolution, etc.; LIMS exposure preferred.
Which role requires OSD-specific experience?
QA Executive (IPQA/Process Validation/CSV) requires minimum 3 years in OSD unit.
What documents should I carry to the walk-in?
Photocopies of last three months’ salary slips, increment letter, resume, educational certificates, and experience documents.
Where is the walk-in venue?
Sayaji Hotel, Vijay Nagar, Indore, Madhya Pradesh – candidates should arrive between 9 AM and 3 PM on 22nd March 2026.
