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RPG Life Sciences Limited, a leading pharmaceutical company, is conducting a walk-in interview for talented professionals to join our Quality Control Department at our manufacturing facility in Ankleshwar, Gujarat. This is a prime opportunity for candidates with expertise in pharmaceutical quality control to contribute to a dynamic team in a reputed organization.
Event Details
- Date: Sunday, June 1, 2025
- Time: 09:00 AM to 04:00 PM
- Venue:
RPG Life Sciences Ltd
Plot No. 3102/A, GIDC, Ankleshwar, Gujarat
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Open Positions and Requirements
We are seeking skilled professionals for the Quality Control Department with experience in Oral Solid Dosage (OSD) formulation or API plant operations. Below is a detailed breakdown of the roles, qualifications, experience, and desired skills:
| Sr. No | Department | Designation | Qualification | Experience | Vacant Positions | Desired Profile |
|---|---|---|---|---|---|---|
| 1 | Quality Control (Analyst) | Executive | B.Sc. / M.Sc. | 2–7 Years | 10 | Experience in analysis of Raw Material (RM), Finished Products, In-Process, and Stability samples using instruments like HPLC, UV, Dissolution Apparatus, GC, IR, and AAS. |
| 2 | Quality Control (Reviewer) | Sr. Executive / Assistant Manager | B.Sc. / M.Sc. | 8–12 Years | 2 | Expertise in reviewing GMP documents such as analytical worksheets for stability, RM, In-Process, and Finished Products. |
Key Requirements
- Candidates must have exposure to regulatory audits (e.g., USFDA, MHRA).
- Experience in OSD formulation or API plant is mandatory.
- Familiarity with Good Manufacturing Practices (GMP) and quality control processes.
Key Responsibilities
- Analyst (Executive):
- Conduct analysis of RM, Finished Products, In-Process, and Stability samples.
- Operate and maintain analytical instruments like HPLC, UV, Dissolution Apparatus, GC, IR, and AAS.
- Ensure compliance with regulatory standards and GMP guidelines.
- Reviewer (Sr. Executive/Assistant Manager):
- Review GMP documents including analytical worksheets for stability, RM, In-Process, and Finished Products.
- Ensure accuracy and compliance with regulatory audit requirements.
- Support quality control processes in OSD formulation or API plant settings.
Mandatory Documents to Bring
To facilitate a smooth interview process, please bring the following documents:
- Updated resume
- Salary breakup or last 3 months’ salary slips
- Passport-size photograph
- Copy of Aadhar card (mandatory)
How to Apply
- In-Person: Attend the walk-in interview at the specified venue with all required documents.
- Outstation Candidates: Email your resume to hr1ankleshwar@rpgls.com.
Why Join RPG Life Sciences?
- Industry Leader: Be part of a trusted name in the pharmaceutical industry with a focus on OSD formulations and APIs.
- Career Growth: Opportunities to work on regulatory-compliant projects and enhance your expertise in quality control.
- Collaborative Environment: Join a team dedicated to innovation, quality, and excellence in pharmaceutical manufacturing.
About RPG Life Sciences Ltd
Established as a pioneer in the pharmaceutical sector, RPG Life Sciences specializes in API manufacturing and formulation development, delivering high-quality products globally. With a commitment to innovation and regulatory compliance, we strive to make a positive impact on healthcare.