February 28, 2026

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group.

Piramal Pharma Limited is a part of the Piramal Group, a global business conglomerate with diverse interests in pharma, financial services, and real estate. The Group has offices in over 30 countries and a global brand presence in more than 100 markets, and operates with over 10,000 people worldwide from 21 diverse nationalities.

DATE AND TIME:

Date: 28th February (Saturday)
Time: 9:00 AM – 2:00 PM

Venue: Plot 67 & 70, Pithampur Industrial Area, Sector II,
Pithampur, Madhya Pradesh – 454775


Contact Person: Ashish Singh – 9644700970

Job Details

1. QC Executive – FG / Stability / RM

Total Experience : Minimum 3 Years
Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)

 Responsibilities:

  • Analysis of Finished Goods (FG), Raw Materials (RM), and Stability samples
  • Handling QC instruments such as:
    • LCMS
    • HPLC
    • GC
    • Dissolution
    • Malvern 3000
  • Documentation as per GMP guidelines
  • Exposure to LIMS preferred

2.QC Executive / Dy. Manager – Lab QA

Total Experience : Minimum 5 Years
Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)

 Job Responsibilities:

  • Analytical data review
  • Audit trail review of QC instruments
  • Handling laboratory investigations
  • Ensuring compliance with regulatory requirements
  • GMP documentation and QA procedures

3. QC – Dy. Manager (LIMS)

Total Experience Required: Minimum 2 Years in LIMS
Qualification: B.Pharm / M.Pharm / M.Sc (Chemistry)

 Responsibilities:

  • LIMS implementation
  • Master data creation
  • LIMS data review
  • Ensuring proper electronic documentation and compliance

 Documents

  • Updated Resume
  • Photocopies of last 3 months salary slips
  • Increment letter

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