MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA.
The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following:
- More than 900+ national and international patents
- Product portfolio featuring over 450 + APIs
- 300+ Formulations, covering over 35 major therapies
- Won the trust of more than 40 Million patients across 80+ countries globally
Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.
DATE AND TIME:
- Date: 13th May 2025 (Tuesday)
- Time: 9:00 AM – 3:00 PM (Arrive early; official window: 9:00 AM – 1:00 PM)
- Venue:
MSN Laboratories Pvt Ltd., R&D Center
Pashamylaram, Isnapur, Patancheru,
Sangareddy District
Contact: 040-30438786
JOB DESCRIPTION:
- Position: Executive / Senior Executive – FDQA (Formulation Development Quality Assurance)
- Experience Required: 2 to 7 years
- Qualification: B.Pharma / M.Pharma
- Industry: Pharmaceutical & Life Sciences
- Employment Type: Full Time, Permanent
Responsibilities
- Manage issuance and review of Batch Manufacturing Records and analytical raw data.
- Maintain and archive bio-batch documentation and raw data.
- Control, distribute, retrieve, and archive GMP documentation.
- Review SOPs, equipment qualification, calibration, supplier qualification, and analytical validation documents.
- Handle change controls, incidents, and out-of-specification (OOS) reports.
- Support licensing applications and departmental schedule preparation.
- Serve as document control lead and QA approver in the absence of Head FDQA.
SKILLS:
- Background in pharmaceutical quality assurance with hands-on experience in development QA.
- Familiar with GMP documentation, eDMS, and technology transfer processes.
- Strong organizational and documentation skills.
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