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;27 June – 5th July
TIME: 10.00 AM – 4.00 PM
VENUE:Sy No- 317& 323, Rudraram (Village ), Patancheru (Mandal Sangareddy(District, Telangana 502329 (View on map)
JOB DETAILS:
- Department: Senior Executive/Junior Manager – Validation -API
- Qualification : B.Pharma in Any Specialization, B.Sc in Chemistry/M.Pharma in Pharmacy, MS/M.Sc(Science) in Bio-Chemistry, Chemistry
- Experience: 5-10 Years
- Openings: 30
Desired Candidate Profile:
- Hands-on experience in analytical techniques (HPLC/GC) is a must.
- Good knowledge of regulatory guidelines (ICH, WHO, USFDA, etc.)
- Strong documentation and communication skills.
- Experience in a regulated API manufacturing unit is preferred.
Responsibilities:
- Perform analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) as per approved specifications and SOPs.
- Operate and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc.
- Review and verify analytical data and ensure proper documentation in line with cGMP and GLP guidelines.
- Prepare and standardize volumetric solutions and reagents.
- Carry out stability studies and maintain stability data as per ICH guidelines.
- Ensure timely calibration of laboratory instruments.
- Perform method validation/transfer activities as per regulatory and internal requirements.
- Involve in investigations related to OOS/OOT/Deviations and CAPA implementation.
- Coordinate with cross-functional departments like QA, Production, and R&D for smooth workflow.
- Comply with all safety protocols and maintain a clean and organized lab environment.
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