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PHARMA JOBS POST > Formulations > Join MSN Labs: Walk-In Interview for Formulation Regulatory Affairs – April 26
FormulationsRegulatory Affairs

Join MSN Labs: Walk-In Interview for Formulation Regulatory Affairs – April 26

ARPITA
Last updated: April 18, 2025 2:49 pm
ARPITA 2 months ago 204 Views
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MSN Laboratories Pvt. Ltd. is one of India’s fastest-growing research-based pharmaceutical companies, established in 2003. With a strong presence in over 65 countries, MSN is committed to delivering affordable and high-quality medicines across the globe. The company operates in major segments such as APIs (Active Pharmaceutical Ingredients), formulations, and contract manufacturing.

Contents
Requirement Details :Work location :Interview location:Job Description:

WALK-IN a Bengaluru
Saturday @ 26-04-2025 9:00 AM To 4:00 PM

Requirement Details :

Department: Formulation
Regulatory Affairs-Department

Qualitication:M Sc | B pharmacy I M Pharmacy

Designation: Executive To Senior Manager

Experience: 1 to 15 Years

Work location :

Work Location:- MSN Laboratories Pvt Ltd, R&D Center, Hyderabad

Interview location:

Interview Location:
BloomSuites | Electronic City, 56/A, Opp. Wipro Gate No. 5, Electronic City Phase – 1, Hosur Road, Bengaluru, 560100.

REACH US:
Y Umadevi,9154704771
B V V Narasimha Raju,9100376029
narasimharaju.manthena@msnlabs.com


Please Note :
Candidates Are Requested to Bring Resume, Photo Copy of Educational Certificates, Latest Increment Letter, Last Three Months Pay Slips, Last Six Months Bank Statements,
Passport size photograph, Adhar card copy

Job Description:

JOB DESCRIPTION:
• International Product filing Registrations and life-cycle management
Expertise in Regulatory Norms for regulated markets / emerging market. dossiers, renewal & variation applications for various markets based on CTD, ACTD and/or other region-specific requirements.
Respond to queries raised by regulatory agencies and/or local partners of the above regions.
Review and give regulatory feedback on technical documents like process validation, AMV, Stability and composition, labeling, batch records, specification or test methods, etc. Ensure accuracy and compliance of documentation.

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DEFINE ACADEMY DRUG REGULATORY AFFAIRSDEFINE ACADEMY DRUG REGULATORY AFFAIRS
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