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MSN Labs Hiring B.Pharm, M.Pharm, MSc in Regulatory Affairs

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Job Title: Regulatory Affairs Vacancies – Pharma Formulation

Location: R&D Center, Pashamylaram, Hyderabad

Company: MSN Laboratories Pvt Ltd
Job Type: Full-time


About MSN Laboratories

MSN Laboratories is a global leader in the pharmaceutical industry, known for its innovative approaches and commitment to quality. Specializing in the formulation of pharmaceutical products, MSN Labs has consistently pushed the boundaries in drug development, delivering cutting-edge solutions to meet global health challenges.

We are hiring professionals with expertise in Regulatory Affairs to join our R&D Center located in Hyderabad. This role provides the opportunity to be a part of MSN Labs’ mission to ensure regulatory compliance and contribute to life-cycle management of pharmaceutical formulations.


Position Overview

MSN Labs is seeking qualified candidates for multiple roles in Regulatory Affairs – Pharma Formulation. These positions are crucial for overseeing product filings, handling regulatory submissions, and managing the documentation process. If you have experience in regulatory processes and product lifecycle management, we encourage you to apply.

Available Job Positions:

  • Executive
  • Senior Executive
  • Manager
  • Assistant Manager

Key Responsibilities

  • Product Filings & Registrations:
    Handle the preparation and submission of dossiers for international product filings, ensuring all documentation complies with regulatory standards like ICH guidelines.
  • Life-cycle Management:
    Oversee the complete life-cycle management of pharmaceutical products, from development to post-market surveillance.
  • Documentation & Dossier Preparation:
    Prepare, review, and update dossiers for product renewals and variation applications, ensuring compliance with CTO and ACTD requirements.
  • Query Resolution:
    Act as the point of contact for regulatory agencies, responding to queries and providing necessary information.
  • Regulatory Compliance:
    Ensure all products meet international regulatory requirements and adhere to applicable standards.

Qualifications Required

Candidates applying for these positions must possess the following qualifications:

QualificationRequirement
EducationB.Pharm, M.Pharm, or M.Sc in a relevant field
Experience3 to 10 years of experience in the formulation industry, with specific knowledge of regulatory affairs processes

Skills & Expertise

  • In-depth knowledge of ICH guidelines and international regulatory requirements.
  • Experience in dossier preparation and life-cycle management of pharmaceutical products.
  • Proficiency in handling documentation for renewals, variation applications, and regulatory queries.
  • Strong communication and organizational skills.

Salary and Benefits

  • Salary: Not disclosed (based on experience and qualifications)
  • Location: R&D Center, Pashamylaram, Hyderabad
  • Job Type: Full-time

Walk-In Interview Details

Venue: R&D Center, MSN Laboratories Pvt Ltd, Pashamylaram, Hyderabad
Date: 13th September 2024 (Friday)
Time: 09:00 AM onwards

Important: Please bring the following documents:

  • Photocopy of educational certificates
  • Latest increment letter
  • Last three months’ pay slips
  • Last six months’ bank statements
  • Passport-sized photographs
  • Aadhar card copy

How to Apply

Interested candidates can directly attend the walk-in interview at our R&D Center in Hyderabad. For further details, you can reach out to Narasimha Raju at narasimharaju.manthena@marlabs.com. Additionally, scan the QR code provided in the official posting for precise location details.


About Regulatory Affairs in Pharma

Regulatory Affairs professionals play a critical role in the pharmaceutical industry by ensuring that products comply with all legal and regulatory standards. They work to navigate the complex regulatory landscape, ensuring that drugs and medical products meet the safety and efficacy standards of the countries in which they are marketed.


Why Join MSN Laboratories?

  • Opportunity to work in a cutting-edge research and development environment.
  • Engage with a dynamic team of experts in regulatory affairs and pharmaceutical formulation.
  • Contribute to the global health sector by ensuring the safety and compliance of new medical products.

This posting provides all the necessary details regarding the role, qualifications, and interview process. We look forward to seeing qualified professionals join our team at MSN Labs.

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