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Mediwin Pharma Hiring Freshers in Regulatory Affairs

Published on

B Pharm, M Pharm

Ahmedabad

0 - 2 Years

Verified Job

Online Application

Are you a fresh graduate or an early-career professional with a passion for Regulatory Affairs in the pharmaceutical industry? Pharmabharat.com is excited to announce an opening for a Junior Regulatory Affairs Executive at a leading Pharmaceutical Formulation Company. If you have a B.Pharm or M.Pharm degree and 0-2 years of experience, this is your chance to kickstart your career in a dynamic and rewarding environment!


About the Company

At Mediwin Pharma, we are dedicated to connecting talented professionals with top-tier pharmaceutical companies. Our partner company is a well-established player in the pharmaceutical formulation sector, known for its commitment to quality, innovation, and compliance with global regulatory standards. Join a team that values growth, collaboration, and excellence in regulatory affairs.

Job Description

As a Junior Regulatory Affairs Executive, you will play a crucial role in ensuring the company’s compliance with regulatory guidelines. You will work closely with senior regulatory affairs professionals to prepare, review, and submit regulatory documents. This is an excellent opportunity to gain hands-on experience in CTD/ECTD dossier preparation and contribute to the company’s success in global markets.

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Key Responsibilities:

  • Prepare and assemble CTD/ECTD dossier documents as per the current guidelines of specific countries.
  • Support senior RA professionals in preparing and reviewing regulatory documents.
  • Provide regular updates and reports to senior RA team members.
  • Execute other regulatory affairs-related tasks as assigned.
  • Ensure compliance with cGMP, GLP, ICH, and USFDA guidelines.

Requirements

Qualifications:

  • B.Pharm or M.Pharm degree from a recognized institution.

Experience:

  • 0-2 years of experience in regulatory affairs within a pharmaceutical formulation company.

Required Skills:

  • Basic knowledge of CTD/ECTD dossier preparation.
  • Familiarity with cGMP, GLP, ICH, and USFDA guidelines.
  • Proficiency in Microsoft Word, Excel, and PowerPoint.
  • Strong verbal and written communication skills in English and Hindi.
  • Good interpersonal skills and a team-oriented mindset.

Why Join Us?

  • Gain hands-on experience in regulatory affairs and dossier preparation.
  • Work in a supportive and collaborative environment.
  • Opportunity to grow your career in the pharmaceutical industry.
  • Be part of a company that values innovation and compliance.

How to Apply

Application Link

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