sun pharma regulatory affairs job vacancies

Sun Pharma Regulatory Affairs Job Vacancies: Shaping the Future of Pharmaceuticals

Sun Pharma, a pioneering pharmaceutical company dedicated to innovation, quality, and excellence. With a commitment to shaping the future of healthcare, Sun Pharma is at the forefront of research and development in the pharmaceutical industry. Renowned for its USFDA, EU-GMP, and COFEPRIS approvals, Sun Pharma continues to be a trusted name in Active Pharmaceutical Ingredients (APIs), Mineral Actives, and Premixes.

Company Vacancies List

• Company Name: Sun Pharmaceutical Industries Ltd
• Company Address: Sun Pharma Road, Tandalja, Baroda – 390016

Position Title: Executive – Regulatory Affairs API

• Qualification: MSc-Chemistry
• Experience: 2-4 Years
• Role Category: Regulatory Affairs API

Position Title: Executive/Sr. Executive – Regulatory Affairs Formulation – US

• Qualification: M.Pharm
• Experience: 3-6 Years
• Role Category: Regulatory Affairs Formulation – US

Position Title: Sr. Officer/Executive – Regulatory Affairs Formulation – US (Labeling)

• Qualification: BSc/B.Pharm/M.Pharm
• Experience: 1-6 Years
• Role Category: Regulatory Affairs Formulation – US (Labeling)

Position Title: Sr. Officer/Executive – Regulatory Affairs Formulation – US (eCTD)

• Qualification: BSc/B.Pharm
• Experience: 1-6 Years
• Role Category: Regulatory Affairs Formulation – US (eCTD)

Detailed Job Description

Role: Regulatory Affairs API

As an Executive in Regulatory Affairs API, you will be responsible for:

• Compilation and review of registration dossiers for API Plant or corporate.
• Preparation of dossiers in eCTD format for ANDA, EU-MA application.
• Dossier applications for various health authorities.
• Life cycle management of ANDA, EU-Application, and emerging markets.

Role: Regulatory Affairs Formulation – US

As an Executive/Sr. Executive in Regulatory Affairs Formulation – US, your responsibilities will include:

• Reviewing data and documents related to product registrations for various health authorities.
• Compiling registration dossiers for submission to health authorities like US-FDA, Health Canada, Europe, Australia/New Zealand, Japan, and Israel.
• Preparing responses to deficiency letters and maintaining life-cycle changes for drug product registration dossiers.

Role: Regulatory Affairs Formulation – US (Labeling)

As a Sr. Officer/Executive in Regulatory Affairs Formulation – US (Labeling), you will be involved in:

• Labeling development for original applications (NDA/ANDA) based on RLD labeling and current FDA guidance.
• Responding to labeling queries and patent amendments.
• Tracking RLD labeling changes and initiating labeling revision activities.

Role: Regulatory Affairs Formulation – US (eCTD)

As a Sr. Officer/Executive in Regulatory Affairs Formulation – US (eCTD), your duties will include:

• Regulatory submission/publishing activities for eCTD global submission dossiers.
• Electronic document publishing, including PDF file preparation and compilation/publishing in software.

How to Apply

Interested candidates are invited to attend the walk-in drive at Sun Pharmaceutical Industries Ltd, Sun Pharma Road, Tandalja, Baroda, on Sunday, 3rd December 2023, from 9:30 am to 1:00 pm. Please bring an updated resume, last degree, PAN card, Aadhar card, and current CTC proof to the venue.