sun pharma regulatory affairs job vacancies
- Sun Pharma Regulatory Affairs Job Vacancies: Shaping the Future of Pharmaceuticals
- Company Vacancies List
- Position Title: Executive – Regulatory Affairs API
- Position Title: Executive/Sr. Executive – Regulatory Affairs Formulation – US
- Position Title: Sr. Officer/Executive – Regulatory Affairs Formulation – US (Labeling)
- Position Title: Sr. Officer/Executive – Regulatory Affairs Formulation – US (eCTD)
- Detailed Job Description
- Role: Regulatory Affairs API
- Role: Regulatory Affairs Formulation – US
- Role: Regulatory Affairs Formulation – US (Labeling)
- Role: Regulatory Affairs Formulation – US (eCTD)
- How to Apply
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: M.Sc-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: B.Sc/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: B.Sc/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.
To apply for this job please visit attend%20the%20walk-in%20drive.
