Are you a Regulatory Affairs professional eager to advance your career in the pharmaceutical industry? July 2025 has presented several exciting job openings at top pharmaceutical and biopharma companies in India.
Whether you prefer remote work or are interested in positions in industry hubs like Navi Mumbai or Ahmedabad, here are three valuable opportunities in the dynamic field of regulatory affairs that are worth applying for.
1. Regulatory Associate (EU Market) – Syneos Health (Remote)
Location: India (Remote)
Company: Syneos Health
About the Role:
Syneos Health is seeking a Regulatory Associate (EU Market) to support global CMC dossier submissions and lifecycle regulatory documentation. This work-from-home opportunity is ideal for individuals with one or more years of experience in Regulatory Affairs and a keen interest in international markets.
Key Responsibilities
- Prepare and review CMC dossiers, variation applications, post-approval changes.
- Assist in compiling components for INDs, NDAs/MAAs, DMFs, renewals, and MATs.
- Conduct regulatory research to support submission and development activities.
- Perform quality checks on documents and assist with other regulatory submissions.
- Compile reports, coordinate with cross-functional teams, and maintain data integrity.
Key Requirements:
- M.Pharm (preferred) or MSc in Science or Healthcare
- 1+ year experience in Global Regulatory Affairs (CMC focus)
- Strong knowledge of regulatory systems across the EU, the US, LATAM, and APAC
- Hands-on dossier preparation, post-approval changes, and IND/NDA submissions
- Excellent communication and technical writing skills
2. Regulatory Affairs Associate I – Teva Pharmaceuticals, Navi Mumbai
Location: Navi Mumbai, Maharashtra
Company: Teva Pharmaceuticals
About the Role:
Teva Pharmaceuticals, a global leader in generic and specialty medicines, is hiring for a Regulatory Affairs Associate I at their Navi Mumbai location. This role focuses on post-approval regulatory activities in the European region, helping maintain Marketing Authorization (MA) compliance across EU markets.
Key Requirements:
- Master’s in Pharmacy or Life Sciences
- 2–3 years of experience in post-approval Regulatory Affairs
- Familiarity with EU submission processes and document management
- Proficient in electronic databases, dossier tracking, and stakeholder coordination
- Ability to handle multiple procedures and meet regulatory timelines
3. Associate – Regulatory Affairs (Document Publishing) – Amneal Pharma, Ahmedabad
Location: Ahmedabad, Gujarat
Company: Amneal Pharmaceuticals
About the Role:
Amneal Pharmaceuticals is hiring for the role of Associate – Regulatory Affairs with a focus on Document Level Publishing (DLP). This role is integral to the preparation of high-quality electronic submission documents for regulatory authorities, ensuring compliance, accuracy, and timely delivery.
Key Requirements:
- Strong understanding of PDF publishing tools, especially ISI Toolbox
- Hands-on experience in eCTD submission preparation
- Expertise in bookmarking, TOC generation, hyperlinking, and PDF quality control
- Detail-oriented mindset and ability to meet regulatory timelines
- Collaborative approach to working in global regulatory publishing teams
Quick Comparison Table
| Company | Role | Location | Key Experience Required |
|---|---|---|---|
| Syneos Health | Regulatory Associate (EU Market) | Remote (India) | ≥1 yr Global RA, CMC dossier |
| Teva Pharma | Regulatory Affairs Associate I | Navi Mumbai | 2–3 yrs EU post-approval RA |
| Amneal Pharma | RA Associate – Document Publishing Specialist | Ahmedabad | PDF tools, ISI Toolbox, eCTD |
Final Thoughts
Each of these roles provides distinct advantages. For instance, Syneos Health offers flexible remote work, while Teva provides structured post-approval regulatory affairs experience. Meanwhile, Amneal focuses on technical document publishing. Whether you’re a recent graduate with internship experience or an established regulatory professional seeking your next significant opportunity, these private sector positions available in July 2025 present excellent chances for growth in the pharmaceutical industry.
Also Read: Process Validation in Pharma: Lifecycle, GMP Guidelines, 2025 Trends & Mistakes to Avoid
Found this post helpful?
Share it with your friends & colleagues.
Follow us on WhatsApp & Telegram for job updates, interview tips, and study material:
Subscribe to PharmaSpectacle to stay ahead in the pharmaceutical world with valuable pharma knowledge and professional growth tips.
Published by PharmaSpectacle – Your trusted lens into pharmaceutical careers and compliance.
