Novumgen Hiring Regulatory Affairs Executive
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Novumgen?
- FAQs – Novumgen Regulatory Affairs Executive
- Summary Table
Regulatory Affairs Executive – B.Pharm/M.Pharm – Ahmedabad
Apply for Regulatory Affairs Executive at Novumgen, Ahmedabad. B.Pharm/M.Pharm with 2+ years of experience in UK/EU submissions.
Novumgen, a rapidly expanding global pharmaceutical company, is inviting skilled professionals to join its Regulatory & Scientific Affairs team in Ahmedabad. This is an excellent opportunity for candidates passionate about global regulatory operations, documentation excellence, and compliance with international guidelines. If you have the experience and drive to support submissions for UK and EU markets, Novumgen offers a dynamic and collaborative environment to grow your career.
Company Overview
Novumgen is a multinational pharmaceutical company focused on developing, manufacturing, and marketing high-quality healthcare products that improve patients’ lives across the world. With operations across multiple regions, including the UK and EU, Novumgen has established itself as a trusted name in global regulatory excellence, quality assurance, and innovative product development.
The company’s Regulatory Affairs division plays a vital role in ensuring that all medicinal products comply with stringent international quality and safety standards, positioning Novumgen as a leader in pharmaceutical compliance and research-driven innovation.
Job Role & Responsibilities
As an Executive – Regulatory & Scientific Affairs, you will contribute to the preparation and management of regulatory submissions for UK and EU regions. The role requires meticulous attention to detail, strong communication skills, and proficiency in regulatory documentation.
Key Responsibilities:
- Coordinate with cross-functional teams including Development, Clinical, Nonclinical, Pharmacovigilance, Quality, and Manufacturing to compile necessary data and justifications.
- Prepare, review, and finalize responses to UK/EU regulatory authority queries for Marketing Authorization Applications (MAAs).
- Ensure regulatory compliance with MHRA, EU, and ICH guidelines.
- Maintain submission integrity through eCTD formatting, version control, and document referencing.
- Contribute to internal SOP development and quality system improvements for the Regulatory Affairs department.
Eligibility / Qualifications
- Education: B.Pharm or M.Pharm from a recognized university.
- Experience: Minimum 2 years of experience in Regulatory Affairs, preferably handling submissions for UK/EU markets.
- Skills Required:
- Strong understanding of global regulatory frameworks (MHRA, EMA, ICH)
- Proficiency in regulatory documentation tools and eCTD compilation
- Excellent written and verbal communication
- High attention to detail and ability to manage timelines effectively
Location & Salary
- Location: Ahmedabad, Gujarat
- Department: Regulatory & Scientific Affairs
- Employment Type: Full-Time
- Salary: Competitive and commensurate with experience; includes performance-based incentives.
Application Process
Interested candidates meeting the eligibility criteria can send their updated CVs to the email below:
isha.patel@novumgen.com
www.novumgen.com
Apply early to secure your opportunity with one of India’s most dynamic pharma innovators!
Why Join Novumgen?
- Work with global teams on regulatory submissions across UK and EU.
- Gain exposure to international pharmaceutical compliance and documentation standards.
- Grow your career in an organization that emphasizes innovation, research, and quality excellence.
- Be part of a company contributing to global healthcare improvement.
FAQs – Novumgen Regulatory Affairs Executive
1. What is the minimum experience required?
You need at least 2 years of experience in Regulatory Affairs, ideally managing UK/EU submissions.
2. What qualifications are required?
A degree in B.Pharm or M.Pharm is mandatory.
3. Where is the job location?
The role is based in Ahmedabad, Gujarat.
4. What kind of submissions will I handle?
You will work primarily on Marketing Authorization Applications (MAAs) and regulatory responses for UK/EU agencies.
5. How do I apply?
Email your resume to isha.patel@novumgen.com and mention “Application – Regulatory Affairs Executive” in the subject line.
Summary Table
| Category | Details |
|---|---|
| Company | Novumgen Pharmaceuticals |
| Vacancies | Executive – Regulatory & Scientific Affairs |
| Required Education | B.Pharm, M.Pharm |
| Experience | Minimum 2 years (UK/EU Regulatory Affairs) |
To apply for this job email your details to isha.patel@novumgen.com
