Freyr is currently hiring for two distinct roles in the regulatory domain, offering excellent opportunities for both fresh graduates and experienced professionals in pharma and life sciences. These include a Medical Device (SaMD) Regulatory Affairs Intern role and a Regulatory Data Governance Specialist position.
If you’re aiming to build a career in regulatory affairs, pharmacovigilance, or regulatory data management, these roles provide valuable exposure to global regulatory processes, tools, and compliance standards.
Role 1: Medical Device (SaMD) Regulatory Affairs Intern (Unpaid)
Overview
Freyr is seeking a regulatory student or recent graduate for an internship focused on regulatory marketing research and regulatory content writing in the medical device domain (SaMD).
Key Responsibilities
- Conduct regulatory marketing research in medical devices (SaMD)
- Assist in drafting regulatory content and documentation
- Support regulatory intelligence and compliance tracking
- Collaborate with internal regulatory teams
Qualifications
- Background in Pharmacy, Life Sciences, or related field
- Strong interest in medical device regulatory affairs
- Good writing and analytical skills
- Freshers and recent graduates preferred
Benefits
- Hands-on regulatory affairs experience
- Exposure to real-world regulatory projects
- Opportunity to work with an experienced regulatory team
- Networking and career-building opportunity
How to Apply
Interested candidates can apply by:
- Sending a message on LinkedIn
- Emailing: prashil.panchal@freyrsolutions.com
Note: Hiring window is open for 7 days. Early application is recommended.
Role 2: Regulatory Data Governance Specialist (3โ5 Years Experience)
Overview
Freyr is hiring experienced professionals for a Regulatory Data Governance role focusing on EudraVigilance database management and pharmacovigilance systems.
Key Responsibilities
- Manage and maintain EudraVigilance database with high data integrity
- Resolve adverse event reporting issues in pharmacovigilance systems
- Develop and maintain regulatory documentation and SOPs
- Train teams on tools like ServiceNow and JIRA
- Collaborate with cross-functional regulatory and IT teams
Qualifications
- 3โ5 years of experience in pharma/life sciences
- Expertise in EudraVigilance and E2BM standards
- Experience with ServiceNow, JIRA, or similar tools
- Strong data management and analytical skills
- Willingness to work night shifts
Benefits
- Remote working opportunity
- Exposure to global pharmacovigilance systems
- Career growth in regulatory data governance
- Competitive salary package
Salary (Estimated)
โน6,00,000 โ โน10,00,000 per annum (based on experience)
How to Apply
