IQVIA, one of the world’s leading clinical research and healthcare intelligence organizations, is hiring Regulatory Affairs Officer II professionals for its India operations. This is an excellent opportunity for experienced Regulatory Affairs professionals with expertise in EU Clinical Trial Regulation (EU CTR), Chemistry Manufacturing & Controls (CMC), Lifecycle Maintenance, Marketing Authorization, Regulatory Publishing, and Technical Writing.
Candidates with strong knowledge of global regulatory requirements and 3–6 years of Regulatory Affairs experience are encouraged to apply.
Job Details
| Details | Information |
|---|---|
| Position | Regulatory Affairs Officer II |
| Company | IQVIA |
| Location | Thane, Maharashtra & Bangalore, Karnataka |
| Work Mode | Hybrid / Remote (Role dependent) |
| Job Type | Full-Time |
| Experience | 3–6 Years |
| Qualification | Bachelor’s or Master’s Degree in Life Sciences or related discipline |
| Application Deadline | August 7, 2026 |
IQVIA is a global leader in clinical research services, healthcare intelligence, commercial insights, and technology solutions. The company supports pharmaceutical, biotechnology, and medical device organizations by accelerating the development and commercialization of innovative therapies while maintaining global regulatory compliance.
As a Regulatory Affairs Officer II, you will:
- Lead Regulatory Affairs activities for assigned projects.
- Prepare and review regulatory submissions and technical documentation.
- Support Chemistry Manufacturing & Controls (CMC) documentation.
- Handle Lifecycle Maintenance activities.
- Work on Marketing Authorization Transfer projects.
- Support Regulatory Publishing and Labeling activities.
- Act as a Subject Matter Expert (SME) for regulatory processes.
- Coordinate with global clients regarding regulatory requirements.
- Participate in bid defense meetings and customer discussions.
- Review regulatory SOPs and recommend process improvements.
- Train junior regulatory professionals.
- Ensure project timelines, quality standards, and compliance requirements are achieved.
Applicants should possess:
- Bachelor’s Degree in Life Sciences or related discipline
- OR Master’s Degree in Life Sciences or related discipline
Eligible educational backgrounds include:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Biomedical Sciences
- Other relevant Life Science disciplines
IQVIA’s official job posting mentions:
- Minimum 3–4 years of relevant Regulatory Affairs experience.
The hiring communication additionally indicates preference for professionals having:
- 5–6 years of Regulatory Affairs experience
- Strong experience with EU Clinical Trial Regulation (EU CTR)
Candidates with the following skills will have an advantage:
- Regulatory Affairs
- EU CTR
- Clinical Trial Regulation
- Regulatory Submissions
- Chemistry Manufacturing & Controls (CMC)
- Lifecycle Maintenance
- Marketing Authorization Transfer
- Regulatory Publishing
- Regulatory Labeling
- Technical Writing
- Microsoft Office
- Regulatory Compliance
- Project Management
- Client Communication
- SOP Management
Joining IQVIA offers several benefits:
- Global pharmaceutical projects
- Hybrid working opportunities
- Career growth in Regulatory Affairs
- Exposure to international regulatory submissions
- Opportunity to work with leading pharmaceutical and biotechnology companies
- Learning from experienced global regulatory experts
- Professional development and internal training
Interested candidates who meet the eligibility criteria can:
- Apply through the official IQVIA Careers portal.
- Candidates matching the required experience may also share their updated resume with:
Email: anuraj.kr@iqvia.com
Apply before August 7, 2026.
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