IQVIA, a global leader in clinical research, healthcare intelligence, and regulatory services, has announced a new job opening for the position of Regulatory Affairs Officer 2. The company is inviting applications from experienced regulatory professionals with 3–4 years of experience in Regulatory Affairs and Life Sciences.
The position is available at Thane, Maharashtra and Bengaluru, Karnataka, making it an excellent opportunity for candidates seeking a career in regulatory affairs, chemistry, manufacturing and controls (CMC), labeling, publishing, and lifecycle management.
IQVIA Recruitment 2026 – Overview
| Particulars | Details |
|---|---|
| Company Name | IQVIA |
| Job Role | Regulatory Affairs Officer 2 |
| Job Location | Thane, Maharashtra / Bengaluru, Karnataka |
| Employment Type | Full-Time |
| Experience | 3–4 Years |
| Qualification | Bachelor’s or Master’s Degree in Life Sciences or Related Discipline |
| Application Mode | Online |
| Last Date to Apply | 7 August 2026 |
Job Responsibilities
The selected candidate will be responsible for:
- Lead regulatory activities for assigned projects as a Regulatory Team Leader.
- Prepare, review, and submit regulatory documents in accordance with global regulatory requirements.
- Coordinate with clients to discuss regulatory strategies, project updates, and compliance requirements.
- Provide subject matter expertise in Chemistry, Manufacturing & Controls (CMC), lifecycle maintenance, labeling, marketing authorization transfers, and publishing activities.
- Manage project timelines, deliverables, and assigned budgets.
- Review technical documents prepared by junior team members and provide constructive feedback.
- Support the training and development of junior regulatory professionals.
- Participate in client meetings and regulatory presentations.
- Review and contribute to Regulatory Standard Operating Procedures (SOPs).
- Deliver regulatory training sessions to internal teams when required.
- Assist in process improvement initiatives and support regulatory compliance across projects.
- Perform additional responsibilities assigned by Regulatory Management.
Educational Qualification
Candidates should possess one of the following qualifications:
- Bachelor’s Degree in Life Sciences or a related discipline
- Master’s Degree in Life Sciences or a related discipline
Experience Required
Applicants should have:
- 3 to 4 years of relevant experience in Regulatory Affairs.
- Practical knowledge of pharmaceutical product development and global regulatory requirements.
- Experience in handling regulatory documentation and lifecycle management activities.
Required Skills
The ideal candidate should possess:
- Strong understanding of the pharmaceutical Research & Development process.
- Knowledge of Chemistry, Manufacturing & Controls (CMC).
- Experience with Lifecycle Maintenance and Marketing Authorization Transfers.
- Knowledge of Labeling and Regulatory Publishing.
- Regulatory documentation preparation and review skills.
- Good communication and client management abilities.
- Strong organizational and project management skills.
- Proficiency in Microsoft Office and regulatory publishing tools.
- Ability to manage multiple projects simultaneously.
- Knowledge of regulatory guidelines and quality systems.
- Excellent analytical and problem-solving skills.
- Ability to work independently as well as within cross-functional teams.
Salary Details
IQVIA has not officially disclosed the salary for this position.
Based on current industry standards, professionals with 3–4 years of Regulatory Affairs experience may receive an estimated annual salary ranging between ₹8 LPA and ₹14 LPA, depending on qualifications, skills, and interview performance.
Additional employee benefits may include:
- Competitive salary package
- Health and insurance benefits
- Learning and professional development programs
- Global project exposure
- Career advancement opportunities
- Employee wellness benefits as per company policy
Job Locations
Selected candidates may be posted at either of the following locations:
- Thane, Maharashtra
- Bengaluru, Karnataka
How to Apply
Interested and eligible candidates can apply online through IQVIA’s official careers portal before the application deadline.
Last Date to Apply: 7 August 2026
Applicants should ensure that all educational qualifications, work experience, and supporting information are correctly mentioned while submitting their online application.
Why Join IQVIA?
IQVIA is one of the world’s leading organizations in clinical research, healthcare analytics, and regulatory consulting. Employees get the opportunity to work on global regulatory projects, collaborate with international clients, and contribute to the development and commercialization of innovative healthcare products. The company also offers continuous learning, career growth, and exposure to advanced regulatory technologies.
Frequently Asked Questions (FAQs)
What is the job role offered by IQVIA?
IQVIA is hiring for the position of Regulatory Affairs Officer 2.
What qualifications are required?
Candidates should have a Bachelor’s or Master’s Degree in Life Sciences or a related discipline.
How much experience is required?
Applicants should have 3–4 years of relevant Regulatory Affairs experience.
What are the job locations?
The vacancies are available in Thane, Maharashtra and Bengaluru, Karnataka.
What is the last date to apply?
The last date to submit the online application is 7 August 2026.
