IQVIA Hiring Regulatory Affairs Specialist
IQVIA, a global leader in health information technology and clinical research, is currently inviting applications for the position of Regulatory Affairs Specialist in Bangalore, India. This hiring drive is a golden opportunity for experienced professionals in the pharmaceutical and life sciences industries who are seeking growth in the field of regulatory compliance and documentation. IQVIA Hiring Regulatory Affairs Specialist
The position offers a highly competitive salary package ranging from ₹7 LPA to ₹10 LPA, making it one of the most sought-after roles for professionals with 3–4 years of experience in Regulatory Affairs. Let’s explore all the key details about this opportunity including job responsibilities, required qualifications, and how to apply.
About the Role: Regulatory Affairs Specialist at IQVIA
The selected candidate will work as a Regulatory Team Leader, handling complex regulatory projects that involve end-to-end submission preparation, client interaction, technical documentation, and compliance with global regulatory frameworks.IQVIA Hiring Regulatory Affairs Specialist
This role is best suited for professionals who are already familiar with CMC (Chemistry, Manufacturing & Controls), Labeling, Lifecycle Maintenance, and Regulatory Strategy.
Key Responsibilities
As a Regulatory Affairs Specialist, your primary responsibilities will include: IQVIA Hiring Regulatory Affairs Specialist
- Leading regulatory projects and ensuring all deliverables meet global standards and regulatory requirements.
- Preparing and reviewing various regulatory submissions, including IND, NDA, MAA, and others.
- Acting as a Subject Matter Expert (SME) in areas such as CMC, Labeling, or Regulatory Strategy.
- Collaborating directly with clients, managing queries, and presenting key insights and recommendations.
- Overseeing project timelines, budgets, and deliverables while ensuring high-quality output.
- Providing guidance and mentorship to junior team members and conducting internal training sessions.
- Supporting the development of Standard Operating Procedures (SOPs) and continuous process improvement initiatives.
- Keeping up-to-date with global regulatory updates from US FDA, EMA, CDSCO, and other major authorities.
Required Qualifications
Education
To be eligible for this position, candidates must hold a Bachelor’s or Master’s degree in one of the following disciplines: IQVIA Hiring Regulatory Affairs Specialist
- Life Sciences
- Pharmacy
- Biotechnology
- Other related fields
Experience
- 3 to 4 years of hands-on experience in Regulatory Affairs, preferably within the pharmaceutical, CRO (Contract Research Organization), or healthcare sectors.
- Sound understanding of R&D processes, including preclinical, clinical, and CMC-related submissions.
- Prior experience in eCTD publishing, post-approval regulatory changes, or product labeling is considered an advantage.
Essential Skills
Candidates should possess the following skillset: IQVIA Hiring Regulatory Affairs Specialist
- Strong technical writing and documentation skills.
- Proficiency in Microsoft Office and tools such as Veeva Vault, DocuBridge, and other regulatory publishing platforms.
- Excellent communication and interpersonal skills to work in a team and with global clients.
- Ability to independently manage multiple regulatory projects under tight deadlines.
- Analytical thinking with excellent problem-solving capabilities.
Why Choose IQVIA?
IQVIA is a renowned name in the healthcare and clinical research industry, operating in over 100 countries. The organization is known for merging advanced analytics with real-world data to improve clinical outcomes and accelerate product commercialization.
Working at IQVIA offers:
- Opportunities to collaborate with global pharma clients
- Exposure to international regulatory standards
- A fast-paced environment that fosters learning and innovation
- Career advancement through internal training and leadership development programs
Job Location and Salary
- Location: Bangalore, Karnataka, India
- Salary Range: ₹7,00,000 to ₹10,00,000 per annum
- Job Type: Full-Time, Permanent
- Work Mode: Onsite
Important Dates
- Job Posting Date: June 19, 2025
- Last Date to Apply: June 21, 2025
Candidates are encouraged to apply well before the deadline as positions may close early based on the volume of applications received.
How to Apply
Interested and eligible candidates can apply online by visiting the official career page of IQVIA or through verified job platforms like Pharmabharat. Ensure your updated resume highlights relevant Regulatory Affairs experience and certifications, if any. IQVIA Hiring Regulatory Affairs Specialist
Steps to Apply:
- Visit the official IQVIA career portal or a trusted job portal.
- Search for “Regulatory Affairs Specialist – Bangalore”.
- Fill in your personal and professional details.
- Upload your resume and relevant documents.
- Submit your application before the last date.
Also Apply For: Hetero Regulatory Affairs Jobs
In addition to IQVIA, Hetero is also hiring in the Regulatory Affairs domain. Candidates seeking wider opportunities in this sector should explore similar openings to maximize their chances of selection. IQVIA Hiring Regulatory Affairs Specialist
Final Words
If you’re an experienced regulatory professional looking for your next big move in 2025, IQVIA’s Regulatory Affairs Specialist role in Bangalore is a perfect opportunity. With a competitive salary, a global work environment, and exposure to complex regulatory challenges, this role offers both career growth and professional development. IQVIA Hiring Regulatory Affairs Specialist
Apply before June 21, 2025, and take the next step toward a fulfilling career in Regulatory Affairs with one of the world’s most respected clinical research organizations.
Tags: IQVIA Hiring 2025, Regulatory Affairs Specialist Job, Pharma Jobs Bangalore, Clinical Research Jobs, CMC Jobs India, IQVIA Careers, Regulatory Submissions Jobs, Life Sciences Jobs India, Hetero Regulatory Jobs
WhatsApp Group