India's DMPLOI - Jobs & Networking App
ClinChoice, a global leader in clinical research and regulatory services, is seeking motivated and detail-oriented individuals to join its Regulatory Affairs team as Associate – Regulatory Affairs in Chennai, India. This position offers an excellent opportunity for recent graduates or early-career professionals (0–6 months of experience) to begin a rewarding career in regulatory science and compliance.
Job Title: Associate – Regulatory Affairs
Location: Chennai
Experience: 0–6 months
About the Role
As an Associate in Regulatory Affairs, you will play a vital role in ensuring that all raw materials, formulations, and product information meet global and local regulatory standards. You’ll collaborate closely with local operating companies and global partners, providing critical support to maintain product compliance and uphold Johnson & Johnson’s high-quality standards.
This position provides hands-on exposure to regulatory review processes, documentation management, and product lifecycle compliance—key foundations for a long-term career in the life sciences industry.
Key Responsibilities
Collaborate with local and global operating teams to review and approve formulations, raw materials, and their constituent data.
Verify critical information such as trade names, manufacturer details, INCI names, CAS/EINECS numbers, and constituent percentages.
Ensure alignment with both regional and global regulatory requirements.
Evaluate the potential impact of changes on compliance, reporting, and documentation requirements, coordinating with Johnson & Johnson’s personnel when necessary.
Conduct regulatory evaluations for innovation platforms, new product development, and existing marketed products to ensure full compliance with local regulations and internal standards.
Prepare and compile all required documentation, working in close partnership with cross-functional teams.
Develop and manage project implementation plans with the Client’s PR&S DRI’s, ensuring on-time completion of assigned tasks.
Adhere to established best practice documents and work instructions for material and formulation reviews.
Deliverables
Comprehensive regulatory compliance evaluations for new and existing materials and formulations.
Timely and accurate reporting and documentation in alignment with regulatory expectations.
Weekly progress updates to Client’s PR&S DRI’s.
Training and knowledge-sharing sessions for offshore team members.
Conducting periodic portfolio surveys to monitor ongoing compliance.
Who Should Apply
This role is ideal for individuals with an academic background in pharmacy, chemistry, biotechnology, or related life sciences disciplines who are eager to enter the regulatory affairs field. Candidates should possess strong analytical skills, attention to detail, and the ability to work collaboratively in a dynamic, cross-functional environment.
Why Join ClinChoice?
At ClinChoice, you’ll become part of a global organization committed to improving health outcomes and accelerating medical innovation. The company provides a supportive environment that encourages learning, growth, and professional development—making it an excellent starting point for a career in regulatory affairs.
Location: Chennai, India
Employment Type: Contract
Experience Level: 0–6 months
If you’re passionate about ensuring product safety, compliance, and quality, and you’re looking to begin a fulfilling career in regulatory affairs, ClinChoice invites you to apply for this exciting opportunity.
OR
