If you’re a recent graduate or have up to 6 months of experience in Regulatory Affairs, this is your chance to join a leading healthcare organization and play a vital role in ensuring product safety and compliance. The Associate – Regulatory Affairs (Contract) role in Chennai offers an exceptional opportunity to work on product formulations, documentation, and compliance within a globally recognized organization.
Whether you’re passionate about regulatory documentation, product compliance, or pharmaceutical standards, this role is a strong entry point into the world of global regulatory affairs.
Job Details
- Position: Associate – Regulatory Affairs
- Location: Chennai, India
- Employment Type: Contract
- Experience: 0–6 months
- Salary: ₹3,00,000 – ₹4,80,000 per annum (Estimated)
- Posted on: October 31, 2025
- Valid through: November 30, 2025
Roles and Responsibilities
As an Associate – Regulatory Affairs, you will support product compliance activities for formulations, raw materials, and product innovations. Key responsibilities include:
- Collaborate with local operating companies to review and approve product formulations and raw material data.
- Verify information such as trade name, manufacturer, INCI name, CAS/EINECS numbers, and constituent percentages.
- Evaluate potential impacts on regulatory compliance and documentation requirements.
- Ensure all formulations meet local regulations and Johnson & Johnson (J&J) internal standards.
- Prepare and compile necessary documentation for new product development and marketed products.
- Work with cross-functional partners to meet project timelines.
- Maintain accuracy using best practice documents for review and approval processes.
- Provide weekly updates and participate in training sessions for offshore teams.
Key Deliverables
- Regulatory compliance evaluations of new and existing materials.
- Timely completion of documentation and compliance reports.
- Training and guidance for offshore team members.
- Periodic portfolio surveys and process improvements.
Qualifications
- Education: Bachelor’s or Master’s degree in Pharmacy, Chemistry, Life Sciences, or related field.
- Experience: 0–6 months (Freshers encouraged to apply).
- Skills:
- Understanding of regulatory compliance and documentation.
- Strong attention to detail and analytical skills.
- Excellent communication and teamwork abilities.
- Familiarity with global regulatory databases and standards is an advantage.
Why Join
- Exposure to global regulatory frameworks.
- Learn from industry-leading professionals in product compliance.
- Gain hands-on experience with raw material and formulation documentation.
- Opportunity to work on innovation platforms and marketed products.
How to Apply
