ClinChoice Hiring Associate – Regulatory Affairs

Associate – Regulatory Affairs (0–6 Months) | Chennai Openings
Apply for Associate – Regulatory Affairs (Contract Role) in Chennai. Ideal for Life Science graduates with 0–6 months experience. Apply now!

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Working in Regulatory Affairs offers an exciting opportunity to ensure pharmaceutical products meet global compliance standards. If you’re looking to kickstart or advance your career in pharma documentation and regulatory support, this position at ClinChoice, Chennai provides the right platform to grow your expertise in one of the most in-demand fields in the pharmaceutical industry.

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Company Overview

ClinChoice is a trusted global contract research organization (CRO) offering a wide range of services including clinical development, regulatory affairs, pharmacovigilance, and data management. With a strong legacy of working with top pharmaceutical and life sciences companies, ClinChoice focuses on delivering quality-driven and compliant solutions that advance global healthcare. The Chennai branch is expanding its Regulatory Affairs team to support product innovation and compliance for global clients, including Johnson & Johnson.

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Job Role & Responsibilities

As an Associate – Regulatory Affairs, you will support regional and global product compliance by ensuring formulations, raw materials, and associated documentation meet regulatory standards. You’ll collaborate with internal teams and client partners to deliver high-quality, compliant regulatory submissions.

Key Responsibilities:

• Collaborate with local operating companies to review and approve formulations and raw material data.
• Verify and validate critical information, including:
  • Trade name
  • Manufacturer details
  • INCI name
  • CAS/EINECS numbers
  • Percentage of constituent
  • Regional and global regulatory compliance
• Evaluate potential compliance impacts and documentation requirements.
• Assess formulations for new product development, innovation platforms, and marketed products.
• Prepare, compile, and submit required documentation with cross-functional support.
• Manage project implementation plans and workload timelines with the client’s PR&S DRI team.
• Utilize best practice templates and standard operating procedures (SOPs) for reviews and approvals.

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Eligibility / Qualifications

Educational Background:

• Required: B.Pharm, M.Pharm, B.Sc, M.Sc in Chemistry, Biochemistry, Biotechnology, or Life Sciences.
• Preferred: PG Diploma in Regulatory Affairs, Pharma Quality Assurance, or related certifications.

Experience:

• 0 to 6 months (freshers with internship experience in Regulatory Affairs or QA may apply).

Technical & Soft Skills:

• Strong analytical and documentation abilities.
• Basic understanding of regional/global regulatory frameworks.
• Good communication and coordination skills.
• Proficiency in MS Office tools and database management systems.

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Location & Salary

Location: Chennai, Tamil Nadu
Employment Type: Contract (Full-Time)
Salary Range: Competitive, aligned with market standards for entry-level Regulatory Affairs roles.

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Application Process

Interested candidates who meet the above qualifications can apply directly via the official job portal below. Ensure that your resume highlights relevant coursework, project experience, and regulatory exposure.

Apply Here: ClinChoice Regulatory Affairs – Chennai

Application Tip: Apply before 15th November 2025 to secure early interview consideration.

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Why Join ClinChoice?

• Work with leading global healthcare brands such as Johnson & Johnson.
• Gain hands-on experience in international regulatory standards.
• Be part of a culture that values compliance, innovation, and scientific excellence.
• Continuous professional development opportunities through structured training and mentorship.

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Career Growth Opportunities in Regulatory Affairs

Regulatory Affairs professionals play a crucial role in bridging innovation and compliance. In this role, you’ll gain exposure to:

• Global documentation frameworks (USFDA, EMA, CDSCO).
• Lifecycle management of new drug applications.
• Market authorization and label compliance.
• International collaboration across R&D, QA, and manufacturing functions.

With experience, you can progress into roles such as Regulatory Specialist, Regulatory Manager, or Global Compliance Lead, each offering greater responsibility and rewarding career advancement in the pharmaceutical sector.

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FAQs

Q1. Who can apply for this role?
Candidates with degrees in Life Sciences, Pharmacy, or Chemistry with up to 6 months of experience can apply.

Q2. Is this role suitable for freshers?
Yes, freshers with internship or academic project experience in Regulatory Affairs or QA are encouraged to apply.

Q3. What is the mode of employment?
This is a contract-based full-time position with the potential for extension based on performance.

Q4. What is the salary range?
Salary is competitive and varies based on education and interview performance.

Q5. How can I apply?
You can apply directly through ClinChoice’s official career page.

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Summary Table

Category	Details
Company	ClinChoice Pvt. Ltd.
Vacancies	Multiple – Associate (Regulatory Affairs)
Required Education	B.Pharm, M.Pharm, B.Sc, M.Sc (Chemistry, Biochemistry, Biotechnology, Life Sciences)
Experience	0–6 months (Freshers eligible)
Location	Chennai, Tamil Nadu
Employment Type	Contract (Full-Time)
Application Link	Apply Here

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