Regulatory Affairs Associate Vacancy at S3V Vascular Technologies

Looking for a Regulatory Affairs Associate job in Chennai? S3V Vascular Technologies is hiring experienced candidates for its Regulatory Affairs team. Candidates with a background in B.Pharm, M.Pharm, Life Sciences, or Biotechnology and experience in regulatory documentation, dossier preparation, and regulatory submissions are encouraged to apply.

This opportunity is ideal for professionals seeking growth in the medical device regulatory affairs industry with exposure to CTD/eCTD dossiers, lifecycle management, compliance review, and post-market surveillance activities.

About S3V Vascular Technologies

S3V Vascular Technologies is focused on developing innovative cardiovascular medical technologies designed to improve patient outcomes globally. The company works closely with physicians and healthcare professionals to create advanced medical devices and therapies for cardiovascular care.

With a strong emphasis on quality, compliance, and innovation, S3V Vascular Technologies continues to expand its footprint in the Indian healthcare and medical device sector.

Regulatory Affairs Associate Job Details

Job Role: Regulatory Affairs Associate

Company: S3V Vascular Technologies

Location: Chennai, Tamil Nadu

Job Type: Full-Time

Experience: 1–3 Years

Qualification: B.Pharm, M.Pharm, Life Sciences, Biotechnology

Industry: Medical Devices / Regulatory Affairs

Workplace Type: On-site

Key Responsibilities

The selected candidate will be responsible for:

Preparing and reviewing CTD, eCTD, and ACTD dossiers

Managing new product registrations and renewals

Handling lifecycle management activities including variations, amendments, and supplements

Reviewing product labels, IFUs, and promotional materials for regulatory compliance

Coordinating with R&D, QA, and Clinical teams for technical documentation

Supporting post-market surveillance and adverse event reporting

Maintaining audit-ready regulatory databases and trackers

Assisting in drafting responses to health authority queries

Ensuring compliance with applicable regional and international regulatory standards

Eligibility Criteria

Candidates applying for this Regulatory Affairs Executive job in Chennai should possess:

Educational Qualification

B.Pharm

M.Pharm

Life Sciences Degree

Biotechnology Degree

Experience Required

1 to 3 years of experience in Regulatory Affairs

Experience in regulatory documentation and submissions

Knowledge of regulatory compliance standards

Familiarity with medical device or pharmaceutical regulations

Strong analytical and organizational skills

Preferred Skills

Experience with regulatory submissions

Knowledge of medical device regulations

Understanding of post-market surveillance

Excellent communication and coordination abilities

Ability to work effectively with cross-functional teams

Salary and Benefits

Candidates selected for this Regulatory Affairs Associate role can expect:

Competitive salary package

Exposure to global regulatory practices

Career growth in medical devices and regulatory affairs

Collaborative and innovation-driven work environment

Opportunity to work with experienced industry professionals

Expected Salary Range: ₹3.5 LPA – ₹5.5 LPA

How to Apply

Interested candidates can apply directly through the company or contact the hiring team using the details below:

Contact Details

HR Contact: Dilip Kumar

Phone: 8870013482

Email: dilip001jothi@gmail.com

Official Email: Karthikeyan_m@s3vvascular.com

Application Link