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Regulatory Affairs Specialist – Appasamy Associates – Chennai – Entry Level/Experienced

  • Writer: Ai Search
    Ai Search
  • Sep 29
  • 1 min read

🌟 Hiring Alert! Regulatory Affairs Specialist Vacancy for Biomedical Engineers. Join Appasamy Associates, a leading manufacturer of ophthalmic medical devices, dedicated to creating world-class eye care products that improve vision and transform lives.



They are looking for a Regulatory Affairs Specialist to oversee compliance and regulatory activities for our ophthalmic medical device portfolio. The role involves ensuring adherence to global regulatory standards, including ISO 13485, managing product licensing, registration renewals, audits, and inspections. You will work closely with cross-functional teams to maintain accurate documentation, ensure compliance in product labeling and packaging, and support timely product launches. Responsibilities include tracking project timelines, preparing regulatory submissions, and monitoring progress to meet compliance requirements throughout the product lifecycle.This position plays a key role in executing regulatory strategies to deliver safe, effective, and compliant medical devices to the market.



📍Location: Chennai

🛠 Product Segment: Ophthalmic Medical Device Regulatory Affairs

🎓 Eligibility: Bachelor’s/Master’s in Life Sciences, Pharmacy, or Engineering

(B.Tech/Biomedical) with 2–5 years of experience in regulatory affairs.

💰 Salary: 5.0 to 10.0 LPA



🌐 Employer Website: www.appasamy.com




Regulatory Affairs Specialist Vacancy at Appasamy Associates for Chennai for Biomedical Engineers.



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