Meril is inviting applications for the position of Clinical Specialist for professionals interested in medical device clinical evaluation, Clinical Evaluation Reports (CER), CDSCO submissions, ISO 10993 biological evaluation, and regulatory documentation. This opportunity is ideal for candidates with 1–5 years of experience looking to build a career in medical device regulatory affairs and clinical evaluation.

If you have strong analytical, documentation, and research skills with exposure to medical devices or clinical documentation, this Meril recruitment offers an excellent opportunity to work on global regulatory projects.

Job Details

Key Responsibilities

As a Clinical Specialist at Meril, you will:

• Assist in preparing Clinical Evaluation Reports (CERs).
• Perform scientific literature reviews and clinical evidence analysis.
• Prepare clinical performance documentation.
• Support CDSCO regulatory submissions.
• Assist in preparing technical files and clinical evaluation documentation.
• Support Post-Market Surveillance (PMS) documentation.
• Coordinate ISO 10993 biological evaluation testing.
• Follow up with external testing laboratories.
• Maintain accurate regulatory and technical documentation.
• Collaborate with cross-functional regulatory and quality teams.

Eligibility Criteria

Candidates should possess:

• Graduate or Postgraduate degree in Life Sciences, Pharmacy, Biomedical Engineering, Biotechnology, or related disciplines.
• 1–5 years of relevant experience.
• Strong scientific research and analytical skills.
• Excellent documentation and technical writing abilities.
• Good proficiency in Microsoft Office.
• Exposure to Clinical Evaluation Reports (CER), CDSCO documentation, regulatory affairs, or medical device documentation is preferred.

Preferred Skills

• Clinical Evaluation Report (CER)
• Medical Device Documentation
• CDSCO Regulatory Submission
• ISO 10993 Biological Evaluation
• Literature Review
• Clinical Evidence Assessment
• Technical Documentation
• Post-Market Surveillance (PMS)
• Regulatory Affairs
• Medical Writing
• Research Documentation
• Clinical Research

Why Join Meril?

• Opportunity to work with a leading medical device company.
• Exposure to global regulatory documentation.
• Experience in Clinical Evaluation Reports (CER).
• Hands-on work in ISO 10993 biological evaluation.
• Career growth in medical device regulatory affairs.
• Collaborative work environment with experienced professionals.

How to Apply

Application Link