Are you a clinical or regulatory writing professional seeking a rewarding opportunity in the medical device industry? Meril, a global medical technology company, is hiring Sr. Officer / Jr. Executive with experience in Clinical Evaluation Report (CER) writing at their Pardi location in Gujarat, India.
🏢 About Meril – Innovating for Better Lives
Founded in 2006, Meril is a leading Indian medical device company with a global presence in over 100 countries. Headquartered in India with subsidiaries in the USA, Germany, Brazil, Russia, South Africa, and more, Meril is at the forefront of vascular intervention, in-vitro diagnostics, orthopaedic implants, and endo-surgery innovation.
Their mission? To deliver world-class healthcare solutions that improve quality of life through innovative research, advanced manufacturing, and strong collaborations with healthcare professionals worldwide.
📋 Job Details – Sr. Officer / Jr. Executive (CER Writer)
- Job Type: Full-Time
- Location: Pardi, Gujarat, India – 396191
- Experience Required: 1–3 Years
- Industry: Medical Devices / Healthcare Manufacturing
- Department: Regulatory Affairs / Clinical Writing
🧪 Key Responsibilities
- Write, manage, and finalize Clinical Evaluation Reports (CERs) in alignment with MedDev 2.7/1 Rev. 4, MDR, and internal SOPs.
- Analyze clinical data, literature, and regulatory requirements to support medical device safety and performance.
- Collaborate across regulatory, clinical, quality, and engineering teams.
- Assist in other documentation needs across regulatory and product lifecycle.
- Ensure quality and compliance with templates, work instructions, and regulatory standards.
📌 Eligibility Criteria
| Criteria | Requirement |
|---|---|
| Education | Bachelor’s / Master’s / PhD in Life Sciences or related discipline |
| Experience | 1–3 years in CER writing or clinical/regulatory/quality roles |
| Skills Required | – MedDev 2.7/1 Rev. 4 knowledge – Strong MS Office skills – Project management – Excellent communication |
| Other Requirements | Detail-oriented, self-driven, familiar with regulatory frameworks |
🎁 Benefits of Joining Meril
✅ Exposure to global healthcare markets
✅ Skill enhancement via collaboration with R&D and regulatory teams
✅ Diverse work environment
✅ Growth in medical device regulatory writing domain
✅ Knowledge exchange with global teams
