Meril Hiring Executive – Clinical Evaluation Report (CER)
- Meril Hiring Executive – Clinical Evaluation Report (CER) | 1–3 Years Experience | Pardi, Gujarat
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location & Employment Details
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this Executive position at Meril?
- 2. Is prior MedDev 2.7/1 Rev 4 knowledge mandatory?
- 3. Is this role suitable for freshers?
- 4. What industry does this role belong to?
- 5. What long-term career paths are available?
- Recruitment Summary
Meril Hiring Executive – Clinical Evaluation Report (CER) | 1–3 Years Experience | Pardi, Gujarat
Meril is inviting applications for the position of Executive in its Manufacturing and Medical Device division at Pardi, Gujarat. This is a full-time opportunity for professionals with 1–3 years of experience in Clinical Evaluation Report (CER) writing, regulatory affairs, clinical research, or quality systems within the medical device industry. Candidates with a strong scientific background and working knowledge of European medical device regulations will find this role aligned with long-term growth in regulatory writing and global compliance.
If you are looking to build a career in medical device regulatory affairs, clinical data analysis, and global healthcare compliance, this opening offers direct exposure to international standards and innovative medical technologies.
Company Overview
Founded in 2006, Meril is an India-based global medical device company committed to delivering world-class healthcare solutions. With operations in more than 100 countries and subsidiaries across the USA, Germany, Brazil, Russia, South Africa, Bangladesh, and Turkey, the organization has established itself as a major force in medical technology innovation.
Meril focuses on the research, design, and manufacturing of advanced medical devices across vascular interventions, orthopaedics, in-vitro diagnostics, endo-surgery, and ENT segments. With a workforce of over 4,000 professionals worldwide, the company collaborates closely with physicians, researchers, and global healthcare innovators to address unmet clinical needs.
The organization’s strong emphasis on research and development, regulatory compliance, and quality assurance ensures that its products meet international medical standards. By maintaining high manufacturing quality and scientific credibility, Meril continues to contribute meaningfully to global healthcare advancement.
Job Role & Responsibilities
The Executive will primarily be responsible for developing and managing Clinical Evaluation Reports (CERs) for pre-market and post-market medical devices. This role is central to regulatory submissions and compliance under global medical device frameworks.
Key Responsibilities
- Develop, draft, and update Clinical Evaluation Reports in compliance with MedDev 2.7/1 Rev 4 and applicable regulatory standards.
- Review and analyze clinical trial data, scientific literature, and post-market surveillance information.
- Interpret complex medical and scientific data to derive evidence-based conclusions.
- Ensure consistency with internal SOPs, quality management systems, and global regulatory requirements.
- Plan, appraise, and evaluate clinical data to support device safety and performance claims.
- Collaborate with regulatory, quality, clinical, and engineering teams on cross-functional projects.
- Maintain documentation integrity to support audits and regulatory inspections.
- Communicate scientific findings clearly and concisely in written and oral formats.
This position demands strong analytical skills, regulatory knowledge, and the ability to convert large volumes of clinical evidence into structured regulatory documentation.
Eligibility / Qualifications
Educational Qualification
Bachelor’s, Master’s Degree, or PhD (preferred) in a scientific discipline.
Relevant Courses: B.Pharm, M.Pharm, Pharm.D, BSc Biotechnology, MSc Biotechnology, BSc Life Sciences, MSc Life Sciences, Biomedical Engineering, Clinical Research, Regulatory Affairs, Medical Writing, Microbiology, Biochemistry, Biomedical Sciences.
Experience
- 1–3 years of experience in CER writing within the medical device industry.
- 1–3 years of experience in clinical, regulatory, quality, or engineering roles.
- Solid knowledge of MedDev 2.7/1 Rev 4 guidelines.
Required Skills
- Strong understanding of medical device regulations and global compliance frameworks.
- Ability to read, interpret, and implement regulatory standards and guidance documents.
- Experience in scientific writing and regulatory documentation.
- Advanced proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong project management skills including multitasking and prioritization.
- Excellent written and verbal communication abilities.
- Ability to work independently with high attention to detail.
Candidates with prior experience in clinical evaluation, regulatory submissions, quality assurance systems, or medical writing will be strongly preferred.
Location & Employment Details
Location: Pardi, Gujarat, India
Job Type: Full-Time
Industry: Medical Device Manufacturing
Experience Required: 1–3 Years
Application Process
Interested candidates can apply directly through the official Meril career portal using the link below:
Apply Here:
https://merillife.zohorecruit.in/jobs/merilcareer/26825000016891225/Executive?source=CareerSite
Applicants are advised to highlight CER writing experience, regulatory compliance exposure, and scientific data interpretation skills in their resumes.
Frequently Asked Questions (FAQs)
1. Who can apply for this Executive position at Meril?
Candidates with a Bachelor’s or Master’s degree in a scientific discipline and 1–3 years of CER writing or regulatory experience in medical devices can apply.
2. Is prior MedDev 2.7/1 Rev 4 knowledge mandatory?
Yes. Working knowledge of MedDev 2.7/1 Rev 4 guidelines is essential for this role.
3. Is this role suitable for freshers?
No. A minimum of 1 year of relevant industry experience is required.
4. What industry does this role belong to?
This position is within the medical device manufacturing and regulatory affairs domain.
5. What long-term career paths are available?
Professionals can advance into Senior Regulatory Affairs Specialist, Clinical Evaluation Manager, Medical Writer, or Global Compliance roles.
Recruitment Summary
| Company | Meril |
|---|---|
| Vacancies | Executive – Clinical Evaluation Report (CER) |
| Required Education | Bachelor’s/Master’s/PhD in Scientific Discipline |
| Experience | 1–3 Years in CER Writing, Clinical, Regulatory or Quality Roles |
To apply for this job please visit merillife.zohorecruit.in.
