Meril is hiring for the position of Regulatory Affairs Officer for its medical-device regulatory function. The role is suitable for candidates with a background in life sciences, biotechnology, microbiology, biomedical sciences, pharmacy, or related disciplines.
The vacancy is open to candidates with 0–1 years of experience, while the detailed profile mentions relevant experience in medical writing, clinical research, clinical evaluation, or regulatory documentation. Candidates with 6 months or more of medical writing experience are preferred.
The position focuses on Clinical Evaluation Reports (CERs), systematic literature reviews, clinical evidence assessment, EU MDR requirements, PMS, PMCF, and regulatory documentation for medical devices.
Meril Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Meril |
| Position | Regulatory Affairs Officer |
| Job Locations | Valsad, Vapi, Daman & Diu |
| Employment Type | Full Time, Permanent |
| Experience | 0–1 Years listed; relevant experience preferred |
| Relevant Experience | Medical Writing / Clinical Research / Clinical Evaluation / Regulatory Documentation |
| Qualification | M.Sc. / relevant Life Science qualification |
| Vacancies | 1 |
| Salary | ₹2.5–4.5 LPA |
| Industry | Pharmaceutical & Life Sciences |
| Department | Legal & Regulatory |
| Job Category | Regulatory Affairs |
About Meril
Meril operates in the healthcare and medical-device sector. This Regulatory Affairs position is focused on the scientific and regulatory documentation required to evaluate the clinical evidence associated with medical devices.
The role combines scientific literature research, clinical evidence assessment, medical writing, regulatory documentation, and collaboration with teams such as Regulatory Affairs, R&D, Quality Assurance, and Clinical functions.
Meril Regulatory Affairs Officer Job Description
The Regulatory Affairs Officer will support the preparation, review, and maintenance of clinical evaluation documentation for medical devices.
The selected candidate will work with scientific literature and clinical evidence to assess the safety, performance, intended purpose, clinical benefits, and benefit-risk profile of medical devices.
The position also involves maintaining traceable evidence and supporting responses to regulatory or Notified Body questions related to clinical evaluation.
Clinical Evaluation and Regulatory Documentation
Key activities include:
- Prepare, review, and update Clinical Evaluation Reports (CERs).
- Support preparation and maintenance of Clinical Evaluation Plans (CEPs).
- Work on Clinical Literature Reviews (CLRs) and related clinical evaluation documents.
- Ensure regulatory documentation is scientifically sound and properly referenced.
- Maintain consistency and traceability across clinical evaluation records.
- Support documentation in accordance with applicable regulatory requirements and internal procedures.
Educational Qualification
The preferred educational background includes:
- M.Sc. in Zoology
- M.Sc. in Life Sciences
- M.Sc. in Biotechnology
- M.Sc. in Microbiology
- M.Sc. in Biomedical Sciences
- M.Sc. in Pharmacy
- Related scientific or life-science discipline
The job listing also contains education categories for Biomedical Engineering and B.Sc. Agriculture under its general education section. Candidates should verify the specific qualification accepted for this position with the employer.
Experience Requirements
The vacancy headline lists 0–1 years of experience.
The detailed candidate profile mentions 2 years of relevant experience in areas such as:
- Medical writing
- Clinical research
- Clinical evaluation
- Scientific writing
- Regulatory documentation
Candidates with 6 months or more of medical writing experience are specifically preferred.
Because the listing contains different experience indications, candidates should confirm the applicable experience requirement with Meril before applying.
Required Knowledge and Skills
Candidates should have an understanding of:
- Medical devices
- Clinical evaluation principles
- Scientific literature research
- Clinical evidence assessment
- Scientific writing
- Regulatory documentation
- Clinical publications
- Medical-device safety and performance
- Benefit-risk assessment
Familiarity with the following is also beneficial:
- EU MDR 2017
- Clinical evaluation requirements
- Post-Market Surveillance (PMS)
- Post-Market Clinical Follow-up (PMCF)
- Medical-device clinical evidence requirements
Scientific Literature Research Skills
The role requires the ability to perform systematic searches and review scientific information.
Candidates should be comfortable using resources such as:
- PubMed
- Google Scholar
- ClinicalTrials.gov
- Other relevant scientific databases
The selected candidate will need to identify relevant scientific evidence, critically assess published literature, and determine its relevance and applicability to medical-device clinical evaluation.
Key Responsibilities
1. Clinical Literature Research
- Conduct systematic searches of scientific literature.
- Search relevant medical and scientific databases.
- Identify publications related to medical devices and their intended uses.
- Review scientific papers and clinical evidence.
- Assess the relevance and quality of published information.
- Maintain accurate references and literature records.
2. Clinical Evidence Evaluation
- Identify and summarize clinical and scientific evidence.
- Evaluate information related to device safety and performance.
- Review evidence concerning clinical benefits.
- Support assessment of the benefit-risk profile of medical devices.
- Consider state-of-the-art information relevant to clinical evaluation.
3. Clinical Evaluation Documentation
- Prepare and update Clinical Evaluation Reports.
- Support Clinical Evaluation Plans.
- Prepare or contribute to Clinical Literature Reviews.
- Maintain evidence tables and supporting documentation.
- Ensure information is traceable and consistently documented.
- Keep clinical evaluation records aligned with applicable regulatory requirements.
4. Review of Clinical and Post-Market Information
- Review clinical investigation data.
- Assess relevant Post-Market Surveillance information.
- Support review of PMCF data.
- Review vigilance information where applicable.
- Incorporate relevant clinical evidence into evaluation documentation.
5. Regulatory and Cross-Functional Support
- Coordinate with Regulatory Affairs teams.
- Work with R&D and Quality Assurance teams.
- Collaborate with Clinical and other relevant departments.
- Collect and review clinical information required for regulatory documentation.
- Support responses to Notified Body questions.
- Assist with responses to regulatory authority queries concerning clinical evidence.
6. Regulatory Knowledge Development
- Keep updated with relevant medical-device regulatory requirements.
- Follow developments related to EU MDR.
- Maintain awareness of clinical evaluation requirements.
- Stay informed about PMS and PMCF requirements.
- Track scientific and regulatory expectations concerning medical-device clinical evidence.
Required Soft Skills
The role requires:
- Strong written English
- Scientific writing ability
- Analytical thinking
- Critical literature-review skills
- Attention to detail
- Accurate documentation
- Ability to manage references
- Ability to handle multiple documents
- Deadline management
- Cross-functional communication
- Ability to interpret scientific publications
- Organized working approach
Software Skills
Candidates should be comfortable working with:
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Experience with scientific literature databases and clinical research platforms is also useful.
Work Location and Work Environment
The vacancy lists the following locations:
- Valsad, Gujarat
- Vapi, Gujarat
- Daman & Diu
The listing does not specify a remote or hybrid work arrangement. Candidates should confirm the exact work location and applicable working arrangement during the recruitment process.
Salary / CTC
The advertised salary range for the Regulatory Affairs Officer position is:
₹2.5 lakh to ₹4.5 lakh per annum (LPA).
Actual compensation may depend on the candidate’s qualifications, relevant experience, skills, and the employer’s hiring terms.
Selection Process
The source vacancy does not provide a detailed selection process.
Candidates should confirm the applicable interview, assessment, or evaluation stages with Meril during recruitment.
How to Apply
Interested and eligible candidates can apply through the recruitment platform where the current Meril Regulatory Affairs Officer vacancy is listed.
Candidates should ensure that their resume highlights relevant experience or knowledge in medical writing, clinical evaluation, scientific literature review, medical devices, EU MDR, regulatory documentation, or clinical research.
Important Details Before Applying
- Position: Regulatory Affairs Officer
- Company: Meril
- Job locations: Valsad, Vapi, and Daman & Diu
- Vacancies: 1
- Advertised experience: 0–1 years
- Detailed profile mentions relevant experience in medical writing, clinical research, clinical evaluation, or regulatory documentation.
- Candidates with 6+ months of medical writing experience are preferred.
- Relevant M.Sc./life-science qualifications are preferred.
- Knowledge of EU MDR 2017 is beneficial.
- PubMed and Google Scholar experience is useful.
- Clinical evaluation and scientific writing skills are important.
- MS Word, Excel, and PowerPoint proficiency is expected.
- Advertised salary: ₹2.5–4.5 LPA.
- The source contains different experience indications; candidates should verify the applicable requirement before applying.
Frequently Asked Questions
1. What position is Meril hiring for?
Meril is hiring for a Regulatory Affairs Officer position.
2. What is the job location?
The listing mentions Valsad, Vapi, and Daman & Diu as possible locations.
3. What is the advertised salary?
The advertised salary range is ₹2.5–4.5 LPA.
4. How much experience is required?
The listing headline shows 0–1 years, while the detailed profile mentions relevant experience and states 2 years for medical writing, clinical research, clinical evaluation, or regulatory documentation. Candidates should verify the exact requirement with the employer.
5. Is medical writing experience preferred?
Yes. Candidates with 6 months or more of medical writing experience are specifically preferred.
6. What educational qualifications are preferred?
Relevant M.Sc. qualifications in areas such as Life Sciences, Biotechnology, Microbiology, Biomedical Sciences, Zoology, or Pharmacy are listed.
7. What is a Clinical Evaluation Report?
A Clinical Evaluation Report (CER) is a regulatory document used to assess and document clinical evidence concerning the safety, performance, and clinical benefits of a medical device.
8. Is knowledge of EU MDR required?
Basic understanding of EU MDR 2017, particularly its clinical evaluation and clinical evidence requirements, is listed as preferred.
9. Which databases may be used in this role?
The vacancy mentions PubMed, Google Scholar, ClinicalTrials.gov, and other relevant scientific databases.
10. What software skills are required?
Candidates should have proficiency in MS Word, Excel, and PowerPoint.
Important Note
Vacancy details, eligibility criteria, experience requirements, salary, job location, and recruitment conditions may change during the hiring process. The source listing contains a difference between the headline experience range and the detailed experience requirement, so candidates should confirm the latest eligibility criteria with Meril before applying.