Medtronic is hiring for the position of Clinical Evaluation Medical Writer in Hyderabad. This is a full-time role with a flexible work arrangement for experienced medical and clinical writers with a background in medical devices, pharmaceuticals, life sciences or related scientific disciplines.
The selected professional will support the preparation and maintenance of clinical and regulatory documentation related to medical devices. The role focuses on clinical evidence evaluation, medical writing, literature research, regulatory documentation and collaboration with global cross-functional teams.
Medtronic Clinical Evaluation Medical Writer Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Medtronic |
| Job Title | Clinical Evaluation Medical Writer |
| Location | Nanakramguda, Hyderabad, India |
| Job Type | Full Time |
| Work Arrangement | Flexible Work Arrangement |
| Experience | 4–8 Years |
| Qualification | B.Pharm + M.Pharm, M.Sc./Master’s, MBBS, or Doctorate in Relevant Sciences |
| Industry | Medical Devices / Pharmaceutical |
| Key Area | Clinical Evaluation & Medical Writing |
| Requisition ID | R72925 |
| Salary | Competitive; Exact Amount Not Specified |
| Incentive | Eligible for Medtronic Incentive Plan (MIP) |
About Medtronic
Medtronic is a global healthcare technology company focused on developing medical technologies designed to support patient care. The company operates across numerous countries and works in areas including medical devices, clinical research, healthcare technology and patient-focused innovation.
The Clinical Evaluation Medical Writer will be part of Medtronic’s medical writing function and will contribute to clinical and regulatory documentation supporting medical device safety, performance and compliance.
Job Description
The Clinical Evaluation Medical Writer will be responsible for preparing, reviewing and maintaining clinical evaluation and regulatory documents for assigned medical device portfolios.
The role involves gathering and critically assessing clinical evidence from scientific literature and other credible sources, preparing regulatory reports and working with cross-functional teams to support the safety and performance evaluation of medical devices.
The position may cover devices including Class III and implantable devices, Class IIb and Class IIa medical devices.
Key Responsibilities
Clinical Evaluation and Regulatory Writing
- Prepare and maintain Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER).
- Develop and maintain Summary of Safety and Clinical Performance (SSCP) documentation.
- Support preparation of Periodic Safety Update Reports (PSUR) and related clinical documentation.
- Prepare and review clinical and regulatory documents required for submissions and internal activities.
- Develop responses to questions raised by Notified Bodies.
- Prepare clear and accurate responses to audit and regulatory submission queries.
- Support clinical documentation associated with assigned medical device portfolios.
Clinical Evidence Research and Analysis
- Conduct comprehensive searches of scientific and peer-reviewed literature.
- Identify relevant clinical evidence from available credible sources.
- Critically evaluate the quality and relevance of clinical data.
- Analyze and summarize evidence for inclusion in clinical evaluation documentation.
- Maintain databases containing relevant literature and clinical evidence.
- Develop assessments reflecting the current state of knowledge for assigned product families.
- Ensure clinical evidence is aligned with the intended purpose of the relevant products.
Medical and Scientific Writing
Depending on business requirements, the role may involve preparing and editing:
- Clinical study reports and summaries
- Scientific reports
- Manuscripts
- Abstracts
- Medical communication materials
- Special data summaries
- Monographs
- Comprehensive reviews
- Scientific exhibits
- Other documents supporting regulatory submissions or internal use
Cross-Functional Collaboration
- Work with cross-functional teams to gather and evaluate clinical and safety information.
- Analyze data related to medical device safety and performance.
- Provide evidence-based recommendations to support assigned projects.
- Collaborate with stakeholders involved in clinical, regulatory, quality and medical activities.
- Communicate scientific findings clearly to relevant teams.
Regulatory and Compliance Responsibilities
- Monitor changes in medical device safety regulations and guidance.
- Keep track of relevant industry expectations and regulatory developments.
- Apply applicable quality and risk-management standards to clinical evaluation activities.
- Support continued compliance of clinical and regulatory documentation.
- Apply knowledge of ISO 13485, ISO 14971, EU MDR and relevant product-specific standards.
Educational Qualification / Eligibility Criteria
Candidates should have one of the relevant educational backgrounds specified by Medtronic, including:
- B.Pharm + M.Pharm
- M.Sc. or Master’s degree in Pure or Applied Sciences
- Biochemistry
- Biotechnology
- Microbiology
- Nursing
- Other relevant Life Sciences disciplines
- MBBS
- Doctorate in Pure or Applied Sciences
The qualification should be relevant to clinical, medical, scientific or healthcare-related work.
Experience Requirements
Candidates should have:
- 4–8 years of experience as a medical or clinical writer.
- Experience in the medical device and/or pharmaceutical industry.
- A combination of medical device and pharmaceutical experience is preferred where applicable.
Experience in clinical evaluation, regulatory medical writing or clinical evidence assessment can be relevant to the position.
Required Technical Knowledge
Candidates should have knowledge of applicable medical device and quality-system regulations, including:
- US and EU quality-system regulations
- ISO 13485
- ISO 14971
- 21 CFR Part 820
- 21 CFR Part 11
- EU MDR
- Product-specific industry standards
- Clinical evaluation principles
- Medical device clinical evidence
- Scientific literature evaluation
- Regulatory medical writing
Required Skills
The role requires:
- Strong medical and scientific writing skills
- Excellent written and verbal English
- Strong literature research capabilities
- Critical evaluation of clinical evidence
- Data analysis and interpretation
- Strong attention to detail
- Effective planning and organization
- Ability to manage multiple priorities
- Ability to work under time-sensitive conditions
- Strong communication skills
- Learning agility
- Commitment to continuous professional development
- Team-oriented working approach
Preferred Skills
The following qualifications or experience are considered beneficial:
- Experience working with global cross-functional teams
- Relevant medical writing industry certifications
- Experience in medical device clinical evaluation
- Familiarity with international regulatory environments
Work Location and Work Arrangement
Location: Nanakramguda, Hyderabad, India
Job Type: Full Time
Work Arrangement: Flexible Work Arrangement
The exact working arrangement and applicable flexibility will be subject to Medtronic’s employment policies and business requirements.
Salary and Benefits
Medtronic states that the position offers competitive compensation and a flexible benefits package. However, the exact salary amount has not been disclosed in the provided vacancy.
The position is also stated to be eligible for the Medtronic Incentive Plan (MIP), a short-term incentive program.
Specific benefits and compensation terms may depend on the applicable employment conditions.
Selection Process
The detailed recruitment and selection stages are not specified in the provided job listing. Candidates should follow the official Medtronic recruitment process and complete any assessments, interviews or other stages communicated by the company.
How to Apply for Medtronic Clinical Evaluation Medical Writer Recruitment 2026
Interested and eligible candidates can apply through the official Medtronic careers portal.
- Open the official Medtronic job application page.
- Review the complete eligibility and experience requirements.
- Prepare an updated CV/resume highlighting relevant medical writing and clinical evaluation experience.
- Submit the required information through the online application.
- Complete any additional recruitment steps requested by Medtronic.
Important Details Before Applying
- The position is based in Nanakramguda, Hyderabad.
- This is a full-time position.
- A flexible work arrangement is specified.
- Required experience is 4–8 years in medical or clinical writing.
- Medical device and/or pharmaceutical industry experience is required.
- Relevant qualifications include B.Pharm + M.Pharm, M.Sc./Master’s, MBBS or a relevant doctorate.
- Knowledge of ISO 13485, ISO 14971, EU MDR, 21 CFR Part 820 and 21 CFR Part 11 is required.
- Experience with clinical evaluation documentation is relevant.
- Strong English communication and scientific writing skills are required.
- The position is eligible for the Medtronic Incentive Plan (MIP).
- Exact salary has not been disclosed.
Medtronic Recruitment Fraud Alert
Medtronic advises candidates to apply only through its official recruitment channels. Genuine Medtronic recruitment communications use approved Medtronic platforms and official @medtronic.com email addresses.
Candidates should be cautious of anyone asking for payment or sensitive financial information during the recruitment process. Medtronic states that it does not request payment or sensitive personal information such as bank account details during the early stages of hiring.
If a communication appears suspicious, candidates should not respond, click unknown links or open unexpected attachments.
Frequently Asked Questions
1. What position is Medtronic hiring for?
Medtronic is hiring for the position of Clinical Evaluation Medical Writer.
2. Where is the job located?
The position is based at Nanakramguda, Hyderabad, India.
3. What is the required experience?
The vacancy specifies 4–8 years of experience as a medical or clinical writer.
4. Is medical device experience required?
The position requires experience in the medical device and/or pharmaceutical industry, with a preference for relevant medical device experience.
5. What qualifications are accepted?
Relevant qualifications include B.Pharm + M.Pharm, an M.Sc./Master’s degree in relevant sciences, MBBS or a doctorate in pure or applied sciences.
6. What documents will the Medical Writer prepare?
The role includes Clinical Evaluation Plans, Clinical Evaluation Reports, SSCPs, PSURs, clinical study documents, scientific reports and other regulatory or medical communication materials.
7. Does the role involve literature research?
Yes. The position involves comprehensive literature searches and critical assessment of clinical evidence from scientific publications and other credible sources.
8. Which regulations and standards are relevant?
The vacancy mentions ISO 13485, ISO 14971, EU MDR, 21 CFR Part 820, 21 CFR Part 11 and applicable product-specific standards.
9. Is the position full time?
Yes. The job is listed as full time.
10. What is the work arrangement?
The listing specifies a Flexible Work Arrangement.
11. What is the salary?
The exact salary is not disclosed. Medtronic describes the compensation as competitive and states that the position is eligible for the Medtronic Incentive Plan.
12. What is the job requisition number?
The requisition ID is R72925.
Important Note
Job availability, eligibility requirements, compensation, working arrangements and recruitment conditions may change. Candidates should verify the latest information on the official Medtronic careers portal before applying.