Medical Writer Medical Devices Job at Wipro regulatory documentation, CER, PSUR, PMCF roles with attractive salary range.
Company Overview
Wipro is a globally recognized organization with a strong footprint across information technology, healthcare, life sciences, and regulatory services. In the medical devices and healthcare domain, Wipro supports global clients through end-to-end regulatory, clinical, and post-market documentation services. The company is known for its structured work culture, international exposure, and high standards of compliance with global regulatory frameworks. Medical Writer Medical Devices Job at Wipro
As part of its growing medical devices and regulatory documentation practice, Wipro is inviting applications from experienced medical writers for a full-time, office-based role at its Pune location. Medical Writer Medical Devices Job at Wipro
Job Location & Employment Type
- Job Location: Pune, Maharashtra
- Employment Type: Full-time, permanent
- Work Mode: Work From Office (WFO)
- Industry Domain: Medical Devices | Regulatory Affairs | Medical Writing
Open Positions / Department Details
Wipro is hiring for the following position:
Medical Writer – Medical Devices
This role focuses on regulatory and post-market medical writing for global medical device markets, particularly supporting EU MDR and international compliance requirements. The position is suitable for mid-level to senior professionals with hands-on regulatory documentation experience. Medical Writer Medical Devices Job at Wipro
Key Roles & Responsibilities
Selected candidates will be responsible for preparing, reviewing, and maintaining high-quality regulatory and clinical documentation related to medical devices. Core responsibilities include: Medical Writer Medical Devices Job at Wipro
- Authoring and reviewing Clinical Evaluation Reports (CER) in line with EU MDR requirements
- Preparing Periodic Safety Update Reports (PSUR) and Post-Market Clinical Follow-Up (PMCF) documents
- Developing Post-Market Surveillance (PMS) plans and trend analysis reports
- Ensuring all documents comply with global regulatory guidelines and internal quality standards
- Conducting detailed literature searches and clinical data evaluations
- Interpreting clinical, safety, and performance data for medical devices
- Collaborating with cross-functional teams such as Regulatory Affairs, Quality, and Clinical teams
- Supporting regulatory submissions and ongoing lifecycle management activities
- Maintaining consistency, accuracy, and traceability across regulatory documents
This role demands strong technical writing skills and a deep understanding of medical device regulations. Medical Writer Medical Devices Job at Wipro
Eligibility Criteria
Education
Candidates must meet one of the following educational requirements:
- Graduate degree in Pharmacy
- Graduate degree in Biomedical Engineering
- Post-graduate degree in Life Sciences or related disciplines
Experience
- Minimum 2 years of relevant experience in medical device medical writing
- Maximum 15 years of experience for senior-level candidates
Skills Required
- Proven experience in medical device regulatory documentation
- Hands-on exposure to CER, PSUR, PMCF, PMS, and trend reports
- Strong understanding of EU MDR and global post-market surveillance requirements
- Ability to interpret clinical and safety data for medical devices
- Excellent written communication and technical documentation skills
- Capability to work in a structured, compliance-driven environment
- Willingness to relocate to Pune and work from office
⚠️ Candidates without medical device regulatory writing experience are advised not to apply.
Salary & Benefits
- Salary Range: ₹6,00,000 to ₹22,00,000 per annum (based on experience and role fit)
- Opportunity to work with a global healthcare and technology leader
- Exposure to international regulatory projects in the medical devices domain
- Clear career progression paths in medical writing and regulatory affairs
- Structured work environment with defined quality and compliance processes
Medical Writer Medical Devices Job at Wipro
Selection Process
- Resume shortlisting based on qualification and relevant experience
- Technical evaluation focusing on medical device documentation expertise
- HR discussion for shortlisted candidates
Final selection will depend on overall suitability and role requirements.
How to Apply
Eligible and interested candidates should apply via email only.
Send your updated resume to:
📧 simran.sagar@wipro.com
Email Subject Line (mandatory):
Medical Writer – Medical Devices | Pune
Applications without the correct subject line may face delays in shortlisting. Medical Writer Medical Devices Job at Wipro
Important Dates
- Application Mode: Ongoing (apply at the earliest for better consideration)
Why Apply for This Pharma Job?
- High-value role in the fast-growing medical devices regulatory domain
- Attractive salary range for experienced medical writers
- Opportunity to work on EU MDR and global compliance projects
- Strong brand value and professional credibility with Wipro
- Ideal role for professionals looking to advance in regulatory medical writing
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical and life sciences job information platform. We are not affiliated with Wipro or any of its hiring partners. All job details are shared strictly for informational purposes. Candidates are advised to verify role details directly with the employer before applying. Medical Writer Medical Devices Job at Wipro
Final Call-to-Action
If you have hands-on experience in medical device regulatory writing and are ready to work on global compliance projects, this opportunity at Wipro Pune could be your next career milestone. Apply now with a well-updated resume and take the next step in your medical writing career. Medical Writer Medical Devices Job at Wipro
