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Are you an experienced Medical Writer passionate about medical device safety and regulatory compliance?
Wipro is inviting applications for the position of Senior Medical Writer (PMS) at its Pune office.
This is a Work-from-Office opportunity for professionals skilled in drafting Post-Market Surveillance (PMS) reports for medical devices.
This role is ideal for graduates in pharmacy, biomedical engineering, or postgraduates in life sciences who are ready to contribute to Wipro’s excellence in global healthcare documentation.
Key Responsibilities
- Prepare and review Post-Market Surveillance (PMS) reports and documentation for medical devices.
- Ensure compliance with regulatory standards (MDR, ISO 13485, and ISO 14971).
- Collaborate with cross-functional teams for data collection, analysis, and summary of PMS findings.
- Identify product safety trends, summarize complaints, and prepare PMS summaries.
- Maintain and update PMS plans, PSURs, and vigilance reports.
- Ensure timely submission of all regulatory documentation and support audit readiness.
Required Qualifications
- Educational Background:
- Graduate in Biomedical Engineering or Pharmacy, or
- Postgraduate in Life Sciences.
- Experience: 5–8 years of hands-on experience in drafting PMS reports for medical devices.
- Preferred: Immediate joiners are highly encouraged to apply.
- Work Mode: On-site (Wipro Office, Pune).
Why Join Wipro?
- Work with a global leader in healthcare and life sciences technology.
- Opportunity to contribute to regulatory excellence and patient safety.
- Collaborate with industry experts and leading medical device clients.
- Competitive salary and benefits aligned with market standards.
Application Process
If you meet the above qualifications and are ready to make an impact, send your updated CV to:
📧 Simran.sagar@wipro.com
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Location: Wipro Office, Pune, Maharashtra
Employment Type: Full-time, Work-from-Office
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