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Looking to build a high-impact career in medical writing for medical devices and regulatory submissions? BD (Becton Dickinson), a global leader in medical technology, is hiring a Medical Writer to support its Interventional Surgery Business Unit.
This remote medical writing job in India offers an excellent opportunity for professionals experienced in Clinical Evaluation Reports (CER), EU MDR, and regulatory documentation to work on global submissions and clinical strategy.
๐ Job Overview
- Position: Medical Writer
- Company: BD (Becton Dickinson)
- Job ID: R-539573
- Location: Remote (India โ Gurgaon base)
- Department: Clinical Affairs
- Experience: 2โ4 Years
- Job Type: Full-Time
- Mode: Remote
๐ง Key Responsibilities (Medical Writing & Regulatory)
- Prepare and review Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER)
- Conduct systematic literature reviews using PubMed, Embase, Ovid
- Analyze clinical data, real-world evidence, and trial results
- Support global regulatory submissions (EU MDR compliance)
- Collaborate with cross-functional teams:
- Regulatory Affairs
- Product Development
- Quality & PMS
- Ensure compliance with MEDDEV 2.7/1 Rev 4, MDCG, IMDRF guidelines
- Contribute to post-market surveillance reports and safety documentation
๐ Qualifications & Eligibility
- Bachelorโs degree in Life Sciences / Pharmacy / Medical field
- 2โ4 years experience in medical writing (medical devices preferred)
- Experience in end-to-end CER writing is mandatory
- Exposure to Class II / Class III medical devices
- Advanced degree (M.Pharm / MSc / MPH / PhD) โ Preferred
๐งฉ Required Skills
- Strong knowledge of EU MDR & clinical evaluation frameworks
- Expertise in literature search & systematic reviews
- Scientific writing with regulatory accuracy
- Familiarity with tools like DistillerSR (preferred)
- Proficiency in MS Word, Excel, PowerPoint
- Excellent English writing & proofreading skills
- Ability to handle multiple regulatory projects simultaneously
๐ผ Salary & Benefits (Estimated)
- Salary Range: โน8 LPA โ โน14 LPA (based on experience)
- Remote work flexibility
- Global exposure in medical device regulatory writing
- Opportunity to work on high-risk device submissions (EU MDR)
- Career growth in clinical affairs & regulatory writing
๐ Why This Role is High-Value (SEO Insight)
This role is ideal for candidates targeting:
- Medical Writer Jobs in India (Remote)
- CER Writing Jobs (EU MDR)
- Regulatory Writing for Medical Devices
- Clinical Evaluation Report Specialist Roles
- Transition roles from Pharmacovigilance / Clinical Research to Medical Writing
๐ฉ How to Apply
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