4C Pharma Hiring for Medical Writer – Medical Devices

Are you passionate about medical writing and regulatory compliance?
4C Pharma Solutions is hiring a Senior Medical Writer – Medical Devices to join its growing team in Hyderabad, India. This role is perfect for professionals skilled in authoring CERs, CEPs, PMCFs, and PSURs under EU MDR guidelines.

If you have a background in Life Sciences, Pharmacy, or Biomedical Engineering, this is your chance to shape the future of medical device documentation and contribute to patient safety excellence.

🧾 Key Responsibilities

As a Senior Medical Writer (Medical Devices), you will:

• Author and review Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Clinical Follow-up (PMCF) reports, and Periodic Safety Update Reports (PSURs).
• Ensure alignment with EU MDR regulatory requirements and ISO 14155 standards.
• Collaborate with regulatory and safety teams to manage document timelines.
• Conduct literature searches, data analysis, and interpretation for medical devices.
• Maintain high-quality scientific and regulatory documentation.

🎓 Qualifications

• Education: B.Pharm / M.Pharm / Life Sciences / Biomedical / Engineering.
• Experience: 1–3 years in medical writing for medical devices.
• Strong knowledge of EU MDR, clinical evaluation processes, and regulatory documentation.
• Excellent scientific writing, analytical, and communication skills.
• Immediate joiners or those with a 30-day notice period preferred.

💼 Why Join 4C Pharma Solutions?

• Work on diverse global medical device projects.
• Collaborate with regulatory experts and experienced medical writers.
• Competitive salary packages (₹5–8 LPA depending on experience).
• Growth-oriented, supportive work environment.
• Full-time Work from Office (Hyderabad) opportunity.

📩 How to Apply

Send your updated resume to hr@4cpharma.com with the subject line:
“Application – Senior Medical Writer (Medical Devices)”