Medical Writing Job at West Pharmaceutical | Life Science R&D Jobs | Apply Now
If you are searching for a global-level Medical Writing Job, this opportunity at West Pharmaceutical could be your next big move. This high-responsibility R&D Job focuses on clinical and regulatory documentation, literature research, and scientific evaluation, making it ideal for life science and medical professionals aiming to build expertise in regulatory and clinical domains.
About the Company:
West Pharmaceutical has been improving patient lives for more than a century by supporting the safe delivery of injectable medicines worldwide. With a strong focus on innovation and regulatory excellence, West Pharmaceutical continues to lead in clinical documentation, applied life science research, and advanced healthcare solutions.
Job Overview:
This Medical Writing Job is part of the Applied Research & Medical Affairs team in Bangalore. The role involves developing Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), Post-Market Surveillance (PMS) reports, and Periodic Safety Update Reports (PSURs). As an R&D Job, it requires strong literature research skills, competitor analysis, regulatory compliance knowledge, and cross-functional coordination within West Pharmaceutical’s global operations.
Key Responsibilities:
- Develop CERs, CEPs, PMS reports, and PSURs
- Conduct comprehensive literature searches and scientific reviews
- Analyze clinical risks, benefits, and competitor data
- Ensure regulatory compliance with FDA and EU MDR standards
- Coordinate with reviewers and technical teams
- Perform quality checks and documentation validation
- Maintain trackers and project documentation
Educational Requirements:
- Graduate or Postgraduate in Life Sciences or Bio-Medical Engineering
- 3–5 years of experience in medical device clinical affairs domain
Skills Required:
- Experience with working in the pharmaceutical/CRO industry is preferred.
- Substantial understanding of medical devices and broad medical knowledge.
- Familiarity with regulatory frameworks such as FDA, EU MDR, MEDDEV, IMDRF, and MDCG.
- Passionate about technical writing and scientific documentation.
- Proficient written, verbal, and presentation communication skills.
- Keeps informed about the latest scientific developments for their application in ongoing projects.
- Demonstrated ability to think Critically and Analytically
- Ability to work as part of a team as well as independently
- Ability to work on medical literature and research data (via medical journals, and resources like Medline, PubMed, etc.)
If you aim to build a specialized career in a Medical Writing Job, this opportunity at West Pharmaceutical offers global exposure, regulatory expertise, and career advancement in a structured R&D Job environment. Take the next step toward contributing to impactful healthcare innovation.
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