Medical Writer Jobs at West Pharma | Life Science | Apply Now
Medical Writer Jobs at West Pharma present a high-impact opportunity for life science professionals looking to grow their careers in R&D medical writing. This role blends regulatory expertise, clinical documentation, and applied life science knowledge, making it ideal for candidates seeking long-term Life Science Jobs with global exposure, innovation, and patient-centric outcomes.
About the Company:
West Pharmaceutical Services is a global leader in injectable drug delivery systems with a legacy spanning over a century. Driven by innovation and patient safety, West Pharma supports life-saving therapies worldwide while fostering sustainability, diversity, and professional growth across its workforce.
Job Details:
The Medical Writer, R&D role within the Applied Research & Medical Affairs team focuses on preparing and managing clinical and regulatory documentation to support global submissions. The position involves close collaboration with cross-functional teams to ensure regulatory compliance, scientific accuracy, and timely delivery of documentation supporting medical devices and injectable therapies.
Key Responsibilities for Medical Writer Jobs:
- Develop CERs, CEPs, PMS reports, and PSURs
- Conduct comprehensive literature searches and reviews
- Analyze competitor and similar device data
- Summarize clinical risks, benefits, and treatment alternatives
- Coordinate with reviewers and technical leaders
- Ensure regulatory compliance with FDA, EU MDR, and global standards
- Maintain trackers, documentation, and quality systems
Education & Experience for Medical Writer Jobs:
- Graduate or Postgraduate in life sciences or Bio-Medical Engineering with 3 to 5 years’ experience.
- 3+ years of experience in the medical device clinical affairs domain.
Preferred Knowledge, Skills and Abilities:
- 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.).
This Medical Writer Job at West Pharma offers a rewarding career path for life science professionals passionate about regulatory excellence and scientific communication. Join a globally respected organization and contribute to innovations that improve patient lives worldwide.
