Medical Job | Medical Writing Role at Becton Dickinson
Looking to advance your career in medical job with a globally trusted healthcare brand? Becton Dickinson (BD) is hiring a Deputy Manager, Medical Writing-a remote position based in Haryana. This is an excellent opportunity to join one of the top names in Becton Dickinson careers, contributing to clinical and regulatory excellence through high-quality documentation. If you’re passionate about science, writing, and regulatory compliance, explore one of BD’s most rewarding remote medical writing jobs today.
Job Details
- Position: Deputy Manager, Medical Writing
- Company: Becton Dickinson (BD)
- Location: Remote, Haryana, India (Primary Work Location: IND Gurgaon – Aurbis Summit)
- Job ID: R-529997
About the Company
Becton Dickinson (BD) is a world-leading medical technology company transforming healthcare through innovation and science. With over 70,000 associates in 190+ countries, BD is committed to improving medical discovery, diagnostics, and care delivery. Becton Dickinson careers offer professionals the chance to grow, collaborate, and impact global health outcomes through meaningful medical jobs across diverse functions.
Qualifications and Experience for this Medical Job
Required:
- Bachelor’s or advanced degree in medicine or a related field.
- 1–3 years of medical device experience (or 5+ years total industry experience).
- Strong English writing, communication, and analytical skills.
- Expertise in Microsoft Office and ability to manage multiple projects independently.
- Understanding of clinical research principles and regulatory writing requirements.
Preferred:
- Experience authoring CERs, CEPs, and PMCF documentation.
- Familiarity with European MDR and MEDDEV 2.7.1 guidelines.
Job Description
As part of BD’s expanding portfolio of medical job, this Deputy Manager, Medical Writing role involves developing and maintaining regulatory and clinical documentation, including Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), and Post-Market Clinical Follow-up (PMCF) Plans and Reports. You will collaborate with cross-functional teams across Regulatory, R&D, and Quality to ensure documents meet global standards and regulatory requirements. This flexible, remote medical writing job is ideal for professionals seeking autonomy, scientific engagement, and impactful healthcare communication.
Medical Job – Key Responsibilities
- Conduct comprehensive clinical evaluations, including data analysis, literature review, and report preparation.
- Author and maintain CERs, CEPs, and PMCF documents following EU MDR and MEDDEV 2.7.1.
- Collaborate with internal teams to gather technical, clinical, and regulatory information.
- Ensure all documentation meets accuracy, compliance, and timeline expectations.
- Conduct systematic literature reviews and summarize data for technical files.
- Provide quality control (QC) and peer review support for documents authored by team members.
- Stay updated on evolving regulatory and medical device standards.
- Support continuous improvement by revising templates and contributing to SOP development.
