17/08/2025) Deputy Manager, Medical Writing

Summary We are the makers of possible BD is one of the largest global medical technology companies in the world Advancing the world of health TM is our Purpose and it s no small feat It takes the imagination and passion of all of us from design and engineering to the manufacturing and marketing of our billions of MedTech products per year to look at the impossible and find transformative solutions that turn dreams into possibilities Why Join Us A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive growth-centered and rewarding culture You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time To find purpose in the possibilities we need people who can see the bigger picture who understand the human story that underpins everything we do We welcome people with the imagination and drive to help us reinvent the future of health At BD you ll discover a culture in which you can learn grow and thrive And find satisfaction in doing your part to make the world a better place Become a maker of possible with us As a Medical Writer Scientific Affairs - Medical Affairs you will be responsible for the evaluation of clinical data and in the writing creation of clinical and scientific reports These documents are used in regulatory submissions to support safety and performance of our products to help define clinical endpoints for New Product Development Teams and to aid in the identification of new indications and unmet needs This role will support the BD Interventional Surgery Business Unit within the Scientific Affairs - Medical Affairs Function This individual will report to the Manager Medical Writing within this team If you would like to part of a talented and dynamic team and love working on challenging projects come join the BD family Essential Duties and Position Responsibilities Independently prepares writes and edits documents to support global regulatory submissions and associated communications with regulatory authorities The primary focus is independent writing of Clinical Evaluation Plans and Reports CEP CERs and associated documentation such as Post Market Clinical Follow-up PMCF Plans and Evaluation Reports and State of the Art literature reviews per the European Union EU Medical Device Regulation MDR Works with cross functional teams such as Regulatory Affairs R D Post-Market Surveillance PMS Quality and Marketing to create new or update existing CEPs CERs and PMCF documents and support PMS documents Responsible for critically analyzing and interpreting clinical data e g literature real world data clinical trials etc and writing a thorough and accurate analysis of such data in the clinical evaluation documents Ensures documents are produced in accordance with corporate business unit procedures regulations guidance and medical writing templates and style guides Provides technical mentorship and guidance to junior level medical writing associates as applicable Qualifications Knowledge and Skills Required Bachelor s Degree in the sciences with 3 years of experience in the medical device pharmaceutical industry and clinical scientific or literature research experience required Advanced degree in a scientific discipline preferred e g PhD PharmD MPH MSPH etc Published works is a plus At least 1 year of experience writing Clinical Evaluation Reports CERs beginning to end is required Ability to evaluate complex clinical data sets and write clear evidence-based summaries about safety and performance of medical devices with impeccable accuracy Excellent English Language communication skills Exceptional writing skills strong grasp of medical terminology and grammar and ability to quickly learn and write about varied therapeutic areas Highly skilled in Microsoft Word Excel Outlook and PowerPoint Thorough knowledge of medical device regulations and guidance including EU MDR MEDDEV 2 7 1 Rev 4 MDCG and IMDRF required Experience with high risk Class II and Class III medical devices preferred Working knowledge of clinical literature review clinical research device development regulatory requirements good clinical and data management practices and scientific or clinical research and methods Demonstrated expertise conducting literature searches using Embase PubMed Medline or other similar medical literature databases Experience with DistillerSR a plus Demonstrated ability to meet project goals within a matrixed environment Must be able to handle a variety of projects at the same time and complete deliverables on time Ability to communicate and collaborate in a remote team environment and also to work independently with minimal supervision Ability for potential travel up to 10 Click on apply if this sounds like you Becton Dickinson and Company is an Equal Opportunity Affirmative Action Employer We do not unlawfully discriminate on the basis of race color religion age sex creed national origin ancestry citizenship status marital or domestic or civil union status familial status affectional or sexual orientation gender identity or expression genetics disability military eligibility or veteran status or any other protected status To learn more about BD visit Required Skills Optional Skills Primary Work Location IND Gurgaon - 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