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About the role

Overview: In this role you drive clinical evidence strategy and medical safety across the product lifecycle, collaborating with cross-functional teams and external experts. You translate safety signals into actionable decisions, supporting regulatory documentation and risk-benefit analyses. You’ll work on new product introductions, post-market safety, and scientific communications, shaping evidence-based decisions that underpin patient safety and product success. This position offers meaningful impact in a health-technology company focused on improving oral healthcare. Compensation / Benefits comprehensive Philips Total Rewards benefits program generous PTO 401k with up to 7% match HSA with company contribution stock purchase plan education reimbursement
Responsibilities: Support clinical evidence generation and medical safety activities across the product lifecycle Analyze clinical trial protocols and studies to inform development Ensure data integrity and rigorous interpretation of results Evaluate safety information from trials, post-market data, literature, and real-world data Identify potential safety risks and support ongoing safety monitoring Collaborate on New Product Introduction projects, post-market initiatives, and regulatory documentation Provide clinical and medical safety input to stakeholders and translate findings for clear decision-making
Key requirements: 7+ years of medical device industry experience in safety risk assessment or clinical research Experience in oral healthcare or dentistry preferred Strong knowledge of medical device standards (ISO, IEC) Understanding of Health Hazard Evaluations, Issue Impact Assessments, and Risk-Benefit Analyses in a medical device context Solid understanding of clinical research and relevant standards in medical devices PhD in scientific research in the medical devices space or Doctoral degree in Dentistry/Dental Hygiene preferred Excellent communication and ability to influence cross-functional stakeholders excellent communicator cross-functional collaboration influence and stakeholder management medical device safety risk assessment clinical development strategy post-market surveillance and real-world data analysis

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JOB OVERVIEW

Experience level

Lead

Location

Bothell, WA

Occupation

Occupational Health and Safety Specialists

Industry

Dental Equipment and Supplies Manufacturing

Posted

today

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