
10,000+ employees
🏥 Healthcare
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare • Healthcare Insurance • Biotechnology
Philips is a global health technology company committed to improving people's health and well-being through meaningful innovation. They focus on various domains including personal health, diagnosis and treatment, and connected care, striving to provide advanced technologies and solutions that enhance health outcomes for individuals and healthcare providers alike.
🔥 16 hours ago
🍂 Massachusetts, Washington – Remote
💵 $133k - $237k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
👻 Ghost score 0%
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10,000+ employees
🏥 Healthcare
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare • Healthcare Insurance • Biotechnology
Philips is a global health technology company committed to improving people's health and well-being through meaningful innovation. They focus on various domains including personal health, diagnosis and treatment, and connected care, striving to provide advanced technologies and solutions that enhance health outcomes for individuals and healthcare providers alike.
• Independently oversee comprehensive medical product safety evaluations using post-marketing surveillance, literature reviews, and clinical trial data • Identify and assess potential risks and safety signals to support patient well-being • Provide safety insights and recommendations for Health Hazard Evaluations, Risk-Benefit Analyses, and recall procedures • Support New Product Introduction, clinical studies, and post-marketing activities with safety perspectives • Collaborate on regulatory submissions and prepare safety documentation, including RBAs, protocols, Clinical Study Reports, and Clinical Evaluation Reports • Respond to safety inquiries from healthcare professionals, patients, and internal stakeholders • Support safety policies, procedures, and programs that promote compliance • Monitor evolving medical product safety regulations and guidelines • Provide input into safety studies and vigilance activities throughout the product lifecycle
• 5+ years of experience with a bachelor’s degree, or 3+ years of experience with a master’s degree or higher, in Medical/Clinical Affairs/Medical Safety in the Medical Device industry strongly preferred • Bachelor’s/master’s degree or higher in Medical Science, Nursing or equivalent • Strong knowledge of relevant medical device industry standards and regulations, including ISO and IEC • Strong knowledge of Health Hazard Evaluations, Issue Impact Assessments, and Risk-Benefit Analyses in a medical device environment • Prior bedside-related clinical experience preferred • Related specialized clinical experience preferred • MD/PhD preferred • Certified Professional in Patient Safety (CPPS) preferred • Excellent communication and ability to influence cross-functional stakeholders using clinical expertise and knowledge of standard of care and medical device standards • Ability to meet minimum physical, cognitive, and environmental job requirements with or without accommodation • US work authorization required; candidates requiring current or future visa sponsorship will not be considered • Must reside in or within commuting distance to posted locations
• Generous PTO • 401k with up to 7% match • HSA with company contribution • Stock purchase plan • Education reimbursement • Annual incentive bonus, sales commission or long-term incentives may be offered • Comprehensive Philips Total Rewards benefits program
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