Medical Safety Manager – Hospital Patient Monitoring

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $133k - $237k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 0%

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Philips

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🔧 Hardware

💰 Post-IPO Equity - Philips on 2025-03

Healthcare • Hardware

Philips is a global health technology company (Koninklijke Philips N. V. ) that develops medical imaging systems (MR, CT, handheld ultrasound), patient monitoring and critical care solutions, and consumer health products such as Sonicare and the Pregnancy+ app. The company emphasizes delivering solutions that help clinicians provide faster, better care and also offers consumer-focused personal care and oral-health products. Philips positions itself around healthcare equipment, clinical informatics and connected care, and patient-facing health technologies.

📋 Description

• Conduct comprehensive evaluations of safety information from Post-Marketing Surveillance and literature searches • Contribute insights and recommendations to Risk Management, Health Hazard Evaluations, Risk-Benefit analyses, and recall procedures • Provide safety perspectives for New Product Introduction projects, clinical studies, and Post-Marketing Surveillance efforts • Supply safety inputs for regulatory submissions, Risk-Benefit Analyses, protocols, Clinical Study Reports, and Clinical Evaluation Reports • Conduct literature reviews and surveillance activities to identify emerging safety issues • Answer safety-related inquiries from healthcare professionals, patients, and internal stakeholders • Contribute to implementation of safety policies, procedures, and programs • Maintain awareness of evolving medical product safety regulations and guidelines and ensure compliance • Provide input into safety studies and medical device vigilance activities throughout the product lifecycle • Analyze clinical trial and post-market surveillance data to identify safety signals and trends

🎯 Requirements

• 5+ years of experience with a Bachelor’s OR minimum 3+ years of experience with a Master’s in Medical/Clinical affairs in the Medical Device/Biotech industry or equivalent • Critical Care and/or Telemetry experience required • Experience as a practicing clinician required • Strong knowledge of relevant medical device industry standards and regulations (ISO, IEC, etc.) • Strong knowledge of Health Hazard Evaluations, Issue Impact Assessments, and Risk-Benefit Analyses in a medical device environment • Bachelor’s/master’s degree in medical, Nursing, or equivalent • Excellent communication skills and ability to influence cross-functional stakeholders using clinical expertise and knowledge of standard of care and medical device standards • Willingness and ability to travel up to 25% based on business needs • Ability to successfully perform minimum physical, cognitive, and environmental job requirements with or without accommodation • US work authorization required; candidates requiring current or future sponsorship will not be considered • EDT and CDT time zone preferred

🏖️ Benefits

• Generous PTO • 401k with up to 7% match • HSA with company contribution • Stock purchase plan • Education reimbursement • Annual incentive bonus may be offered • Sales commission may be offered • Long-term incentives may be offered • Company relocation benefits will not be provided