Medical Safety Manager – Ultrasound

Philips

. Independently oversee comprehensive medical product safety evaluations using post-marketing surveillance, literature reviews, and clinical trial data .

Posted 9/23/2026full-timeRemote • United StatesMid-LevelSenior💰 $133,000 - $237,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in medical product safety evaluations, including Health Hazard Evaluations and Risk-Benefit Analyses, while ensuring compliance with industry standards and regulations. Strong ability to communicate safety insights and collaborate with cross-functional teams to support patient well-being.

Highest-signal resume keywords

Medical Product Safety EvaluationsHealth Hazard EvaluationsRisk-Benefit AnalysesISO and IEC StandardsCertified Professional in Patient Safety (CPPS)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Post-Marketing SurveillanceClinical Trial Data AnalysisSafety Documentation PreparationClinical Study ReportsClinical Evaluation Reports

Soft Skills

Excellent CommunicationInfluencing Stakeholders

Certifications & Qualifications

Certified Professional in Patient Safety (CPPS)

Industry Keywords

Medical Device IndustryRegulatory SubmissionsSafety PoliciesComplianceClinical Affairs

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

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