Medical Safety Manager, Ambulatory Monitoring – Diagnostics

Philips

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

Posted 10/23/2026full-timeRemote • United StatesMid-LevelSenior💰 $133,000 - $237,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in conducting safety evaluations and risk assessments within the medical device industry, with a strong focus on regulatory compliance and clinical safety standards. Proficient in providing safety insights for product lifecycle management and regulatory submissions.

Highest-signal resume keywords

Medical Device Industry ExperienceHealth Hazard EvaluationsRisk-Benefit AnalysesISO and IEC Standards KnowledgeCertified Professional in Patient Safety (CPPS)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Safety EvaluationsRisk ManagementClinical Trial Data AnalysisPost-Marketing SurveillanceRegulatory SubmissionsClinical Study ReportsClinical Evaluation ReportsIssue Impact AssessmentsSafety Policies ImplementationVigilance Activities

Soft Skills

Excellent Communication SkillsInfluencing Cross-Functional Stakeholders

Certifications & Qualifications

Certified Professional in Patient Safety (CPPS)

Industry Keywords

Medical AffairsMedical SafetyClinical ExperienceMedical Device StandardsPost-Marketing EffortsSafety SignalsRegulatory ComplianceField-Based RolePatient SafetyHealthcare Professionals

About the role

Key responsibilities & impact

Independently conduct comprehensive safety evaluations using post-marketing surveillance, literature reviews, and clinical trial data
Identify and assess potential risks and safety signals
Provide safety insights and recommendations for Health Hazard Evaluations, Risk-Benefit Analyses, risk management activities, and recall procedures
Support New Product Introduction, clinical studies, and post-marketing efforts
Provide safety input for regulatory submissions, RBAs, protocols, Clinical Study Reports, and Clinical Evaluation Reports
Respond to safety-related inquiries from healthcare professionals, patients, and internal stakeholders
Support implementation of safety policies, procedures, and programs
Monitor evolving medical product safety regulations and guidelines
Provide input into safety studies and vigilance activities throughout the product lifecycle
Work in a field-based role outside the company’s main facilities, generally at customer or supplier locations

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
Prior bedside related clinical experience required
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
Bachelor’s/master’s degree or higher in Medical Science, Nursing, or equivalent
MD/PhD strongly preferred
Related specialized clinical experience preferred
Certified Professional in Patient Safety (CPPS) preferred
Ability to perform the minimum physical, cognitive, and environmental job requirements with or without accommodation
Excellent communication skills and ability to influence cross-functional stakeholders using clinical expertise and knowledge of standard of care and medical device standards
US work authorization required; candidates requiring visa sponsorship now or in the future will not be considered
Must reside in or within commuting distance to the posted locations

Benefits

Comp & perks

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