Senior Medical Safety Manager HPM (all genders)

Philips
Germany
Workplace: HybridFull timeFunction: Healthcare (Clinical, Medical, Wellness)Experience: 7-10 yearsSkills: ["Stakeholder communication","Proactive risk management"]

Ensure patient safety and medical device regulatory compliance across the Hospital Patient Monitoring product lifecycle. You’ll oversee adverse event reporting and safety surveillance, analyze clinical and post-market safety data to detect signals and emerging risks, and prepare safety submissions and safety-related documentation such as risk-benefit analyses, CSR, protocols, and CERs. Partner with cross-functional teams to implement risk management strategies, conduct literature reviews, and respond to safety inquiries.

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Philips
Philips
1 month ago

Senior Medical Safety Manager HPM (all genders)

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Source: Company careers pageValidated by: Fursa AI
Last checked: 27 days agoStatus: Live

Job Summary

Ensure patient safety and medical device regulatory compliance across the Hospital Patient Monitoring product lifecycle. You’ll oversee adverse event reporting and safety surveillance, analyze clinical and post-market safety data to detect signals and emerging risks, and prepare safety submissions and safety-related documentation such as risk-benefit analyses, CSR, protocols, and CERs. Partner with cross-functional teams to implement risk management strategies, conduct literature reviews, and respond to safety inquiries.
Location: Germany
Workplace: Hybrid
Employment Type: Full time
Job Function: Healthcare (Clinical, Medical, Wellness)
Seniority: Manager level

Key Responsibilities

  • •Support timely and accurate evaluation, documentation, and reporting of adverse events from post-market surveillance, literature reviews, and real-world data.
  • •Analyze safety data from clinical trials and post-market surveillance to identify safety signals, trends, and emerging risks for early mitigation.
  • •Prepare and submit safety reports and safety-related content for regulatory submissions and key documents (RBA, CSR, protocols, CERs).
  • •Collaborate cross-functionally during product development and post-market phases to assess safety risks and implement risk management strategies.
  • •Conduct scientific literature reviews and ongoing safety surveillance; respond to safety inquiries from healthcare professionals, patients, and internal stakeholders.
Travel: Medium travel

Pay and Benefits

Perks:Annual LeavePensionPaid Leave

Key Requirements

  • •Bachelor’s or Master’s degree in Medical Science, Nursing, Clinical Science, or an equivalent discipline.
  • •7–10 years of experience in Medical or Clinical Affairs within the Medical Devices or Biotech industry.
  • •Clinical experience in adult or pediatric ICU, operating room, or telemetry environments.
  • •Willingness and ability to travel internationally approximately 10–25% annually for meetings.
  • •Certified Professional in Patient Safety (CPPS) (preferred).
Experience:7-10 yearsMedical devicesBiotechClinical affairsPost-market surveillance
Education:
Skills:Stakeholder communicationProactive risk management
Certifications:Certified Professional in Patient Safety (CPPS)
Languages:English

Company Brief

Philips
Global health technology company focusing on diagnostic imaging, patient monitoring, and consumer health products. Philips develops medical devices, healthcare informatics, and solutions to improve patient care and personal well-being.
Industry: HealthTech
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Amsterdam, Netherlands
Founded: 1891
Glassdoor
Glassdoor: 3.8
WebsiteLinkedIn