577050 Medical Safety Manager (all genders)

Medical Safety Manager (all genders)

In this role, you will have the opportunity to ensure patient safety and regulatory compliance across the full product lifecycle by supporting medical product safety surveillance, adverse event reporting, and proactive risk management activities. You will contribute to timely and accurate safety reporting to regulatory authorities and internal stakeholders, analyze safety data from clinical and post‑market sources, and collaborate cross‑functionally to identify, assess, and mitigate potential safety risks. Your work will play a key role in safeguarding patient well‑being and maintaining compliance with global regulatory standards.

Your Job

• Support the timely and accurate evaluation, documentation, and reporting of adverse events from multiple sources, including post‑market surveillance, literature reviews, and real‑world data, in accordance with applicable regulatory requirements.
• Analyze safety data from clinical trials and post‑market surveillance to identify potential safety signals, trends, and emerging risks, enabling early detection and proactive risk mitigation actions.
• Assist in the preparation and submission of safety reports and safety‑related content for regulatory submissions and key documents such as Risk‑Benefit Analyses (RBA), Clinical Study Reports (CSR), protocols, and Clinical Evaluation Reports (CERs).
• Collaborate with cross‑functional teams during product development and post‑market phases to assess safety risks and contribute to the development and implementation of effective risk management strategies.
• Conduct scientific literature reviews and ongoing safety surveillance activities to identify new or evolving safety issues and ensure continuous compliance with regulatory standards.
• Respond to safety‑related inquiries from healthcare professionals, patients, and internal stakeholders, ensuring transparent, accurate, and professional communication regarding product safety.
• Support the implementation and continuous improvement of safety‑related processes, policies, and procedures, and maintain up‑to‑date knowledge of evolving medical device safety regulations and guidelines.

You Should bring the following

• Bachelor’s or Master’s degree in Medical Science, Nursing, Clinical Science, or an equivalent discipline.
• 3–5 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 internal and external meetings.

Technical & Functional Skills

• Regulatory Compliance
• Risk Management and Risk‑Benefit Analysis
• Adverse Event Reporting and Signal Detection
• Safety Data Analysis and Interpretation
• Documentation and Regulatory Reporting
• Scientific Literature Review
• Strong business and stakeholder communication skills
• Certified Professional in Patient Safety (CPPS) (Preferred)

Philips benefits for you

• Annual leave: 30 days
• Mobility and devices: subsidized Germany ticket, leasing opportunities for private use (bicycles, cars, smartphones,…)
• Philips University & Philips in Balance: Wide range of professional training courses and for personal development & Healthcare
• “Partnerzeit” – two paid weeks off after your partner has given birth
• PhilipsMyShop: Discount on Philips products
• Free drinks and low prices in our canteen and Café
• Culture: Informal culture, a paid day for voluntary work, various team/cultural activities (on sustainability, diversity, …), etc.

How We Work Together

We believe that we achieve better results when we work together rather than apart. For this role this means to be on‑site at least 3 days a week.