Job Title
Senior Toxicologist
Job Description
Exciting opportunity to play an important role in improving and saving lives around the world through generating Toxicological Risk Assessments for Philips Sleep & Respiratory care devices/products, ensuring they are safe for use by the intended patient population.
Your role:
- Preparation of toxicological risk assessments and dossiers using Organization for Economic Co-operation and Development (OECD), European Chemicals Agency (ECHA) and Restriction of Chemicals (REACH) guidance and any other regulatory agencies databases.
- Lead and/or manage the design, monitoring, and interpretation of In Vitro, In Vivo, or pre-clinical bio-compatibility studies conducted under Good Laboratory Practices (GLP). Interpreting the results of Biological/Volatile Organic Compound tests for impacts to patient safety and preparation of expert reports on toxicology/patient risk in the support of regulatory documentation.
- Reporting to the Manager-Biological Safety Engineering, you will work cross-functionally and collaborate with R&D, NPD, CRO's, Regulatory Agencies internal/external scientists and other stake holders.
- This role may require travel up to 10%.
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- You've acquired a minimum of 3 years' experience in Toxicological/Biological Risk Assessments, with proven experience in Toxicological/Biological test methods for compliance to ISO 10993 (required) and ISO 18562 (desired).
- Your skills include conducting biological assessments and documenting test evidence to support regulatory agency submittals, as well as interaction with Regulatory Agencies to address test strategies and questions related to toxicological assessments.
- You have a minimum of a Bachelor's degree in Toxicology or related fields (Required), MS or PhD desired . DABT or other health science/medical professional certifications desired. Knowledge of FDA 2020 Guidance Document "Use of International Standard ISO 10993-1". (Required)
- You have experience documenting biological risk assessments, analyzing results from Contract Resource Organizations (CRO's) and communicating with NPD teams and CROs to explain the results of toxicological assessments. Assist development teams in selecting proper materials for use in medical devices.
- You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position .
- US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
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- Discover our rich and exciting history.
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- Read more about our employee benefits .
Philips Transparency Details:
The pay range for this position is $92,000 to $158,000, annually. The actual base pay offered may vary depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
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This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates. Interested candidates are encouraged to apply as soon as possible to ensure consideration.
Philips is an Equal Employment and Opportunity Employer/Disabled/Veteran and maintains a drug-free workplace.