INTERNSHIP DETAILS

Co-op - Biological Safety Engineering - Murrysville, PA - January-June 2027

CompanyPhilips
LocationMurrysville
Work ModeOn Site
PostedNovember 5, 2026
Internship Information
Core Responsibilities
The co-op will support biological safety evaluations of materials and devices to ensure compliance with medical device regulatory standards. They will also assist in conducting verification and validation testing while curating data for Biological Evaluation Plans and Reports.
Internship Type
full time
Salary Range
$26 - $55
Company Size
72921
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Over the past decade we have transformed into a focused leader in health technology. At Philips, our purpose is to improve people’s health and well-being through meaningful innovation. We aim to improve 2.5 billion lives per year by 2030, including 400 million in underserved communities. We see healthcare as a connected whole. Helping people to live healthily and prevent disease. Giving clinicians the tools they need to make a precision diagnosis and deliver personalized treatment. Aiding the patient's recovery at home in the community. All supported by a seamless flow of data. As a technology company, we – and our brand licensees – innovate for people with one consistent belief: there’s always a way to make life better. Visit our website: http://www.philips.com/ Follow our social media house rules https://www.philips.com/a-w/about-philips/social-media.html
About the Role

Job Title

Co-op - Biological Safety Engineering - Murrysville, PA - January-June 2027

Job Description

Are you interested in a co-op opportunity with Philips? We welcome individuals who are currently pursuing an undergraduate (BS) and/or graduate (MS) or PhD degree to participate in 6 month paid co-op opportunities at our site in Murrysville, PA. Through this role you will gain meaningful, hands-on experience working for a HealthTech company.


Your role:

As a Co-op Biological Safety Engineer within the Biocompatibility Group, you will contribute directly to the design and development of new respiratory care products—including CPAPs, ventilators, respiratory masks, drug delivery devices, oxygen concentrators, and respiratory care accessories.

Key responsibilities include:

  • Supporting biological safety evaluations of materials, components, and finished devices used in sleep and respiratory care products, under direct supervision.
  • Assisting in reviewing material composition data, supplier documentation, and manufacturing process information to support biological risk assessments and compliance with ISO 10993, ISO 18562, and other related medical device regulatory standards.
  • Conducting verification and validation testing, analyzing material stability, and providing data to guide product development decisions.
  • Organizing, tracking, and curating biological safety data and test reports to ensure traceability and accessibility for ongoing and future evaluations.
  • Contributing to the development of Biological Evaluation Plans (BEPs) and Biological Evaluation Reports (BERs) by compiling background data, drafting sections, and ensuring adherence to applicable standards and company policies.

You're the right fit if:

  • You are currently pursuing a Bachelor’s or Master’s/PhD degree in Biomedical Engineering, Bioengineering, Materials Science & Engineering, or Chemical Engineering.
  • Your skills include strong engineering principals as well as analyzing chemical and physical properties of materials to draw scientific conclusions.
  • You’ve acquired 2+ years of experience in University and/or previous internships or coops and you are comfortable using test instrumentation and equipment in and out of a lab environment.
  • You thrive in a collaborative environment and can work effectively across technical disciplines, external partners, and global teams.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position.

How we work together


We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.


This is an office role.


About Philips

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.


Philips Transparency Details

The hourly pay range for this position is Bachelor Level: $26.00 to $29.00 an hour; Masters/PhD Level: $33.00 to $55.00 an hour plus overtime eligible. The actual base pay offered may vary depending on multiple factors including, job-related knowledge/skills, experience, business needs, geographical location, and internal equity. 


Details about our benefits can be found here. 


At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. 


Additional Information

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.

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 including Disability/Vets and maintains a drug-free workplace.

Key Skills
Biomedical EngineeringBioengineeringMaterials ScienceChemical EngineeringBiological SafetyISO 10993ISO 18562Regulatory StandardsVerification And ValidationMaterial StabilityBiological Evaluation PlansBiological Evaluation ReportsData AnalysisLaboratory InstrumentationTechnical DocumentationRisk Assessment
Categories
EngineeringHealthcareScience & ResearchManufacturing