Intern - Regulatory Affairs - Colorado Springs, CO - Summer 2026

8 Minutes ago • All levels • $52,000 PA - $58,240 PA
Legal

Job Description

Philips is seeking a Regulatory Affairs Intern for a 3-month internship in Colorado Springs, CO, starting Summer 2026. This role is for undergraduate engineering students interested in healthcare solutions, specifically within the Image Guided Therapy (IGT) team. The intern will support regulatory filings and department projects, preparing post-market submissions, assisting senior specialists with new product filings and changes, and ensuring compliance with global medical device regulations like FDA, ISO, and EU standards. This position offers hands-on experience in a medical device manufacturing environment, contributing to the next generation of healthcare solutions.
Must Have:
  • Currently pursuing an undergraduate degree in engineering, Regulatory Affairs, or a science-related field.
  • Prepare post-market submissions (PMA annual reports, technical files, updates/submissions).
  • Support senior RA Specialists in preparing regulatory filings for new products, post-market changes, and line extensions.
  • Review regulatory issues with RA Management.
  • Obtain knowledge in global regulatory requirements.
  • Follow Spectranetics Quality System procedures for compliance with US CFR, ISO 13485, MDD/MDR, CMDR, MDSAP, and other applicable regulations.
  • Apply FDA, ISO, EU, and other applicable regional regulations.
  • Ability to manage multiple tasks with accuracy and high attention to detail.
  • US work authorization is a precondition of employment.
  • Must reside in or within commuting distance to Colorado Springs, CO.

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Intern – Regulatory Affairs – Colorado Springs, CO – Summer 2026

We welcome individuals who are currently pursuing an undergraduate degree in engineering to join Philips as a Regulatory Affairs Intern in our Colorado Springs location for a 3-month long internship to play a role in creating our next generation of healthcare solutions. You will have the opportunities to join the Philips Image Guided Therapy (IGT) team, a medical device manufacturer offering healthcare solutions in the field of cardiovascular imaging and interventional hemodynamics. The Regulatory Affairs Intern performs specific regulatory tasks in support of a regulatory filing or department project with direct support from management or more senior regulatory affairs specialists.

Your role:

Under the supervision of the Regulatory Affairs (RA) Manager or a more senior Regulatory Affairs Specialist, a Regulatory Affairs Intern is responsible for:

  • Preparing post-market submissions i.e. PMA annual reports, updating technical files, and similarly scoped updates/submissions.
  • Support more senior RA Specialists in the preparation of regulatory filings for new products, as well as post market changes and line extensions.
  • Reviews regulatory issues with RA Management.
  • Obtaining knowledge in global regulatory requirements.
  • Following Spectranetics Quality System procedures to ensure compliance with US CFR, ISO 13485, MDD/MDR, CMDR, MDSAP and all other applicable regulations.
  • Applying FDA, ISO, EU, and other applicable regional regulations

You're the right fit if:

  • You are working towards a degree in engineering, or preferably in Regulatory Affairs and/or a science related field.
  • You have general knowledge of medical device regulations (21CFR), FDA law, MDD, other global laws and regulations and standards, including ISO14971, IEC 60601 and related particular standards.
  • You have strong written, oral, and interpersonal skills.
  • You are able to manage multiple tasks and perform with accuracy and a high attention to detail.
  • You are proficient in computer skills, especially in Microsoft Office.
  • 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 onsite role.

Philips Transparency Details

The hourly pay range for this position is $25.00 - $28.00. 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.

Company relocation benefits will not be provided for this position. For this position, you must reside in or within commuting distance to job posting location.

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.

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