Regulatory Affairs Intern Job at MicroSurgical Technology, Washington DC

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  • MicroSurgical Technology
  • Washington DC

Job Description

Founded in 1976 and headquartered in Redmond, Washington, MicroSurgical Technology's passion is creating exceptional surgical devices and instruments used to restore or improve sight for patients all over the world. MST is part of UK based Halma PLC, a global company whose healthcare division helps provide technologies and solutions that enhance the quality of patients’ lives.

Our products are surgeon-designed and meticulously crafted to instill confidence and assurance in Cataract and Glaucoma procedures and include a wide range of surgical instruments such as forceps, scissors, hooks, spatulas, and knives, all designed for the delicate and intricate procedures required in microsurgery.

Together, we create a place where we are successful, motivated by our mission and inspire each other. This is where you can do your best work!

Job Title: Regulatory Affairs Intern

Reports To : Sr. Director, Regulatory Affairs

Hybrid – Redmond, WA

Job Summary:

Micro Surgical Technology, Inc., is seeking a motivated Regulatory Affairs Intern to support our Regulatory Affairs team with day-to-day compliance activities, data management, and regulatory documentation. This internship offers hands-on experience in the medical device industry, with a focus on Global Unique Device Identification Database (GUDID) support, UDI spreadsheet maintenance, and EU product code verification. This is an excellent opportunity for someone looking to build or strengthen a career in regulatory affairs within the medical device sector.

Key Responsibilities:

  • Assist with data entry and updates in the FDA’s Global Unique Device Identification Database (GUDID).
  • Support the clean-up and organization of the UDI master spreadsheet, ensuring accuracy, consistency, and alignment with product documentation.
  • Verify and apply appropriate GMDN (Global Medical Device Nomenclature) codes and other code nomenclature for medical devices.
  • Coordinate with cross-functional teams (e.g., QA, engineering, product management) to gather or verify data needed for regulatory process improvement initiatives.
  • Track and document changes to regulatory data and ensure version control.
  • Support the preparation and submission of regulatory documentation as needed.
  • Maintain internal regulatory databases and filing systems.
  • Provide general administrative support to the Regulatory Affairs team, including document formatting, compliance tracking, and support of special projects.

Qualifications:

  • Bachelor’s degree and working towards MS of Science in Biomedical Regulatory Affairs
  • Minimum of 2 years of experience in a regulatory, administrative, or data management capacity preferred.
  • Familiarity with UDI, GUDID, and GMDN terminology is a plus.
  • Proficient in Microsoft Excel; ability to manage and clean large datasets.
  • Strong organizational skills and attention to detail.
  • Excellent written and verbal communication skills.
  • Ability to work independently and in a team-oriented environment.

Internship Details:

  • Type: Paid Internship
  • Duration: 3–6 months
  • Location: Hybrid/Redmond, WA
  • Pay: Starting at $22.00/hour based on experience
  • Hours: 40 hours /week, flexible around class schedules

MicroSurgical Technology Inc. is an equal opportunity employer and does not discriminate based on gender, sex, age, race and color, religion, marital status, national origin, disability, sexual orientation, gender identity or expressions, veteran status, or any other category that is protected by applicable law.

Please note that only qualified candidates will be contacted for further consideration.

No agencies or recruiters please.

Job Tags

Flexible hours,

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