Quality Ops Intern: Regulated Medical Devices

Boston Scientific Gruppe; Netherlands; Remote; EUR 10,000 - 12,000; Part time

Benefits offered by this job

Hands-on Quality ops experience

Mentorship from Quality professionals

Diverse, collaborative team

Job summary

Boston Scientific invites students to join the Quality Operations team in Kerkrade for a hands-on internship focused on ensuring compliance with internal procedures and global standards.

As an intern, you will review processes, document findings, and collaborate with stakeholders to update procedures and align local practices with global requirements. This role offers exposure to regulated environments in medical device operations and mentorship from seasoned professionals.

Qualifications

• Strong attention to detail and accuracy.
• Critical mindset and problem-solving.
• Team player with interpersonal and collaboration skills.
• Initiative, commitment and customer/patient orientation.
• Strong communication and reporting skills.
• Proficiency with Microsoft Office (Excel, Word, Adobe).
• Proficiency in English (spoken and written).

Responsibilities

• Conduct Practice vs. Procedure reviews within Quality Operations.
• Identify gaps or non-conformities between documented requirements and execution.
• Document findings clearly and objectively.
• Support or lead updates to procedures and related documentation.
• Collaborate with stakeholders to validate proposed changes.
• Assist in harmonizing local procedures with global standards.

Skills

Detail orientation

Critical mindset

Team player

Initiative & commitment

Communication skills

MS Office

English proficiency

Education

BSc/MSc student in Life Sciences / Industrial Engineering / Quality Management / Biomedical Sciences / Supply Chain

Job description

Boston Scientific invites students to join the Quality Operations team in Kerkrade for a hands-on internship focused on ensuring compliance with internal procedures and global standards.

As an intern, you will review processes, document findings, and collaborate with stakeholders to update procedures and align local practices with global requirements. This role offers exposure to regulated environments in medical device operations and mentorship from seasoned professionals.