At Terumo, we advance lifesaving medical technologies to benefit society. Are you eager to make a difference with us? Here, you’ll grow your expertise while staying true to your personal aspirations.
Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement. If you see yourself in our values, keep reading; this might be the opportunity you're looking for
Department Info
The Quality Regulatory (QR) Department is dedicated to ensuring that our products consistently meet the highest quality standards and adhere to regulatory requirements. Within QR, there are five specialized subgroups:
- Quality Systems
- QA Development
- Quality Operations
- Regulatory Affairs
- Complaint & Vigilance
Job Summary
As a QC Inspector, you will play a key role in ensuring the quality and compliance of both finished and semi-finished products before they reach the market. You will be responsible for executing tests and inspections, evaluating results, and supporting continuous improvements in line with Good Laboratory Practice (GLP) and Good Documentation Practice (GDP) standards. This position will initially operate in day shift (until 2027) and transition to a 2-shift system from 2027 onward.
Job Responsibilities
-
Conduct physical, functional, dimensional, and visual tests/inspections in accordance with prescribed procedures for monitoring, stability studies, validation, and engineering requests.
-
Document all activities and results accurately, ensuring compliance with GLP/GDP guidelines.
-
Perform administrative processing, including evaluation of results against specifications, investigating out-of-spec findings (OOS), and creating non-conformity reports within the ERP system.
-
Maintain a clean and compliant working environment, monitor lab parameters and equipment, and ensure correct maintenance and verification.
-
Collect, archive, and manage retention samples, batch records, and test results. Support semi-automatic line testing where required.
-
Accurately interpret results, report findings, and collaborate closely with colleagues in Quality and Production to address issues promptly.
-
Enter and process results in SAP or summary files for release and trend analysis. For raw materials, ensure timely release in SAP.
Profile Description
-
Education: Bachelor’s degree in (Clinical/Industrial) Chemistry, Food, Biomedical Laboratory Technology, Process Technology, or equivalent experience.
-
Strong ability to work independently with a high degree of quality awareness and attention to detail.
-
Fluent in Dutch. Practical knowledge of English (written and spoken).
-
Comfortable working with IT systems (SAP and general office applications).
-
Flexible to transition from a day-shift role (until 2027) into a 2-shift system.
Offer
At Terumo, we believe in offering more than just a job. It's an opportunity to make a difference, contribute to society, and be a part of our passionate and high-performing team.
Rewards That Match Your Dedication: We offer a competitive salary and benefits package that sets the benchmark for rewarding your commitment.
Join a Passionate Team: Become a valued member of our passionate and high-performing team where everyone is treated with respect. We are dedicated to creating a diverse, equal, and inclusive work environment.
Invest in Your Development: At Terumo, we invest in our associates by providing a wide range of development opportunities to help you grow both personally and professionally.
Connect with Us: During the recruitment process, you'll have the opportunity to engage in meaningful conversations with the hiring manager and other enthusiastic Terumo associates.
Contact Person
Jarne Jans - Talent Acquisition Business Partner
Working at Terumo means advancing healthcare with heart. Here, you are empowered to grow your own way, inspired to create to innovate, and supported as we get there together. Join us in shaping a healthier future for our patients, society, and each other.
