Senior quality assurance engineer (fulltime)
- Logistic/ Transport / Procurement
- North Limburg
- MBO ,
- HBO
Function content
For a fast-growing international company in Venlo, we are looking for an experienced
Quality Assurance Engineer (Fulltime)
This company is known for its innovative products and solutions in the healthcare industry and is one of the world's leading companies in medical devices. Together with your 6 colleagues you will be part of the Central Distribution Center (CDC) QA Team with a mandate to set-up and maintain labeling processes, implement quality standards, ensure, and execute compliance on every stage of the process. Assess potential risks and gives recommendations. Takes responsibility for all quality control aspects of the process.
Your responsibilities are:
- Process Task Ownership including where applicable tasks regarding Training, Document and Record Control;
- NC/CAPA support and where applicable NC/CAPA ownership;
- Process reporting to stakeholders in and outside CDC;
- Driving improvements regarding Labeling, Process, and Quality in general;
- Assisting on internal and external auditing;
- Supporting the CDC QA labeling group with implementation and maintenance of Value-Added Service initiatives including labeling, kitting, and other as applicable;
- Collaborating with internal & external stakeholders and their Company Design Divisions regarding labeling process set-up, execution & improvements;
- Any other QA activities as defined by the Associate QA Manager.
What you get in return
- Direct contract at our client with excellent working condition;
- Great career possibilities with meaningful growth opportunities;
- 27 vacation day (+ 3 days if not sick for 12 months);
- 8,5% holiday allowance;
- 10% bonus opportunity;
- Attractive stock purchase plan;
- Travel allowance;
- Working at home is possible.
Function requirements
- Education and/or experience equivalent to a MBO+ level or degree;
- Experience of working in Medical Devices Industry in a Quality Assurance Engineering function;
- Experience of working in an ISO13485, FDA QSR or other regulated Quality function environment;
- Customer and Service minded, hands-on mentality;
- Working proactively and independently with minimal supervision;
- Team player and able to positively influence others;
- Structured, eye for detail, precise, able to prioritize;
- Excellent knowledge of the English language;
- Administrative and analytical skills (create and review reports, compare the data);
- MS Office/Excel advanced experience;
- Team player, quick learner, able to work in a dynamic organization, and be able to work from home.
More info
Want to know more? Then contact René van den Borst on 06 - 1881 7501.
Apply
Interested? Then click on the application button or send your resume to r.vdborst@suc6recruitment.nl
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