QA Manager

**GC Corporation** was founded in 1921 in Japan and has developed itself into one of the most prominent companies in the development, production and distribution of a very wide range of dental products. Since 1972 GC Europe NV, our European Headquarter is located at the Researchpark Haasrode in Leuven. **GC Europe NV** supports and leads our different sales offices and dealers. Our warehouse spreads our products to Europe and the Middle East. Next to this we produce some leading products for dental technicians.

We are currently looking for a:
**QA Manager**

**Purpose of the job**

As Manager of the Quality Assurance (QA) department at GC Europe, you will oversee the QA System. Together with the QA team you will work in collaboration with other departments to achieve a lean and compliant QA system and promote the continuous improvement culture within the company.

**What is your mission?**
- Develop and implement quality assurance policies and procedures to ensure consistent and reliable product quality
- Lead a team of Quality Assurance Specialists and Assistants and ensure they are trained and equipped to perform their roles effectively
- Conduct regular audits to ensure that all processes are being followed and all products meet required standards
- Collaborate with other departments to identify areas for improvement and ensure that changes are effectively implemented
- Develop and maintain key metrics to track and report on the performance of the Quality Management function
- Stay up to date with industry developments and trends in quality assurance and implement best practices as appropriate

**Requirements**:

- A university degree in Engineering, Chemistry, Dentistry, or an equivalent Life Science degree. A postgraduate degree in Management or Business is a plus
- At least a 3 years tracking record in a team lead QA responsibility within the Medical Device / Pharma / Life Science industry
- Knowledge of relevant regulations and standards, such as ISO 13485, 9001, 14971
- Practical knowledge of EU Medical Device Regulation and FDA requirements
- Experience with QA standard operating procedures such as, NCR and CAPA management processes, and conducting internal and external audits
- Strong leadership and organizational skills, with the ability to manage an experienced team with multiple priorities and meeting tight deadlines
- Excellent analytical and communication skills
- Proficient with MS Office tools
- You speak and write Dutch and English fluently. Knowledge of other European languages is an asset.

**We offer you**:

- A challenging job in a growing international company in Leuven
- Full time employment with a permanent contract
- Flexible working hours & possibility to work from home
- Competitive salary & benefits (Hospital insurance, group insurance, meal vouchers, company car)
- Stunning offices and a great company culture, based on respect and comradeship
- An opportunity to contribute to a better, healthier world in collaboration with colleagues who are passionate about what they do.

**Interested?**

When applying, be sure to upload your CV and motivational letter to your profile
- GC is an equal opportunity employer that evaluates applicants regardless of their race, nationality, gender, age or disability._