Quality Manager (ISO 13485, MDR)

What we do

Working at Cryo means working with an interesting client base, including biomedical companies, IVF clinics, and (university) hospitals. Our team consists of 25-30 highly motivated and driven individuals. We offer a pleasant, hands-on culture in an open work environment with short communication lines.

What we are looking for

As Quality Manager at Cryo Products, you will be responsible for safeguarding and improving quality systems, focusing on ISO 13485 and compliance with the European Medical Device Regulation (MDR). You will play a key role in quality assurance for medical devices and support internal teams in complying with all relevant laws and regulations. You will also contribute to the management of distributors to ensure they meet quality standards and regulatory requirements.

Job requirements

• You have completed at least a higher professional education.
• You have at least 2-5 years of experience in a similar position within the medical device industry where experience with ISO 13485 and MDR is required.
• You have thorough knowledge of quality management systems (ISO13485, ISO9001) and relevant norms and standards.
• You are analytical and have an eye for detail and process improvement.
• You have excellent written and oral communication skills in Dutch and English.
• You are proactive and solution-oriented.
• You have strong organizational and administrative skills.
• You are a team player with an independent working attitude.

Offer

• A challenging and varied position within an innovative organization.
• A market-conform salary, depending on experience and education.
• Ample opportunities for personal development and training.
• Pleasant working environment.

Application procedure

Are you enthusiastic and do you recognize yourself in this profile? Send your CV and cover letter to dvaessen@cryo-products.com or fill out the contact form on www.werkenbijcryo.nl.