If you are passionate about building your team up, setting clear goals and strive to achieve them in the field of Regulatory Affairs and Product Compliance – you are the candidate we are looking for! This is a challenging position where you must use your leadership skills, manage people and use of your experience in delivering high-quality products in a fast-growing, innovative medical company that specializes in the field of hearing diagnostics and balance disorders.

Working with us you will receive:

• a significant role in our Global Quality Department;
• independence in leading the team and tools to motivate and develop them;
• full-time work agreement in an international organization;
• opportunity to work closely with cross-functional teams, and will be expected to collaborate effectively with people at all levels of the organization;
• Scandinavian culture – we are informal and care about equality, independence, open dialog and work-life balance;
• social benefits: a social package (Multisport card on preferential financial terms and Medicover medical package), free buses to Rosówek;
• close cooperation with your team and internal stakeholders, but also your manager- (4) Flemming Vinding | LinkedIn

What tasks are waiting for you?

• Regulatory Affairs and Product Compliance Manager for DGS Diagnostics and leader for all employees in the team.
• Ensuring strong link between business needs and regulatory affairs / product compliance.
• Supporting and developing the structure of regulatory documentation.
• Ensuring unified procedures for documentation are in place and followed across projects.
• Ensuring communication towards stakeholders.
• Developing and implementing our regulatory affairs and product compliance strategy.
• Acting as project manager for prioritized initiatives.
• Acting as contact person for one of the brands we are supporting.

It would be great if you:

• have strong communication & relationship management skills, enthusiastic & self-driven, with a high degree of commitment;
• have strong people management skills, able to identify individuals’ motivations and profiles and utilize that understanding to build strong teams;
• have regulatory and product compliance knowledge in the field of medical devices;
• have ability to build up strong relationships towards critical stakeholders;
• have quality focus and thoroughness in general.

Please send your CV in English and kindly inform you that we will contact selected candidates.