Senior Manager, RA Processes, Systems and Tools

Radiometer

Copenhagen, Denmark

The Senior Manager, RA Processes, Systems and Tools for Radiometer is responsible to drive process improvements as well as implementation of systems and tools within the Regulatory Affairs to support an efficient regulatory support to the organization and growth of the company.

You will be a part of the Regulatory Affairs leadership team and report to the Sr Director Regulatory Affairs responsible for global regulatory strategy and tactical planning, providing guidance and support to the organization during product development as well as post market and through market expansions globally with our product portfolio. The Regulatory affairs team assures that defined regulatory strategies are effectively implemented and maintained in line with changing regulatory and business needs. If you thrive in an amazing, multifunctional, leadership, fast paced, supporting role working with stakeholders across the global organization and want to work to build a world-class regulatory affairs team - read on.

In this role, you will have the opportunity to:

Oversee and direct an awesome team of highly engaged associates and focus on continuous development of the team.
Drive process improvements for RA owned processes and procedures.
Implement systems and tools that supports the Regulatory Affairs organization towards a more efficient way of working.
Work with key stakeholders and a cross-functional team monitoring, interpreting, and implementing new/changed legislation, standards, and guidance’s though the Regulatory Intelligence process and other processes such as MAPSS (Marketing, Advertising, Promotional, Scientific, and Sales) material.
Establish and drive Daily Management in RA as well as the improvement opportunity funnel.

The essential requirements of the job include:

Minimum bachelor’s degree in a technical field such as chemistry, biochemistry, biology, or related required.
Knowledge and experience in global IVD/MD regulations, quality standards such as ISO 13485, US FDA 21 Part 820, IVDR/MDR, design control, risk management, etc. required.
Minimum 7 years of regulatory experience related to medical device/in vitro diagnostics required.
Demonstrates excellent negotiation skills, problem-solving skills and builds consensus.
Demonstrates effective communication skills in written and oral channels both within Regulatory and across the organization.
Able to deliver challenging messages effectively without compromising important business relationships.
Experience working in a complex matrix environment.