Vice President, Global Quality Assurance & Regulatory Affairs
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About the Role
Greater Munich, Germany Area (On-site)
The Company is seeking a Vice President for Global Quality Assurance and Regulatory Affairs. This key leadership role is pivotal in the strategic development and alignment of quality and regulatory processes on a global scale. The successful candidate will be responsible for defining and implementing quality objectives and strategies, managing audits, and ensuring compliance with international regulatory requirements within the medical device industry. This includes the further development of quality management systems, regulatory approval processes, and compliance structures. The role also involves close collaboration with the executive board on strategic issues, budget management, and representing the company to various stakeholders. Applicants for the Vice President position at the company should hold a degree in a technical field, with additional qualifications as a quality manager and auditor. A minimum of several years' professional and management experience in quality assurance and regulatory affairs, particularly within the medical device industry, is required. The ideal candidate will have a strong background in international regulatory requirements, modern quality management methods, and relevant IT systems. Strategic thinking, excellent communication skills, and a proactive, analytical, and customer-focused approach are essential. The role demands a leader with a modern mindset, strong leadership skills, and the ability to develop people and organizations within a value-driven corporate culture.
Functions:
- Operations
About the Company
Traditional, globally active family-run company providing sophisticated medical technology solutions
Industry
Medical Devices
Type
Privately Held
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