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Quality & Regulatory Affairs Manager

BioSpace Recruitment Services
53719, Madison
Start date
Mar 16, 2023


  • Develops and implements regulatory strategy and plans for projects, as assigned to ensure client and agency needs are met. Actively drives interactions with regulatory bodies, as assigned ensuring information meets agency requirements for form and content in collaboration with client
  • Provides regulatory support for the development of technical files conforming to regulatory body requirements.
  • Assesses regulatory files to determine conformance to applicable regulatory requirements. Provides guidance to project teams on addressing any compliance issues or risks.
  • Assists in the preparation, coordination, and management of simple and complex regulatory submissions for medical device in accordance with applicable regulations.
  • Translates regulatory agency requirements into practical, workable requirements; assists in the coordination of internal/external authoring/review/comment adjudication and finalization of submission related documents.
  • Provides regulatory expertise in comments during document review, mindful of regulatory requirements pertaining to document content.
  • Interfaces with internal and external functional groups in the preparation, review, compilation, finalization submission and posting of regulatory submissions supporting its quality and regulatory obligations to clients. Acts as liaison between regulatory and other functional areas; represents regulatory in cross-functional team meetings providing expertise on regulatory guidelines and requirements.
  • Assists with developing corporate quality objectives and plans to ensure the quality management system (QMS) is implemented and managed to meet the quality objectives and applicable standards and regulations. This includes managing changes to the QMS ensuring its integrity.
  • Develops, implements, improves and maintains the QMS by ensuring its effectiveness and compliance with regulatory requirements, corporate quality policies, and applicable industry quality standards for the company and its client.
  • Identify key performance indicators/metrics and preventive measures; monitors key processes and develops and implements corrective actions and verification activities to ensure QMS effectiveness.
  • Provides reports to leadership regarding the effectiveness of the quality management system and provides identified areas of the QMS for improvement.
  • Drives quality culture companywide by providing quality and regulatory support to internal cross-functional teams and clients ensuring compliance to applicable processes, procedures, regulations, standards, and guidance.
  • Provides awareness of regulatory requirements and trains teams on quality and regulatory principles, requirements, regulations, standards, and good practices facilitating company-wide adherence.
  • Drives continuous improvement by supporting internal and external audits, and championing root cause analysis and CAPA to make change and reinforce the company’s quality culture.
  • Provides regulatory and quality support when selecting and qualifying suppliers and vendors by ensuring compliance with internal procedures and regulatory requirements.
  • Organizes and maintains the document control processes ensuring document accuracy, integrity, security, and quality. This includes managing changes to documents and records reviewing them for adequacy prior to issuance.



  • Maintains and increases job knowledge by studying the state-of-the-art, ongoing research in the field, etc.; participate in educational opportunities; read professional publications; maintain personal networks; participate in professional organizations.
  • Adheres to stated policies and procedures relating to health and safety, and quality management ensuring highest quality project deliverables to clients.



  • BA or BS degree in health or science related discipline.
  • 5 years of professional quality and regulatory experience in medical device or drug.
  • Experience in managing quality systems and regulatory submissions (pre-submissions, 510(k), De Novo, PMA). Extensive experience in FDA and EU medical device regulations also required.
  • Demonstrated experience as a self-starter and a fast learner; must work efficiently responding to changing priorities, able to work independently and within a team; must have excellent problem solving skills, analytical and research skills and attention to details.
  • Must consistently meet deadlines, manage projects across several collaborators and handle multiple projects simultaneously.
  • Excellent written and verbal communication skills are required and must be able to write clear reports, proposals, etc., and efficiently discuss the same with other scientists, engineers, and clients.

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