Senior Quality Engineer, ISO 13485, FDA, GMP,QMS,QE

Senior Quality Engineer, ISO 13485, FDA, GMP,QMS,QE

I have an excellent opportunity to work on a truly unprecedented project which is the largest life-science quality remediation project globally. The role, although initially a short term contract would most likely offer extension simply due to the huge scope of work currently with the company.

You MUST HOLD A VALID EU PASSPORT for this role and be available within 1 months notice.

Job description:

- Independently lead local and regional projects in accordance with the assignment of the Steering Committee
- Leading project teams
- Project planning, reporting, administration and controlling
- Initiate projects (prepare project scope documents, proposal for the Local Management & Quality Organization)
- Assessment and selection of solutions for internal and external processes
- Assure the knowledge transfer within and outside of the department
- Management and coordination of the external suppliers in projects
- Know and follow all laws and policies that apply to one's job and maintain the highest levels of professionalism, ethics and compliance at all time
- Support of the Quality and Process Manager in special tasks
- Management of the project portfolio Local Quality Department
- Follow the Quality standards and regulatory requirements

a) Professional education with three years work experience and additional professional training (eg Meister, Technician, HF) or
b) Technical college

- Quality Management as an advantage
- Project Management Education
- Project Management in regulated Industries (Medical Device/Pharma)

Senior Quality Engineer, ISO 13485, FDA, GMP,QMS,QE