Description
Project: Freelance Quality Specialist (m/f/d)Industry: Medical technology
Project start: Asap
Project duration: 24 months
Location: Rhône-Alpes region (2-3 days per week on Site)
Tasks:
MSA/ audit planning/ process risk/ statistics
Perform gap analyses between the DHF/DMR documents and production requirements (e.g. drawings, pFMEAs, inspections, MSA, PCPs...)
Acquire knowledge of requirements and processes related to these documents
Collaborate with SMEs to update or create DHF/DMR documents
Lead the execution/creation of new documents
Liaise with functional managers to establish clear acceptance criteria for each document prior to execution
Qualifications:
5+ years of relevant experience
Experience in medical technology required
Team player
Motivated, engaged, influential
Very strong communication skills
French speaker highly preferred