This position is no longer open for applications

Essential duties and responsibilities:

• Write process verification/validation test protocols

• Run machine test protocols (commissioning, process characterization and qualification) including record management

• Manage deviations including root cause analysis, change management and implementation

Requirements:

Minimum 5 years’ experience with process validation within the Medical Device or Pharma industry.

• Education Level: M.Sc Engineer or equivalent
• Language requirement: Excellent in English and Swedish (write, read and speak)
• Good communication skills
• Experience with technical advanced equipment
• Experience of working in teams and building teamwork
• Experience of Working in virtual teams are beneficial