Informacje o stanowisku

Main responsibilities:

• Product inspection after certain steps of the production process
• Final product testing and approval
• Product release and blocking in the ERP system
• Review and approval of production process documentation
• Creation and archive of DHR (device history record) per batch of product
• Participation in Quality Control of document creation (instruction, forms) and internal projects
• Follow the hygienic rules implemented at Lina Medical (cleanroom class 8)
• Participation in all quality processes like nonconformity, corrective and preventive actions, audits (internal and external), risk analysis, validations

Requirements:

• One year of work experience in the ISO area (preferable ISO13485; acceptable ISO9001)
• Any experience from Medical Device / Pharmaceutical area will be an advantage
• Fluent English both writing and speaking
• Driving license cat. B
• Familiar with basic IT tools (Microsoft Office)

We offer:

• Full-time job contract
• Opportunity to work in an international environment
• A number of benefits (private medical care, sports card, flexible working time)
• Great atmosphere in the office and interesting challenges
• Opportunity to grow with the organization and build a successful career path

Poznań - Oferty pracy w okolicznych lokalizacjach