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Agnieszka Kawalec
Talent Acquisition Consultant at Coopers Group AG - Life Science
Start date: As soon as possible
Duration: 1 year/possible extension
Workload: 100%
For our medical device client we are looking for a QA Manager.
Responsibilities:
QA supervision of qualification- and validation-activities for GMP-relevant equipment (including CSV), Analytics, infrastructure
Review and approval of GMP relevant Documents like Plans, Reports, SOPs, Change Control, Discrepancy Management, CAPA (corrective action and preventive action), Risk Analysis
Provide technical and quality assurance input to review and approval of manufacturing and Quality related documents as appropriate, Serve as a Subject Matter Expert (SME) in support of departmental functions and build partnerships and collaborate with stakeholders in other areas of the business to ensure success of the quality.
Leading of complex risk assessments Leading resolutions of quality issues and establish work priorities to meet targets and timelines
Creation and periodic review of quality agreements (QAGs) with contract organizations including quality agreements
Cost conscious working and optimization of processes. Ensure the efficient use of the available resources (staff, equipment, machinery, working spaces, materials).
Requirements:
Degree in Engineering, Chemistry, Life Science, Pharmacy or equivalent
Min. 5 years of Quality Management related experience in the medical device industry
Fluent Enlgish. German an advantage
Karrierestufe
Management
Beschäftigungsverhältnis
Zeitarbeit
Tätigkeitsbereich
Qualitätssicherung
Branchen
Herstellung medizinischer Geräte
Mit einer Empfehlung lassen sich Ihre Chancen auf ein Vorstellungsgespräch bei Coopers Group AG verdoppeln.