QA Professional managing quality assurance and audits in pharmaceutical logistics. Responsible for documentation and compliance with regulatory standards in a decentral location.
Responsibilities
Support for qualification and validation activities within the GDP environment
Local document management including creation, maintenance and administration of quality documents
Local QA contact for operational units
Responsibility for local deviation management
Participation in QA projects
Preparation of quality-relevant documents (SOPs, qualification documentation, CAPA, Change Control) in German and English
Support in the implementation of new clients at the site
Conducting initial and refresher training in GDP
Responsibility for local change control processes
Management and oversight of automated temperature-monitoring systems
Requirements
University degree in natural sciences or engineering (e.g., biosciences, pharmacy, chemistry, medical engineering, biotechnology) or equivalent qualification
Alternatively: Completed vocational training in the pharmaceutical field or equivalent, with several years of professional experience and/or further qualification in GDP/GMP quality management
Relevant professional experience in quality assurance (GDP or Medical Devices), ideally in pharmaceutical wholesale
Strong knowledge of regulatory requirements in the pharmaceutical environment
Experience in pharmaceutical quality assurance (GDP and/or GMP) is required
Business-fluent German (C2) and very good English skills (at least C1), both written and spoken
Benefits
30 days of vacation per year
Employer contribution to company pension scheme and company disability insurance
Employee discounts via Corporate Benefits - bike leasing through JobRad - Wellpass - Nilo Health - staff parking
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