QA Professional managing quality assurance activities in pharmaceutical logistics. Working with Loxxess Pharma to ensure regulatory compliance and oversee documentation processes.
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-related 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 monitoring of automated temperature monitoring
Requirements
Degree in natural sciences or engineering (e.g., biosciences, pharmacy, chemistry, medical technology, biotechnology) or a comparable qualification
Alternatively: Completed vocational training in the pharmaceutical field or equivalent, with many 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
Solid knowledge of regulatory requirements in the pharmaceutical environment
Experience in pharmaceutical quality assurance (GDP and/or GMP) is mandatory
Business-fluent German (C2) and very good English (at least C1), both written and spoken
Benefits
Personal development: We support your professional growth through training in relevant and other interesting topics
Flexible workplace: After completion of onboarding, the option to work from home up to two days per week
Vacation: 30 days of annual leave
Benefits: Employer contribution to the company pension scheme and company disability insurance
Additional benefits: Employee discounts via Corporate Benefits; bike leasing through JobRad; Wellpass; Nilo Health; and employee parking
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