Description
A specialist pharmaceutical manufacturing company is urgently looking for a QA Specialist (Danish speaking) to support the compliance of its production activities.Location: Copenhagen area, Denmark
Duration: 3-4 months +
Role and Responsibilities:
• Managing the closure of non-conformances within the production area - liaising between the QA and production departments
• Identifying critical deviations and leading root cause investigations into these
• Ensuring that deviations are fully closed out and robust CAPAs are implemented
• Writing summary reports for the QA department
Requirements:
• Degree educated in scientific or engineering discipline, or equivalent experience
• Experience working with pharmaceutical production processes within a QA or compliance role
• Experience in CAPA management
• Strong knowledge of EU and FDA GMP regulations
This is an opportunity to play a critical role in the regulatory compliance of a site, paying highly competitive rates.