Qualified Person (QP) for ATMPs | Southern Germany

Just in time for Christmas, you can secure your place in a leading Clinical Research Organisation based in a beautiful part of Southern Germany, famous for its amazing Christmas markets and phenomenal work life balance.

This opportunity isn’t only fantastic because of the career progression that goes with it, but it is also an amazing opportunity for someone with the right requirements to join a leading clinical research organisation in the heart of the EU.

Take a look below to see whether you could be this company’s next hire.

ROLE

• Release decision for clinical medicinal products
• Support client projects
• Audit management
• QP declaration creation
• SOP approval
• Complain handling and processing
• Approval for commissioning contract laboratories
• Deviations
• Root Cause Analysis for deviations
• Manufacturing documentation and validation review (documents)

REQUIRED (Essential)

• Pharmaceutical studies with 2 years’ experience in pharmaceutical QC
• An EU certified QP in accordance with the German Medicines Act
• At least 2 years work experience in an field involving analysis and QC of medicinal products
• Fluency in German and English

REQUIRED (Preferred)

• ATMP experience is preferred

REMUNERATION

• Basic Salary of £95K - £120K Per Annum depending on experience

RESPOND

• Call Terry Blaney on +44 (0)1580 211221 to Learn More about this Career Opportunity or e-Mail terry@arxconsultancy.com with Your Application, Including Your Current CV