Job Description
As a QC Associate you will be responsible for ensuring products and business processes meet GMP, Novo Nordisk A/S and local requirements, QC documentation and performing practical analyses.
• Perform practical activities during installation, qualification, calibration, and maintenance all
types of lab equipment
• Support the simple functional tests in QC, that includes creation (and timely update) of
procedures (SOP), participation in transfer of analytical procedures from supporting
laboratories to LMT, creation of verification protocols/reports for analytical methods
• Control, review and approve QMS documentation for QC with focus on proper documenting of
test results
• Perform needed actions on DVs/CRs related to Employee’s area of responsibility
• Register OOS, participate in investigations of OOS results, initiate LI (lab investigation) and
implement corrective actions when required