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 of all types of lab equipment.
● Support the simple functional tests in QC, which includes creation (and timely update) of procedures (SOP), participation in the 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 a focus on proper documenting of test results.
● Perform needed actions on DVs/CRs related to the employee’s area of responsibility.
● Register OOS, participate in investigations of OOS results, initiate LI (lab investigation), and implement corrective actions when required.