QC Coordinator

Major accountabilities:

• OOx/Deviation handling.
• CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) – protocol preparation, evaluation, report preparation.
• Reporting (Trend analysis, evaluation) -Performance of protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release) -Provide expert Support for site qualification and validation activities -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

• The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis & documentation of the results.
• Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
• Individual performance is assessed using the PMP performance dialog together with the manager

Minimum Requirements:
Work Experience:

• Functional Breadth.
• 5 years experience in Pharma/Manufacturing sector in analytical lab in.
• Collaborating across boundaries.
• A GMP environment/equivalent.

Skills:

• Continuous Learning.
• Dealing With Ambiguity.
• Decision Making Skills.
• Gxp.
• Industry Standards.
• Laboratory Equipment.
• Laboratory Excellence.
• Quality Control (QC) Testing.
• Quality Control Sampling.
• Self-Awareness.
• Technological Expertise.
• Total Quality Management.

Languages:

• English.