QC Analyst IV

Summary

This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.

About the Role

Major accountabilities:

• Sample storage and management - Analytical testing/documentation of drug product/finished product/complaints/stability/packaging material samples to GxP standards.
• Reporting of technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours of receipt.
• Distribution of marketing samples (where applicable).

Key performance indicators:

• Orders are processed correctly and quickly.
• No waiting times due to wrong or delayed order.
• Deadline adherence rate: orders completed on time, all missed deadlines reported in good time.
• Ensure constant readiness for inspection, no critical complaints from superiors and inspectors.
• Consistently follow the GMP and GSU guidelines, as well as the SOPs, with no critical irregularities.
• Finding and implementing optimization options to reduce costs.
• Completed training plan.

Minimum Requirements:

Work Experience:

• Sound technical & scientific knowledge of pharmaceutical/chemical.
• Working experience in Laboratory environment in the Pharmaceutical industry.
• Analytics/QC/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.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Learn more