QC Analyst II

Job Description 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.

 

Job Description

• Sample storage and management -Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards Stability -Testing/Sample storage and management .
• Analytical documentation of stability samples to GxP standards -Reporting of technical complaints / adverse events .

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, the shortest possible lead 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, no critical irregularities -Finding and implementing optimization options to reduce costs -Completed training plan

Minimum Requirements: 
Work Experience:

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

Language: Englisch

 

Skills Desired