Job Description Summary
This role utilizes chemistry laboratory skills to test and measure products or materials, ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods, and current Compendia.
Job Description
Sample storage and management - Analytical testing and documentation of drug products, finished products, complaints, stability, and packaging material samples to GxP standards. Includes stability testing and sample storage management.
Analytical documentation of stability samples to GxP standards.
Reporting of technical complaints and adverse events.
Key Performance Indicators:
Orders are processed correctly and promptly.
No waiting times due to incorrect or delayed orders.
Deadline adherence: orders completed on time, with timely reporting of any missed deadlines. Maintain the shortest possible lead time.
Ensure constant readiness for inspections, with no critical complaints from superiors or inspectors.
Consistently follow GMP, GSU guidelines, and SOPs, avoiding critical irregularities.
Identify and implement optimization options to reduce costs.
Complete training plans.
Minimum Requirements:
Experience working in a pharmaceutical laboratory environment.
Strong technical and scientific knowledge of pharmaceutical or chemical industries.
Experience in analytics, QC, or an equivalent role.
Language: English
Skills Desired
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