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
Major accountabilities:
- 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:
- Sound technical & scientific knowledge of pharmaceutical/ chemical.
- Working experience in Laboratory environment in the Pharmaceutical.
- analytics/QC/ equivalent.
- industry.
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 :
Skills Desired
Continued Learning Dealing With Ambiguity Decision Making Skills Gxp Industry Standards Laboratory Equipment Laboratory Excellence Quality Control (Qc) Testing Quality Control Sampling SelfAwareness Technological Expertise Total Quality Management
Required Experience:
IC