Lab Analyst
3 months ago
Responsibilities:
- Sample storage and management
- Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
- Ensure all activities in compliance with cGxP, incl. data integrity
- Stability (when not centralized)
- Testing/Sample storage and management
- Analytical documentation of stability samples to cGxP standards
- Comply with all HSE guidelines
- Detect and report potential accident, risks and propose solutions
- Responsible for participating in initial training and retraining
About You:
- At least 3-4 years relevant experience in a laboratory environment in the pharmaceutical industry (quality assurance, production), QC Raw material or Analytical testing experience, aseptic technique.
- Has completed apprenticeship as a laboratory assistant or equivalent training
- Collaboration; result-oriented
- Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
- Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
- Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; related industry GxP standards and processes; Laboratory Excellence; Quality decision making
Job Type: Contract
Contract length: 06 months. Option to extend/convert subject to performance review.
Normal Shift Job.
Tell employers what skills you have
GxP
Pharmaceutical Industry
Sampling
Quality Control
Operational Excellence
Quality Assurance
GMP
Compliance
Packaging
Decision Making
API
Laboratory
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