QC Analyst
Date Posted: February 13, 2026
Job Description
The QC Analyst executes essential laboratory tasks within the Quality Control department to support pharmaceutical manufacturing. In this role, you take ownership of the analytical testing and documentation for APIs, drug substances, and finished products, ensuring every action meets strict cGxP regulations. You manage the full lifecycle of laboratory activities—from sample storage to equipment calibration—maintaining a constant state of inspection readiness. Working within a rotating shift pattern, you play a vital role in ensuring data integrity and operational excellence in a high-stakes production environment.
Key Responsibilities
- Lead Analytical Testing by performing rigorous analysis and documentation of APIs, drug substances, drug products, and packaging materials.
- Manage Sample Lifecycle including the secure storage and handling of stability samples, complaint samples, and finished products.
- Maintain Laboratory Excellence by overseeing the maintenance, calibration, and qualification of complex analytical equipment.
- Ensure cGxP Compliance by executing all tasks in strict accordance with data integrity principles and Standard Operating Procedures (SOPs).
- Drive Stability Programs by testing and managing stability samples to ensure long-term product quality and compliance.
- Uphold HSE Standards by complying with safety guidelines, reporting potential risks, and proposing solutions to maintain a zero-harm workplace.
- Optimize Lead Times by processing orders efficiently to ensure zero waiting time and adherence to strict project deadlines.
- Support Continuous Improvement by identifying optimization initiatives to reduce costs and improve laboratory throughput.
Required Qualifications and Skills
- Completed an apprenticeship as a laboratory assistant or hold an equivalent technical qualification.
- Experienced in a pharmaceutical laboratory environment, ideally within Quality Assurance or Production.
- Possess hands-on skills in QC testing, sampling, and the use of sophisticated laboratory equipment.
- Preferred background in aseptic techniques and working within sterile environments.
- Deep understanding of cGxP standards, TQM, and data integrity requirements.
- Comfortable using digital laboratory systems and technology to document and track analytical results.
- Resilient, results-oriented collaborator with strong administrative capabilities and a commitment to continuous learning.
If you are keen to grow your career with this job, apply with us and send us your resume now. All shortlisted candidates will be contacted shortly.
Reference no.: 122-4948-2918-NW
Registration no.: 968446516E