Join a dynamic Pharmaceutical Organization as a key member of the QC Laboratory Team
Duties:
* Movement of materials across the network.
* System transactions including movement and shipping of samples across QC labs within the network.
* A strong understanding of systems such as GLIMS, LIMS and SAP is essential for success.
* Inspection of primary packaging to ensure quality standards are met.
* Contribute to the development and maintenance of accurate operational procedures, training materials and maintenance procedures for various Quality systems; ensuring compliance with regulatory requirements.
* Review, approve and trend test results where applicable.
* Peer review other analysts documentation, ensuring high-quality testing outcomes are achieved.
* Participate in daily meetings and communicate effectively with colleagues regarding testing progress, deviations etc.
* Ensure adherence to all Quality Systems within the department on a daily basis.
* Complete all documentation in accordance with GMP and GxP standards.
* Utilize problem-solving skills to identify root causes of issues.
* Support audit/inspection requirements to ensure department readiness.
* Collaborate with colleagues by sharing your expertise and skill-set.
* Pursue continuous improvement, perform root cause analysis on system failures e.g. FMEA, Fishbone diagrams, 5 whys etc,
Requirements:
* Degree in Science or Engineering.
* 1 - 3 years' experience in the Pharmaceutical industry or similar environment with a background in Quality functions.
* Previous Analytical Experience.