Mission
For our client operating in the medical sector, we are seeking a Quality Control Associate.
They are responsible for the verification activities of raw materials, intermediate and final products. These verification activities include the control according to the specifications, the statement of the usage decision and the management of the non-conformities.
Challenges we trust you with
· Perform the control activities of raw materials, intermediate and final products and the recordings of the control evidences.Products responding to the quality requirements (international standards)
· Contribute to verification protocols improvement
· Verification Protocol order (VPO) are reviewed in order to comply with Quality Control Process requirements
· Identify and register the non-conformities
· Non-conformities identified during Quality Control or reported to Quality Control team are recorded managed according to their urgency and priority
· Respect the Quality Control Planning
· Control activities shall respect the priorities and due date set in the Quality Control Planning
· Maintain equipment and work space
· Equipment and workspace are clean, tidy and in order
· Respect of Quality Management system, safety, security, radioprotection procedures for quality control
· Quality Management documents and Quality Standards, GMP and internal guidelines respected. All safety issues are directly reported to managers. Safety procedures are applied (electrical consignment, radioprotection, wearing individual protection equipment…)
· Give technical trainings to QC colleagues
· Knowledge transfer of own technical expertise to colleagues
You have
· University Degree in Science or an equivalent demonstrated by experience
· A minimum of 3 years of experience in Quality in Medical Devices/Pharmaceutical industries
· Excellent level of oral & written communication skills enabling to act as a facilitator with strong leadership skills.
· Proficient English and French
& Also you are
· Adaptable and willing to take on multiple new tasks and responsibilities
· Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real time
· Process orientated, logical, analytical, meticulous, highly organized and able to analyze