-Logistics Coordination -Batch record executions -Equipment use logs -Work order initiation and tracking -Support Projects -Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP. -Adheres to established regulations and follows cGMP established by site. -Reports abnormalities and deviations in a timely and accurate manner. -Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately. -Maintains production areas according to predefined standards (5s). -Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification. -Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs. | |||
| Skills: | -1 or more years of experience in cGMP regulated industry. -Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and Right the first-time mindset. -Strong written and verbal communication skills. -Ability to work with computer-based systems and manufacturing execution systems (MES). -Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards. -Ability to work as part of a high performing team and collaborate effectively with staff. -Must be able to read and see clearly. PHYSICAL DEMANDS: - Duties of this position may require the incumbent to exert some physical effort. -Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds. - Employees required to participate and have acceptable result from vision testing including color blindness. | ||
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