GerTEK is an engineering consultancy company specialising in project management, talent solutions and commissioning qualification and validation services. We partner with many of the world's largest life science & technology companies who entrust in us to deliver their most strategic and important projects with our technically strong personnel ensuring all important activities meet both current requirements and client's needs. We have multiple projects that we support, and we are looking to add to our team, we are interested in talking to you if you fit the criteria outlined below: Title: Product Inspection Technician Responsibilities: Major Duties and Responsibilities The Tablet Inspection Operator performs functions related to the visual inspection of drug products. The position incumbent is expected to adhere to all cGMP compliance and regulatory mandates and quality requirements and comply with all SOPs and internal policies and procedures in the performance of job duties. The Tablet Inspection Operator correctly follows SOPs to complete tasks and applies skills and knowledge to recognize issues that impact production efficiency, throughput, quality, and/or the fulfilment of the assigned production targets. The Tablet Inspection Operator is responsible for the safe, compliant, and efficient execution of job duties in a team environment. The role may also require working in Class C cleanroom environment. Qualification & Experience: Actively highlight any safety concerns to assist in the reduction of accidents or near misses. Support and adhere to established manufacturing scheduling processes and production targets. Handle raw materials and/or intermediate or finished products according to applicable SOPs. Gowning correctly and wearing of assigned PPE, Perform AQL sampling. Complete all required production data entries and calculations for manufactured batches on the BMR/EBR worksheets/SIC logs with detail and accuracy in real time. Observe established escalation process for issues impacting established production-related Service Level Agreements (SLAs) and/or fulfilment of production goals. Recognize and report to immediate supervisor any process or equipment anomalies and/or deviations from accepted standards. Provide status updates on manufacturing activities and operational challenges according to defined procedures. Perform master cleans and surface cleans of manufacturing equipment and production areas according to established SOPs and SLAs. Execute changeovers between batches according to established SOPs and SLAs. Keep work area neat and orderly and observe all safety and compliance procedures. Seek process innovation and continuous process improvement in production area. Complete and conform to all training requirements for job role, including company-required and machine-specific training. Carry out and assist in the ongoing training of new and existing personal as required in the area of manufacture. Can work equally well in a large or small team environment, where communication and feedback between team members and across shifts is critical. May participate in department initiatives and projects. Requirements: Secondary School Leaving Cert, or equivalent Exposure to pharmaceutical manufacturing equipment or equivalent Basic Microsoft Excel and Word skills EBR and TrackWise knowledge desirable May need to undergo a yearly test for 20/20 vision and colourblindness. We offer competitive compensation packages and opportunities for professional growth in a dynamic and innovative work environment. If you are a motivated Inspection Technician seeking an exciting challenge in the biopharmaceutical industry, we encourage you to apply. To start the process click the Continue to Application or Login/Register to apply button below.