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 VISUAL INSPECTION TECHNICIAN Dept: Operations Reports to: Manufacturing Team Lead Responsibilities ? To work as a team member to support biologics operation in pharma operations in line with all safety, regulatory and organizational requirements. ? Visual Inspection Technician will be assigned to the daily production operations. ? Documentation of all activities in line with cGMP requirements. ? Perform final product visual inspection. ? Perform product intermediary packaging, as applicable. ? Perform in process testing methods. ? Monitor Process Alarms. ? Material receipt from warehouse, verifying all pertinent documentation. ? Transfer of final material to warehouse inventory. ? Ensure all manufacturing documentation is completed on a timely manner without errors, following cGMP's. ? Diagnose and resolve events or exceptions of VI process. ? Disposal of domestic, biomedical, and hazardous waste from their respective area as applicable, ensuring compliance with regulations following the procedures and policies of the plant, division, and the corporation. ? Keep detailed records, manual or electronic, of the operations carried out during the work shift. ? Active Participation in Factory Acceptance testing, Site Acceptance Testing and commissioning and qualification of equipment. ? Adhering to all relevant policies relating to Quality & Safety. ? Ensure successful external inspections, and Division and Corporate audits. ? Active participant in the development of batch records and electronic batch records for the site. ? Work with Engineering, Quality and other departments in the development and update of Standard Operating Procedures. Requirements ? Leaving Certificate and 1 years' experience in GMP manufacturing ? 1 year plus of Knowledge of GMP and regulatory requirements relating to the pharma/biologics industry. ? 1 year in Batch processing operations in an FDA/ HPRA regulated industry is highly desirable. ? Essential: Requires annual visual test certification for colour blindness and 20/20 vision. ? A good knowledge of cGMP and regulatory requirements relating to the biologics/pharmaceutical industry is desirable. ? Experience in handling of dangerous chemicals is highly desirable. ? Good I.T. skills are required. ? Possessing previous Inspection experience in a Pharma/Biologics facility is a distinct advantage for operators assigned to VI. To start the process click the Continue to Application or Login/Register to apply button below.