Dental lab technician h1.location_city

3rd SHIFT: Sunday-Thursday, 10:00PM to 6:30AM, 15% Shift Differential Contact - 6-36 months Excellent employment opportunity for a MFG Associate-Filling & Visual Inspection in the Fremont, CA area. 3rd SHIFT: Sunday-Thursday, 10:00PM to 6:30AM, 15% Shift Differential Ability to independently and accurately prepare all assigned records, calculations, and documentation. Demonstrated ability to independently and properly handle and dispose of hazardous waste. Ability to read and follow schedules, procedures, and documents. Demonstrated knowledge of safety precautions and procedures. Will be required to assist in training other employees in an area of responsibility as assigned. Assist staff in developing new procedures and methods or improving old ones. Ability to practice aseptic techniques independently. Ability to perform media fills with (process simulation testing) with passing results per applicable SOP. Ability to perform clean room gowning and pass clean room garment validation consecutively. Ability to independently prepare disinfectants and sanitizing solutions. Ability to independently clean and sanitize production equipment, rooms and areas. Demonstrated knowledge of an aseptic operation and the relationship of laminar flow systems and environmental monitoring. Ability to assist in performing environmental monitoring, such as but not limited to, independently placing settling plates and air sampling. Ability to use basic hand tools. Ability to independently set-up, operate, maintain and troubleshoot steam sterilizers, capping machines, stoppering machines, bottle washers, sterilizing tunnels, equipment washing machines, sterile filtration equipment, L bar sealers/Bundler, vision systems, inkjets, vacuum check equipment as needed. Ability to wear a respirator if required of the job, no pulmonary restrictions. Ability to independently use and understand computer assisted data entry. Ability to independently perform sterile filtration. Ability to aseptically gather and transfer samples for QC testing. Ability to independently perform filter integrity and prepare accurate documentation Experience: High School diploma or GE and 2 years’ experience Basic operator functions New to GMP Ability to lift fifty (50) pounds. Demonstrated knowledge of: Federal, State, and international regulations, such as cGMP, USDA, DOT, EPA, OSHA Corporate guidelines and Policies related to the employee's work. Standard Operating Procedures (SOPs) Material Safety Data Sheets (MSDSs), safety procedures, and hazardous materials procedures. Aseptic processing procedures related to the employee's work. Team process and leadership principles. Appropriate processes and theory related to the employee's work. Documentation related to the employee's work. Equipment as defined in Duties Additional education and/or equivalent experience. Successful completion of National Career Readiness Work Keys assessment. Traffic Patterns. Working with BPE Methods. Understanding of Basic GMP/Documentation practices. Ability and understanding of safe working habits. Ability to work in a team environment. • Candidate needs to have experience working in a pharmaceutical/biopharmaceutical manufacturing or GMP-regulated production environment • Candidate needs to have experience working in aseptic processing and cleanroom environments, including gowning and sterile techniques • Candidate needs to have experience with filling operations, visual inspection, and production equipment used in sterile manufacturing • Candidate needs to have experience with documentation, batch records, and data entry in compliance with SOPs and regulatory requirements • Candidate needs to have experience handling, cleaning, and sanitizing equipment, as well as managing hazardous materials and waste safely • Candidate needs to have experience supporting training activities and collaborating with teams to improve processes and procedures