General Electric QC Lab Technician in South Plainfield, New Jersey
Job Description Summary
Description: As a member of a dedicated team, this role is responsible to provide support to various laboratories. To perform Stability, Raw Material, Chemistry Testing and Microbiology Support on a daily basis. To ensure that there are sufficient quantities of consumables as to meet logistical requirements. To keep track of deliveries and to organize and maintain the store room. To ensure that all data is archived, maintaining the archive system.
Key Responsibilities/Essential Functions Include:
Analyze products or raw materials, in compliance with documented procedures and in accordance with the stipulated deadlines
Understand and comply with the requirements of Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) carrying out all tasks to standards accepted as GxP
Comply with Good Laboratory Practices and Good Manufacturing Practices to include required methods of achieving sterility such as depyrogenation of glassware, cleaning of incubators and fridges and fogging of the sterility test suite
Maintain the working environment in a safe and tidy condition based on the defined standards rules and schedules (such as performing periodic Dick and Bowie and Leak rate required tests for the laboratory autoclave)
Generate microbiology regulatory documentation
Maintain accurate and inspect able paper and electronic records through archive logbook, and collection and returns from the provider of data protection, data recovery and archiving software
Maintain and monitor stock levels of consumables to include tracking of deliveries and dealing with suppliers issues
Predict and co-ordinate purchasing requirements of the Microbiology group
Archive all data within the laboratory
Responsible for training and mentoring Lab Assistant when required
Assist more senior staff with non-routine analyses, when required
Comply with EHS regulations and policies
Can assist in training more junior lab technicians as required
Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality and Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Knowledge and understanding of requirements for software and hardware verifications and validations, electronic signature, document control, configuration change control, good documentation practices, calibration and Preventative Maintenance as applicable to assigned tasks. 5. Training: Aware of and comply with GEHC training requirements
- High school diploma or local equivalent 2. 2 year degree in biotechnology or a biological science 3. Minimum of 3 years experience in relevant environment 4. Good written and oral communication, 5. Experience in dealing with ordering, deliveries, computer experience 6. Knowledge and preferably experience in a GxP environment 7. Excellent record keeping and organizational skills
- Bachelor degree and/or 4 years laboratory experience 2. Exceptional attention to detail
GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an Equal Opportunity Employer (https://assets.phenompeople.com/CareerConnectResources/GE11GLOBAL/en_global/desktop/assets/images/poster_screen_reader_optimized_w_supplement.pdf) . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
Relocation Assistance Provided: No