QC Technician II

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information: 3175 Staley Road, Grand Island NY BioProduction Division Position is for 1st shift, Monday - Friday How Will You Make an Impact?: The Finished Product Testing QC Technician II performs routine Quality Control testing of finished products to ensure they meet established specifications, customer requirements, and applicable regulatory requirements. Testing is performed using approved methods and SOPs in accordance with cGMP, Good Documentation Practices (GDP), data integrity expectations, and laboratory safety requirements. We are seeking a self-motivated individual with strong communication, technical, and operational skills who can coordinate and execute laboratory testing with limited supervision or guidance. The successful candidate will demonstrate strong attention to detail, sound judgment, and the ability to work both independently and collaboratively within the Microbiology Quality Control Laboratories. This position supports a variety of QC activities, including aseptic testing, sterility testing, finished-product testing, and other microbiological laboratory activities. The technician plays an important role in maintaining compliant laboratory operations and supporting the timely release of quality products to our customers. A Day in the Life: Perform finished-product Quality Control testing using approved procedures and aseptic techniques, including sterility, endotoxin, pH, osmolality, powder reconstitution, and other miscellaneous QC testing as required. Accurately document testing activities and results in accordance with cGMP and GDP requirements. Support laboratory inventory management and upkeep by monitoring testing supplies and materials, maintaining appropriate stock levels, identifying inventory needs, and helping ensure materials are available to support uninterrupted laboratory operations. Contribute to a culture of continuous improvement by supporting Lean and 5S principles, maintaining organized and efficient laboratory workspaces, identifying opportunities to reduce waste and improve workflow, and participating in team improvement initiatives. Demonstrate a positive, collaborative, and customer-focused attitude while working independently and with cross-functional teams. Communicate effectively, take ownership of assigned responsibilities, and contribute to timely, right-first-time testing that supports quality, operational excellence, and customer satisfactio n . Education: High school diploma or equivalent required. AAS degree preferred or 1-2 years of relevant lab experience Experience: Experience (2+ years) in MS Excel, Word, and Outlook, Microsoft Teams Proficient oral and written communication skills are required to be effective in this role Knowledge, Skills, Abilities: Strong people skills, team focused. Strong written, verbal, and organizational skills, and the ability to work independently. Ability to work in a fast-paced environment and prioritize tasks as necessary Individual should be comfortable working a in a cGMP clean room environment for extended periods of time. Physical Requirements / Work Environment: Work within a Quality Control laboratory environment while adhering to applicable cGMP, safety, and laboratory requirements. Wear required Personal Protective Equipment (PPE) based on assi…

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