**Work Schedule** Other **Environmental Conditions** Laboratory Setting **Job Description** **Job Responsibilities** As a QC Technician II, you will play a crucial role in ensuring the flawless quality of our GeneChip products. Your responsibilities will include: + Performing QC testing of GeneChip products to ensure strict compliance with ISO 13485, MDSAP, and 21-CFR-820 requirements. + Conducting target preparation for Cytoscan and Axiom with outstanding accuracy. + Supporting lab investigations related to product failures and participating in the implementation of corrective actions as necessary. + Conducting experiments and analyses to support new product releases and improve test methods. + Assisting FQC Shift Leads and Supervisors in accomplishing assigned tasks. **Job Requirements** To successfully compete for this role, you must meet the following requirements: + Proven experience in a manufacturing or quality control environment, preferably within the medical device industry. + Strong understanding of ISO 13485, MDSAP, and 21-CFR-820 standards will be most advantageous. + Ability to perform meticulous lab work and maintain detailed records. + Excellent problem-solving skills and the ability to determine root causes of product issues. + Ability to work collaboratively in a team-oriented environment. + Able to work 12h rotating shift. **Why You'll Love Working With Us** At Thermo Fisher Scientific, we value diverse experiences and perspectives. We are dedicated to encouraging an inclusive and collaborative environment. Join us in our mission to accelerate research and solve complex scientific challenges. Be part of something outstanding! Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.