Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting Job Description When you are part of the team at Thermo Fisher Scientific, you'll do important work. And you'll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world. Position Summary *: Leads by example, within a team of manufacturing operators in a world class manufacturing operation. Hands-on involvement in assembly/ manufacturing of Rapid product line, including Rapid Hit Cartridges, Primary Cartridges and Gel Cartridges within a cleanroom environment, working with DNA reagents according to SOPs, with due regard to product availability and integrity. Position may include performing quality control testing of Rapid manufactured goods. The position impacts the ability to fulfil production schedules. Decisions taken affect quality and integrity of products. Responsibilities - Work in ISO 7 clean rooms with Tyvek gowning and personal hood PPE. - Perform multi-stage, semi-automated assembly of Rapid Hit cartridges on a production line within a team. - Support the assembly of Gel cartridges, Primary cartridges, Newton house ladder cartridges, and bead cleaning. - Submit regular samples to QC, ensuring clear communication. - Conduct quality control testing of intermediates and finished goods. - Train and support new operators to achieve confident unsupervised proficiency. - Calibrate laboratory instruments and monitor the calibration schedule for designated equipment. - Liaise with Engineering to report and resolve breakdowns promptly, minimizing production downtime. - Adhere to and support the Company safety and hazardous waste management program. - Maintain clean, orderly, and safe laboratory work areas. - Participate in regular particle reduction cleans to uphold the ISO 7 cleanroom standards. - Assist with environmental monitoring of cleanrooms (swab preparation/taking). - Continuously improve understanding of quality and efficiency concepts as they apply to all work performed. - Support continuous improvement activities and projects. - Raise and manage PRs or equivalent experience in Trackwise and lead/support investigations when problems arise. - Manage change orders on the OCPLM system to facilitate improvement activities and corrective actions, including updating documents and crafting new SKUs. Minimum Requirements/Qualifications - Proven experience in manufacturing within a clean production environment. - Awareness of COSHH and experience working with hazardous materials. - Ability to follow written and verbal instructions, meet targets, and complete necessary paperwork to GDP standards. - Capable of managing manual handling tasks with good manual dexterity. - Strong ability to work independently and collaboratively within a team. - Flexible approach to work with possible changes in duties at short notice. - Willingness to learn and adapt to shift work/overtime requirements. - Excellent time management and organizational skills. - Strong communication and problem-solving skills. - Proficient in using office equipment, including operating a computer terminal throughout the day. - Demonstrates interest/experience in scientific and/or engineering processes. At Thermo Fisher Scientific, each of our 100,000 outstanding minds has an unusual story to tell. Join us and contribute to our outstanding mission-enabling our customers to make the world healthier, cleaner, and safer. Apply today! 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.