Work Schedule12 hr shift/daysEnvironmental ConditionsCleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowedJob DescriptionDESCRIPTION: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:This position is part of the Pharma Services Group (PSG) and is located in our Greenville, NC facility. You will be working specifically on vial line 9, utilizing state-of-the-art equipment in a critical production area. The Greenville site is a key location for our pharmaceutical manufacturing operations, offering opportunities to work on cutting-edge projects in drug development and production.How Will You Make an Impact?:As a Sr Formulation Technician in the PSG, you will play a crucial role in ensuring the quality and efficiency of our pharmaceutical manufacturing processes. Your expertise will contribute directly to the production of life-saving medications and therapies. Shift hours are 6am-6pm on a 2-2-3 rotating schedule.A Day in the Life:Operate and monitor advanced equipment on vial line 9Ensure compliance with cGMP regulations and company SOPsCollaborate with cross- functional teams to optimize production processesTroubleshoot technical issues and implement solutionsEducation:High school diploma or equivalent required.Equivalent combinations of education, training, and relevant work experience may be considered. Experience:Required: Minimum of 2 years of work experience in a pharmaceutical manufacturing, operations, production, lab setting or related fieldPreferred: Experience in a cGMP environmentPreferred: Experience working in a clean room environmentPreferred: Experience with aseptic processing and sterile drug manufacturingKnowledge, Skills, Abilities:Strong understanding of pharmaceutical manufacturing processesProficiency in following SOPs and maintaining accurate documentationExcellent attention to detail and ability to work in a highly regulated environmentStrong problem-solving and communication skillsPhysical Requirements / Work Environment: Must be able to stand for extended periods, lift up to 25 pounds, and work in a clean room environment. May require wearing personal protective equipment (PPE) for extended periods.