QC Technician II Sample Management (Mon-Friday 8hr days) at Thermo Fisher Scientific

Work ScheduleStandard (Mon-Fri)Environmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cold Room/Freezers -22degreesF/-6degrees C Fluctuating Temps hot/cold Laboratory Setting Office Various outside weather conditionsJob DescriptionAs part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.Location/Division Specific InformationGreenville NC/ Drug Product Division - The Drug product Division is one of the divisions that make up the Pharma Services Group. We specialize in both small and large molecule method development and commercial drug product services. This allows us to serve the Contract Manufacturing needs of Small/Emerging Mid-Sized and Large Pharma sectors globally.Discover Impactful Work:The QC Technician II Sample Management will work on a team of technicians committed to supporting QC sampling functions at this site. This team is responsible for the pickup of GMP manufacturing samples and transport to various lab storage locations within QC. Additionally the team handles packing and coordinates the logistic aspects of shipping samples to offsite customer sites and test laboratories.The team also will use the sites LIMS systems to print labels and record GMP transactions for samples. This team works in parallel with the QC Laboratory Support functional team. Shift hours are 7am - 4pm Monday-Friday.A day in the Life:Transport samples from the manufacturing areas to quality control testing/storage areas. Report sample issues to the appropriate management as the need arises per procedures.Receive samples into the analytical and microbiology laboratories. Receive samples for storage into the QC Sample Management storage units.Documentation of all activities to meet cGMP/cGDP requirements.Performs all duties in strict compliance with Standard Operating Procedures Good Manufacturing Practices Good Laboratory Practices and Safety guidelines. Maintains the vital compliance status required by company and facility standards.Clearly and accurately communicates status of samples (picked up for testing for send-out) to cross-functional area teams.Maintain up to date training records.Effectively train department employees in the execution of Sample Management tasksAuthor Sample Management documents in the site electronic document management systemInvestigate and complete investigation of minor sample management deviations.Assist with additional laboratory support duties as necessary to meet departmental goals.Keys to Success:Education:High school diploma or equivalent required.Experience:Required: Minimum of 1 year of work experience in QA QC or related field; or may consider an Associates degree or higher in Science or Technology in lieu of experiencePreferred: Experience in a cGMP environmentKnowledge Skills AbilitiesKnowledgeSolid understanding of GMP regulations in a GMP environmentKnowledge of cGMP practices and aseptic techniquesSkillsMS OfficeDetail orientedResults oriented.Safety MindsetElectronic document systemTrackWise or equivalent deviation systemElectronic Sample Management System (LIMS)SAPAbilitiesAble to read write and communicate in English.Able to understand and carry out instructions.ReliableStrong communication (written and verbal)Effectively multi-taskAble to work in an environment of change.Experienced in performing tasks both independently and within a team setting.Able to recognize problems developing not just occurring.Occasional heavy lifting or moving required.BenefitsWe offer competitive remuneration annual incentive plan bonus healthcare and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative forward-thinking organization and outstanding career and development prospects. We offer an exciting company culture that stands for integrity intensity involvement and innovation!Required Experience:IC Key Skills Laboratory Experience,Aseptic Technique,ELISA,FDA Regulations,PCR,High-Performance Liquid Chromatography,Microbiology,Quality Control,GLP,cGMP,Laboratory Information Management Systems,QA/QC Employment Type : Full-Time Experience: years Vacancy: 1