{"schemaVersion":"jobsearcher.job.v1","id":"fb250bd8d4c78fa7eadbde8a","url":"https://jobsearcher.com/jobs/fb250bd8d4c78fa7eadbde8a","canonicalUrl":"https://jobsearcher.com/jobs/fb250bd8d4c78fa7eadbde8a","title":"Senior Quality Control Technical Analyst","description":"About the Department\nThe Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. The CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado facility and works closely with our teams in Lexington, Massachusetts. Together, we are driving change. Are you ready to make a difference.\n\nThe Position\nNovo Nordisk, CMC Boulder, is building a Phase 1 and 2 API Pilot facility for oligonucleotide manufacturing in Boulder Colorado. As such, the Quality Control team is seeking a Senior Quality Control Technical Analyst to support both the successful start‑up and ongoing operation of the Quality Control laboratory supporting early phase manufacturing. The Senior Quality Control Technical Analyst will own all activities related to the establishment & operation of Novo Nordisk's Global LIMS platform for support all aspects of the QC Chemistry laboratory implementation of instruments, reagents, methods, workflows supporting analysis of raw materials, in‑process, final product samples, as well as routine stability samples. In addition, this position is responsible for the oversight and SME for iStability representing the system to Boulder as well as other Novo sites throughout the world. This position is for a hands‑on analyst familiar with Novo systems (iStability and Global LIMS) and processes as they relate to GMP Quality Control.\n\nRelationships\nReports to Associate Director, Quality Control.\n\nEssential Functions\n\nServe as QC Global LIMS Site SuperUser and Site Builder responsible for training and building QC methods\n\nServe as the Global lead for iStability, responsible for training other Novo sites\n\nServe as the Boulder QC lead for iStability responsible for managing the system, generation of reports and data as requested by internal groups\n\nWrite/revise SOPs, technical protocols, change control and other quality related reports\n\nLead & coach team members, other specialists, providing leadership in problem solving for process & quality issues\n\nEvaluate and support corporate initiatives for new technology and process improvements\n\nUnderstand the processes of data evaluation and trending, to include reporting findings to leadership\n\nRepresent Boulder QC on global and site level as needed for collaboration with other NN sites\n\nInteract professionally with external vendors to solicit new technology\n\nInteract closely with all areas to improve the flow of information & products\n\nFollow all safety & environmental requirements in the performance of duties\n\nOther accountabilities, as required\n\nPhysical Requirements\nAbility to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time.\n\nQualifications\n\nHigh School Diploma or GED and 8+ years of experience, or Associate's degree with 6+ years of experience, or Bachelor's degree from an accredited university and 4+ years of experience, or Master's degree and 2+ years of experience is required\n\nQC experience in a pharmaceutical or related (regulated) environment required\n\nExperience with computerized laboratory systems (iStability, Global LIMS, etc.) preferred\n\nDemonstrated expert understanding of processes, procedures & products associated with assigned areas required. Able to perform detailed analysis of events & processes, develop appropriate responses to situational needs, & convey information/results to various organizational levels as appropriate required\n\nDemonstrated knowledge of adult learning methodologies & is able to use multiple methods to train & coach others within the department & organization preferred\n\nExcellent verbal & written communication skills, investigative writing skills, & computer skills required (MS Word, Outlook, Excel, PowerPoint, Global LIMS, iStability and Microsoft Project)\n\nDemonstrated experience in practical problem solving & process improvement methods required\n\nDemonstrated ability to manage multiple tasks/deadlines & prioritize properly based on process needs & events. Demonstrated effectiveness in systematic follow‑up required\n\nUnderstand the processes and products at an advanced level required\n\nDemonstrates understanding of project management and NN gate process flow preferred\n\nExpert level of knowledge & understanding regarding departmental SOP's & their high‑level inter‑relationships required (i.e. how they work together to establish a system)\n\nCompensation & Benefits\nThe base compensation range for this position is $125,000 to $145,000. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.\n\nNovo Nordisk offers long‑term incentive compensation and or company vehicles depending on the position's level or other company factors.\n\nEmployees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex‑able vacation policy, and parental leave policy.\n\nEqual Opportunity Employer\nNovo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.\n\n#J-18808-Ljbffr","company":"Merck","rawCompany":"merck","city":"Boulder","state":"CO","isRemote":false,"isActive":false,"createdAt":"2026-06-17T04:17:13.856Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Senior Quality Control Technical Analyst","description":"About the Department\nThe Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. The CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado facility and works closely with our teams in Lexington, Massachusetts. Together, we are driving change. Are you ready to make a difference.\n\nThe Position\nNovo Nordisk, CMC Boulder, is building a Phase 1 and 2 API Pilot facility for oligonucleotide manufacturing in Boulder Colorado. As such, the Quality Control team is seeking a Senior Quality Control Technical Analyst to support both the successful start‑up and ongoing operation of the Quality Control laboratory supporting early phase manufacturing. The Senior Quality Control Technical Analyst will own all activities related to the establishment & operation of Novo Nordisk's Global LIMS platform for support all aspects of the QC Chemistry laboratory implementation of instruments, reagents, methods, workflows supporting analysis of raw materials, in‑process, final product samples, as well as routine stability samples. In addition, this position is responsible for the oversight and SME for iStability representing the system to Boulder as well as other Novo sites throughout the world. This position is for a hands‑on analyst familiar with Novo systems (iStability and Global LIMS) and processes as they relate to GMP Quality Control.\n\nRelationships\nReports to Associate Director, Quality Control.\n\nEssential Functions\n\nServe as QC Global LIMS Site SuperUser and Site Builder responsible for training and building QC methods\n\nServe as the Global lead for iStability, responsible for training other Novo sites\n\nServe as the Boulder QC lead for iStability responsible for managing the system, generation of reports and data as requested by internal groups\n\nWrite/revise SOPs, technical protocols, change control and other quality related reports\n\nLead & coach team members, other specialists, providing leadership in problem solving for process & quality issues\n\nEvaluate and support corporate initiatives for new technology and process improvements\n\nUnderstand the processes of data evaluation and trending, to include reporting findings to leadership\n\nRepresent Boulder QC on global and site level as needed for collaboration with other NN sites\n\nInteract professionally with external vendors to solicit new technology\n\nInteract closely with all areas to improve the flow of information & products\n\nFollow all safety & environmental requirements in the performance of duties\n\nOther accountabilities, as required\n\nPhysical Requirements\nAbility to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time.\n\nQualifications\n\nHigh School Diploma or GED and 8+ years of experience, or Associate's degree with 6+ years of experience, or Bachelor's degree from an accredited university and 4+ years of experience, or Master's degree and 2+ years of experience is required\n\nQC experience in a pharmaceutical or related (regulated) environment required\n\nExperience with computerized laboratory systems (iStability, Global LIMS, etc.) preferred\n\nDemonstrated expert understanding of processes, procedures & products associated with assigned areas required. Able to perform detailed analysis of events & processes, develop appropriate responses to situational needs, & convey information/results to various organizational levels as appropriate required\n\nDemonstrated knowledge of adult learning methodologies & is able to use multiple methods to train & coach others within the department & organization preferred\n\nExcellent verbal & written communication skills, investigative writing skills, & computer skills required (MS Word, Outlook, Excel, PowerPoint, Global LIMS, iStability and Microsoft Project)\n\nDemonstrated experience in practical problem solving & process improvement methods required\n\nDemonstrated ability to manage multiple tasks/deadlines & prioritize properly based on process needs & events. Demonstrated effectiveness in systematic follow‑up required\n\nUnderstand the processes and products at an advanced level required\n\nDemonstrates understanding of project management and NN gate process flow preferred\n\nExpert level of knowledge & understanding regarding departmental SOP's & their high‑level inter‑relationships required (i.e. how they work together to establish a system)\n\nCompensation & Benefits\nThe base compensation range for this position is $125,000 to $145,000. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.\n\nNovo Nordisk offers long‑term incentive compensation and or company vehicles depending on the position's level or other company factors.\n\nEmployees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex‑able vacation policy, and parental leave policy.\n\nEqual Opportunity Employer\nNovo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.\n\n#J-18808-Ljbffr","datePosted":"2026-06-17T04:17:13.856Z","dateModified":"2026-06-17T04:17:13.856Z","hiringOrganization":{"@type":"Organization","name":"Merck","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Boulder","addressRegion":"CO","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fb250bd8d4c78fa7eadbde8a"},"url":"https://jobsearcher.com/jobs/fb250bd8d4c78fa7eadbde8a"}}