NewGlobal Quality Manager LINCOLN TECHNOLOGY SOLUTIONS, Inc.Global Quality ManagerCary, NC$100,000–$125,000Full timeYou’ll lead and mentor the quality team while working closely with engineering, manufacturing, and customers to ensure product performance, manage returns and failure analyses and maintain precise documentation that protects LTS’s reputation and contractual interests. The ideal candidate is a hands-on problem solver who understands both engineering principles and customer expectations, and who can translate complex technical issues into clear, actionable reports that drive effective, closed-loop corrective actions.
NewAssociate Director, Quality for Capital Programs (Microbiology) #26-15319 US Tech Solutions, Inc.Associate Director, Quality for Capital Programs (Microbiology) #26-15319Durham, NCReporting to the Director of Sterility Assurance and Contamination Control, the Associate Director of Quality for Capital Programs is responsible for quality assurance oversight from early design phase through to Commissioning and Qualification ensuring quality and GMP requirements are met for sterile manufacturing capital programs. As a member of the capital program project team, the candidate will act as primary quality representative for key capital programs and collaborate with Client’s site and engineering cross functional teams, ensuring the principles of GMP and contamination control are upheld.
Senior / Project Quality Assurance Lead - US/Canada - Remote Worldwide Clinical Trials Holdings IncSenior / Project Quality Assurance Lead - US/Canada - RemoteNCRemote$65,500–$130,500 / yearBachelor's degree or equivalent with concentration in biological, physical, health, pharmacy or other related science and 5+ years of relevant GCP experience or 3+ years of relevant GCP with a M.S. or equivalent in a scientific or allied health field preferably within a Clinical Research Organization (CRO) or pharmaceutical company setting. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
QA Lead Expert In Recruitment SolutionsQA LeadDurham, NCTwo (2) years' experience (cumulative) developing QA strategies, test plans, test cases, and metrics to measure quality and readiness. Collaborate with program management, business analysts, developers, and vendors to prioritize defect resolution and testing scope.
Lead Process Technician - QA Floor Support Eli Lilly and CoLead Process Technician - QA Floor SupportResearch Triangle Park, NC$28.84–$46.54 / hourOur current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). The Lead QA Floor Support Lead Tech works as a team member supporting multiple production functions (formulation, filling, and visual inspection), from operations to maintenance, to achieve site goals while providing Quality oversight and guidance.
Lead QA Engineer - Tax Product Development (SDET) BDO USA PCLead QA Engineer - Tax Product Development (SDET)NC$140,000–$210,000 / yearThe annual allocation to the ESOP is fully funded by BDO through investments in company stock and grants employees the chance to grow their wealth over time as their shares vest and grow in value with the firm's success, with no employee contributions. The Lead Engineer leads the development and execution of comprehensive test plans, while mentoring junior team members and collaborating with cross-functional teams to deliver high-quality solutions.
QA Automation Team Lead - Qforce - RTP Vast Data IncQA Automation Team Lead - Qforce - RTPNCLead a team responsible for Test Automation Development, design automation tests and pipelines integrating with SW tools from the ground up, interfacing to various systems and tests (Python-based). We are building the enterprise software infrastructure to capture, catalog, refine, enrich, and protect massive datasets and make them available for real-time data analysis and AI training and inference.
Quality Assurance Automation Lead Faro Health IncQuality Assurance Automation LeadNCWe are a hybrid workplace where San Diego employees work from their homes as well as in our stunning main headquarters enjoying a gym with classes and (early next year) spa services, outdoor lawn work area, and steeply discounted food hall. Faro is a mission driven company seeking world class people who share our passion for improving drug availability and patient outcomes through better clinical trial design.
QA Engineer - Patient Systems Legal, Quality & Regulatory · US Raleigh Ascom Holding AGQA Engineer - Patient Systems Legal, Quality & Regulatory · US RaleighRaleigh, NCThis role focuses on supporting product quality across the lifecycle-working closely with R&D, regulatory, and cross-functional teams to uphold Ascom's Integrated Management System while enabling efficient and compliant product development. By ensuring adherence to design controls, supporting risk management, and driving resolution of product and process nonconformities, you will help safeguard patient safety, maintain regulatory confidence, and improve operational effectiveness.
NewQuality & Organizational Excellence Leader - Quality Assurance UNC HealthQuality & Organizational Excellence Leader - Quality AssuranceNC$33.37–$47.97 / hourClinical Experience associated with leading quality improvement efforts may be assessed as equivalent to direct quality improvement experience both in determining minimum requirements, as well as level of experience. Professional Experience Requirements: If a Bachelors degree: Three (3) years of experience in quality team facilitation, project management, process improvement or quality data analysis role.
Traveling Quality Assurance - Quality Control Manager - MSG - Pharmaceutical Turner Construction CoTraveling Quality Assurance - Quality Control Manager - MSG - PharmaceuticalRaleigh, NC$120,000–$217,000 / yearDevelop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements. Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents.
Principal QA Specialist KBI Biopharma IncPrincipal QA SpecialistDurham, NCDemonstrated solid Body of Knowledge of Quality systems and functions supporting drug or related FDA governed manufacturing obtained from professional Quality roles Includes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus. Ability to work effectively with others and communicate in customer-facing forums to progress issues and obtain positive results Able to navigate conflict to achieve deliverables and drive to targeted outcomes Ability to work professionally and facilitate positive interdepartmental interactions with a diverse group of people Voluntarily communicates needs and suggestions clearly and effectively Listens and is attentive to others' ideas and contributions.
Quality Assurance - Quality Control Manager Turner Construction CoQuality Assurance - Quality Control ManagerRaleigh, NC$145,000–$217,000 / yearDevelop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples documentation, and tracking of potential cost changes documentation, and tracking of approved change orders within budgetary requirements. Position Description: Responsible for planning, coordinating, and developing the project-specific Quality Assurance/Quality Control (QAQC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents.
QA Validations Analyst Leadstack IncQA Validations AnalystResearch Triangle Park, NC$45–$54 / hourJob Responsibilities: The Validations Contractor GMP Quality Assurance, reporting to the Associate Director, GMP Quality Assurance, will be responsible for ensuring the compliant onboarding, qualification, and validation of equipment, instruments, and computerized systems against corporate procedures, and applicable GMP national, international, and state regulations. Provide timely quality support and thorough reviews and approvals of various records including, but not limited to; equipment and computer system qualification and validation documents, SOPs, Change Controls, non-conformities, Deviations and Corrective Action/Preventive Action (CAPAs).
KBI: US - Principal QA Specialist KBI Biopharma IncKBI: US - Principal QA SpecialistDurham, NC$113,000–$156,000 / yearProvides QA oversight of analytical and microbial laboratory activities including but not limited to method qualification, method transfers, method validations, creation and revision of test methods, specifications, stability studies, laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external customers by ensuring patient safety and regulatory compliance while supporting product lifecycle activities for timely delivery of products to clients for patients.
QRM Support Manager - National Tax Quality Assurance (NTQA), Quality Risk Deloitte Touche Tohmatsu LtdQRM Support Manager - National Tax Quality Assurance (NTQA), Quality RiskNC$93,000–$191,000 / yearp>Information for applicants with a need for accommodation: https://www2.deloitte.com/us/en/pages/careers/articles/join-deloitte-assistance-for-disabled-applicants.html. Our team supports client-facing teams in how they approach the marketplace, develop service offerings, evaluate and onboard prospective clients, contract for services, deliver quality client service, and fulfill post-engagement and other recurring obligations.
Quality Assurance Auditor IQVIA Holdings IncQuality Assurance AuditorDurham, NC$43,400–$108,500 / yearJob Summary: Assist lead auditors and audit liaisons in conducting, hosting, and reporting quality assurance audits by performing defined audit tasks under the supervision of senior QA staff. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Sr. QA Auditor - 41779 IQVIA Holdings IncSr. QA Auditor - 41779Durham, NC$75,400–$188,600 / yearReview, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closures for quality events arising from Quality Issues, Audits, Inspections or during simillar QA activities. Manage/oversee quality events updates in eQMS and/or Maintains the electronic quality management system (eQMS) and provides support in relation to the audit lifecycle.
Supervisor II/III - Quality Assurance Grifols SASupervisor II/III - Quality AssuranceClayton, NCEducation and Requirements: Candidates for the Supervisor II-QA: BS/BA degree preferably in a STEM (Science, Technology, Engineering, and Mathematics) discipline with minimum of 5 years relevant experience, or equivalent combination of education and experience. Candidates for the Supervisor III-QA: BS/BA degree preferably in STEM (Science, Technology, Engineering, and Mathematics) discipline with a minimum of 6 years relevant experience, or equivalent combination of education and experience.
Technician - Process Quality Assurance Floor Support (Night Shift) Eli Lilly and CoTechnician - Process Quality Assurance Floor Support (Night Shift)Research Triangle Park, NC$18.02–$38.61 / hourOur current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Troubleshoot and provide QA systems support to reconcile issues in systems, such as, inventory control systems (SAP), laboratory LIMS system (Darwin) and other systems as required (TrackWise.
KBI: US - Supervisor, QA KBI Biopharma IncKBI: US - Supervisor, QADurham, NCOversee the Quality Support (Shop Floor QA) function at KBI Biopharma supporting the manufacture of biopharmaceuticals, providing QA support on the manufacturing floor. Level load work across team in support of batch release dates, daily manufacturing release schedules, and project priorities.
Quality Assurance Specialist - Lab IntelliPro GroupQuality Assurance Specialist - LabResearch Triangle Park, North CarolinaExamples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical and preclinical studies, qualification and/or validation of methods, equipment/software validation, laboratory processes, etc. Must be able to effectively collaborate cross-functionally with peers, scientific and technical staff; and be comfortable working in a matrixed team.
Executive Director, Clinical Pharmacology Services Quality Assurance (United States or United Kingdom) FortreaExecutive Director, Clinical Pharmacology Services Quality Assurance (United States or United Kingdom)Durham, North Carolina$220,000–$245,000 / yearLeads the design, implementation, and continuous improvement of audit, inspection readiness, and quality oversight programs across CPS, including clinical pharmacology operations, GMP pharmacy activities, and early-phase clinical development, while fostering a strong culture of quality, compliance, and operational excellence. Provides executive leadership for Quality Assurance (QA) and Regulatory Compliance within the Clinical Pharmacology Services (CPS) business unit, ensuring a robust, risk-based, and inspection-ready quality management system aligned with global regulatory expectations and Fortrea business strategy.
Principal QA Specialist KBI BiopharmaPrincipal QA SpecialistDurham, North CarolinaIncludes a balance of, from such areas as Supplier Quality Assurance, Compliance, Audits/Inspections, Shop Floor Support, Batch / Material release, Quality document control, review and approval, Validation, QC, Deviations, Prior direct regulatory agency, and audit management /r support experience a plus. Minimum 5 years prior experience in the Pharmaceutical/Biotechnology industry with a thorough knowledge of Quality Systems, Quality Assurance and Quality Control including solid knowledge of global GMP Quality and Regulatory requirements.
Salesforce QA Engineer SS&C Technologies Holdings IncSalesforce QA EngineerNCRemotep>Our team is highly collaborative and cross-functional, bringing together product owners, developers, administrators, and QA engineers to deliver high-quality applications that drive efficiency, enable data-driven decision-making, and provide a strong user experience. To further explore this opportunity, please apply through our careers page on the corporate website at https://www.ssctech.com/careers/join-ssc.
GMDP Quality Assurance Manager WEP ClinicalGMDP Quality Assurance ManagerMorrisville, North CarolinaThe GMDP Quality Manager will also act as a primary expert and interface between supply chain and logistics, project management and other departments to drive delivery of client solutions with respects to Post Approval Named Patient/Expanded Access Program and Clinical Trial supply service lines for the site. Our Services Include:Access ProgramsClinical Trial ServicesPatient Site SolutionsClinical Trial SupplyMarket Access and Commercialization Data Privacy Notice:WEP Clinical is committed to protecting your personal information throughout the recruitment process.
Sr. Supervisor / Supervisor III, QA (Filling and Utilities) Grifols SASr. Supervisor / Supervisor III, QA (Filling and Utilities)Clayton, NCResponsibilities may also include advanced roles (such as author, reviewer, approver, administrator or coordinator) in all quality systems such as Change Control, Discrepancy Management, Quarantine, Batch Release, SAP, SAP Quality Module, Documentation, and Annual Product Reviews as well as provide Quality input for Validation projects, capital engineering projects, clinical studies, stability studies, ETPs, and Regulatory submissions. Specific duties will depend on the assignment and may include; review of manufacturing or testing records, preparation or review of failure investigations, product/raw material sampling and/or testing, sampling/testing/data analysis of environmental monitoring samples and data, auditing, data analysis for stability, etc.
Quality Assurance Manager Harris Computer SystemsQuality Assurance ManagerNC5+ years of experience in software delivery, QA, or test engineering 2+ years of experience in QA leadership or people management Hands-on experience with automated testing frameworks (Playwright, Selenium, Cypress, etc.) Strong understanding of Agile delivery and embedded QA collaboration within scrum teams Ability to introduce structure and rigor without creating bureaucracy Experience using quality metrics as tools for visibility, learning, and accountability Excellent communication and partnership skills across Engineering, Product, and Support A calm, steady leadership style with strong ownership and follow-through. Own QA execution and release readiness • Lead day-to-day QA delivery across multiple product teams, ensuring testing is well planned, visible, and aligned with sprint and release goals • Provide clear quality signals to Engineering and Product partners, supporting informed tradeoffs and predictable delivery • Maintain a strong pulse on testing progress and risk across teams through thoughtful engagement in key Agile ceremonies and targeted check-ins • Ensure effective defect triage, validation, and collaboration on high-priority production or customer-impacting issues.
Quality Assurance Specialist II TalentBurst, Inc.Quality Assurance Specialist II20 TW Alexander Dr, Research Triangle Park,, NC$30–$32 / hourExamples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analysis from clinical and preclinical studies, qualification and/or validation of methods, equipment/software validation, laboratory processes, etc. Education/ Qualifications:Quality Assurance Specialist - Bachelor's degree, in a health care or relevant scientific field and 3+ years of relevant industry experience.
NewQuality Assurance Inspector 1st Shift TalentBurst, Inc.Quality Assurance Inspector 1st ShiftClayton, NC$17–$25 / hourQuality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
NewQuality Assurance Inspector 2nd Shift TalentBurst, Inc.Quality Assurance Inspector 2nd ShiftClayton, NC$17–$25 / hourQuality Assurance Inspectors work with manufacturing operations during the production process, by approving the raw materials and associated documentation for incoming plasma shipments from donor collection centers and the in-process production batches (Production Units - PUs) at the Plasma Logistics Center (PLC). Quality Assurance Inspectors identify and document deviations of both materials and the manufacturing process and ensure these deviations are corrected to ensure a better finished product for prospective customers.
Director, Clinical Quality Assurance Cellectis SADirector, Clinical Quality AssuranceNC$190,000–$234,000 / yearThe Director, Clinical Quality Assurance is primarily responsible for establishing and leading the Clinical QA function and providing independent oversight of Good Clinical Practices (GCP) activities to ensure compliance with FDA, EMA, ICH, and other applicable global and national regulatory requirements across Cellectis' clinical programs. Knowledge and understanding of regulations regarding cell/gene therapies including but not limited to ICH guideline, GCP, and GMP as defined by the US Food and Drug Administration and European Medicines Agency.
Pharma GMP Quality Assurance IntelliPro GroupPharma GMP Quality AssuranceResearch Triangle Park, North CarolinaProviding deliverables and resolving issues; Draft SOPs/controlled documents as well as perform quality unit review and approval of Quality Management Systems requests/ records related to Learning Management, Non-Conformance Management, CAPA management, and metric/KPI reporting. Minimum Requirement:Bachelor’s degree in a scientific field and 4+ years of experience in GMP based Quality Assurance, particularly in support/oversight of a company QMS, or 10+ years of GMP based Quality Assurance experience using a company QMS.
NewQuality Assurance Inspector (2nd shift) RD PartnersQuality Assurance Inspector (2nd shift)Clayton, North Carolina$41,600–$52,000Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor. Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
NewQuality Assurance Inspector (1st shift) RD PartnersQuality Assurance Inspector (1st shift)Clayton, North Carolina$41,600–$52,000Approves incoming plasma shipment documentation and raw materials by confirming specifications, rejects and returns unacceptable materials as directed by QA Supervisor. Responsible for inspecting final outgoing plasma lot shipments to ensure all pallets are properly packaged and loaded for sales and distribution.
Senior Quality Assurance Engineer Hewlett Packard Enterprise CoSenior Quality Assurance EngineerDurham, NC$120,500–$276,500 / yearp>Please note that Hewlett Packard Enterprise (HPE), its direct and indirect subsidiaries and affiliated companies, and its authorized recruitment agencies/vendors will never charge any candidate a registration fee, hiring fee, or any other fee in connection with its recruitment and hiring process. We help companies connect, protect, analyze, and act on their data and applications wherever they live, from edge to cloud, so they can turn insights into outcomes at the speed required to thrive in today's complex world.
KBI: US - Principal QA Specialist KBI BiopharmaKBI: US - Principal QA SpecialistDurham, North CarolinaProvides QA oversight of analytical and microbial laboratory activities including but not limited to method qualification, method transfers, method validations, creation and revision of test methods, specifications, stability studies, laboratory investigations and laboratory deviations. The Principal QA Specialist provides exemplary service to both internal and external customers by ensuring patient safety and regulatory compliance while supporting product lifecycle activities for timely delivery of products to clients for patients.
Mission Critical - QA Foreman Adams Electric CompanyMission Critical - QA ForemanRaleigh, NCDirectly supervise, manage, and coordinate activities of electricians, apprentices, helpers, and temporary workers. Overlook the crew and direct work in logical steps and budget time required to meet.
Senior QA Technical Specialist FujifilmSenior QA Technical SpecialistResearch Triangle Park, NCThe Senior QA Technical Specialist acts independently and provides QA subject matter knowledge in the GMP domain to systems and projects with focus on key quality activities and deliverables in accordance with company policies/SOPs and regulatory requirements. Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
Director of Quality Assurance Forge NanoDirector of Quality AssuranceRaleigh, NCThis role is a critical leadership position responsible not only for managing quality, but for building and scaling the quality function from early-stage ramp through full production in a high-growth, next-generation battery manufacturing environment. Forge Battery is a rapidly growing company that is building a multi-GWh battery plant in Morrisville, NC, and is seeking a highly skilled and experienced Director of Quality Assurance (QA), to lead the QA resources and assets.
Software Test (QA) Engineer Mechanical Licensing CollectiveSoftware Test (QA) EngineerRaleigh, NCRemoteYou will build and maintain automated testing frameworks and perform exploratory validation across workflows, APIs, integrations, and user-facing components to ensure the system behaves as intended and that changes do not introduce regressions. Experience testing machine learning or probabilistic systems, building testing frameworks from scratch, or working with orchestration tools such as Dagster or Airflow is a plus.
Quality Assurance Area Specialist III - Finished Production Novo Nordisk ASQuality Assurance Area Specialist III - Finished ProductionClayton, NCDemonstrated expertise in Regulations & quality systems in one or more of the following: product disposition, DV/CAPA, Change Control, Audits, Supplier Management, Project Management, Validation, laboratory method and equipment validation, warehouse/logistics, and IT preferred. Quality oversight, review & approval of validation activities and documents associated with projects, new systems, changes to existing systems & maintaining validated state of equipment, processes, and systems.
QA Area Specialist I - SDF (1st shift) Novo Nordisk ASQA Area Specialist I - SDF (1st shift)Durham, NCOur Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. Knowledge of Quality and one or more of the following: Aseptic Production, Business Support, QC, Production Support, Warehousing/Transport, API, and/or Finished Production processes preferred.
QA Area Specialist I - SDF (2nd shift) Novo Nordisk ASQA Area Specialist I - SDF (2nd shift)Durham, NCOur Emerging Technologies -Solid Dosage Forms US facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. Knowledge of Quality and one or more of the following: Aseptic Production, Business Support, QC, Production Support, Warehousing/Transport, API, and/or Finished Production processes preferred.
NewSpecialist, Quality Assurance FujifilmSpecialist, Quality AssuranceResearch Triangle Park, NCp>Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place.
Associate III, Quality Assurance (On The Floor, Swing Shift) BiogenAssociate III, Quality Assurance (On The Floor, Swing Shift)Research Triangle Park, North CarolinaThis includes but is not limited to Review and Approval of executed BPRs, PRCDs/WIs, Formulas, Recipes, Validity Rules (FRRV/BOM), existing/revised MPRs, MSLRs, MSMs, PCDs, PFDs, PARs; on the Manufacturing floor record review and observations, performing WORCs, performing inspection readiness walkthroughs, and oversight of Manufacturing operations. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
QA 135 RTS/AWR Inspector Fly Exclusive, LLCQA 135 RTS/AWR InspectorRaleigh, NCUpdate items in work orders and ensure all tracked inspections, maintenance and parts are tracked correctly updated in records tracking system at all times. Summary and Objective The QA 135 RTS/AWR Inspector is responsible for ensuring all maintenance paperwork for all aircraft, engines, and APU are correct and accounted for.
Head of Product and Quality Assurance EnrollHereHead of Product and Quality AssuranceRaleigh, North CarolinaThe right person in this role will directly influence product innovation, customer satisfaction, platform adoption, and company growth while helping ensure we continue to deliver at a pace that sets us apart from the market. EnrollHere is seeking a highly driven Head of Product & Quality to lead product execution, customer engagement, quality assurance, and delivery across our platform.
Sr. Manager, Compliance - Quality Assurance Biogen IncSr. Manager, Compliance - Quality AssuranceResearch Triangle Park, NC$127,000–$170,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. As a key member of the Site Quality Leadership Team, this leader partners closely with cross-functional stakeholders to strengthen compliance oversight, risk management, and data integrity while fostering a strong quality culture.
Sr. Specialist I, Product Quality Assurance Beam Therapeutics IncSr. Specialist I, Product Quality AssuranceDurham, NC$140,000–$185,000 / yearBeams suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. The role will provide Quality oversight of routine manufacturing, testing, and related operations to ensure that systems and processes are maintained in compliance with Good Manufacturing Practices (GMP), and ultimately to Good Distribution Practices (GDP) as the programs move to the commercial phase.