18 information technology jobs found in Durham

Biogen About This Role: As a Senior Associate III in Inspection Management within our Quality Assurance team, you play a pivotal role in maintaining and enhancing quality systems at the RTP facility. Your expertise in GMP activities ensures that our quality systems remain compliant with industry standards. You will lead the charge in managing site inspections, regulatory requests, and overseeing the creation and approval of GMP documents. Your ability to balance departmental workload, mentor team members, and manage key projects will significantly contribute to our team's success. This position not only ensures compliance but also drives continuous improvement, reinforcing our commitment to quality and excellence. What You'll Do: Manage regulatory and partner inspections, ensuring timely inspection setup, support, and closure Lead inspection readiness activities, including planning and execution Process regulatory requests to support submissions and approvals...

Biogen This is a full time on-site position with M-F business hours About This Role The Sr. Associate II is responsible for the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. This individual has advanced understanding of the Quality Management Systems and applies that knowledge by coaching peers and ensuring continuous improvement cross-functionally. The Sr. Associate II provides guidance regarding regulatory compliance, technical expertise, independent assessment and expert consultation to Manufacturing, Quality Control, Engineering, Validation, and other supporting departments in a mannerconsistent with site and Corporate policies, cGMP, safety, environmental and humanresources policies and procedures. This individual will assist with regulatory and third party audits, aid in the development and implementation of GlobalQualitySystems, and manage Quality projects and other...

Biogen This is a full time, on-site position with a schedule of 12 noon to 12 midnight on a rotating 2-2-3 schedule About This Role The QA Sr Associate I has the working understanding, full knowledge and ability in their primary discipline. They are able to apply technical principles, concepts and understanding of systems and procedures in order to conduct quality and compliance related activities. They are proficient in their understanding of the Biogen Quality Systems. The QA Sr Associate I has working knowledge of GxP regulations and adheres to all regulatory licenses and regulations as well as internal SOPs. The Associate identifies and resolves issues through collaboration with others. They partner with colleagues in identifying and resolving potential compliance concerns. The QA Sr Associate I performs all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures. The Associate should be...

Fidelity Investments Job Description: Note: Fidelity will not provide immigration sponsorship for this role. The Role The Fidelity Institutional Technology (FIT) group is looking for a highly motivated, self-driven systems analyst to be part of its diverse, globally distributed team of IT professionals responsible for the development and maintenance of Fidelity's Institutional Client Platforms and Products in the rapidly growing and evolving Wealth Management space. The focus of this position will involve analysis and support of managed discretionary solutions products and tools. The systems analyst will need to collaborate extensively with other teams within the same product area and domain as well as across the enterprise partnering with a varied set of business and technology partners. They will be a key member of a delivery team and will be actively involved in all aspects of the technical product vision and design. The individual will gain a deep end-to-end...

Fidelity Investments Job Description: Director, Observability Platform Engineering Technical Lead The Role We are seeking a highly experienced, hands-on Technical Lead and Build Owner to lead a dedicated team of software engineers responsible for delivering core platform capabilities within Fidelity's Enterprise Observability Platform. This is not an SRE role; instead, you will focus on building and evolving the observability platform that Site Reliability Engineering and development teams depend on. In this role, you will define and drive the Observability Integrations roadmap , emphasizing scalable automation, security-by-design, and enterprise readiness across a complex hybrid-multi-cloud environment. You will lead the design, development, and support of enterprise-grade observability integrations with SaaS solutions such as Datadog , as well as open-source frameworks including OpenTelemetry (OTel) and Prometheus . The Expertise and Skills You Bring...

Fidelity Investments Job Description: Note: Fidelity will not provide immigration sponsorship for this position The Team Come join Fidelity as we have our Better Way of Working! Your mission, if you choose to accept it, is to join the Fidelity Wealth Solutions Engineering chapter focused on greater delivery, efficiency, and quality. Our engineering team is innovative, diverse, passionate, and self-driven. We work in a very dynamic, agile environment. You will work in a Squad focused on enabling Wealth Management business in Fidelity through Flexible, Scalable platforms and report to a Chapter Leader (your manager), whose primary focus is to help you develop in your career and skills as we drive towards increased automation, continuous delivery with quality. Chapter Leaders drive the 'how': skills & mastery, while your Squad drives the 'what'. This is the next evolution of Agile development! The Purpose As a systems analyst on the team, you will be expected to...

Fidelity Investments Job Description: Job Title Principal Quant Development The Role We are seeking Principal Quant Engineering to join our Quantitative Research & Investments Technology (QRIT) team in Fidelity Asset Management Technology. This role will partner with the quant research and investments teams to design, build, enhance, and support a comprehensive Systematic Fixed Income research and portfolio construction ecosystem. This individual will include hands on development collaborating with team of software engineers and quantitative developers. The Expertise and Skills You Bring Bachelor's degree in a computational field such as Computer Science, Master's degree is preferred Minimum of 5 years of proven professional experience working in financial services (Asset Management experienced preferred) Proven experience engaging with senior internal and external clients and partners Experience with Python and micro-services / RESTful APIs...

The Nature Conservancy What We Can Achieve Together: The CPRG Peatlands Project Lead manages and implements climate pollution reduction restoration projects. The focus of this work is acquisition and hydrological restoration of pocosin peatland properties as part of the deliverables associated with the five-year $200 million Climate Pollution Reduction Grant (CPRG) from the EPA to TNC in 2024. The Peatlands Project Lead will coordinate and implement acquisition and restoration work across eastern NC to deploy and scale peatland protection and restoration as a natural climate solution that reduces greenhouse gas emissions. They will work closely with the CPRG Project Steering Committee, Project Team and staff in NC, and will be responsible for building strong internal and external partnerships in order to ensure the timely execution of projects. The Peatlands Project Lead will establish objectives and key results to track progress and make sure projects meet key...

Biogen This application is for a 6-month student role from July - December 2026. Resume review begins in January 202. Cell Culture Development works to create high quality, robust processes that are manufacturing-ready. We use carefully designed experiments to target areas for improvement identified from previous biological process knowledge/experience. We balance understanding/fundamental science with efficiency to make risk-based decisions that ensure safety/success of any process. Members of this team have the opportunity to contribute directly to current challenges in the group. While performing diverse, hands-on experiments, an individual will learn about a wide variety of research areas, including bioprocess development, process analytical technology, and control strategy. What You'll Do: This co-op is onsite and lab-based. Perform and document a variety of functions in support of the development of new technologies for cell culture manufacturing processes of...

Biogen This onsite, 1st shift role runs Monday to Friday, with some weekend and off-shift support as needed About This Role We are seeking a highly experienced and motivated Biochemistry Senior Associate II to join the Biochemistry team at our RTP biologics drug substance manufacturing facility. The role will support advancing biochemistry laboratory activities, including method execution, troubleshooting, instrument validation, data interpretation, and participation in project teams. This role primarily works independently with minimal supervision as needed, consults with management on key decisions. What You'll Do Act as the primary team lead and represent the team in absence of Manager Conduct laboratory investigations (i.e. invalids, OOS, and atypical) and deviations Reviews tests, approves release data, and issues certificates Authors and review protocols, change control requests, and SOPs Serve as a technical resource for the workgroup or project...

Biogen About This Role As a Sr. Engineer III in Manufacturing Sciences, you will be an integral member of the global Manufacturing Sciences team. Your primary focus will be on leading, facilitating, and coordinating biologic molecule technology (tech) transfer activities at our Bio Site in RTP. You will create, drive, and communicate technology transfer deliverables while managing the overall tech transfer schedule and metrics. By utilizing technical rigor, analyzing complex issues and identifying business process optimization opportunities, you will provide technical leadership, strategic insights and direction. Your role also involves communicating transfer plans and risk mitigations to senior leadership, ensuring alignment with departmental priorities. This position is pivotal for driving successful tech transfers, supporting both internal programs and those of our strategic partners, and enhancing the value to our business What You'll Do: Coordinate and lead tech...

Biogen About This Role Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts (either Days or Nights) on a 2-2-3 calendar rotation. Shift Details: 12-hour shifts Nights: 6:00 PM - 6:00 AM Rotating 2-2-3 schedule The Manufacturing Associate, Lead plays a critical hands-on leadership role within a cGMP manufacturing environment, performing and documenting daily manufacturing operations while ensuring compliance, quality, and efficiency. This role works closely with the Manufacturing Supervisor to coordinate shift activities, allocate resources, and support production, validation, and continuous improvement initiatives. What You'll Do Execute manufacturing processing steps and manufacturing support activities in accordance with batch records, SLRs, control systems, and standard operating procedures. Monitor and control processes, serving as a subject matter expert (SME) for assigned unit operations and process steps. Coordinate and,...

Biogen About This Role As a Principal Risk Based Quality Management Data Monitor, you will play a critical role in shaping how clinical trial data is monitored, protected, and elevated to the highest quality standards. You will be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies-ensuring patient safety, regulatory compliance, and data integrity across all phases of clinical research. You'll collaborate closely with biostatistics, data science, safety/pharmacovigilance, clinical operations, and vendors to detect and triage signals early, optimize KRIs/QTLs, and drive continuous process and technology improvements across the portfolio. This position is ideal for someone who thrives on analytical thinking, cross-functional collaboration, and using RBQM and advanced analytics to keep clinical trials running smoothly and safely. What You'll Do Partner with cross functional teams to identify critical data and processes (CDPs) and associated...

Biogen About This Role Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts (either Days or Nights) on a 2-2-3 calendar rotation. Shift Details: 12-hour shifts Nights: 6:00 PM - 6:00 AM Rotating 2-2-3 schedule Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Product (Parenteral Filling) facility in Research Triangle Park (RTP). These teams are the backbone of our operations-each playing a critical role in delivering life-changing therapies to the patients who need them. Our teams are organized by key steps in the biomanufacturing process. Parenteral Filling Manufacturing Associates execute critical aseptic operations in a controlled cleanroom environment governed by Current Good Manufacturing Practices (cGMP). What You'll Do Parenteral Filling Operations Include Aseptic filling of drug product into vials, syringes, or cartridges Operation of automated and semi-automated...

Biogen About the Role: This application is for a 6-month student role from July - December2026. Resume review begins in February2026. TheManufacturing Technical Operations (MTO) team is a critical technical function within manufacturing sites. Its primary mission is to ensure that manufacturing processes, documentation, and systems are robust, compliant, and continuously improved. The group acts as a bridge between Manufacturing, Quality, Engineering, and Manufacturing Sciences, supporting operational readiness and technology implementation.This position would support theLarge ScaleManufacturing Facility in RTP. WhatYou'llDo: The role will offer an opportunity for cross functional collaboration withQuality, Automation, Engineering, and Manufacturing Sciences.Working in MTOwill allow thecandidategainexperiencein a GMP facility at a15,000L Bioreactor scale. They will gain experience in a GMP facility workingto support manufacturing.This is anoffice-basedrole and can...

Merck Job Description Our company is launching a highimpact global Supply Planning Transformation and seeking a Manufacturing Network Supply Planning Lead with a strongpharmaceutical or drug development manufacturingbackground to help shape how we plan and supply across a multisite network. In this role, you will lead theprocess and solution designof an enterprisewideAdvanced Planning System (APS), identifying and closing gaps in current supply planning practices, harmonizing ways of working across sites, and building scalable, futureready planning models. You will work endtoend-from design through deployment and hypercare-driving change adoption, elevating planning capabilities, and partnering with crossfunctional and global teams to deliver a stepchange in service, agility, and reliability for our global manufacturing network. This role is for a builder-someone who thrives in ambiguity, moves with speed, and brings the intensity required to reshape how we plan, operate,...

Biogen About This Role Biogen studies highly complex, devastating, and burdensome diseases and there are still significant challenges in how we understand and treat them. In the Quantitative Sciences Development Organization we aspire to transform patients' lives by accelerating disease research using best in breed and emerging techniques. Leveraging applied machine learning and emerging technologies, we drive solutions to advance research, clinical care, and patient empowerment. We stand with our colleagues across Biogen developing pioneering treatments. We believe that now, more than ever, biology and technology should go hand-in-hand to better meet patient needs, while enabling a shift towards more prevention-focused, affordable, and equitable care. What You'll Do As a Machine Learning Engineer, Operations and Health Systems Research, you will: Design, develop, and implement complex end-to-end data pipelines, engineer features and disease models to...

Biogen About This Role As a Principal Application Specialist, you will play a critical role in designing, building, implementing, and maintaining Veeva Vault Document Management System. Biogen is undergoing a business transformation with technology as a core enabler. Veeva Vault QualityDocs is a critical component of this transformation, and you will be the ultimate driver, leveraging your expertise to ensure high-quality service delivery, optimal system performance, and seamless user experiences. Acting as the IT System Owner for Veeva Vault QualityDocs, you will collaborate closely with cross-functional teams, including business analysts, technical architects, system configurators and project managers, to deliver upgrades, enhancements, new modules, and other initiatives aligned with strategic business roadmaps. Your work will directly support Biogen's Employee Experience and GxP compliance, ensuring that our document management system meets regulatory requirements and user...