Lumen Bioscience jobs - 15,491 jobs

Join Lumen Bioscience as a Clinical Operations Manager to play a vital role in overseeing and coordinating the clinical operations activities within our growing biopharmaceutical company. In this role, you'll collaborate with cross-functional teams, and manage CROs and clinical research sites, while ensuring the successful execution of clinical trials, adherence to regulatory guidelines, and the timely delivery of high-quality clinical data. This position combines hands-on leadership of clinical operations activities with clinical trial oversight, relationship management, clinical sample management, clinical trial supply management, documentation and data management, and process improvement. You'll oversee the planning, implementation, and execution of clinical trials in collaboration with cross-functional teams, collaborate with CROs and clinical trial sites, and oversee and supervise clinical trial sample management life cycle to maintain chain-of custody in a GxP compliant setting. You'll assist with forecasting and managing inventory of investigational product, manage relationships with third-party vendors, oversee investigational product shipments domestically and internationally, and oversee the collection, processing, and archival of clinical trial data and documents while identifying opportunities to streamline clinical operations processes, enhance efficiency, and optimize resource allocation. If you have strong leadership skills, in-depth knowledge of clinical research processes, and thrive in a fast-paced environment, we encourage you to apply. Duties & Responsibilities: * Clinical Trial Oversight: * Oversee the planning, implementation, and execution of clinical trials in collaboration with cross-functional teams, including regulatory affairs, medical writing, production and development, and data management. * Ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and relevant regulatory requirements. * Monitor clinical trial progress, identify potential issues, and proactively develop and implement corrective actions. * Relationship Management: * Collaborate with Contract Research Organizations (CROs) and clinical trial sites to ensure efficient study start-up, enrollment, and conduct. * Facilitate effective communication and build strong relationships with external partners, including investigators, site personnel, and vendors. * Serve as the main point of contact for clinical trial-related inquiries and issue resolution. * Clinical Sample Management: * Oversee and supervise clinical trial sample management life cycle to maintain chain-of custody in a GxP compliant setting * Work closely with CRO, external lab vendors and internal teams to plan and execute sample processing, tracking and shipment of clinical samples * Oversee sample receiving procedures and sample testing timelines * Clinical Trial Supply Management: * Assist with forecasting and managing inventory of investigational product needed for upcoming and ongoing clinical trials * Establish packaging, labeling and distribution timelines * Manage relationships with third-party vendors, e.g., shipping companies and IRT providers. * Oversee investigational product shipments domestically and internationally, including coordination of import/export documentation, permits and licenses to ensure timely and compliant delivery of investigational product to drug depots and clinical research sites. * Documentation and Data Management: * Oversee the collection, processing, and archival of clinical trial data and documents, ensuring accuracy, completeness, and traceability. * Collaborate with the data management team to implement efficient data capture and reporting processes. * Ensure compliance with data protection regulations and maintain data confidentiality. * Process Improvement: * Identify opportunities to streamline clinical operations processes, enhance efficiency, and optimize resource allocation. * Contribute to the development and implementation of standardized operating procedures (SOPs) and best practices. * Stay up to date with industry trends and regulatory changes to ensure the adoption of current best practices. Qualifications & Requirements: * Education and Experience: * Bachelor's degree in life sciences or a related field (advanced degree preferred). * Minimum of 8 years of experience in clinical operations, with a demonstrated track record of managing clinical trials. * Strong knowledge of GCP guidelines, FDA regulations, and other relevant regulatory frameworks. * Proven experience in leading and managing teams, with excellent organizational and interpersonal skills. * Skills and Attributes: * Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software applications. * Excellent written and verbal communication skills, with the ability to effectively communicate complex information to diverse stakeholders. * Detail-oriented, with strong problem-solving and decision-making abilities. * Ability to work effectively in a fast-paced, dynamic environment and manage multiple priorities simultaneously. * Demonstrated ability to adapt to changing circumstances and proactively drive process improvements. Physical Requirements: * Ability to work on-site in Seattle, WA * Ability to sit for extended periods of time (2 or more hours) Benefits at Lumen Bioscience: * Stock bonus * Health, Dental, and Vision premiums fully covered by Lumen * 401k match up to 4% * Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure * Monthly wellness program to support your health and well-being * Free onsite parking or public transportation subsidies * Comprehensive parental leave policies * Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range $80,000 - $120,000 USD Create a Job Alert Interested in building your career at Lumen Bioscience? Get future opportunities sent straight to your email. Create alert

Wellspring Nurse Source is seeking a travel Ultrasound Technologist for a travel job in Aberdeen, Washington. Job Description & Requirements Specialty: Ultrasound Technologist Discipline: Allied Health Professional Start Date: 01/26/2026 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Job Title: Ultrasound Technologist Job Summary: An Ultrasound Technologist (also known as a Sonographer) performs diagnostic imaging procedures using specialized ultrasound equipment to produce detailed images of internal organs, tissues, and blood flow. These images assist physicians in diagnosing and monitoring a wide range of medical conditions. The Ultrasound Technologist plays a critical role in patient care by ensuring accurate imaging, patient comfort, and effective communication with the healthcare team. Key Responsibilities: Perform general ultrasound examinations, including abdominal, pelvic, obstetric, vascular, and small parts imaging, as ordered by physicians. Operate ultrasound equipment to capture diagnostic-quality images, adjusting settings based on patient needs and clinical requirements. Prepare patients for ultrasound procedures by explaining the process, positioning them correctly, and ensuring their comfort. Analyze and interpret ultrasound images to identify normal and abnormal findings, documenting results for physician review. Monitor patient vitals, including heart rate, blood pressure, and oxygen levels, during procedures to ensure patient safety. Collaborate with radiologists, physicians, and other healthcare professionals to provide diagnostic information and contribute to patient care plans. Maintain and clean ultrasound equipment and ensure compliance with infection control protocols. Educate patients about procedures, post-procedure care, and the significance of imaging results. Stay current on advancements in ultrasound technology, imaging techniques, and patient care standards through continuing education. Qualifications: Education: Associate's or Bachelor's degree in Diagnostic Medical Sonography or a related field. Certification: Registered Diagnostic Medical Sonographer (RDMS) certification from the American Registry for Diagnostic Medical Sonography (ARDMS) preferred. Basic Life Support (BLS) certification required. Experience: Previous experience as an Ultrasound Technologist Wellspring Nurse Source Job ID #35440906. Pay package is based on 10 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied Ultrasound Technologist About Wellspring Nurse Source Wellspring is nurse owned and operated which means that we get you, we stand behind you, and we advocate for you. We are 100% committed to helping you find your best job at the best rate. We are unwavering in our commitment to supporting our clinicians on every step of their travel adventure, assisting with everything from onboarding and payroll to on-the-job clinical support with a dedicated Clinician Success Team. You're not just a number at Wellspring, you're a valued member of our family. Join us and experience the Wellspring difference.

This position is for a local contract Registered Nurse (RN) specializing in home health care in Spokane Valley, Washington. The role involves providing in-home nursing care for a 13-week assignment, working 40 hours per week in 8-hour shifts. Host Healthcare supports the nurse with benefits such as medical coverage, housing, and continuing education opportunities. Host Healthcare is seeking a local contract nurse RN Home Health for a local contract nursing job in Spokane Valley, Washington. Job Description & Requirements Specialty: Home Health Discipline: RN Start Date: Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Type: Local Contract Host Healthcare Job ID #La1fVJrcXYAQ. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: RN - Home Health About Host Healthcare At Host Healthcare, we provide a truly comfortable experience as you explore your travel nursing, therapy, or allied career. We make your travel healthcare journey easy by taking care of all the details, so you don't have to. We are on a mission to help others live better and we do this by helping the healers of the world be as comfortable as possible. With access to tens of thousands of travel nursing, therapy, and allied jobs in all 50 states, our responsive and friendly recruiters find your dream position based on what's important to you. During your assignment, get access to premium benefits, including Day 1 medical that continues up to 30 days between assignments, 401K matching, travel reimbursements, dedicated housing support, and more. We also offer 24/7 support from our team and access to our on-staff clinicians so you can feel comfortable and confident throughout your entire assignment. Travel comfortably with Host Healthcare. Benefits Referral bonus School loan reimbursement Vision benefits Wellness and fitness programs Company provided housing options License and certification reimbursement Life insurance Medical benefits Mileage reimbursement Pet insurance Discount program Employee assistance programs Guaranteed Hours Health savings account Holiday Pay 401k retirement plan Continuing Education Dental benefits Keywords: Registered Nurse, Home Health Care, Contract Nursing, Patient Care, Healthcare Staffing, Travel Nursing, Medical Benefits, Licensed RN, In-Home Care, Washington Healthcare Jobs

Access Healthcare is seeking a travel CVOR Technologist for a travel job in Everett, Washington. Job Description & Requirements Specialty: CVOR Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Access Healthcare Job ID #75256875. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About Access Healthcare Access Healthcare aims to provide superior service to our nursing family by providing around the clock support, competitive pay packages and an unmatched benefits package! Unlike other agencies, we offer a true family feel and work with you to find the placement that is right for you. We offer one of the top leading pay packages in the industry and we are ready to get you the money you deserve! Access Healthcare was founded by two travel nurses, Danielle and Diego, who had a dream and a shared vision of creating an agency which all nurses would want to work with. Our passion has led us to where we are today as one of the top 10 agencies in our home state of New Jersey, with access to contracts in all 50 states! We encourage you to join our team and we cannot wait to get to know you!

Wellspring Nurse Source is seeking a travel Speech Language Pathologist for a travel job in Tacoma, Washington. Job Description & Requirements Specialty: Speech Language Pathologist Discipline: Therapy 40 hours per week Shift: 8 hours, days Employment Type: Travel Wellspring Nurse Source Job ID #35417858. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied Speech Language Pathologist About Wellspring Nurse Source Wellspring is nurse owned and operated which means that we get you, we stand behind you, and we advocate for you. We are 100% committed to helping you find your best job at the best rate. We are unwavering in our commitment to supporting our clinicians on every step of their travel adventure, assisting with everything from onboarding and payroll to on-the-job clinical support with a dedicated Clinician Success Team. You're not just a number at Wellspring, you're a valued member of our family. Join us and experience the Wellspring difference.

Join Lumen Bioscience as a QC Specialist, Microbiology to help establish and perform microbiological quality control testing that supports process development, manufacturing, and product release in an early-stage GMP environment. In this role, you will execute routine and non-routine microbiological assays, including bioburden testing, microbial limits per USP, and environmental monitoring, while helping maintain a compliant QC microbiology lab. This position is a strong fit for someone who enjoys hands-on lab work and brings solid quality and compliance fundamentals. You will prepare media, reagents, and cultures, document results accurately using Good Documentation Practices, interpret results and trends, and escalate OOS, OOT, or atypical findings. You will also support method qualification and validation, equipment qualification, calibration, and maintenance, and contribute to quality systems by authoring and revising SOPs, test methods, and controlled documents. You will assist with deviation investigations, CAPAs, and change controls as needed, and partner closely with Process Development, Manufacturing, Quality Assurance, and external partners to support lot release and program timelines. If you are detail-oriented, organized, proactive, and comfortable building structure in an evolving environment, with a strong commitment to quality and compliance, we encourage you to apply. Duties & Responsibilities: This position requires working under the 21 CFR part 210/211 standard pharmaceutical cGXP quality system processes. * Microbiology Testing & Analysis * Perform routine microbiological assays, including bioburden testing, microbial limits per USP, and environmental monitoring. * Conduct adventitious agent screening or support external testing as needed. * Prepare media, reagents, and microbiological cultures following SOPs and GMP requirements. * Document results accurately in compliance with Good Documentation Practices (GDP). * Interpret results, identify trends, and escalate out-of-specification (OOS), out-of-trend (OOT), or atypical findings. * Quality Systems & Compliance * Author and revise SOPs, test methods, and other controlled documents. * Support qualification, calibration, and maintenance of microbiology laboratory equipment. * Participate in method qualification/validation and QC readiness for GMP manufacturing. * Assist with deviation investigations, CAPAs, and change controls as needed. * Ensure work is performed in compliance with cGMP, GLP, and company quality policies. * Environmental Monitoring & Facility Support * Perform routine environmental monitoring. * Trend EM data and support investigation of excursions. * Coordinate sample submission to external contract testing labs when required. * Cross-Functional Collaboration * Work closely with Process Development, Manufacturing, Quality Assurance, and external partners to support lot release and overall program timelines. * Provide microbiology subject matter insights to support risk assessments, contamination control strategy, and process improvements. Qualifications & Requirements: * Education and Experience: * Minimum 6 years of work experience in Quality Control in a regulated (cGXP) organization. * -OR- a PhD in biochemistry, microbiology, or related scientific field plus 2 years of hands-on microbiology experience in a pharmaceutical, biotech, or regulated laboratory environment. * -OR- a bachelor's or master's degree in biochemistry, microbiology or related scientific field plus 5 years of hands-on microbiology experience in a pharmaceutical, biotech, or regulated laboratory environment. * Knowledge of relevant cGxP, ISO 9001, and ICH requirements for document control and quality records. * Skills and Attributes: * Hands-on, detail-oriented, and organized. * Strong communication skills across technical and non-technical teams. * Comfortable building structure in ambiguous or evolving environments. * Proactive problem-solver who enjoys continuous improvement. * High level of integrity and commitment to quality. * Experience supporting clinical-stage or commercial GMP operations. * Familiarity with method validation, equipment qualification, and QC lab setup. * Experience with regulatory inspections or QA/QC audits. * Hands-on, detail-oriented, and organized. * Ability to support weekend or off shift testing as needed in a startup environment. Physical Requirements: * Ability to work on-site in Seattle, WA * Ability to sit/stand for extended periods of time (2 or more hours) * Occasionally lift or carry up to 23 kg Benefits at Lumen Bioscience: * Stock bonus * Health, Dental, and Vision premiums fully covered by Lumen * 401k match up to 4% * Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure * Monthly wellness program to support your health and well-being * Free onsite parking or public transportation subsidies * Comprehensive parental leave policies * Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range $85,000 - $95,000 USD Create a Job Alert Interested in building your career at Lumen Bioscience? Get future opportunities sent straight to your email. Create alert

Join Lumen Bioscience as a Project Coordinator to play a vital role in supporting the successful execution of projects within our expanding biopharmaceutical company's clinical activities. In this role, you'll work closely with Project Managers to ensure the smooth coordination and implementation of various projects while assisting in project planning, tracking progress, facilitating communication, and managing project documentation. This position combines hands-on project support with documentation and reporting, communication and collaboration, risk management, and administrative support. You'll coordinate project activities, maintain accurate and up-to-date project documentation, act as a primary point of contact for project-related inquiries, and assist in identifying potential risks and issues that may impact project timelines or objectives. If you are highly organized and detail-oriented, and enjoy collaborating with cross-functional teams, we encourage you to apply. Duties & Responsibilities: Project Support: Assist Project Managers in developing project plans, timelines, and deliverables. Coordinate project activities, ensuring adherence to established timelines and quality standards. Monitor project progress and update relevant stakeholders on key milestones and potential risks. Facilitate communication and information exchange among project team members. Documentation and Reporting: Maintain accurate and up-to-date project documentation, including project plans, meeting minutes, and progress reports. Prepare regular status reports to track project activities, milestones, and risks. Assist in the development of presentations and materials for project meetings and stakeholder updates. Communication and Collaboration: Act as a primary point of contact for project-related inquiries from internal teams and external stakeholders. Foster effective communication and collaboration among project team members to ensure alignment and synergy. Schedule and coordinate meetings, workshops, and other project-related activities. Risk Management: Assist in identifying potential risks and issues that may impact project timelines or objectives. Contribute to the development and implementation of risk mitigation strategies. Monitor project-related risks and proactively communicate updates to the Project Managers. Administrative Support: Provide administrative assistance to Project Managers, including scheduling meetings, managing calendars, and arranging travel if necessary. Assist in budget tracking and expense management for projects. Support the coordination of vendor contracts and agreements, as needed. Qualifications & Requirements: Education and Experience: Bachelor's degree in a relevant scientific or healthcare discipline is preferred 2+ years of experience in a project coordination or administrative support role, preferably in the biopharmaceutical or clinical research industry Skills and Attributes: Demonstrated ability to coordinate and support multiple projects concurrently Exceptional organizational skills with a keen eye for detail and accuracy Strong written and verbal communication abilities to facilitate effective collaboration Proactive and self-motivated approach to work, demonstrating initiative and problem-solving skills Ability to work well under pressure and meet tight deadlines Collaborative mindset with a focus on teamwork and building positive relationships Proficient in Microsoft Office Suite, project management software (e.g., Smartsheets) and reference software (e.g., Zotero) Ability to adapt quickly to changing priorities and requirements Strong ethics and integrity, ensuring compliance with regulatory guidelines and company policies Physical Requirements: Ability to work on-site in Seattle, WA Ability to sit for extended periods of time (2 or more hours) Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$33.75-$38.50 USD

Join Lumen Bioscience as a Security Engineer & Analyst to be the guardian of our hybrid cloud infrastructure and endpoint ecosystem. In this role, you'll own security architecture, monitoring, and incident response across Microsoft 365/Entra ID, Azure, AWS, and a diverse endpoint fleet (Windows 11/mac OS). This position requires balancing stringent biotech regulatory and compliance requirements with practical, scalable security solutions that enable scientific innovation. If you enjoy building secure-by-design environments, leading incident response, and partnering with cross-functional teams to protect sensitive data and systems, we encourage you to apply. Duties & Responsibilities: * Cloud & Identity Security (~40%) * Architect and maintain security posture across Azure, AWS, and Microsoft 365/Entra ID environments. * Design and implement Zero/Low Implicit Trust architecture with Conditional Access policies, MFA enforcement, and Privileged Identity Management (PIM). * Configure and maintain Azure Security Center, AWS Security Hub, and native cloud security controls. * Implement secure baselines for cloud workloads, storage, and networking components. * Manage identity lifecycle, RBAC, and least-privilege access models across cloud and SaaS platforms. * Endpoint Security & Management (~30%) * Administer endpoint protection platforms (EDR/XDR) across Windows 11 and mac OS devices. * Deploy and maintain Intune policies for Windows endpoints including BitLocker encryption, Windows Defender, and compliance baselines. * Implement mac OS security controls using MDM solutions (Jamf/Kandji or Intune for Mac). * Secure shared laboratory and manufacturing endpoints using kiosk modes and restricted profiles. * Orchestrate patch management, software deployment, and configuration drift monitoring for endpoints. * Security Operations & Incident Response (~20%) * Design and tune SIEM alerting rules (e.g., Azure Sentinel, Splunk, or similar) to minimize false positives while detecting critical events. * Lead incident response activities including communication with MDR vendor, triage, forensics, containment, eradication, and recovery. * Conduct threat hunting exercises and security investigations based on logs, alerts, and intelligence. * Maintain incident response runbooks and coordinate tabletop exercises. * Generate security metrics, KPIs, and executive-level reporting. * Governance, Risk & Compliance (~10%) * Support FDA, SOC 2, CMMC, and GxP audit activities through evidence collection, documentation, and remediation tracking. * Perform vulnerability assessments and coordinate remediation efforts with relevant teams. * Conduct vendor security assessments and manage third-party risk. * Develop and maintain security policies, standards, and procedures. * Partner with QA/Compliance teams on 21 CFR Part 11 and data integrity requirements. Required Qualifications: * Technical Skills: * Endpoint Management: Strong Intune experience for Windows; familiarity with mac OS MDM solutions (e.g. Intune, Jamf, or similar). * Security Tools: Hands-on experience with EDR/XDR platforms such as Huntress, CrowdStrike, Defender for Endpoint, or SentinelOne. * SIEM/Monitoring: Experience with Azure Sentinel, Splunk, or similar platforms, including log analysis and correlation. * Scripting: Proficiency in PowerShell and Python for security automation and orchestration. * Networking: Understanding of network segmentation, firewalls, VPNs, and zero-trust principles. * Professional Skills: * Clear technical writing skills for documentation, procedures, and audit artifacts. * Ability to translate security risks into business impact for non-technical stakeholders. * Strong problem-solving skills with high attention to detail. * Self-motivated with the ability to work independently in a hybrid environment. Desirable Qualifications: * Industry & Compliance Experience: * Preferred 2+ years in biotech, pharma, medical device, or healthcare IT environments * AZ-500, SC-200, SC-300, AWS Security Specialty, CISSP, CCSP, or comparable security certifications * Advanced Skills: * Experience with Infrastructure as Code (e.g., Terraform, ARM templates) * Container security experience (e.g., Docker, EC2-based workloads) * DevSecOps practices and CI/CD pipeline security * Experience with Data Loss Prevention (DLP) and Cloud Access Security Broker (CASB) solutions Physical Requirements: * Ability to work on-site in Seattle, WA * Ability to sit for extended periods of time (2 or more hours) * Occasionally lift or carry items up to 50 lb/23 kg Benefits at Lumen Bioscience: * Stock bonus * Health, Dental, and Vision premiums fully covered by Lumen * 401k match up to 4% * Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure * Monthly wellness program to support your health and well-being * Free onsite parking or public transportation subsidies * Comprehensive parental leave policies * Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range $115,000 - $130,000 USD Create a Job Alert Interested in building your career at Lumen Bioscience? Get future opportunities sent straight to your email. Create alert

Join Lumen Bioscience as a Service Desk Manager to transform our IT support function into a world-class service organization. In this role, you'll lead a small, high-performing team while designing and implementing scalable processes that support a rapidly growing environment. This position combines hands-on technical leadership with strategic service management. You'll architect processes aligned to business goals (e.g., Incident, Problem, Change, Knowledge Management) while also rolling up your sleeves to troubleshoot complex technical issues across Microsoft 365, endpoint management, and identity platforms. If you thrive as a "player-coach" in a fast-paced setting and enjoy improving both systems and people, we encourage you to apply. Duties & Responsibilities: * Service Delivery Leadership (~35%) * Lead and mentor a team of 2-3 Service Desk analysts (with plans to grow the team over time). * Establish and maintain SLAs/OLAs with clear performance metrics (e.g., MTTR, FCR, CSAT). * Implement and maintain compliance-aware Incident, Problem, Change, and Knowledge Management processes. * Drive continuous improvement using data-driven insights and root cause analysis. * Build and maintain a service catalog and self-service portal to reduce ticket volume and improve user experience. * Create and maintain a comprehensive knowledge base and troubleshooting guides to support first-contact resolution. * Technical Operations (~30%) * Oversee endpoint lifecycle management for 150+ devices (Windows 11 via Intune; mac OS via MDM), including provisioning, configuration, patching, and decommissioning. * Manage Microsoft 365 tenant administration, including Exchange Online, SharePoint, Teams, and OneDrive. * Coordinate Entra ID (Azure AD) identity management, including user provisioning, group policies, SSO, MFA, and periodic access reviews. * Implement automation using PowerShell and Microsoft Graph API (and similar tools) to streamline repetitive tasks, reporting, and service workflows. * Optimize and improve ticketing system workflows, queues, and reporting. * Team Development (~20%) * Recruit, onboard, and develop Service Desk talent, including creating training plans and mentoring team members. * Create career development paths and skills matrices for Service Desk staff. * Foster a partnership-centric culture that emphasizes empathy, customer focus, and first-contact resolution. * Coordinate cross-training to ensure coverage, knowledge redundancy, and continuity of service. * Lead by example with hands-on support during peak periods or critical incidents. * Strategic Initiatives (~15%) * Partner with the Security team on endpoint compliance, incident response, and security-related policies. * Collaborate with the Infrastructure team on monitoring, proactive maintenance, and reliability initiatives. * Support the CSV Engineer with validated system requirements and change control processes. * Drive process initiatives aimed at improving the overall employee experience with IT. * Manage vendor relationships and optimize software licensing usage and costs. Required Qualifications: * Leadership Experience: * 3+ years managing IT Service Desk or technical support teams. * Proven track record of improving service metrics (e.g., MTTR, first-contact resolution, CSAT). * Experience building teams and processes in growing organizations. * Strong project management skills with the ability to juggle multiple initiatives and priorities. * Technical Skills: * Microsoft 365: Advanced administration of Exchange Online, SharePoint, Teams, and OneDrive. * Endpoint Management: Hands-on Intune experience for Windows; familiarity with mac OS MDM solutions. * Identity Management: Entra ID/Azure AD administration, including SSO and MFA. * Ticketing Systems: Experience improving and optimizing service desk/ticketing platforms. * Scripting: Proficiency with PowerShell (and shell or Python) for automation and reporting. * Professional Skills: * Exceptional communication skills (written, verbal, and presentation) with the ability to communicate clearly at all levels. * Strong analytical and problem-solving abilities. * Customer service mindset with high emotional intelligence and empathy for end users. * Ability to translate complex technical concepts into language understandable to non-technical stakeholders. Desirable Qualifications: * Industry & Compliance Experience: * Background in biotech, pharma, or healthcare IT environments * Understanding of GxP, 21 CFR Part 11, CMMC, and/or SOC 2 requirements * Advanced Skills: * Experience with IT asset management systems * Knowledge of network fundamentals and IoT systems * Familiarity with laboratory and scientific computing environments * Experience with business analysis and process improvement methodologies Physical Requirements: * Ability to sit for extended periods of time (2 or more hours) * Occasionally lift or carry items up to 50 lb/23 kg Benefits at Lumen Bioscience: * Stock bonus * Health, Dental, and Vision premiums fully covered by Lumen * 401k match up to 4% * Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure * Monthly wellness program to support your health and well-being * Free onsite parking or public transportation subsidies * Comprehensive parental leave policies * Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range $110,000 - $125,000 USD Create a Job Alert Interested in building your career at Lumen Bioscience? Get future opportunities sent straight to your email. Create alert

Wellspring Nurse Source is seeking a travel Mammography Technologist for a travel job in Snoqualmie, Washington. Job Description & Requirements Specialty: Mammography Technologist Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Wellspring Nurse Source Job ID #34799284. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied Mammography Technologist About Wellspring Nurse Source Wellspring is nurse owned and operated which means that we get you, we stand behind you, and we advocate for you. We are 100% committed to helping you find your best job at the best rate. We are unwavering in our commitment to supporting our clinicians on every step of their travel adventure, assisting with everything from onboarding and payroll to on-the-job clinical support with a dedicated Clinician Success Team. You're not just a number at Wellspring, you're a valued member of our family. Join us and experience the Wellspring difference.

Triage Staffing is seeking a travel nurse RN PCU - Progressive Care Unit for a travel nursing job in Puyallup, Washington. Job Description & Requirements Specialty: PCU - Progressive Care Unit Discipline: RN Start Date: ASAP Duration: 16 weeks 36 hours per week Shift: 12 hours, nights Employment Type: Travel Travel Nursing: Progressive Care Unit Puyallup Location: Puyallup Start Date: 12/15/2025 Shift Details: 12H Days (12:00 AM-12:00 PM) 36 hours per week Length: 16 WEEKS Apply for specific facility details.Stepdown/PCU RN Triage Staffing Job ID #4T4HXRXU. Posted job title: Nursing: Progressive Care Unit About Triage Staffing At Triage, we prefer to be real. Real about expectations-both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great-or grating-your next supervisor may be. Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too. We staff all five major divisions of acute care-nursing, lab, radiology, cardiopulmonary and rehab therapy, offering: - Competitive, custom pay packages - One point of contact for both travelers and facilities (per division) - A reliable recruiter who's got your back throughout your entire assignment - In-house compliance and accounting specialists - A clinical liaison team available 24/7 to offer medical and professional support and career development - A mentoring program that is run and managed by actual clinicians-yeah, you read that right - And more (because of course there's more) Are we the biggest? No. Are we the best? That's rather subjective, but we're trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will. Benefits: Day One comprehensive, nationwide insurance plans for health, vision and dental and life-including a HSA option Day One 401(k) program with employer-matching contributions once eligible Facility cancelling protection-your time is money on and off-the-clock Guaranteed hours Weekly paychecks via direct deposit Earned vacation bonuses for time worked Paid holidays Employee assistance program (EAP)-your mental health is important, too Continuing education, certification and licensing reimbursement Workers comp-because accidents happen Top-rated professional liability insurance Company provided housing options Referral bonus-$750 in your pocket after they've completed a 13-week assignment

Triage Staffing is seeking a travel nurse RN OR - Operating Room for a travel nursing job in Pasco, Washington. Job Description & Requirements Specialty: OR - Operating Room Discipline: RN Duration: 13 weeks 40 hours per week Shift: 8 hours, days Employment Type: Travel Travel Nursing: OR Pasco Location: Pasco Start Date: 2/9/2026 Shift Details: 8H Days (7:00 AM-3:30 PM) 40 hours per week Length: 13 WEEKS Apply for specific facility details.OR RN Triage Staffing Job ID #3WPCFV39. Posted job title: Nursing: OR About Triage Staffing At Triage, we prefer to be real. Real about expectations-both ours and yours. Real about how a decision you make today could affect your tomorrows. Real about how compensation actually works. Real about how great-or grating-your next supervisor may be. Being real allows everyone at Triage to be ready. Ready to serve you with real honesty. So if that gig near the ocean is really no day at the beach, or that third shift comes with a second-class rate, we tell you. So you can be ready, too. We staff all five major divisions of acute care-nursing, lab, radiology, cardiopulmonary and rehab therapy, offering: - Competitive, custom pay packages - One point of contact for both travelers and facilities (per division) - A reliable recruiter who's got your back throughout your entire assignment - In-house compliance and accounting specialists - A clinical liaison team available 24/7 to offer medical and professional support and career development - A mentoring program that is run and managed by actual clinicians-yeah, you read that right - And more (because of course there's more) Are we the biggest? No. Are we the best? That's rather subjective, but we're trying to be. Will we work like hell to get you as close to your idea of heaven as possible? Yes. Yes, we will. Benefits: Day One comprehensive, nationwide insurance plans for health, vision and dental and life-including a HSA option Day One 401(k) program with employer-matching contributions once eligible Facility cancelling protection-your time is money on and off-the-clock Guaranteed hours Weekly paychecks via direct deposit Earned vacation bonuses for time worked Paid holidays Employee assistance program (EAP)-your mental health is important, too Continuing education, certification and licensing reimbursement Workers comp-because accidents happen Top-rated professional liability insurance Company provided housing options Referral bonus-$750 in your pocket after they've completed a 13-week assignment

Lumen Bioscience is hiring a Production Lead to manage day-to-day operations on our production floor, including growing and harvesting algae in Lumen's photobioreactor system following written SOPs. Primary responsibilities include managing daily Production operations, building and maintaining production schedules, maintaining Production inventories and stock levels, and supporting Production activities in a clean, food-grade environment. This role focuses on safe and compliant Production under cGMP and Lumen's QMS. The Production Lead will perform cleaning, inspection, and light maintenance in production areas; manage wet, dry, and/or powder processes; conduct daily sampling and sample processing; and accurately complete GMP paperwork and lot/batch records. This position also trains Production Assistants and Production Associate's in all aspects of Production operations and includes Saturday and Sunday workday on a rotating basis. If you bring strong commercial food or beverage production experience, are safety-minded and mechanically competent, and enjoy working as part of a cross-functional team, we encourage you to apply. Duties & Responsibilities: Production Operations: Manage day-to-day operations on the Production floor. Assist with inoculations, transfers, harvests, and cleaning activities in Lumen's photobioreactor system following written SOPs. Manage wet, dry, and/or powder processes following Standard Operating Procedures. Operate under current Good Manufacturing Practices (GMP), requiring careful attention to detail and the ability to conduct operations strictly according to procedure under hygienic conditions. Strictly adhere to food and personal safety standards and protocols to ensure a safe working environment for both the operator and other team members, and production of a safe and compliant food product. Complete GMP paperwork accurately and in a timely manner. Work a schedule that includes either a Saturday or Sunday workday as part of the regular work schedule. Scheduling & Inventory Management: Build and maintain production schedules. Act as point person for Production inventories and stock levels. Coordinate with the Production Head and Food Safety Team to schedule operations and ensure that operations are compliant with Lumen's quality management system (FSSC 22000). Cleaning, Maintenance & Sampling Clean, inspect, and conduct light maintenance in production areas. Conduct daily sampling and sample processing, recording results in lot/batch records. Use pipettes, mechanical pipettors, balances, and spectrophotometer as required by Production activities. Training & Team Support Train Production Assistants and Production Associate's in all aspects of Production operations. Communicate across multiple cross-functional levels to support Production operations. Qualifications & Requirements: Education and Experience: 4-6 years experience in a commercial food or beverage production environment or equivalent with clean operations experience. Some coursework in biology and/or a scientific background in a biology field (preferred). Some experience working in a production environment that is governed by a quality assurance system such as ISO 9001 or the like, including: Document control systems. Batch/lot recordkeeping processes. Rigorously documented operating procedures. Regular cleaning and quality testing procedures. Skills and Attributes: Ability to understand, follow and give detailed operational procedures and work instructions. Attention to detail and enthusiasm for maintaining the working environment. Good office-type computer skills. Mechanical competence, including ability to use pumps and hoses for transfer of liquids. Safety-minded: safe and hygienic workplace practices are mandatory. Ability to communicate across multiple cross-functional levels. Basic knowledge of high-level operations. Excellent interpersonal skills and team focus, along with a desire to learn new processes. Physical Requirements: Ability to work on-site in Seattle, WA Ability to work Saturday & Sunday on a rotating basis Ability to stand for extended periods of time (2 or more hours) Ability to lift and carry up to 30 kg Ability to safely manipulate hoses, air lines, and sanitary tri-clamps & ability to use step stools and ladders in accordance with Lumen's workplace safety protocols Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$36-$38.50 USD

Join Lumen Bioscience as a QC Specialist, Microbiology to help establish and perform microbiological quality control testing that supports process development, manufacturing, and product release in an early-stage GMP environment. In this role, you will execute routine and non-routine microbiological assays, including bioburden testing, microbial limits per USP, and environmental monitoring, while helping maintain a compliant QC microbiology lab. This position is a strong fit for someone who enjoys hands-on lab work and brings solid quality and compliance fundamentals. You will prepare media, reagents, and cultures, document results accurately using Good Documentation Practices, interpret results and trends, and escalate OOS, OOT, or atypical findings. You will also support method qualification and validation, equipment qualification, calibration, and maintenance, and contribute to quality systems by authoring and revising SOPs, test methods, and controlled documents. You will assist with deviation investigations, CAPAs, and change controls as needed, and partner closely with Process Development, Manufacturing, Quality Assurance, and external partners to support lot release and program timelines. If you are detail-oriented, organized, proactive, and comfortable building structure in an evolving environment, with a strong commitment to quality and compliance, we encourage you to apply. Duties & Responsibilities: This position requires working under the 21 CFR part 210/211 standard pharmaceutical cGXP quality system processes. Microbiology Testing & Analysis Perform routine microbiological assays, including bioburden testing, microbial limits per USP, and environmental monitoring. Conduct adventitious agent screening or support external testing as needed. Prepare media, reagents, and microbiological cultures following SOPs and GMP requirements. Document results accurately in compliance with Good Documentation Practices (GDP). Interpret results, identify trends, and escalate out-of-specification (OOS), out-of-trend (OOT), or atypical findings. Quality Systems & Compliance Author and revise SOPs, test methods, and other controlled documents. Support qualification, calibration, and maintenance of microbiology laboratory equipment. Participate in method qualification/validation and QC readiness for GMP manufacturing. Assist with deviation investigations, CAPAs, and change controls as needed. Ensure work is performed in compliance with cGMP, GLP, and company quality policies. Environmental Monitoring & Facility Support Perform routine environmental monitoring. Trend EM data and support investigation of excursions. Coordinate sample submission to external contract testing labs when required. Cross-Functional Collaboration Work closely with Process Development, Manufacturing, Quality Assurance, and external partners to support lot release and overall program timelines. Provide microbiology subject matter insights to support risk assessments, contamination control strategy, and process improvements. Qualifications & Requirements: Education and Experience: Minimum 6 years of work experience in Quality Control in a regulated (cGXP) organization. -OR- a PhD in biochemistry, microbiology, or related scientific field plus 2 years of hands-on microbiology experience in a pharmaceutical, biotech, or regulated laboratory environment. -OR- a bachelor's or master's degree in biochemistry, microbiology or related scientific field plus 5 years of hands-on microbiology experience in a pharmaceutical, biotech, or regulated laboratory environment. Knowledge of relevant cGxP, ISO 9001, and ICH requirements for document control and quality records. Skills and Attributes: Hands-on, detail-oriented, and organized. Strong communication skills across technical and non-technical teams. Comfortable building structure in ambiguous or evolving environments. Proactive problem-solver who enjoys continuous improvement. High level of integrity and commitment to quality. Experience supporting clinical-stage or commercial GMP operations. Familiarity with method validation, equipment qualification, and QC lab setup. Experience with regulatory inspections or QA/QC audits. Hands-on, detail-oriented, and organized. Ability to support weekend or off shift testing as needed in a startup environment. Physical Requirements: Ability to work on-site in Seattle, WA Ability to sit/stand for extended periods of time (2 or more hours) Occasionally lift or carry up to 23 kg Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$85,000-$95,000 USD

Join Lumen Bioscience as a Project Coordinator to play a vital role in supporting the successful execution of projects within our expanding biopharmaceutical company's clinical activities. In this role, you'll work closely with Project Managers to ensure the smooth coordination and implementation of various projects while assisting in project planning, tracking progress, facilitating communication, and managing project documentation. This position combines hands-on project support with documentation and reporting, communication and collaboration, risk management, and administrative support. You'll coordinate project activities, maintain accurate and up-to-date project documentation, act as a primary point of contact for project-related inquiries, and assist in identifying potential risks and issues that may impact project timelines or objectives. If you are highly organized and detail-oriented, and enjoy collaborating with cross-functional teams, we encourage you to apply. Duties & Responsibilities: * Project Support: * Assist Project Managers in developing project plans, timelines, and deliverables. * Coordinate project activities, ensuring adherence to established timelines and quality standards. * Monitor project progress and update relevant stakeholders on key milestones and potential risks. * Facilitate communication and information exchange among project team members. * Documentation and Reporting: * Maintain accurate and up-to-date project documentation, including project plans, meeting minutes, and progress reports. * Prepare regular status reports to track project activities, milestones, and risks. * Assist in the development of presentations and materials for project meetings and stakeholder updates. * Communication and Collaboration: * Act as a primary point of contact for project-related inquiries from internal teams and external stakeholders. * Foster effective communication and collaboration among project team members to ensure alignment and synergy. * Schedule and coordinate meetings, workshops, and other project-related activities. * Risk Management: * Assist in identifying potential risks and issues that may impact project timelines or objectives. * Contribute to the development and implementation of risk mitigation strategies. * Monitor project-related risks and proactively communicate updates to the Project Managers. * Administrative Support: * Provide administrative assistance to Project Managers, including scheduling meetings, managing calendars, and arranging travel if necessary. * Assist in budget tracking and expense management for projects. * Support the coordination of vendor contracts and agreements, as needed. Qualifications & Requirements: * Education and Experience: * Bachelor's degree in a relevant scientific or healthcare discipline is preferred * 2+ years of experience in a project coordination or administrative support role, preferably in the biopharmaceutical or clinical research industry * Skills and Attributes: * Demonstrated ability to coordinate and support multiple projects concurrently * Exceptional organizational skills with a keen eye for detail and accuracy * Strong written and verbal communication abilities to facilitate effective collaboration * Proactive and self-motivated approach to work, demonstrating initiative and problem-solving skills * Ability to work well under pressure and meet tight deadlines * Collaborative mindset with a focus on teamwork and building positive relationships * Proficient in Microsoft Office Suite, project management software (e.g., Smartsheets) and reference software (e.g., Zotero) * Ability to adapt quickly to changing priorities and requirements * Strong ethics and integrity, ensuring compliance with regulatory guidelines and company policies Physical Requirements: * Ability to work on-site in Seattle, WA * Ability to sit for extended periods of time (2 or more hours) Benefits at Lumen Bioscience: * Stock bonus * Health, Dental, and Vision premiums fully covered by Lumen * 401k match up to 4% * Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure * Monthly wellness program to support your health and well-being * Free onsite parking or public transportation subsidies * Comprehensive parental leave policies * Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range $33.75 - $38.50 USD Create a Job Alert Interested in building your career at Lumen Bioscience? Get future opportunities sent straight to your email. Create alert

Join Lumen Bioscience as a Security Engineer & Analyst to be the guardian of our hybrid cloud infrastructure and endpoint ecosystem. In this role, you'll own security architecture, monitoring, and incident response across Microsoft 365/Entra ID, Azure, AWS, and a diverse endpoint fleet (Windows 11/mac OS). This position requires balancing stringent biotech regulatory and compliance requirements with practical, scalable security solutions that enable scientific innovation. If you enjoy building secure-by-design environments, leading incident response, and partnering with cross-functional teams to protect sensitive data and systems, we encourage you to apply. Duties & Responsibilities: Cloud & Identity Security (~40%) Architect and maintain security posture across Azure, AWS, and Microsoft 365/Entra ID environments. Design and implement Zero/Low Implicit Trust architecture with Conditional Access policies, MFA enforcement, and Privileged Identity Management (PIM). Configure and maintain Azure Security Center, AWS Security Hub, and native cloud security controls. Implement secure baselines for cloud workloads, storage, and networking components. Manage identity lifecycle, RBAC, and least-privilege access models across cloud and SaaS platforms. Endpoint Security & Management (~30%) Administer endpoint protection platforms (EDR/XDR) across Windows 11 and mac OS devices. Deploy and maintain Intune policies for Windows endpoints including BitLocker encryption, Windows Defender, and compliance baselines. Implement mac OS security controls using MDM solutions (Jamf/Kandji or Intune for Mac). Secure shared laboratory and manufacturing endpoints using kiosk modes and restricted profiles. Orchestrate patch management, software deployment, and configuration drift monitoring for endpoints. Security Operations & Incident Response (~20%) Design and tune SIEM alerting rules (e.g., Azure Sentinel, Splunk, or similar) to minimize false positives while detecting critical events. Lead incident response activities including communication with MDR vendor, triage, forensics, containment, eradication, and recovery. Conduct threat hunting exercises and security investigations based on logs, alerts, and intelligence. Maintain incident response runbooks and coordinate tabletop exercises. Generate security metrics, KPIs, and executive-level reporting. Governance, Risk & Compliance (~10%) Support FDA, SOC 2, CMMC, and GxP audit activities through evidence collection, documentation, and remediation tracking. Perform vulnerability assessments and coordinate remediation efforts with relevant teams. Conduct vendor security assessments and manage third-party risk. Develop and maintain security policies, standards, and procedures. Partner with QA/Compliance teams on 21 CFR Part 11 and data integrity requirements. Required Qualifications: Technical Skills: Endpoint Management: Strong Intune experience for Windows; familiarity with mac OS MDM solutions (e.g. Intune, Jamf, or similar). Security Tools: Hands-on experience with EDR/XDR platforms such as Huntress, CrowdStrike, Defender for Endpoint, or SentinelOne. SIEM/Monitoring: Experience with Azure Sentinel, Splunk, or similar platforms, including log analysis and correlation. Scripting: Proficiency in PowerShell and Python for security automation and orchestration. Networking: Understanding of network segmentation, firewalls, VPNs, and zero-trust principles. Professional Skills: Clear technical writing skills for documentation, procedures, and audit artifacts. Ability to translate security risks into business impact for non-technical stakeholders. Strong problem-solving skills with high attention to detail. Self-motivated with the ability to work independently in a hybrid environment. Desirable Qualifications: Industry & Compliance Experience: Preferred 2+ years in biotech, pharma, medical device, or healthcare IT environments AZ-500, SC-200, SC-300, AWS Security Specialty, CISSP, CCSP, or comparable security certifications Advanced Skills: Experience with Infrastructure as Code (e.g., Terraform, ARM templates) Container security experience (e.g., Docker, EC2-based workloads) DevSecOps practices and CI/CD pipeline security Experience with Data Loss Prevention (DLP) and Cloud Access Security Broker (CASB) solutions Physical Requirements: Ability to work on-site in Seattle, WA Ability to sit for extended periods of time (2 or more hours) Occasionally lift or carry items up to 50 lb/23 kg Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$115,000-$130,000 USD

Join Lumen Bioscience as a Clinical Operations Manager to play a vital role in overseeing and coordinating the clinical operations activities within our growing biopharmaceutical company. In this role, you'll collaborate with cross-functional teams, and manage CROs and clinical research sites, while ensuring the successful execution of clinical trials, adherence to regulatory guidelines, and the timely delivery of high-quality clinical data. This position combines hands-on leadership of clinical operations activities with clinical trial oversight, relationship management, clinical sample management, clinical trial supply management, documentation and data management, and process improvement. You'll oversee the planning, implementation, and execution of clinical trials in collaboration with cross-functional teams, collaborate with CROs and clinical trial sites, and oversee and supervise clinical trial sample management life cycle to maintain chain-of custody in a GxP compliant setting. You'll assist with forecasting and managing inventory of investigational product, manage relationships with third-party vendors, oversee investigational product shipments domestically and internationally, and oversee the collection, processing, and archival of clinical trial data and documents while identifying opportunities to streamline clinical operations processes, enhance efficiency, and optimize resource allocation. If you have strong leadership skills, in-depth knowledge of clinical research processes, and thrive in a fast-paced environment, we encourage you to apply. Duties & Responsibilities: Clinical Trial Oversight: Oversee the planning, implementation, and execution of clinical trials in collaboration with cross-functional teams, including regulatory affairs, medical writing, production and development, and data management. Ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and relevant regulatory requirements. Monitor clinical trial progress, identify potential issues, and proactively develop and implement corrective actions. Relationship Management: Collaborate with Contract Research Organizations (CROs) and clinical trial sites to ensure efficient study start-up, enrollment, and conduct. Facilitate effective communication and build strong relationships with external partners, including investigators, site personnel, and vendors. Serve as the main point of contact for clinical trial-related inquiries and issue resolution. Clinical Sample Management: Oversee and supervise clinical trial sample management life cycle to maintain chain-of custody in a GxP compliant setting Work closely with CRO, external lab vendors and internal teams to plan and execute sample processing, tracking and shipment of clinical samples Oversee sample receiving procedures and sample testing timelines Clinical Trial Supply Management: Assist with forecasting and managing inventory of investigational product needed for upcoming and ongoing clinical trials Establish packaging, labeling and distribution timelines Manage relationships with third-party vendors, e.g., shipping companies and IRT providers. Oversee investigational product shipments domestically and internationally, including coordination of import/export documentation, permits and licenses to ensure timely and compliant delivery of investigational product to drug depots and clinical research sites. Documentation and Data Management: Oversee the collection, processing, and archival of clinical trial data and documents, ensuring accuracy, completeness, and traceability. Collaborate with the data management team to implement efficient data capture and reporting processes. Ensure compliance with data protection regulations and maintain data confidentiality. Process Improvement: Identify opportunities to streamline clinical operations processes, enhance efficiency, and optimize resource allocation. Contribute to the development and implementation of standardized operating procedures (SOPs) and best practices. Stay up to date with industry trends and regulatory changes to ensure the adoption of current best practices. Qualifications & Requirements: Education and Experience: Bachelor's degree in life sciences or a related field (advanced degree preferred). Minimum of 8 years of experience in clinical operations, with a demonstrated track record of managing clinical trials. Strong knowledge of GCP guidelines, FDA regulations, and other relevant regulatory frameworks. Proven experience in leading and managing teams, with excellent organizational and interpersonal skills. Skills and Attributes: Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and other relevant software applications. Excellent written and verbal communication skills, with the ability to effectively communicate complex information to diverse stakeholders. Detail-oriented, with strong problem-solving and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment and manage multiple priorities simultaneously. Demonstrated ability to adapt to changing circumstances and proactively drive process improvements. Physical Requirements: Ability to work on-site in Seattle, WA Ability to sit for extended periods of time (2 or more hours) Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$80,000-$120,000 USD

Wellspring Nurse Source is seeking a travel MRI Technologist for a travel job in Olympia, Washington. Job Description & Requirements Specialty: MRI Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Wellspring Nurse Source Job ID #35423909. Pay package is based on 10 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Allied MRI Technologist About Wellspring Nurse Source Wellspring is nurse owned and operated which means that we get you, we stand behind you, and we advocate for you. We are 100% committed to helping you find your best job at the best rate. We are unwavering in our commitment to supporting our clinicians on every step of their travel adventure, assisting with everything from onboarding and payroll to on-the-job clinical support with a dedicated Clinician Success Team. You're not just a number at Wellspring, you're a valued member of our family. Join us and experience the Wellspring difference.

Join Lumen Bioscience as a Service Desk Manager to transform our IT support function into a world-class service organization. In this role, you'll lead a small, high-performing team while designing and implementing scalable processes that support a rapidly growing environment. This position combines hands-on technical leadership with strategic service management. You'll architect processes aligned to business goals (e.g., Incident, Problem, Change, Knowledge Management) while also rolling up your sleeves to troubleshoot complex technical issues across Microsoft 365, endpoint management, and identity platforms. If you thrive as a “player-coach” in a fast-paced setting and enjoy improving both systems and people, we encourage you to apply. Duties & Responsibilities: Service Delivery Leadership (~35%) Lead and mentor a team of 2-3 Service Desk analysts (with plans to grow the team over time). Establish and maintain SLAs/OLAs with clear performance metrics (e.g., MTTR, FCR, CSAT). Implement and maintain compliance-aware Incident, Problem, Change, and Knowledge Management processes. Drive continuous improvement using data-driven insights and root cause analysis. Build and maintain a service catalog and self-service portal to reduce ticket volume and improve user experience. Create and maintain a comprehensive knowledge base and troubleshooting guides to support first-contact resolution. Technical Operations (~30%) Oversee endpoint lifecycle management for 150+ devices (Windows 11 via Intune; mac OS via MDM), including provisioning, configuration, patching, and decommissioning. Manage Microsoft 365 tenant administration, including Exchange Online, SharePoint, Teams, and OneDrive. Coordinate Entra ID (Azure AD) identity management, including user provisioning, group policies, SSO, MFA, and periodic access reviews. Implement automation using PowerShell and Microsoft Graph API (and similar tools) to streamline repetitive tasks, reporting, and service workflows. Optimize and improve ticketing system workflows, queues, and reporting. Team Development (~20%) Recruit, onboard, and develop Service Desk talent, including creating training plans and mentoring team members. Create career development paths and skills matrices for Service Desk staff. Foster a partnership-centric culture that emphasizes empathy, customer focus, and first-contact resolution. Coordinate cross-training to ensure coverage, knowledge redundancy, and continuity of service. Lead by example with hands-on support during peak periods or critical incidents. Strategic Initiatives (~15%) Partner with the Security team on endpoint compliance, incident response, and security-related policies. Collaborate with the Infrastructure team on monitoring, proactive maintenance, and reliability initiatives. Support the CSV Engineer with validated system requirements and change control processes. Drive process initiatives aimed at improving the overall employee experience with IT. Manage vendor relationships and optimize software licensing usage and costs. Required Qualifications: Leadership Experience: 3+ years managing IT Service Desk or technical support teams. Proven track record of improving service metrics (e.g., MTTR, first-contact resolution, CSAT). Experience building teams and processes in growing organizations. Strong project management skills with the ability to juggle multiple initiatives and priorities. Technical Skills: Microsoft 365: Advanced administration of Exchange Online, SharePoint, Teams, and OneDrive. Endpoint Management: Hands-on Intune experience for Windows; familiarity with mac OS MDM solutions. Identity Management: Entra ID/Azure AD administration, including SSO and MFA. Ticketing Systems: Experience improving and optimizing service desk/ticketing platforms. Scripting: Proficiency with PowerShell (and shell or Python) for automation and reporting. Professional Skills: Exceptional communication skills (written, verbal, and presentation) with the ability to communicate clearly at all levels. Strong analytical and problem-solving abilities. Customer service mindset with high emotional intelligence and empathy for end users. Ability to translate complex technical concepts into language understandable to non-technical stakeholders. Desirable Qualifications: Industry & Compliance Experience: Background in biotech, pharma, or healthcare IT environments Understanding of GxP, 21 CFR Part 11, CMMC, and/or SOC 2 requirements Advanced Skills: Experience with IT asset management systems Knowledge of network fundamentals and IoT systems Familiarity with laboratory and scientific computing environments Experience with business analysis and process improvement methodologies Physical Requirements: Ability to sit for extended periods of time (2 or more hours) Occasionally lift or carry items up to 50 lb/23 kg Benefits at Lumen Bioscience: Stock bonus Health, Dental, and Vision premiums fully covered by Lumen 401k match up to 4% Industry-leading PTO policy, paid refresh days, and paid year-end holiday office closure Monthly wellness program to support your health and well-being Free onsite parking or public transportation subsidies Comprehensive parental leave policies Life insurance, short & long-term disability, and access to employee assistance programs At Lumen Bioscience, we foster a workplace built on collaboration, innovation, and professional growth. This role offers a significant opportunity to contribute directly to cutting-edge biotechnology and the advancement of global health solutions. Join us to shape innovative solutions and drive operational excellence. Compensation Range$110,000-$125,000 USD