3BMedical Inc. d/b/a React HealthSenior Regulatory Affairs Specialist 3BMedical Inc. d/b/a React HealthSenior Regulatory Affairs SpecialistBothell, WA$133,707.08–$133,707.08 / yearFull timeRecall administration; - Participate in/lead internal audits; - Stay current on international regulatory requirements and lead appropriately regulatory approvals; Lead CE mark requirement definition/implementation; - Support maintaining a c GMP compliant Quality Management System to ensure the Quality System is established and maintained in accordance with FDA 21 CFR 820, c GMP, (MDD 93/42/EEC, MDR 2017 /745,) and ISO 13485 regulatory requirements; - Develop relevant regulatory procedures and work instructions as necessary; - Lead audit readiness initiative. Investigate and document issues relating to the product, process, or Quality System relevant to the regulatory compliance; - Attends and participates in departmental meetings; - Attends seminars and training sessions necessary to maintain appropriate level of professional competence; - Ensures all department compliance guidelines are met; - Attends all meetings, in-services training, or continuing education as delegated by the supervisor; - Provides customer focused interactions; - Performs all duties necessary for the department as per department policies and procedures; - Performs other duties and responsibilities as delegated by the supervisor within the scope of practice and the responsibilities in the department.
Carl Zeiss Meditec, IncSenior Advisor, Regulatory and Clinical Affairs Carl Zeiss Meditec, IncSenior Advisor, Regulatory and Clinical AffairsSeattle, WA$183,000–$228,800 / yearFull timeThe individualis responsible forregulatory strategy andsupportofa variety of FDA submissionsincluding pre-submissions (Q-subs), pre-market notifications(510(k)s), pre-market approvalapplications (PMAs)andinvestigational device exemptions (IDEs). This roleacts as an advisorand subject matter expertfor US regulatoryand clinicalquestions, specifically interpreting US FDA's perspective,at all levels, from senior management to single contributors;for all functions (e.g.
DLA Piper LLP (US)Pursuits & Directories Manager - Regulatory & Government Affairs DLA Piper LLP (US)Pursuits & Directories Manager - Regulatory & Government AffairsSeattle, WAFull timeActs as project manager throughout the pitch and proposal response lifecycle including, but not limited to: conducting opportunity assessments; tracking opportunities; developing project plans; organizing and conducting kick-off calls with lawyers and colleagues; gathering and drafting relevant content; coordinating with client pricing, BD and other business professional colleagues; incorporating competitive intelligence to tailor responses; and ensuring high quality/error free proposals are submitted. This position can sit in our Washington DC, Atlanta, Austin, Baltimore, Boston, Chicago, Dallas, Houston, Los Angeles, Miami, Minneapolis, New York, Northern Virginia, Philadelphia, Phoenix, Raleigh, San Diego, Seattle, Short Hills, or Wilmington office and offers a hybrid work schedule.
JouléAdministration Coordinator JouléAdministration CoordinatorRedmond, WA$22–$24 / hourServe as a member of the divisional PFA team to establish, implement, and maintain global regulatory and quality processes and documents supporting the Global QMS. High school diploma or equivalent required; additional education or certifications in regulatory affairs or related fields are a plus.
Fresenius Kabi USA, LLCDirector, Medical Affairs (Nutrition) Fresenius Kabi USA, LLCDirector, Medical Affairs (Nutrition)Seattle, WA$185,000–$220,000 / yearFull timeThe Director, Medical Affairs will lead the field clinical education team and ensure that the respective territory engagement plans are effectively executed per defined targets, following Fresenius Kabi compliance rules and code of conduct and that relevant medical and scientific insight is routinely shared to optimize the Medical Affairs strategy for the nutrition portfolio. 3+ years of hands-on experience in patient care and in hospital and/or clinic and/or home infusion settings is required, with demonstrated expertise in clinical nutrition including experience in managing formula selection for oral nutritional supplement use and tube feeding regimens.
Fred Hutchinson Cancer CenterRegulatory Affairs Associate/Senior Regulatory Affairs Associate Fred Hutchinson Cancer CenterRegulatory Affairs Associate/Senior Regulatory Affairs AssociateSeattle, Washington$80,172–$114,940 / yearThe RAA oversees communications with industry sponsors and the Fred Hutch IRB, prepares regulatory documentation, coordinates regulatory submissions and monitoring, maintains regulatory files, and facilitates regulatory oversight for all related studies. The Regulatory Affairs Associate (RAA)/Regulatory Affairs Associate Sr. is responsible for supporting investigators and staff within the Infectious Disease Sciences (IDS) Program in the Vaccine and Infectious Disease Division on regulatory issues and requirements through the full cycle of clinical trials and human subjects research.
Columbia DistributingDirector of External Affairs - Kent, WA Columbia DistributingDirector of External Affairs - Kent, WAWoodmont Beach, WA$115,000–$135,000 / yearFull timeThe Director of External Affairs will serve as a strategic partner to the Vice President of External Affairs & Communications, helping to shape and support Columbia Distributing's engagement and communications strategy. The Director will serve as an important bridge between the company and key stakeholders, including teammates, media, community organizations, suppliers, retail partners, industry associations, and policymakers.
Systimmune IncAssociate Director / Director, Regulatory Affairs - IHC Companion Diagnostics (CDx) Systimmune IncAssociate Director / Director, Regulatory Affairs - IHC Companion Diagnostics (CDx)Redmond, WA$150,000–$230,000 / yearBachelor's degree or higher in Life Sciences, Pathology, Molecular Biology, or related field • 8+ years (Associate Director) or 10+ years (Director) of regulatory affairs experience in IVD/CDx • Demonstrated experience leading FDA CDRH interactions for Companion Diagnostics • Strong background in IHC-based CDx development, including understanding of scoring systems and clinical cutoffs • Proven ability to lead cross-functional teams and influence without authority • Prior experience managing or building regulatory teams • Oncology CDx experience supporting patient selection strategies • Experience working with automated IHC platforms and external diagnostic partners • Familiarity with global CDx regulations (EU IVDR, China NMPA). The successful candidate will set regulatory direction, guide cross-functional teams, and ensure high-quality IDE and PMA submissions, while remaining sufficiently hands-on to provide technical oversight and mentorship when needed.
SystimmuneAssociate Director / Director, Regulatory Affairs – IHC Companion Diagnostics (CDx) SystimmuneAssociate Director / Director, Regulatory Affairs – IHC Companion Diagnostics (CDx)Redmond, WAFull timeThe successful candidate will set regulatory direction, guide cross-functional teams, and ensure high-quality IDE and PMA submissions, while remaining sufficiently hands-on to provide technical oversight and mentorship when needed. We are seeking a Regulatory Affairs leader at the Associate Director or Director level to lead IHC-based Companion Diagnostics (CDx) regulatory strategy and execution in support of our oncology ADC pipeline.
BIO RAD LABORATORIES - 390Clinical Affairs Manager BIO RAD LABORATORIES - 390Clinical Affairs ManagerSeattle, WA$116,100–$159,600 / yearFull timeThis role represents Clinical Affairs collaborates cross-functionally with Regulatory Affairs, R&D, Quality, Marketing, and external partners to deliver high-quality clinical data and evidence supporting product registration and commercialization of Bio-Rad diagnostic products. Work Experience: 5 years' (3 years' with advanced degree) experience in clinical research with at least 3 years of clinical trials execution role, preferably in an IVD company; and 1 year of people management experience.
Company ConfidentialCompliance & Legal Affairs Manager Company ConfidentialCompliance & Legal Affairs ManagerRENTON, WA$75,000–$95,000 / yearFull timeWe are seeking a Compliance & Legal Affairs Manager to oversee regulatory compliance, contract review, and risk management across all areas of our operations. Identify legal and business risks; propose practical mitigation strategies.
Bausch + LombDirector, Regulatory Affairs Bausch + LombDirector, Regulatory AffairsRedmond, WA$165,000–$220,000 / yearQualifications: + Bachelors degree required; advanced degree (Masters, PhD, PharmD) preferred + 10-15+ years in Regulatory Affairs or relevant experience in a regulated environment + Global portfolio management and strategy experience and strong familiarity with registration requirements in exU.S. The Director partners crossfunctionally with Clinical, Nonclinical, CMC, Quality, Safety, and Regulatory Operations to develop global regulatory strategies, lead health authority interactions, ensure highquality submissions, and manage regulatory risk across the product lifecycle.
Umoja BiopharmaSenior Director, Clinical Regulatory Affairs Umoja BiopharmaSenior Director, Clinical Regulatory AffairsSeattle, WA$253,000–$312,500 / yearWe are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. This role will develop and implement regulatory strategies leading to successful registration and life-cycle management of unique and technologically complex products serving patients with cancer and other unmet medical needs.
PhilipsSenior Regulatory Affairs Specialist PhilipsSenior Regulatory Affairs SpecialistBothell, WA$99,000–$157,000 / yearThe actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity. + Lead global regulatory intelligence initiatives, contribute to regulatory and product registration strategies, and help implement global regulatory roadmaps based on the competitive landscape and marketing objectives.
Seattle Children'sRegulatory Affairs Specialist II Seattle Children'sRegulatory Affairs Specialist IISeattle, WA$80,715–$121,073 / yearTogether, we deliver superior patient care, advance new discoveries and treatments through pediatric research, and serve as the pediatric and adolescent, academic medical center for Washington, Alaska, Montana and Idaho - the largest region of any children's hospital in the country. Guides and supports all clinical research team members in adhering to applicable federal regulations, state codes, institutional policies, and Institutional Review Board (IRB) oversight and review requirements when conducting research with human participants.
AmazonWHS Regulatory Response Case Manager, Governance and External Affairs AmazonWHS Regulatory Response Case Manager, Governance and External AffairsBellevue, WAKey job responsibilities - Develop and maintain WHS governance frameworks, policies, and procedures aligned with current legislation and industry's best practices - Lead case assessment processes and implement control measures across various operational areas - Manage complex WHS regulatory cases, including external agency investigations, associate claims and complaints, and execution of programs and procedures. USA, TN, Nashville - 66,800.00 - 116,800.00 USD annually USA, VA, Arlington - 74,200.00 - 129,800.00 USD annually USA, WA, Bellevue - 82,700.00 - 129,800.00 USD annually
AmazonRegulatory Response Case Manager, Governance and External Affairs AmazonRegulatory Response Case Manager, Governance and External AffairsBellevue, WAExperience in governance, legal compliance, paralegal experience, and operational execution is a plus Key job responsibilities - Drafting and refining regulatory response letters - working with sites to compose accurate, legally compliant responses to government agencies (particularly OSHA Complaint Response Letters and similar regulatory inquiries) - Ensuring legal accuracy and compliance - coordinating with your legal team to verify that responses meet specific regulatory requirements - Quality control and documentation - reviewing response letters for spelling, grammar, tone, and clarity before submission; - Managing regulatory documentation - handling attachments and ensuring sensitive information is properly redacted - Site liaison - working collaboratively with site teams to gather required information and ensure their responses are complete and compliant A day in the life You manage regulatory requests from intake through agency submission. USA, TN, Nashville - 109,000.00 - 155,400.00 USD annually USA, VA, Arlington - 121,200.00 - 163,900.00 USD annually USA, WA, Bellevue - 121,200.00 - 163,900.00 USD annually
Danaher CorporationManager, Clinical Science, Medical Affairs Danaher CorporationManager, Clinical Science, Medical AffairsSeattle, WARemote$150,000–$170,000 / yearThe essential requirements of the job include: + Bachelor's degree in Biostatistics, Life Science, Chemistry, Biochemistry or equivalent; MD or PhD preferred + 5-10 years experience in Medical Device/Pharma/IVD companies + Experience in next generation sequencing with proficient knowledge of medical terminology + With minimal supervision, demonstrate a high level of customer service skills, approachability, and sense of urgency with strong collaboration skills (communication, tone, messaging, execution, planning, ownership). Travel, Motor Vehicle Record & Physical/Environment Requirements: + Ability to travel 10% domestically, and internationally It would be a plus if you also possess previous experience in: + a Medical Affairs role, such as a Medical Science Liaison (MSL) + Novel Biomarker Assay Development IDT, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives.
Ste Michelle Wine EstatesRegulatory Compliance Administrator Ste Michelle Wine EstatesRegulatory Compliance AdministratorWoodinville, WAPart timeManages and tracks product label submittals in ~30 state to ensure timely action, monitors current registrations with respect to renewal deadlines, and carefully tracks all information on detailed spreadsheets and within online tracking systems. Provides excellent customer service to internal clients and supports the department with projects and additional duties as assigned, including but not limited to licensing application submissions/renewals, surety bond submissions/renewals, etc.
Verathon, Inc.Manager, Regulatory Compliance Verathon, Inc.Manager, Regulatory ComplianceBothell, WAFull timeThe Manager, Regulatory Compliance will lead Verathon's compliance team with focus on internal/external audits, European compliance, distributor and service partner compliance, sterilization oversight, management reviews, and QMS updates. Lead and coordinate external inspections and audits by regulators, Notified Bodies, and MDSAP Auditing Organizations, including front-room/back-room operations and rapid response management.
Puget Sound Energy, IncTemporary Regulatory Compliance Analyst Puget Sound Energy, IncTemporary Regulatory Compliance AnalystSnoqualmie, WATemporaryContractorFull timeDemonstrated ability to learn and apply new and upgraded computerized systems to job responsibilities, including use of software tracking mechanism for compliance issues, word-processing, spreadsheets and presentation programs. Works cooperatively with staff from other departments to communicate pending or upcoming regulatory proposals and obtains input from others in aligning regulatory proposals with company objectives.
Puget Sound Energy, IncSenior Energy Originator Puget Sound Energy, IncSenior Energy OriginatorClyde Hill, WAFull timeOversee and lead negotiations of commercial deals and agreements critical to PSE's corporate growth strategy, such as ownership and development projects, purchase and sales agreements (PPAs, tolling agreements), O&M agreements, real estate agreements, interconnection agreements, and service agreements. In order to support this effort, PSE is seeking an experienced Senior Energy Originator to join our team to lead the origination and commercial negotiations for energy supply agreements for new renewable energy resources.
AmazonNewWHS Compliance Assurance Risk Manager, Governance, Compliance & External Affairs AmazonWHS Compliance Assurance Risk Manager, Governance, Compliance & External AffairsBellevue, WAThe role will engage, collaborate, and partner with Amazon businesses, geographical units, and technical subject matter experts (SMEs) in Workplace Health and Safety (WHS) and other functions (i.e., field operations, governmental affairs, legal, engineering, data scientists and tech teams (AFT), business intelligence engineers, purchasing) to continually improve compliance. Description The Workplace Health & Safety (WHS) Compliance Assurance Risk Manager will be responsible for managing programs and processes that maintain legal compliance and conformance to internal WHS procedures, including assurance processes design, development, testing, implementation, verification, and continual improvement.
Veterans Affairs, Veterans Health AdministrationPublic Affairs Specialist Veterans Affairs, Veterans Health AdministrationPublic Affairs SpecialistSeattle, WAExamples of specialized experience would typically include, but are not limited to: Skill in writing a variety of communication products (articles, news releases, scripts and speeches); knowledge and skill in digital media production, photography, videography and the equipment to support it; ability to develop marketing and communication strategies, create effective messaging and determine the best method for enhancing understanding; ability to manage briefings and town halls. Position Description/PD#: Public Affairs Specialist/PD415510 and PD415500 Relocation/Recruitment Incentives: Not Authorized Critical Skills Incentive (CSI): Not Approved Permanent Change of Station (PCS): Not Authorized PCS Appraised Value Offer (AVO): Not Authorized Requirements Conditions of Employment You must be a U.S. Citizen to apply for this job To be considered for this position, you must complete all required steps in the process.
OpenAI Inc.Manager, AI Deployment Engineering - Health & Life Sciences OpenAI Inc.Manager, AI Deployment Engineering - Health & Life SciencesSeattle, WA$251,000–$335,000 / yearFull timeFor unincorporated Los Angeles County workers: we reasonably believe that criminal history may have a direct, adverse and negative relationship with the following job duties, potentially resulting in the withdrawal of a conditional offer of employment: protect computer hardware entrusted to you from theft, loss or damage; return all computer hardware in your possession (including the data contained therein) upon termination of employment or end of assignment; and maintain the confidentiality of proprietary, confidential, and non-public information. You will operate at both strategic and technical levels - partnering with executive stakeholders, technical leaders, and cross-functional internal teams to deliver secure, compliant, and high-impact AI deployments.
Trident Seafoods CorporationFSQA TECHNICAL MANAGER SUPPORT CENTER Trident Seafoods CorporationFSQA TECHNICAL MANAGER SUPPORT CENTERSeattle, WA$110,000–$165,000 / yearFull timeServe as a primary technical resource for cross-functional teams, including R&D, Procurement, Sales, and Marketing, to ensure regulatory alignment and support product development and market readiness. For full-time employees, the initial PTO benefit starts at 20 days per year, adjusted commensurate with relevant experience, front loaded on the first of the year, initially prorated quarterly based on hire date.
Puget Sound Energy, IncFinance Business Manager Puget Sound Energy, IncFinance Business ManagerClyde Hill, WAFull timeThe ideal candidate must demonstrate the ability to seamlessly transition between deep analytical work and high-level strategic communication, translating intricate technical details and data patterns into compelling executive summaries that drive informed decision-making. As the region's largest utility serving over 1.2 million customers, we're not just managing budgets-we're strategically investing in the infrastructure, renewable energy projects, and innovative technologies that will define the Pacific Northwest's sustainable future.
Puget Sound Energy, IncDevelopment Manager Puget Sound Energy, IncDevelopment ManagerBellevue, WAFull timeOversees and leads negotiations of business deals critical to PSE's corporate growth strategy, including acquisitions and development projects, purchase and sales agreements, O&M agreements, real estate agreements, interconnection agreements, and service agreements. Leads and coordinates all commercial functions, including negotiations, project oversight, cross functional team management, and management approval in the acquisition, joint development, or self-build development of energy resources, real estate, distribution assets, and transmission assets.
Puget Sound Energy, IncSenior Municipal Land Planner Puget Sound Energy, IncSenior Municipal Land PlannerBothell, WAFull timeWorks in close coordination with other PSE disciplines that support utility siting and construction projects, including Municipal Liaison Managers, Government Relations, Real Estate, Communications, Project Management, Vegetation Management and Legal. Responsible for acquiring necessary permits from various local, state and federal agencies to construct high profile and complex utility infrastructure projects in support of PSE's capital project plan and utility system improvements.
Verathon, Inc.Marketing Coordinator I Verathon, Inc.Marketing Coordinator IBothell, WAFull timeThis work helps enable integrated marketing campaigns, supports customer-facing experiences, and ensures content reaches the right audience without delays or compliance risk. Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility.
Puget Sound Energy, IncManager Resource Planning & Analysis Puget Sound Energy, IncManager Resource Planning & AnalysisClyde Hill, WAFull timeProvides oversight and hands-on support for the development of ISP deliverables, including writing, editing, and reviewing the final ISP document to ensure technical accuracy, regulatory compliance, clarity, and consistency across chapters and analyses. Leads a team of highly qualified analysts and project managers to identify, analyze, and communicate policy, regulatory, and market uncertainties that may affect the Company's long-term resource portfolio strategy.
Comagine HealthClinical Reviewer DC Comagine HealthClinical Reviewer DCSeattle, WA$93,000–$104,000 / yearFull timeProvide daily oversight and monitoring of non-clinical staff during their performance of non-clinical support activities, as appropriate; also provide the supervisor with input regarding employees’ performance of these activities. The Clinical Reviewer position supports utilization management activities by assessing the medical necessity and quality of healthcare services through prospective, concurrent, and retrospective reviews.
Verathon, Inc.Quality Program Manager III Verathon, Inc.Quality Program Manager IIIBothell, WAFull timeThe Quality Program Manager III is responsible for defining, structuring, and leading cross functional projects and programs with a focus on product quality, compliance, and continuous improvement of the Quality Management System (QMS). Verathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility.
Qualis HealthClinical Reviewer DC Qualis HealthClinical Reviewer DCSeattle, WA$93,000–$104,000 / yearFull timeProvide daily oversight and monitoring of non-clinical staff during their performance of non-clinical support activities, as appropriate; also provide the supervisor with input regarding employees' performance of these activities. The Clinical Reviewer position supports utilization management activities by assessing the medical necessity and quality of healthcare services through prospective, concurrent, and retrospective reviews.
Puget Sound Energy, IncSupervisor Merchant Transmission Puget Sound Energy, IncSupervisor Merchant TransmissionClyde Hill, WAFull timeCross-Organizational Coordination in Resource Planning, Self-Build Project Development, and Resource Acquisition: Works collaboratively with Electric Resource Planning, Resource Acquisition, Energy Resource Development, Major Projects, PSE Transmission, Accounting, Risk Control and Regulatory Affairs. Provides merchant transmission and generator interconnection expertise and guidance to support organizational objectives including self-development of new generating resources and assessment of project proposals for All Source RFPs.
Providence St. Joseph HealthCorporate Counsel, Contracting and Transactions - Renton, WA, Irvine, CA or Port Providence St. Joseph HealthCorporate Counsel, Contracting and Transactions - Renton, WA, Irvine, CA or PortSeattle, WAFull timeThe Corporate Counsel position is responsible, under the guidance of Department of Legal Affairs (DLA) Leadership, for providing valued, strategic, and practical legal advice and support for Providence St. Joseph Health ("Providence") with a primary focus on system-wide contracting initiatives and enterprise commercial agreements, including development of contracting strategies, templates, playbooks, and processes that enable consistent and scalable contracting across the organization. Support lead transactional attorneys and internal business teams on a defined set of healthcare transactions (e.g., joint ventures, affiliations, partnerships, divestitures, and select M&A), including drafting, negotiation, and project support.
Jazz PharmaceuticalsMedical Science Liaison Jazz PharmaceuticalsMedical Science LiaisonSeattle, WARemote$160,000–$240,000 / yearFull timeConsistently actstoenhanceJazzPharmaceuticals' image as an advocate of medical advancement by using knowledge of product, disease state and pipeline products to engage healthcare providers in meaningful scientific exchange of information. This is afield-based position coveringNorthern California, Washington, Oregon, Alaska, Idaho, & Montana, and requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence.
Providence St. Joseph HealthSenior Clinical Research Analyst - Tumor Institute Providence St. Joseph HealthSenior Clinical Research Analyst - Tumor InstituteSeattle, WAFull timeIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution.
Verathon, Inc.Quality Inspector III Verathon, Inc.Quality Inspector IIIBothell, WAFull timeVerathon is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality products that endure over time and ensure clinical and economic utility. The Quality Inspector is responsible for supporting the Quality and Operations teams by performing receiving inspection and final release of finished products.
Providence St. Joseph HealthParalegal - Hybrid Providence St. Joseph HealthParalegal - HybridRenton, WAFull timeAssist with drafting and reviewing of wide variety of legal documents and agreements, including, but not limited to settlement agreements, physician/provider agreements, clinical education/affiliation agreements; Non-Disclosure Agreements; letters of intent; Business Associate Agreements; presentations; memos; correspondence; and other documents. Assist with a variety of matters to include but not be limited to, intellectual property matters including copyright, trademark, and patent filings; internal advice matters on a wide variety of subjects; regulatory matters, a wide variety of contracting matters, medical staff matters, and pre litigation disputes.
GlaxoSmithKlineViiV Medical Science Liaison, Pacific Northwest (OR/WA/ID/AK) GlaxoSmithKlineViiV Medical Science Liaison, Pacific Northwest (OR/WA/ID/AK)Seattle, WARemoteFull timeEngagements may include but not limited to emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle. The MSL serves as a scientific expert in HIV treatment and prevention, understands territory and market influences, engages scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic plan.
Providence St. Joseph HealthNewDirector Donor Engagement - Hybrid Providence St. Joseph HealthDirector Donor Engagement - HybridRenton, WAFull timeProvidence Shared Services is a service line within Providence that provides a variety of functional and system support services for our family of organizations across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. Responsible for planning, creating, implementing and promoting a culture of gratitude through a comprehensive, strategic donor relations program, including gift acknowledgment, gift stewardship, donor recognition and donor engagement to further Providence's fundraising goals in Southern California.
T-Mobile USA, IncCorporate Counsel - Investigations, Governance & Standards T-Mobile USA, IncCorporate Counsel - Investigations, Governance & StandardsBellevue, WAFull timeDo you want to work with top-notch legal and compliance partners to provide informed and complex legal advice to T-Mobile teams that investigate and remediate issues related to violations of the T-Mobile Code of Business Conduct, other internal corporate policies, or legal and regulatory requirements? Prior investigations experience, either directly supporting federal, state, or local law enforcement in criminal or complex civil matters or supporting large enterprises in connection with internal or government investigations.
EquinixSenior Manager, Clean Energy & Innovation EquinixSenior Manager, Clean Energy & InnovationSeattle, WAFull time
PhilipsDirector of Regulatory Compliance-Oral Healthcare PhilipsDirector of Regulatory Compliance-Oral HealthcareBothell, WA$172,200–$275,520 / yearYou have demonstrated Global Regulatory Domain knowledge/expertise in overseeing the preparation/submission of regulatory filings/documentation, global product registrations/approvals, and leading others in global regulatory matters of diverse product categories - Class I medical device, consumer goods, and cosmetics. Your Role: Develop global regulatory strategies by creating and implementing regulatory roadmaps aligned with market trends, legislation, product marketing objectives, and staying current on evolving regulations to advise senior leadership on strategic decisions.
WASHINGTON TRUST BANKWMAS Relationship Manager III/IV WASHINGTON TRUST BANKWMAS Relationship Manager III/IVSeattle, WAFull timeResponsible for understanding all banking and financial needs of relationship clients including all products and services offered by the Bank (Commercial, Investments, International Banking, Private Banking, Real Estate, Cash Management, etc). As a member of the Wealth Management and Advisory Services (WMAS) Division, serves as a proactive, client-focused trusted financial partner to clients through a seamless delivery of investment, trust, and fiduciary services.
Premera Blue CrossDirector, Regulatory Compliance Premera Blue CrossDirector, Regulatory ComplianceMountlake Terrace, WA$157,900–$315,900 / yearWhat you'll do:** **Set strategy and lead enterprise compliance** + Lead the design, development, and implementation of an enterprise-wide program to monitor compliance with applicable legal and regulatory requirements, including services delivered by third parties. **Promote a culture of integrity while keeping Premera compliant on the ever-changing regulatory and legal requirements** + Maintain deep knowledge of laws, regulations, enforcement priorities, and industry compliance risks relevant to Premera.
Umoja BiopharmaDirector, CMC Regulatory Umoja BiopharmaDirector, CMC RegulatorySeattle, WA$206,400–$254,900 / yearWe are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. Lead technical modules and sections of global regulatory filings (IND/CTA/BLA/MAA submissions), working with global regulatory lead to set strategy for submissions of product registration documents for health authorities worldwide.
GoogleAssociate Regulatory Counsel, Privacy GoogleAssociate Regulatory Counsel, PrivacySeattle, WAAssociate Regulatory Counsel, Privacy _corporate_fare_ Google _place_ San Francisco, CA, USA; Mountain View, CA, USA; +3 more; +2 more **Advanced** Experience owning outcomes and decision making, solving ambiguous problems and influencing stakeholders; deep expertise in domain. As an Associate Regulatory Counsel in Privacy, you will join a Global team that provides subject matter expertise and engages with regulators and others to consider the role of privacy law in the changing economy, development of new technology, and passage of new laws and regulations.
CoreTechsDairy Regulatory Compliance Specialist CoreTechsDairy Regulatory Compliance SpecialistBellevue, WA$16.26–$45 / hourDesign, develop, and deliver comprehensive training programs on dairy regulatory requirements tailored to various roles—production staff, lab technicians, supervisors, and plant managers. Partner with cross-functional teams (Quality, Production, Maintenance, and HR) to identify root causes of non-compliance and implement effective corrective and preventive actions.