NewTechnical Service Specialist- Controls Parkson Corp.Technical Service Specialist- ControlsDenver, CO$32–$39Full timeField Support: Liaise with customer to provide on-site technical support, site surveys, inspections, maintenance of our equipment for water/wastewater treatment facilities, and provide feedback to Business Units for continuous improvement. Equipment Installation & Maintenance: Install, commission, and maintain water/wastewater treatment systems, pumps, valves, PLCs, HMIs, Controls, and related components.
NewEHS CHILD CARE PARTNERSHIP SPECIALIST CIGEHS CHILD CARE PARTNERSHIP SPECIALISTEnglewood, CO$51,000–$53,000Full timep>Through an Early Head Start–Child Care Partnerships (EHS-CCP) grant, ELV and its collaborators deliver best-in-class, comprehensive early childhood services to eligible children across six Colorado counties — leveraging our model to stretch every resource in support of infant and toddler development. Working hands-on with two to four child care sites, you'll coach leaders, grow great teachers, engage families, and bring comprehensive Early Head Start services to infants and toddlers in high-need communities.
NewProperty Adjuster Specialist - Field CAT Team USAAProperty Adjuster Specialist - Field CAT TeamDenver, CORemote$78,560–$141,410 / yearProactively manages assigned claims caseload comprised of complex damages that require commensurate knowledge and understanding of claims coverage including potential legal liability. 2 years of relevant property claims adjusting experience of moderate complexity losses that includes writing estimates, involving dwelling and structural damages.
Regulatory Affairs Specialist I Highridge IncRegulatory Affairs Specialist IWestminster, COli>Ability to learn and stay abreast of regulations pertinent to medical devices, biologics, drugs and combination products as needed, based on functional area \. Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products.
Regulatory Affairs Specialist Highridge IncRegulatory Affairs SpecialistWestminster, COThis person will be joining a small, but mighty team and will have the opportunity to work on a variety of projects, focused on new product introduction, for the world's largest privately held spine company. Principal Duties and Responsibilities: Become a brand champion, owning regulatory activities for that brand, from new product introduction, to product changes and revisions, and international registration support.
Senior Regulatory Affairs Specialist Stryker CorpSenior Regulatory Affairs SpecialistGreenwood Village, COPreferred: • Bachelors degree in Regulatory Science, or technical discipline (Engineering or Life Sciences) • Experience engaging with regulatory authorities to support submissions, respond to inquiries, and facilitate successful interactions throughout the product lifecycle. In this role, you will develop and implement regulatory strategies, ensure compliance across the product lifecycle, manage regulatory submissions, advise stakeholders on regulatory requirements, and engage with regulatory authorities to resolve issues and support market access.
Regulatory Affairs Specialist - On-site Medtronic PlcRegulatory Affairs Specialist - On-siteLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Regulatory & Clinical Specialist LivaNova PlcRegulatory & Clinical SpecialistDenver, CORemote$85,000–$95,000 / yearli>Manage the overall development and approval process for assigned documents (CEP, CER, etc.) within timelines, including documentation generation, initiation of the review process, discussions on proposed revisions, and document completion in collaboration with other team members. The Regulatory and Clinical Specialist is a liaison with the organization working with various groups to effectively communicate and collaborate on the deliverables and meet the project deadlines in line with the regulatory requirements.
NewPharmacovigilance and Regulatory Specialist University of ColoradoPharmacovigilance and Regulatory SpecialistDenver, CORemote$68,994–$115,911 / yearJob Summary: Meet with PI and study team to review the progress of the application and development of the subsequent trial, assist in the development of applicable protocol materials before submission to the FDA, review any adverse safety events, protocol deviations and exclusions, enrollment and follow-up of participants, missing data and data quality controls, and any new medical advances that may require changes in the study protocol to ensure adherence to the protocol and IND/IDE application. Must have experience in each of the following skills: Pharmacovigilance; Regulatory Affairs; Clinical trial regulatory work; Risk assessment and mitigation; Adverse event (AE) analysis; Databases: Trial Master File database, Oncore or other CTMS, Electronic Data Capture systems; Safety parameters, protocols, and reporting.
Regulatory Affairs Specialist II Zimmer Biomet Holdings IncRegulatory Affairs Specialist IIEnglewood, CO$60,000–$90,000 / yearTo support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. Cross-Functional Collaboration: Partner daily with brilliant minds in Engineering, Quality, and Regulatory Affairs to bring life-changing devices from concept to market.
EH&S Specialist - Regulatory SM Energy CoEH&S Specialist - RegulatoryDenver, COul>Minimum of 3 years of oil and gas experience. SM Energy offers competitive compensation and benefits programs which include, but are not limited to, variable pay, health care coverage, retirement plan, protection coverage, time off and leave programs, training and development opportunities and a range of allowances connected to specific work situations. This role ensures projects meet all applicable regulatory requirements by preparing and submitting permit applications, coordinating with internal teams, and maintaining accurate records throughout the permitting lifecycle.
Specialist Environmental and Regulatory Advisor - Commerce City Suncor Energy IncSpecialist Environmental and Regulatory Advisor - Commerce CityCommerce City, CO$135,000–$157,000 / yearAs a Specialist Environmental and Regulatory Advisor you will support air permitting efforts, including Emission Inventories, support regulatory advocacy and implementation efforts including Environmental program development and management, and you will work with the Colorado Department of Public Health and the Environment (CDPHE). Responsibilities: Collect, assess, and manage environmental data to develop technical solutions that maximize compliance, performance, flexibility, and sustainability; maintain environmental databases, emissions calculations, inventories, and Annual Emissions Inventory Reports.
CONTRACT - Regulatory Compliance Data Specialist - 1099, 20 hours/ week Spectra Logic CorpCONTRACT - Regulatory Compliance Data Specialist - 1099, 20 hours/ weekBoulder, CO$35–$43 / hourLocated in the foothills of the Rocky Mountains in Boulder, Colorado, Spectra is an entrepreneurial, private company with more than 40 years of proven success preserving, protecting and defending the world's data. Collecting and validating supplier environmental compliance documentation, including RoHS, REACH, SCIP, TSCA, PFAS, Prop 65, conflict minerals, and material declarations.
Regulatory and Compliance Finance Specialist Vero NetworksRegulatory and Compliance Finance SpecialistDenver, COFull timeThis role serves as the central finance owner for VB-specific regulatory, payroll, and contract compliance, including USAC/FCC reporting, telecom sales and use tax compliance, tax engine and billing platform support, grant reporting and compliance, regulatory audits, and payroll-related regulatory filings. The Regulatory and Compliance Finance Specialist plays a critical role in mitigating regulatory, tax, payroll, and compliance risk for Vero Broadband, LLC (VB) and in supporting regulatory oversight across the broader Vero Fiber organization.
NewRegulatory Policy Specialist - Grid Modernization, Interconnection and Delivery Xcel Energy IncRegulatory Policy Specialist - Grid Modernization, Interconnection and DeliveryDenver, CO$112,200–$159,400 / yearp>As a leading combination electricity and natural gas energy company, Xcel Energy offers a comprehensive portfolio of energy-related products and services to 3.4 million electricity and 1.9 million natural gas customers across eight Western and Midwestern states. Xcel Energy endeavors to make https://www.xcelenergy.com/ accessible to any and all users.
Regulatory Affairs Supervisor University of ColoradoRegulatory Affairs SupervisorDenver, CO$71,517–$90,970 / yearInterpersonal Skills - Ability to establish and maintain effective working relationships with employees at all level; interacts with people in a friendly, open, honest manner; models a commitment to teamwork; demonstrates respect for the opinions of others; and maintains high level of confidentiality. The Regulatory Research Supervisor ensures regulatory compliance for clinical research studies, provides leadership and mentorship to regulatory personnel, and collaborates with investigators, sponsors, and research teams to support the timely and compliant conduct of clinical trials.
Regulatory Affairs Program Manager University of ColoradoRegulatory Affairs Program ManagerDenver, CO$74,627–$94,925 / yearPrimary duties will include, but not be limited to: submissions to the Institutional Review Board (IRB) of record including amendments, unanticipated problems, continuing reviews, and study closures; maintenance of the investigator site file/regulatory binder and all essential documents including documentation of appropriate training and delegation for all personnel; submissions to internal University and Hospital research portals including SARC, Oncore, InfoEd and others; acting as primary regulatory contact person for department faculty and research staff, sponsors/Contract Research Organizations (CROs)/coordinating centers; maintaining research credentials, training documentation and licenses; The Regulatory Affairs Coordinator will work closely with the Director of Clinical Research, program managers, and clinical research coordinators. Qualifications: Minimum Qualifications: Bachelor's degree in public health, public administration, social/behavioral sciences, physical sciences, nursing, healthcare, finance, accounting, business administration, business, or a directly related field from an accredited institution and 4-6 years of professional experience related to regulatory affairs in research administration.
Sr Regulatory Affairs Spec Medtronic PlcSr Regulatory Affairs SpecLafayette, COThis role will partner closely with Geography Regulatory Affairs to support international submissions, government queries, registration documentation, product approval and clearance activities, product demand and release planning, and post-market regulatory compliance to help ensure continued product availability worldwide. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
Regulatory Affairs Coordinator (Open Rank: Senior-Principal) University of ColoradoRegulatory Affairs Coordinator (Open Rank: Senior-Principal)Denver, CO$59,995–$76,314 / yearPrimary duties will include, but not be limited to: submissions to the Institutional Review Board (IRB) of record including amendments, unanticipated problems, continuing reviews, and study closures; maintenance of the investigator site file/regulatory binder and all essential documents including documentation of appropriate training and delegation for all personnel; submissions to internal University and Hospital research portals; acting as primary regulatory contact person for sponsors/Contract Research Organizations (CROs)/coordinating centers; maintaining research credentials, training documentation and licenses; The Regulatory Affairs Coordinator will work closely with the Director of Clinical Research, program managers, and clinical research coordinators. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.
Sr Regulatory Affairs Manager Medtronic PlcSr Regulatory Affairs ManagerLafayette, CO$154,400–$231,600 / yearIf you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. As the Regulatory Affairs Manager, you will be responsible for establishing strategy for worldwide product approval submission activities, directly responsible for execution of submission activities focused on US/EU and for ensuring regulatory compliance for Acute Care and Monitoring products.
NewAVP, Federal Regulatory Affairs Xcel EnergyAVP, Federal Regulatory AffairsDenver, ColoradoLead enterprise-wide engagement with Commercial Operations, Transmission, Integrated System Planning, Operating Companies, Legal, Regulatory, and other internal stakeholders on federal regulatory issues affecting transmission service, wholesale power transactions, organized wholesale market rules and trading strategies, generator interconnections, open access transmission policies, RTO participation, and transmission and wholesale business decisions. Provide strategic leadership and subject matter expertise on federal regulatory, wholesale market, transmission, reliability, tariff, and compliance matters before the Federal Energy Regulatory Commission (FERC), North American Electric Reliability Corporation (NERC), NERC Regional Entities, Regional Transmission Organizations (RTOs), and other regional organizations.
Prin Regulatory Affairs Spec Medtronic PlcPrin Regulatory Affairs SpecLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Manager, Government and Regulatory Affairs - PJM and MISO Scout Clean EnergyManager, Government and Regulatory Affairs - PJM and MISOBoulder, CO$110,000–$150,000ul>Understanding of state legislative processes and utility commission regulations unique to renewable energy technologies and across multiple disciplines including demand drivers, transmission, interconnection, finance, tax, origination, siting, permitting and land use. This individual will join a small team reporting to the Director, Government and Regulatory Affairs, and will coordinate closely with internal and external subject matter experts to advance Scout’s policy strategy and support execution across the development and operating portfolio.
Manager, Government and Regulatory Affairs - PJM and MISO Scout Clean Energy LLCManager, Government and Regulatory Affairs - PJM and MISOBoulder, COp>This individual will join a small team reporting to the Director, Government and Regulatory Affairs, and will coordinate closely with internal and external subject matter experts to advance Scout's policy strategy and support execution across the development and operating portfolio. Scout Clean Energy is seeking a motivated and collaborative Manager, Government and Regulatory Affairs to advance our legislative and regulatory priorities across assigned states within the MISO and PJM footprints.
NewDirector, Regulatory Affairs 3D Systems CorpDirector, Regulatory AffairsLittleton, CO$177,000–$266,000 / yearUSA-CO-Littleton'','''','''','''',''80127'',''Manager with Direct Reports'',''Manager with Direct Reports'',''Yes, 25 % of the Time'',''Yes, 25 % of the Time'',''Employee'',''Employee'',''Jun 29, 2026, 9:30:20 AM'',''Jun 29, 2026, 9:30:20 AM'',''false'',''170351'',''170351'',''true'',''170351'',''false'',''Submission for the position: Director, Regulatory Affairs - (Job Number: 26000055)'',''false'',''170351'',''false'',''true''. In this position, you will lead the development and execution of global regulatory strategies for a diverse portfolio of patient-specific and additively manufactured medical devices, including implantable solutions, digitally enabled surgical planning technologies, and advanced manufacturing platforms.
Director of Quality and Regulatory Affairs MRINetwork JobsDirector of Quality and Regulatory AffairsDenver, ColoradoDirect experience in and knowledge of business and management principles involved in tactical execution, strategic planning, resource allocation, human resources modeling, leadership techniques, production methods, and coordination of people and resources. As Director of Regulatory Affairs – Compliance Systems and Labeling, you’ll direct regulatory and labeling activities and collaborate with senior teams to define strategy and compliance programs.
Director, Regulatory Affairs - Compliance Systems and Labeling Artech LLCDirector, Regulatory Affairs - Compliance Systems and LabelingLakewood, CO$196,500–$245,600 / yearTarget Pay Range: $196,500.00 to $245,600.00 - Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. Collaborate with senior teams to define strategy and compliance programs, playing an integral role in launching new products and supporting established lines.
NewSenior Regulatory Affairs Manager Medtronic plcSenior Regulatory Affairs ManagerLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Open Rank Regulatory Affairs Coordinator (RAC) (Entry - Senior) University of ColoradoOpen Rank Regulatory Affairs Coordinator (RAC) (Entry - Senior)Denver, CO$52,860–$70,833 / yearThe Regulatory Affairs Coordinator (RAC) will work closely with the HCTU Leadership Team, Principal Investigators, Industry Sponsor/CRO Representatives, IRBs, and other departments on campus to provide support for the Division's clinical trial portfolio. Why Join Us: Investigators in the Division of Hematology's Blood Cancer Program are actively engaged in multiple research activities aimed at improving outcomes for patients with blood cancers and related disorders.
Director, Regulatory Affairs (Medical Devices) System OneDirector, Regulatory Affairs (Medical Devices)Denver, Colorado$195,000–$245,000 / yearA well-established and growth-oriented medical device organization is seeking a strategic regulatory leader to guide global regulatory affairs and labeling strategy across a diverse product portfolio. Required Experience:10+ years of progressive regulatory affairs experience within medical devices (combination product experience strongly preferred).
Regulatory Affairs & Public Policy, Senior Associate Rowan Digital InfrastructureRegulatory Affairs & Public Policy, Senior AssociateDenver, ColoradoRowan is assembling a strategic portfolio of data center sites in Tier 1 markets across the United States at various stages of development, and we’re looking for incredible and passionate people to help us advance our company and our commitment to building a more sustainable future. This role serves as a core analytical and operational resource, enabling the team to monitor, assess, and respond to legislative and regulatory developments that impact project siting, energy procurement, and overall business strategy.
NewDirector of Quality and Regulatory Affairs Shurig SolutionsDirector of Quality and Regulatory AffairsDenver, ColoradoDirect experience in and knowledge of business and management principles involved in tactical execution, strategic planning, resource allocation, human resources modeling, leadership techniques, production methods, and coordination of people and resources. As Director of Regulatory Affairs – Compliance Systems and Labeling, you’ll direct regulatory and labeling activities and collaborate with senior teams to define strategy and compliance programs.
Prin Regulatory Strategy Spec Medtronic PlcPrin Regulatory Strategy SpecCOp>If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).
NewSenior Manager, Global Regulatory Affairs Otsuka America PharmaceuticalSenior Manager, Global Regulatory AffairsDenver, COp>Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle activities for all assigned projects in alignment with the Global Regulatory Lead. Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL).
NewSenior Regulatory Affairs Manager Medtronic PlcSenior Regulatory Affairs ManagerLafayette, COp>The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Senior Regulatory Counsel, Kids Content Google LLCSenior Regulatory Counsel, Kids ContentCOp>As a Senior Regulatory Counsel, Content, you'll join a global team that provides subject matter expertise and engages with regulators, academics, and others to consider the role of Content law in our changing economy, the development of new technology, and passage of new laws and regulations. Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Austin, TX, USA; Boulder, CO, USA; Mountain View, CA, USA; Los Angeles, CA, USA; Washington D.C., DC, USA; San Francisco, CA, USA; Seattle, WA, USA.
Regulatory Associate Highridge IncRegulatory AssociateWestminster, COYou will have the opportunity to attend surgical labs, engage with project teams, learn about regulatory affairs, hone your writing skills, and immerse yourself in a medical device organization committed to its customers. As an RA team member, you will work closely with the rest of the RA team to ensure distribution of product within regulatory guidelines, and work with international team members to facilitate international submissions.
NewSr Environmental and Regulatory Advisor - Commerce City SuncorSr Environmental and Regulatory Advisor - Commerce CityCommerce City, ColoradoAs a Specialist Environmental and Regulatory Advisor you will support air permitting efforts, including Emission Inventories, support regulatory advocacy and implementation efforts including Environmental program development and management, and you will work with the Colorado Department of Public Health and the Environment (CDPHE). Collect, assess, and manage environmental data to develop technical solutions that maximize compliance, performance, flexibility, and sustainability; maintain environmental databases, emissions calculations, inventories, and Annual Emissions Inventory Reports.
Commercial & Healthcare Regulatory Counsel Alto IncCommercial & Healthcare Regulatory CounselCORemote$135,000–$185,000 / yearPhysical requirements for this role include the ability to work at a computer terminal with monitor, keyboard and mouse for extended periods of time, stoop, bend, and reach for equipment and supplies, make frequent repetitive motions required to operate a computer that include the wrists, hands and fingers, and lift, carry, push, pull, and move light objects up to 20 pounds. Issue-spot and provide practical guidance on applicable laws and regulations, such as the Anti-Kickback Statute (AKS), Stark Law, False Claims Act, FDA/DEA requirements relevant to pharmacy and telehealth operations, state pharmacy/professional licensing, PBM contracting/network participation, and HIPAA/HITECH.
Consultant, Rates & Regulatory Black & Veatch Holding CoConsultant, Rates & RegulatoryDenver, CO$103,147–$172,271 / yearp>Recognized by Glassdoor as a 2023 Top 100 place to work and winner of the Newsweek's 2023 America's Greatest Workplaces for Diversity, Black & Veatch allows you to lend your talent and perspective to humanity's biggest challenges in a flexible environment where you are empowered to grow and explore new possibilities. Black & Veatch's Infrastructure Advisory Business provides a portfolio of solutions focused on the asset lifecycle, including Asset Management & Operations & Maintenance, Infrastructure Technology, Cybersecurity Solutions, Planning, and Transactions.
Program Manager, Regulatory Operations Financial Industry Regulatory Authority IncProgram Manager, Regulatory OperationsDenver, COFINRA employees are required to disclose to FINRA all brokerage accounts that they maintain, and those in which they control trading or have a financial interest (including any trust account of which they are a trustee or beneficiary and all accounts of a spouse, domestic partner or minor child who lives with the employee) and to authorize their broker-dealers to provide FINRA with duplicate statements for all of those accounts. Additional insurance includes basic life, accidental death and dismemberment, supplemental life, spouse/domestic partner and dependent life, and spouse/domestic partner and dependent accidental death and dismemberment, short- and long-term disability, long-term care, business travel accident, disability and legal.
Principal, RA Specialist Danaher CorpPrincipal, RA SpecialistCORemote$110,000–$135,000 / yearIn this role, you will have the opportunity to: Author and lead the creation of regulatory documents (regulatory submissions/filings, registration and listing, technical files, etc.) to obtain global approvals to commercially distribute products; collaborates with international colleagues in global regions to submit application/registration documents. Provide guidance and approve regulatory/quality documentation related to new product development deliverables acting as core team member conducting regulatory assessments related to design changes, advising and approving protocols, reports, marketing material, etc.
Key Management Specialist CymertekKey Management SpecialistAurora, ColoradoCryptographic Key Manager, Encryption Specialist, Data Protection Analyst, Information Security Specialist, Cybersecurity Analyst, Cryptography Engineer, Security Operations Specialist, Key Access Control Analyst, Identity and Access Management Specialist, IT Security Specialist, Secure Communications Analyst, Data Security Engineer, Network Security Specialist, Key Lifecycle Manager, Digital Security Specialist, Compliance and Risk Analyst, Secure Storage Engineer, Threat Intelligence Analyst, Security Systems Administrator, etc. Cybersecurity, Computer Science, Information Technology, Information Systems, Computer Engineering, Network Engineering, Data Science, Information Assurance, Cryptography, Security Management, Telecommunications, Applied Mathematics, Systems Engineering, Digital Forensics, Software Engineering, Risk Management, Artificial Intelligence, Secure Communications, Compliance and Regulatory Affairs, Electrical Engineering, etc.
Senior Procedure Development Specialist HistoSonics IncSenior Procedure Development SpecialistCORemoteWork closely with the HistoSonics Education, Marketing, Sales and R&D teams to deliver world-class customer and employee training and education programs that enhance the value of the organization. HistoSonics is a medical device company, founded in 2009, that has developed a non-invasive, sonic beam therapy platform that uses histotripsy, which is capable of destroying targeted liver tumors.
Workforce Data Security Specialist Google LLCWorkforce Data Security SpecialistCOp>Note: By applying to this position you will have an opportunity to share your preferred working location from the following: Chicago, IL, USA; Ann Arbor, MI, USA; Atlanta, GA, USA; Austin, TX, USA; Boulder, CO, USA; Los Angeles, CA, USA; Seattle, WA, USA; Washington D.C., DC, USA. Whether recruiting the next Googler, refining our core programs, developing talent, or simply looking for ways to inject some more fun into the lives of our Googlers, we bring a data-driven approach that is reinventing the human resources field.
Program Specialist U.S. Department of Veterans AffairsProgram SpecialistGolden, CO$68,819–$108,251 / year2) knowledge applying Federal, State laws, rules, and regulations relative to compliance and the conduct of investigative studies, (3) interpreting and analyzing data using discretion to implement a wide range of research policies and procedures, (4) preparing and conducting study presentations, trainings, and briefings (5) reviewing and preparing trial budget, and (6) assisting in developing action plans to resolve problems or improve efficiency, and implementation of new methods. (2) interpreting Federal, State laws, rules, and regulations relative to compliance and the conduct of investigative studies, (3) applying analytical and evaluative principles to resolve issues and accomplish program goals for a clinical, medical, and/or research department/organization, (4) creating, maintaining, and disseminating electronic information and documents/files; effectively communicates, orally and in writing, between agencies and across organizational levels to coordinate research needs and deliver requested information.
Pre-Award Specialist (Open-Rank) University of ColoradoPre-Award Specialist (Open-Rank)Boulder, CO$50,160–$63,804 / yearThere is a lot of training up front as this position must learn a Medicare Coverage Analysis (MCA), oncology clinical trial protocols, processes and procedures of the oncology clinical trial Post Award specialist, the oncology clinical trial finance/billing specialist, clinic staff. Job Summary: The Oncology Clinical Research Pre Award Specialist is responsible for developing, negotiating, finalizing and reviewing budgets for clinical trials conducted by faculty members of the University of Colorado Cancer Center at University of Colorado Hospital (UCH).
CPRG Methane Grant Support Specialist - EPS I State of ColoradoCPRG Methane Grant Support Specialist - EPS IDenver, CO$65,736–$97,104 / yearAs part of this commitment, our agency will assist individuals who have a disability with any reasonable accommodation requests related to employment, including completing the application process, interviewing, completing any pre-employment testing, participating in the employee selection process, and/or to perform essential job functions where the requested accommodation does not impose an undue hardship. The Work Unit: The Policy Innovations Unit within the Office of Innovations in Planning and Air Quality Data develops innovative strategies to achieve long-term air pollution goals, including ozone attainment and the state's greenhouse gas reduction targets.
IT Specialist U.S. Department of Veterans AffairsIT SpecialistDenver, CO$89,508–$116,362 / yearCustomer Service - Works with clients and customers (that is, any individuals who use or receive the services or products that your work unit produces, including the general public, individuals who work in the agency, other agencies, or organizations outside the Government) to assess their needs, provide information or assistance, resolve their problems, or satisfy their expectations; knows about available products and services; is committed to providing quality products and services. The Department of Veterans Affairs performs pre-employment reference checks as an assessment method used in the hiring process to verify information provided by a candidate (e.g., on resume or during interview or hiring process); gain additional knowledge regarding a candidates abilities; and assist a hiring manager with making a final selection for a position.
IT Specialist (SYSANALYSIS) U.S. Department of Veterans AffairsIT Specialist (SYSANALYSIS)Denver, CO$106,437–$138,370 / yearCustomer Service - Works with clients and customers (that is, any individuals who use or receive the services or products that your work unit produces, including the general public, individuals who work in the agency, other agencies, or organizations outside the Government) to assess their needs, provide information or assistance, resolve their problems, or satisfy their expectations; knows about available products and services; is committed to providing quality products and services. Specialized experience is defined as: Experience in the planning, testing and implementation of Directory Services infrastructure technologies in a large multi-domain Active Directory (AD) Environment, including AD object management, user and group management, Group Policy management, support of Domain Name System (DNS) services and user access and authentication.