56 Results for

Regulatory Manager Jobs in Denver, CO

Jobs

Westminster, CO

$146,000–$210,000 / year

As a Senior Manager, Clinical Operations working on the Clinical Affairs team, you will be empowered through meaningful work and career development to provide operational management of the Company’s clinical studies from study initiation through to close-out and supporting data dissemination activities and requires deep knowledge and understanding of clinical regulations and best practices. Cerapedics has two drug-device products approved by the FDA powered by Cerapedics’ proprietary P-15 Osteogenic Cell Binding Peptide: PearlMatrix™ Bone Graft for all major lumbar interbody surgical approaches and i-FACTOR® Bone Graft for single-level anterior cervical discectomy and fusion (ACDF) in the cervical spine.

Today

Boulder, CO

p>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.

30+ days ago

Boulder, CO

$110,000–$150,000

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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.

30+ days ago

Denver, CO

$74,627–$94,925 / year

Primary 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.

12 days ago

Lafayette, CO

$154,400–$231,600 / year

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. 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.

30+ days ago

Lafayette, CO

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.

2 days ago

Lafayette, CO

p>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).

7 days ago

Denver, CO

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).

1 day ago

Denver, CO

$71,517–$90,970 / year

Interpersonal 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.

27 days ago

Lafayette, CO

This 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).

30+ days ago

Denver, CO

$59,995–$76,314 / year

Primary 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.

30+ days ago

Denver, Colorado

Lead 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.

7 days ago

Denver, Colorado

Rowan 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.

30 days ago

Lafayette, CO

21 days ago

Littleton, CO

$177,000–$266,000 / year

USA-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.

2 days ago

Lakewood, CO

$196,500–$245,600 / year

Target 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.

10 days ago

Lafayette, CO

30+ days ago

Denver, Colorado

Direct 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.

1 day ago

Westminster, CO

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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.

16 days ago

Westminster, CO

This 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.

30+ days ago

Greenwood Village, CO

Preferred: • 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.

30+ days ago

Denver, Colorado

30+ days ago

Denver, CO

$52,860–$70,833 / year

The 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.

30+ days ago

Denver, Colorado

$195,000–$245,000 / year

A 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).

30+ days ago

p>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.

28 days ago

Englewood, CO

$60,000–$90,000 / year

To 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.

12 days ago

Westminster, CO

You 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.

30+ days ago

Denver, CO

Remote

$200,000–$230,000 / year

You will be responsible for bringing structure, discipline, and clear operating rhythm to a complex, multi state lobbying network, ensuring our external partners are well coordinated, accountable, and aligned to business priorities. We have an exciting opportunity to join our Government & Industry Affairs team in the United States and are currently looking for a Senior Manager, Government & Industry Affairs Operations to join the team.

30+ days ago

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).

29 days ago

Boulder, CO

12 days ago

Boulder, Colorado

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 herea 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).

13 days ago

Remote

$184,000–$210,000 / year

The Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. Data Analysis and Reporting: Utilize reimbursement data, claims data, and other relevant sources to perform data analysis and generate reports on reimbursement trends, payment patterns, and financial outcomes.

30+ days ago

Denver, CO

$129,000–$183,200 / year

On behalf of the CPD and Major Projects Group, manage collaboration with Corporate Development, Legal, Regulatory Affairs, Supply Chain, Siting & Land Rights, Energy Supply Operations, Energy Supply Asset Analytics, 3rd party development organizations, consultants and others to fully assess and define technical parameters including, but not limited to, performance evaluations, operational requirements, permitting, site suitability assessments, constructability reviews, RFP/RFQ bid package development, environmental studies, project performance parameters, project cost estimates and schedules, project cash flow forecasts and budgets, project risk assessments, and QA/QC requirements.

Provide leadership & coordination of multi-disciplinary, matrixed project teams to perform technical due diligence and engineering development tasks to fully develop project scope, project estimate, project schedule, preliminary engineering, construction, and overall execution strategy.

30+ days ago

Lafayette, Colorado

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).

7 days ago

Lafayette, CO

30+ days ago

Denver, CO

p>As part of working with clients you will help with several aspects of life sciences integrated planning including:

Integrated Planning Strategy: Design and implement IBP/S&OP frameworks tailored to life sciences environments, accounting for regulatory release cycles, CMO/CDMO network complexity, and the distinct planning dynamics of biopharma and med tech product portfolios.
Accenture is a leading solutions and services company that helps the world's leading enterprises reinvent by building their digital core and unleashing the power of AI to create value at speed across the enterprise, bringing together the talent of our approximately 786,000 people, our proprietary assets and platforms, and deep ecosystem relationships.

15 days ago

Denver, CO

$98,448–$168,768 / year

Technical experience required includes the ability to write efficient code to extract, manipulate, and analyze complex datasets using SAS software (Base SAS, Macros, SQL) to generate reports, tables, and listings as well as advanced MS Excel skills (VLOOKUP, pivot tables, Power Query, macros, nested if functions), intermediate MS Access skills (SQL, select/append/make table queries), and experience extracting data from a data warehouse using Snowflake or Python or similar software. For URAC accredited areas, the following professional competencies apply: Associates in this role are expected to have strong oral, written and interpersonal communication skills, problem-solving skills, facilitation skills, and analytical skills.

26 days ago

Denver, CO

$124,000–$144,000 / year

As Manager, Sales Operations, you will be responsible for leading a team directly supporting all origination and sales activities within the WECC, ERCOT, and SPP footprint across all technologies including onshore wind, solar, storage, transmission, thermal, and emerging technologies with utilities as the primary customer base. With 25 years of trusted execution, we deliver reliable, affordable energy through a diverse portfolio that includes natural gas, solar, land-based wind, energy storage, transmission, and domestic manufacturing.

16 days ago

Boulder, CO

$157,227–$178,972 / year

JOB REQUIREMENTS: Requires a Master's degree in Regulatory Affairs, Quality Assurance Compliance, or related and 3 years of related experience which must include some experience in each of the following. Managing qualified external labs for product release and stability testing while ensuring timely material delivery and risk mitigation in sourcing plans.

8 days ago

Denver, CO

$124,000–$144,000 / year

15 days ago

Remote

$110,000–$135,000 / year

In 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.

30+ days ago

$120,200–$140,000 / year

Lead and contribute to end-to-end delivery for Generis CARA and associated regulatory technology platforms - including requirements gathering, solution design, system configuration, content template development, and user acceptance testing. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities.

16 days ago

Denver, Colorado

This executive role will be responsible for establishing and refining our long-term strategy across current and prospective addressable markets, while ensuring strategic vision translates into actionable product development and execution. We believe that associates do their best when they feel safe, understood, and valued, and we work diligently and collaboratively to ensure Broadridge is a company—and ultimately a community—that recognizes and celebrates everyone’s unique perspective.

30+ days ago

Lafayette, CO

28 days ago

Lafayette, Colorado

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29 days ago

Boulder, CO

Operating within a CDMO and regulated pharma environment, this role supports drug development and commercial manufacturing by driving strategic sourcing, supplier lifecycle management, contract execution, and cost optimization while ensuring uninterrupted supply, product quality, and full regulatory compliance. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable.

30+ days ago

Aurora, Colorado

Information Security Auditor, IT Security Auditor, Cybersecurity Auditor, Compliance Analyst, Risk Assessment Specialist, Security Risk Auditor, Internal IT Auditor, Information Assurance Analyst, Vulnerability Assessment Specialist, Network Security Auditor, Data Privacy Auditor, Security Compliance Analyst, Security Operations Auditor, Penetration Testing Auditor, Governance, Risk, and Compliance (GRC) Specialist, IT Risk Manager, Threat Assessment Analyst, Systems Compliance Auditor, Cyber Risk Analyst, etc. Cybersecurity, Information Technology, Computer Science, Information Systems, Computer Engineering, Network Engineering, Systems Engineering, Data Science, Information Assurance, Security Management, Risk Management, Digital Forensics, Telecommunications, Software Engineering, Business Administration (with a focus on IT or security), Compliance and Regulatory Affairs, Applied Mathematics, Cryptography, Audit and Assurance, etc.

30+ days ago

Denver, CO

$65,574–$83,410 / year

Interpersonal Skills - Ability to establish and maintain effective working relationships with employees at all levels; 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. As a member of the research team this position is responsible for conducting key aspects of research for Phase I-IV industry-sponsored, co-operative group and or investigator-initiated clinical trials in accordance with the trial protocols, FDA Regulations, and ICH/GCP Guidelines.

30+ days ago

Denver, CO

$11,200–$12,175 / year

Provide administrative support for program operations, including maintaining program documentation, facilitating student enrollment in courses, record keeping for scholarship awardees, tracking inquiries, and coordinating communications. Monitor and manage the program email account and respond to inquiries from prospective and non-degree seeking students regarding program logistics, enrollment processes, financial aid, and scheduling.

14 days ago

Louisville, CO

$247,400–$305,600 / year

CORE ACCOUNTABILITIES Specific Responsibilities include: Hands‑On Clinical Data Management Execution (as needed while building CDM team) Serve as the primary clinical data management lead for assigned clinical trials, with direct accountability for data quality, timeliness, and inspection readiness from protocol development through database lock. We 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.

30+ days ago

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Regulatory Manager Jobs in Denver, CO

Senior Manager, Clinical Operations Cerapedics Inc

Manager, Government and Regulatory Affairs - PJM and MISO Scout Clean Energy LLC

Manager, Government and Regulatory Affairs - PJM and MISO Scout Clean Energy

Regulatory Affairs Program Manager University of Colorado

Sr Regulatory Affairs Manager Medtronic Plc

Senior Regulatory Affairs Manager Medtronic plc

Senior Regulatory Affairs Manager Medtronic Plc

Senior Manager, Global Regulatory Affairs Otsuka America Pharmaceutical

Regulatory Affairs Supervisor University of Colorado

Sr Regulatory Affairs Spec Medtronic Plc

Regulatory Affairs Coordinator (Open Rank: Senior-Principal) University of Colorado

AVP, Federal Regulatory Affairs Xcel Energy

Regulatory Affairs & Public Policy, Senior Associate Rowan Digital Infrastructure

Regulatory Affairs Specialist - On-site Medtronic Plc

Director, Regulatory Affairs 3D Systems Corp

Director, Regulatory Affairs - Compliance Systems and Labeling Artech LLC

Prin Regulatory Affairs Spec Medtronic Plc

Director of Quality and Regulatory Affairs Shurig Solutions

Regulatory Affairs Specialist I Highridge Inc

Regulatory Affairs Specialist Highridge Inc

Senior Regulatory Affairs Specialist Stryker Corp

Director of Quality and Regulatory Affairs MRINetwork Jobs

Open Rank Regulatory Affairs Coordinator (RAC) (Entry - Senior) University of Colorado

Director, Regulatory Affairs (Medical Devices) System One

Prin Regulatory Strategy Spec Medtronic Plc

Regulatory Affairs Specialist II Zimmer Biomet Holdings Inc

Regulatory Associate Highridge Inc

Senior Manager, Government & Industry Affairs Operations VGW Holdings Ltd

Sr PD Program Manager - EU MDR Leader Medtronic Plc

Sr Manufacturing Operations QA Manager - Boulder Medtronic Plc

Sr Manufacturing Operations QA Manager - Boulder Medtronic

Senior Manager, Reimbursement - Central remote Ceribell Inc

Development Manager Dispatchable Lead Xcel Energy Inc

Sr Program Manager – EU MDR Operations Leader Medtronic

Global Senior Marketing Manager - Pancreaticobiliary (Endoscopy) Medtronic Plc

Life Sciences Supply Chain and Operations - Supply Chain Planning Manager Accenture Plc

Business Change Manager Sr Elevance Health Inc

Manager, Sales Operations (West) Invenergy

Project Manager Corden Pharma International GmbH

Manager, Sales Operations (West) Invenergy LLC

Principal, RA Specialist Danaher Corp

Managed Services Sr. Consultant Deloitte Touche Tohmatsu Ltd

Head of Retirement and Workplace Broadridge

Sr Design Quality Engineer Medtronic Plc

Sr Design Quality Engineer Medtronic

Direct Materials Buyer Corden Pharma International GmbH

System Security Auditor Cymertek

Clinical Research Nurse University of Colorado

QA/RA Program Academic Services Professional (Part-Time) University of Colorado

Senior Director, Clinical Data Management Umoja BioPharma Inc

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