NewRegulatory Affairs Manager - PHCS # 26-22099 US Tech Solutions, Inc.Regulatory Affairs Manager - PHCS # 26-22099Tucson, AZCandidate Requirements 3-5 years’ experience with a PhD degree; 5-7 with Master's degree or 6-8 years with Bachelor's degree in the field of IVDs/Medical Devices/Pharma/Biopharmaceutical with significant experience in Regulatory Affairs or equivalent. Leadership & Team Culture: Foster an inclusive team environment, mentor junior staff, champion data stewardship, and drive the adoption of new technologies to increase productivity.
NewPathology Group Leader Sante Consulting LLCPathology Group LeaderScottsdale, AZThe Pathology Group Leader (PGL) oversees the Company’s growing team of employed and contracted pathologists based in multiple locations including at the Company’s Scottsdale, AZ headquarters and Boston, MA satellite office and performs expert reading of slides for CND’s world-leading cutaneous neurodiagnostics services offered to neurologists and other clinicians nationally. •Leverage CND’s prereader resources and pathology assistance system (NerValence) to support the reading of Case Pair 1. •Upon successful completion of CNDs training programs, serve as a primary reader for the Syn-One Test and consult with CND’s other pathologists on cases when necessary.
Regulatory Affairs Manager - PHCS Tailored ManagementRegulatory Affairs Manager - PHCSTucson, AZ$45–$55 / hourThe ideal candidate will bring a strong background in FDA submissions, regulatory strategy, and cross-functional leadership within the medical device, biotechnology, pharmaceutical, or in-vitro diagnostics industries. Collaborate with cross-functional teams including R&D, Quality, Clinical Affairs, Manufacturing, and Program Management to ensure regulatory requirements are integrated into business processes.
Regulatory Affairs Manager - PHCS Artech LLCRegulatory Affairs Manager - PHCSTucson, AZ$45–$55 / hourCandidate Requirements: 3-5 years experience with a PhD degree; 5-7 with Master's degree or 6-8 years with Bachelor's degree in the field of IVDs/Medical Devices/Pharma/Biopharmaceutical with significant experience in Regulatory Affairs or equivalent. Regulatory Affairs Manager – Software & Hardware: This is an onsite position for an experienced Regulatory Affairs Manager supporting Software and Hardware for PHCS (Personalized Healthcare Solutions).
Director of Rates & Regulatory Affairs Nesco Resource, LLCDirector of Rates & Regulatory AffairsPhoenix, AZ$165,000–$210,000 / yearCollaborate with executive leadership to develop rate cases, oversee regulatory reporting, and ensure compliance, all while supporting the company's financial and operational goals. This pivotal role involves leading rate strategy, regulatory filings, and compliance.
Summer 2027 Internship - Regulatory Affairs - Arizona StrykerSummer 2027 Internship - Regulatory Affairs - ArizonaTempe, ArizonaHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. As a Regulatory Affairs (RA) intern at Stryker, you will gain exposure to global regulatory strategy and compliance while working cross-functionally with teams such as R&D, Supplier Quality, Marketing, and Clinical Affairs.
Principal Regulatory Affairs Specialist Innovative Health LLCPrincipal Regulatory Affairs SpecialistScottsdale, AZFull timePrepare regulatory assessments for manufacturing changes, line extensions, design changes, validation activities, and Class III device lifecycle activities to determine whether additional regulatory submissions or agency notifications are required, including 510(k) submissions, U.S. Letters to File, PMA (i.e PMR) supplements, annual reports, or Canadian license amendments.· Supervisory Responsibilities: None Education, Qualifications and Skills:· Bachelor's degree in life sciences or a related field, with a minimum of 10 years of progressive regulatory affairs experience in the medical device industry; or an equivalent combination of education and experience.· Expert-level knowledge of FDA 21 CFR Part 820 and applicable 510(k) submission requirements.·
Manager, Healthcare Compliance and Regulatory Affairs SuvidaManager, Healthcare Compliance and Regulatory AffairsTucson, ArizonaCoordinate system projects by partnering with accountable business owners and proactively lead efforts to mitigate risks associated with business activities, confirm risk measurement/s and business monitoring and align with internal and regulatory requirements. This includes creating a compliance strategy that ensures business accountability for oversight over the day-to-day monitoring of the business areas as well as supporting business partners in implementing that strategy.
Regulatory Affairs Manager - PHCS MindlanceRegulatory Affairs Manager - PHCSTucson, AZ3-5 years experience with a PhD degree; 5-7 with Master's degree or 6-8 years with Bachelor's degree in the field of IVDs/Medical Devices/Pharma/Biopharmaceutical with significant experience in Regulatory Affairs or equivalent. This is an onsite position for an experienced Regulatory Affairs Manager supporting Software and Hardware for PHCS (Personalized Healthcare Solutions), with a pay range of ***-***/hr and a maximum client bill rate of ***.
Regulatory Affairs Manager Pride GlobalRegulatory Affairs ManagerTucson, AZ$45–$55 / hourThis applies to direct care staff (Examples: RN, LPN, Nurse Aides, Therapists) referred to Kentucky nursing facilities, assisted living communities, or long-term care facilities, in accordance with KRS 216.793. Only applicable for San Francisco Candidates : Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of lactation accommodation rights, and this notice will automatically be given upon hiring, any inquiry of parental leave or lactation accommodation.
Regulatory Affairs Expert - Remote YO AI LabsRegulatory Affairs Expert - RemotePhoenix, AZRemoteThe role involves assessing clinical documents, ensuring compliance with regulatory guidelines, identifying inconsistencies, and providing clear, evidence-based feedback to improve AI-generated regulatory content. We are seeking an experienced Regulatory Affairs Specialist to support AI-driven healthcare projects by reviewing and evaluating regulatory documentation.
NewPrincipal Specialist, Regulatory Affairs West Pharmaceutical Services IncPrincipal Specialist, Regulatory AffairsScottsdale, AZWest solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. In addition, the Principal Specialist mentors team members, and provides support for global regulatory approvals (beyond US and EU), commercialized products, and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements.
US_Regulatory Affairs Manager I_CO MindlanceUS_Regulatory Affairs Manager I_COTucson, AZStakeholder management and influencing: Effectively partners with stakeholders to understand and provide best solutions. External interface management: Effectively partner with stakeholders to understand and provide best solutions.
Manager Sponsor Regulatory Affairs & Institutional Trial Compliance HonorHealthManager Sponsor Regulatory Affairs & Institutional Trial ComplianceArizonaESSENTIAL FUNCTIONS Sponsor Regulatory Strategy and Agency Compliance: Lead implementation of regulatory strategy for institutionally sponsored clinical trials, including drug, device, biologic, behavioral, and observational studies Determine regulatory pathway for each study, including IND, IDE, exempt, abbreviated, or non-FDA regulated status Oversee preparation and submission of INDs, IDEs, amendments, annual reports, safety reports, protocol changes, and closeout filings as required Serve as primary institutional contact with FDA and other regulatory agencies regarding sponsor matters Monitor changes in regulations, guidance, and enforcement trends, then implement required operational changes Ensure fulfillment of sponsor commitments, reporting deadlines, and regulatory obligations Provides guidance to leadership on regulatory risk, escalation items, and remediation strategy. Trial Startup, Lifecycle Management, and Sponsor Oversight: Lead sponsor regulatory and compliance startup processes from concept approval through study activation Oversee regulatory readiness for protocol finalization, informed consent documents, investigator qualifications, site documents, and essential regulatory records Approve activation of internal and external participating sites once sponsor requirements are met Direct amendment implementation processes across all participating sites Oversee study closeout, final reporting, archival readiness, and record retention requirements Support expansion of institutional trials into multi-site networks and affiliated partners Ensure delegation of sponsor responsibilities to CROs, monitors, vendors, or external partners is documented and controlled Ensure trial institutional reporting requirements such as to CT.Gov, registration and reporting are completed within the institutional regulatory guidelines.
NewRegulatory Affairs Project Manager F. Hoffmann-La Roche LtdRegulatory Affairs Project ManagerTucson, AZ$84,600–$157,200 / yearIn this position, you will have a role in working with internal and Roche affiliates for a wide array of innovative medical diagnostic products for researchers, physicians, patients, hospitals, laboratories, and blood banks in high-profile demographic regions, specifically in APAC, LATAM, the Middle East, and Africa. Provide support to currently marketed products, e.g., review engineering changes, labeling, product changes, and documentation for compliance and for changes requiring regulatory agency approval, as per international regulatory requirements.
NewRegulatory Affairs Project Manager RocheRegulatory Affairs Project ManagerTucson, ArizonaIn this position, you will have a role in working with internal and Roche affiliates for a wide array of innovative medical diagnostic products for researchers, physicians, patients, hospitals, laboratories, and blood banks in high-profile demographic regions, specifically in APAC, LATAM, the Middle East, and Africa. Provide support to currently marketed products, e.g., review engineering changes, labeling, product changes, and documentation for compliance and for changes requiring regulatory agency approval, as per international regulatory requirements.
NewSenior Manager Regulatory Affairs - Systems & Software F. Hoffmann-La Roche LtdSenior Manager Regulatory Affairs - Systems & SoftwareTucson, AZ$126,800–$235,000 / yearYou will have the opportunity to navigate complex and evolving regulatory areas-including integrated instrument systems, software, cybersecurity, automation, connectivity, and digital technologies-while helping translate innovation into regulatory strategies that enable successful product development and commercialization. This role offers significant visibility, autonomy, and opportunity to influence, making it ideal for an experienced regulatory professional who enjoys solving complex problems, shaping strategy, and seeing their work directly contribute to the future of pathology and patient care.
Sr. Regulatory Affairs Specialist - Relocation Assistance Provided Innovative Health LLCSr. Regulatory Affairs Specialist - Relocation Assistance ProvidedScottsdale, AZAbility to handle multiple projects and coordinate with cross functional teams; Ability to comfortably and effectively confront difficult situations and issues in a timely and appropriate manner while providing a solution; Ability to recommend technical solutions; Ability to specify regulatory requirements for products; General proficiency in Microsoft Word and other applications (Excel, PowerPoint, Adobe Acrobat, and Visio). Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for the submission of FDA 510(k)s, periodic updates, Canadian applications and registrations to regulatory agencies.
NewRegulatory Affairs Associate Arizona Nutritional Supplements LLCRegulatory Affairs AssociateChandler, AZABOUT THE COMPANY: ANS provides industry-leading nutritional solutions to promote health and wellbeing, enabled by a world class team dedicated to service, excellence, quality, and innovation. Maintain and monitor spreadsheets used to track certification program compliance for raw material and finished product certifications.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaAZ$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.