Senior Principal Regulatory Affairs Specialist Balt GroupSenior Principal Regulatory Affairs SpecialistIrvine, CaliforniaPrincipal Regulatory Affairs Specialist is a seasoned expert, responsible for completing and maintaining regulatory approvals/clearances for new and modified medical devices, license renewals, and annual registrations. Serves as a Regulatory representative on specific multi-discipline teams, responsible for organizing and leading meetings and acts independently to identify and resolve problems that may be complex in nature.
Associate Principal Scientist, Innovation - Scientific Affairs Liquid I.V.Associate Principal Scientist, Innovation - Scientific AffairsEl Segundo, CaliforniaWe know that the happiest and highest performing teams include people with diverse perspectives that encourage new ways of solving problems, so we strive to attract and develop talent from all backgrounds and create workplaces where everyone feels seen, heard, and empowered to bring their full, authentic selves to work. Our team members enjoy a flexible and inclusive working environment, a highly collaborative and innovation-forward culture, generous benefits and perks that empower employees to champion their wellbeing every day, as well as an infinite supply of Liquid I.V. for extraordinary hydration.
Senior Director, Rates & Regulatory Affairs Liberty UtilitiesSenior Director, Rates & Regulatory AffairsDowney, CAThe position has direct reporting relationships with the regional regulatory Directors and managers and as such is expected to be the expert on US regulation and all related matters; including being an expert witness representing company interests in each regulatory jurisdiction. At Algonquin, our vision is to be the most trusted utility service provider in North America - a premium regulated utility, known for our customer focus, commitment to sustainability, and strong community partnerships.
Medical Affairs LancesoftMedical AffairsSanta Monica, CA$30–$36.72 / hourThe individual contributes to the operational execution of treatment-use and clinical support activities by coordinating study- and program-related deliverables, managing vendors and external partners, supporting site and investigator communications, tracking key milestones and risks, and helping ensure activities are conducted in alignment with applicable regulations, internal procedures, and program requirements.\. May assist in the review of study-related and essential start-up documents, as delegated by the study manager, including clinical protocols, informed consent forms, investigator brochures, pharmacy manuals, monitoring plans, case report forms, CRF completion guidelines, and other relevant study plans and charters.
Associate Principal Scientist, Innovation - Scientific Affairs Liquid IVAssociate Principal Scientist, Innovation - Scientific AffairsEl Segundo, CA$116,100–$174,100 / yearWe know that the happiest and highest performing teams include people with diverse perspectives that encourage new ways of solving problems, so we strive to attract and develop talent from all backgrounds and create workplaces where everyone feels seen, heard, and empowered to bring their full, authentic selves to work. Functions and duties of this role include, but not limited to: Serve as a Scientific Affairs lead in the innovation engine, partnering with R&D, Regulatory, Brand Innovation, and other cross-functional teams to shape early-stage concepts and sprint work.
Sr Regulatory Affairs Specialist Masimo CorporationSr Regulatory Affairs SpecialistIrvine, CA$85,000–$130,000 / yearSr Regulatory Affairs Specialist is an accomplished regulatory professional with a successful work history with leading regulatory initiatives and partnering with Sales and Marketing teams in obtaining domestic and internal regulatory clearances for Masimo products to meet business objectives. The individual in this position will be capable of providing supported regulatory assessments of medical device regulations to help effective application of regulatory requirements to future products to ensure compliance of the product to pre-market regulatory clearances.
»Regulatory Affairs Allwin Medical Devices Inc»Regulatory AffairsCAEnsures compliance with ISO and Applicable regulatory requirements and Council of European Communities Regulations for medical devices. Coordinates & Conducting awareness of applicable regulatory and quality management requirement throughout the organization.
NewJr. Regulatory Affairs Specialist ConsultNetJr. Regulatory Affairs SpecialistIrvine, CA$30–$31.25 / hourFor over 25 years, we have connected thousands of consultants with meaningful roles through a personal, communication-driven approach, partnering with a diverse client base to build high-performing teams and create lasting impact. Experience in industrial hygiene/safety, government regulations, EU MDR, ISO, MDSAP, operational auditing, work flow analysis, technical writing, and manufacturing operations preferred.
NewSr. Regulatory Affairs Spec FujifilmSr. Regulatory Affairs SpecSanta Ana, California$106,185.25–$120,000 / yearThe Senior Regulator Affairs Specialist will be responsible for providing regulatory support and expertise including but not limited to the following product lines: Cell and Gene Therapy, Bioproduction, recombinant growth factors and Wako Lab Chemicals, Wako endotoxin testing reagents. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world’s biggest health challenges.
Regulatory Affairs Specialist Scale MediaRegulatory Affairs SpecialistBurbank, CARemote$75,000–$85,000 / yearPrepare and present industry updates at recurring team meetings (e.g., a monthly regulatory round-up), keeping cross-functional partners aware of what's happening and why it matters. Comfort with quality or product documentation basics — reviewing specifications or Certificates of Analysis (COAs) and meeting the documentation timelines that gate product release.
Coord 3, Regulatory Affairs Pyramid, IncCoord 3, Regulatory AffairsIrvine, CA$50–$54 / hourFull timeParticipate in providing guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and labeling content. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners.
VP of Quality & Regulatory Affairs Alliance Medical ProductsVP of Quality & Regulatory AffairsIrvine, CaliforniaThe Vice President of Quality Assurance will be responsible for the design, build, and implementation of the strategic framework of the Irvine Quality organization with a focus on driving effective and efficient business results, operational consistency, and cross-functional alignment. Change management –Champion innovation with the design and execution of changes in operating models as the Quality Unit scale up and develop strategies that impact the work of the Quality team.
Regulatory Affairs Specialist II Prolacta BioscienceRegulatory Affairs Specialist IIDuarte, CA$43–$49This position manages assigned deliverables, timelines, records, and documentation packages with focus on accuracy, completeness, traceability, and inspection readiness; identifies routine to moderately complex risks or gaps, supports mitigation activities, participates in assigned health authority interactions, provides practical regulatory support to stakeholders, and escalates complex or high-risk issues to management. A minimum of 3 years of Regulatory Affairs or relevant regulated industry experience, preferably in biologics, biopharmaceutical, pharmaceutical, infant formula, nutrition, medical product, or similarly regulated environment, with exposure to submissions, registrations, product dossiers, renewals, notifications, health authority correspondence, lifecycle management, controlled documentation, or regulatory operations.
Jr. Regulatory Affairs Specialist- 100% onsite ConsultNetJr. Regulatory Affairs Specialist- 100% onsiteIrvine, CA$30–$31.25 / hourFor over 25 years, we have connected thousands of consultants with meaningful roles through a personal, communication-driven approach, partnering with a diverse client base to build high-performing teams and create lasting impact. Experience in industrial hygiene/safety, government regulations, EU MDR, ISO, MDSAP, operational auditing, work flow analysis, technical writing, and manufacturing operations preferred.
VP of Quality & Regulatory Affairs SiegfriedVP of Quality & Regulatory AffairsIrvine, CaliforniaThe Vice President of Quality Assurance will be responsible for the design, build, and implementation of the strategic framework of the Irvine Quality organization with a focus on driving effective and efficient business results, operational consistency, and cross-functional alignment. Change management –Champion innovation with the design and execution of changes in operating models as the Quality Unit scale up and develop strategies that impact the work of the Quality team.
Medical Affairs Operations Rep - HCP Training Roth Staffing CompaniesMedical Affairs Operations Rep - HCP TrainingIrvine, California$28–$30.75 / hourQualifications: * Bachelor's degree in Computer Science, Information Technology, Healthcare Informatics, etc & 2+ years of experience in digital solutions, project management, or a similar role . * Partner with NCD Strategy leadership (SME3) to ensure training and proctor sign-off documentation is processed.
Senior Manager, Diagnostics Public Affairs (Public Relations) AbbottSenior Manager, Diagnostics Public Affairs (Public Relations)Lake Forest, California$129,300–$258,700 / yearThis role will also work in partnership with Public Affairs colleagues in countries outside the U.S. to support the development and execution of external public relations strategies and approaches for key product launches/filings, key clinical and real-world data, product awareness programs/outreach and influencer programs. The Public Affairs senior manager for Abbott's Core Diagnostics has global responsibility for public relations, external communications activities and issues management for key priorities in the business, including Abbott and the Big Ten’s We Give Blood competition.
Government Affairs and Public Policy Manager, Cities ZooxGovernment Affairs and Public Policy Manager, CitiesLos Angeles, CAWork closely with other teams at Zoox, including Legal, Communications, and Safety teams, to ensure up-to-date knowledge of company plans and report on policy/political developments with clear analysis. Anchored on facilitating our expansion to Los Angeles, this exciting new role will build on our positive political reputation and help guide our local operations from testing to commercial deployment.
Government Affairs And Public Policy Manager, Cities ZooxGovernment Affairs And Public Policy Manager, CitiesLos Angeles, CA$130,000–$178,000 / yearWork closely with other teams at Zoox, including Legal, Communications, and Safety teams, to ensure up-to-date knowledge of company plans and report on policy/political developments with clear analysis. Anchored on facilitating our expansion to Los Angeles, this exciting new role will build on our positive political reputation and help guide our local operations from testing to commercial deployment.
Chemical Regulatory & Compliance Engineer Apollo Professional SolutionsChemical Regulatory & Compliance EngineerEl Segundo, CAThis role offers an exciting opportunity to work at the intersection of chemical safety, consumer product compliance, and regulatory affairs, helping ensure products meet evolving safety, environmental, and legal requirements worldwide. Working closely with regulatory, product safety, and cross-functional teams, you will help navigate complex global chemical regulations and contribute to the development of safe, compliant, and trusted consumer products.