NewQuality Assurance/Regulatory Affairs Manager TEMPO Employment ServicesQuality Assurance/Regulatory Affairs ManagerMaineDevelop, implement, and maintain the quality management system to align with the organization’s strategic direction and ensure devices and products comply with customer, quality, regulatory, and statutory requirements. Proven ability to manage complex quality management systems, including ISO 9001, EN ISO 13485, 21 CFR 820, MDD, MDR, MHLW, and KFDA.
NewSenior R&D Manager - New Product Development & Regulatory Licensing IDEXX LaboratoriesSenior R&D Manager - New Product Development & Regulatory LicensingWestbrook, MEYou will educate internal stakeholders - including R&D partners, business leaders, and senior leadership - on regulatory requirements, project risks, timelines, and scope to enable informed decision-making and prioritization, translating complex regulatory frameworks and product attributes into clear, actionable insights for both technical and executive audiences. In this role as Senior R&D Manager - New Product Development & Regulatory Licensing, you will lead a team of talented scientists through the development and regulatory licensing of newly developed diagnostic products, partnering closely with Regulatory Affairs to bring those products to market in the US and around the world.
Government Affairs Manager - Water - North America Idexx Laboratories IncGovernment Affairs Manager - Water - North AmericaMEAn innovation leader in every industry we serve since 1983, our team members help pet owners worldwide keep their companion animals healthy and happy, ensure safe drinking water for billions, and help farmers protect livestock and poultry from disease. A dynamic and exciting career that utilizes your veterinary practice experience and technical skills, allows you to travel, meet new people, expand your knowledge and skill set, all while positively impacting the lives of pets and their owners.
NewProject Manager - Healthmark QMS, Defined Term (Remote in EST) Getinge ABProject Manager - Healthmark QMS, Defined Term (Remote in EST)Augusta, MERemote$120,160–$150,000 / yearRequired Knowledge, Skills and Abilities: Expert-level working knowledge of FDA 21 CFR Part 820 / Quality Management System Regulation (QMSR), including its incorporation of ISO 13485:2016 effective February 2026. The project manager will serve as the primary driver of project(s) execution across a group of QMS workstreams, coordinating cross-functional teams and ensuring delivery against defined milestones.
Regulatory Specialist HealthfirstRegulatory SpecialistME$68,900–$99,620 / yearCompliance is promoted ensuring regulatory updates are evaluated, implemented and by performing monitoring to evaluate compliance with regulatory requirements required by, Centers for Medicare and Medicaid Services (CMS) and State Department of Health (DOH) regulations, and business requirements. Relevant previous work experience and knowledge of Department of Health (DOH) and Local Department of Social Services and Center for Medicare & Medicaid Services (CMS) regulations pertaining to managed care; etc.
Environmental Analyst Casella Waste Systems IncEnvironmental AnalystMEli>Collaborates with facility management to maintain local, state, and federal permits for assigned facilities by identifying permitting needs, anticipating permit renewals, preparing, and submitting applications within an appropriate time frame, and managing electronic and hard copy filing of documents. Participates in frequent field site visits, completes data collection, analyzes findings, and interprets findings by producing technical reports, tabulating data, and preparing charts, graphs, and sketches in support of facility engineering and compliance projects.
Environmental Analyst Willimantic Waste Paper Co., Inc.Environmental AnalystMECollaborates with facility management to maintain local, state, and federal permits for assigned facilities by identifying permitting needs, anticipating permit renewals, preparing, and submitting applications within an appropriate time frame, and managing electronic and hard copy filing of documents. Participates in frequent field site visits, completes data collection, analyzes findings, and interprets findings by producing technical reports, tabulating data, and preparing charts, graphs, and sketches in support of facility engineering and compliance projects.
Quality Assurance Specialist Maine Molecular Quality Controls IncQuality Assurance SpecialistSaco, MEMMQCI has developed technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products. markets unique quality control products used by hospital laboratories to monitor the accuracy of tests for inherited disease, pharmacogenetics, oncology, and infectious diseases.
Quality Assurance Specialist MMQCIQuality Assurance SpecialistSaco, MEFull timeMaine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and sells unique quality control products used by hospital laboratories and manufacturers to monitor the accuracy of tests for genetic, oncologic, and infectious diseases. MMQCI has proprietary technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products.
NewQuality Assurance Specialist MmqciQuality Assurance SpecialistSaco, MaineMaine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and sells unique quality control products used by hospital laboratories and manufacturers to monitor the accuracy of tests for genetic, oncologic, and infectious diseases. MMQCI has proprietary technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products.