{"schemaVersion":"jobsearcher.job.v1","id":"89f2f694dead64cf08aa2ae3","url":"https://jobsearcher.com/jobs/89f2f694dead64cf08aa2ae3","canonicalUrl":"https://jobsearcher.com/jobs/89f2f694dead64cf08aa2ae3","title":"Compliance Manager","description":"SCR Compliance Engineer (Safety, Compliance & Regulatory Engineer)\r\nJob Summary\r\nThe Compliance Engineer is responsible for ensuring that Oral Healthcare products comply with applicable global regulatory, safety, environmental, chemical, packaging, labeling, and market-access requirements throughout the product lifecycle. The role serves as the primary compliance representative within cross-functional product development teams and is responsible for identifying compliance risks, implementing regulatory requirements, supporting certification activities, and ensuring products can be legally marketed in intended countries\r\nKey Responsibilities\r\nProduct Compliance & Regulatory Strategy\r\nRepresent the Safety, Compliance & Regulatory (SCR) function within product development teams.\r\nTranslate regulatory and standards requirements into product requirements and design inputs.\r\nEnsure compliance with applicable international, regional, and country-specific regulations and standards.\r\nEvaluate regulatory implications of design changes, material changes, labeling changes, packaging changes, and software updates.\r\nIdentify and communicate regulatory and compliance risks throughout development and sustaining activities\r\nStandards & Requirements Management\r\nMaintain awareness of evolving regulations, standards, and industry guidance.\r\nAssess impact of new or revised standards on existing and developing products.\r\nSupport creation and maintenance of\r\nStandards & Compliance Plans (SCPs)\r\nCompliance assessments\r\nMarket-access evaluations\r\nDrive implementation of new regulatory requirements into development processes\r\nProduct Safety & Certification\r\nCoordinate safety and compliance testing activities.\r\nReview and approve test plans and test reports.\r\nSupport certification activities with external laboratories, certification bodies, and approval agencies.\r\nMaintain technical files and compliance evidence supporting regulatory submissions and certifications.\r\nServe as primary contact for country approval and approbation activities where required.\r\nLabeling, Packaging & Environmental Compliance\r\nReview product labeling, packaging, user documentation, and marketing claims for compliance.\r\nEnsure compliance with applicable requirements such as\r\nElectrical Safety\r\nEMC\r\nChemical compliance (RoHS, REACH, POPs, Prop 65, etc.)\r\nBattery regulations\r\nPackaging regulations (including EU PPWR)\r\nEnvironmental sustainability requirements\r\nCountry-specific labeling requirements\r\nApprove regulatory aspects of engineering change orders and product releases.\r\nRisk Management & Issue Resolution\r\nInvestigate safety and compliance issues.\r\nPerform root cause analysis using structured methodologies (e.g., 8D).\r\nSupport corrective and preventive actions.\r\nAssess potential impact of field issues, customer complaints, standards changes, and regulatory findings.\r\nAudits & Quality System Support\r\nSupport internal audits, external audits, regulatory inspections, and certification reviews.\r\nEnsure compliance activities are performed in accordance with Quality Management System requirements.\r\nSupport maintenance of compliance records and technical documentation.\r\nSupport departmental metrics and continuous improvement initiatives.\r\nCross-Functional Collaboration\r\nPartner with\r\nRegulatory Affairs\r\nR&D\r\nSystems Engineering\r\nQuality\r\nManufacturing\r\nProcurement\r\nMarketing\r\nSupply Chain\r\nSustainability teams\r\nProvide regulatory and compliance guidance to project teams and leadership.\r\nSupport project gate reviews and product release decisions.\r\nRequired Qualifications\r\nEducation\r\n* Bachelor's degree in Engineering, Regulatory Affairs, Quality Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or related scientific discipline.\r\nExperience\r\n3–7+ years of experience in product compliance, regulatory affairs, quality, safety engineering, certification, or related fields.\r\nExperience working within regulated product environments.\r\nExperience supporting product development projects from concept through commercialization.\r\nTechnical Knowledge\r\nKnowledge of one or more of\r\nIEC/EN/UL standards\r\nElectrical Safety\r\nEMC\r\nRisk Management\r\nProduct Labeling\r\nChemical Compliance\r\nEnvironmental Compliance\r\nMarket Access Requirements\r\nQuality Management Systems\r\nRegulatory Submission Processes\r\nCertification and Approval Processes\r\nPreferred Qualifications\r\nExperience with Philips Personal Health products.\r\nKnowledge of Oral Healthcare products including power toothbrushes and oral irrigators.\r\nExperience with\r\nSCP development\r\nRMM management\r\nMarket access assessments\r\nSustainability regulations\r\nGlobal packaging and labeling regulations\r\nRegulatory intelligence programs\r\nHow We Work Together\r\nWe believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company's facilities. Field roles are most effectively done outside of the company's main facilities, generally at the customers' or suppliers' locations.\r\nFor this project, you'll be contracted via a Randstad company as a temporary worker/contractor and placed at Philips.\r\nThe hourly pay range for this role is $55.00-60.00\r\nAs a contractor, you'll enjoy cutting-edge challenges and unexpected experiences that make you a more in-demand professional.\r\nEqual Opportunity Employer\r\nRandstad is an equal opportunities employer and does not discriminate against Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.\r\nAt Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact kari.carapella@randstadsourceright.com\r\nJ-18808-Ljbffr","company":"Socket","rawCompany":"socket","city":"Bothell","state":"WA","isRemote":false,"isActive":false,"createdAt":"2026-08-14T01:32:57.569Z","occupations":[{"code":"11-9199.01","title":"Regulatory Affairs Managers","slug":"regulatory-affairs-managers"},{"code":"11-9199.02","title":"Compliance Managers","slug":"compliance-managers"},{"code":"13-1041.07","title":"Regulatory Affairs Specialists","slug":"regulatory-affairs-specialists"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Compliance Manager","description":"SCR Compliance Engineer (Safety, Compliance & Regulatory Engineer)\r\nJob Summary\r\nThe Compliance Engineer is responsible for ensuring that Oral Healthcare products comply with applicable global regulatory, safety, environmental, chemical, packaging, labeling, and market-access requirements throughout the product lifecycle. The role serves as the primary compliance representative within cross-functional product development teams and is responsible for identifying compliance risks, implementing regulatory requirements, supporting certification activities, and ensuring products can be legally marketed in intended countries\r\nKey Responsibilities\r\nProduct Compliance & Regulatory Strategy\r\nRepresent the Safety, Compliance & Regulatory (SCR) function within product development teams.\r\nTranslate regulatory and standards requirements into product requirements and design inputs.\r\nEnsure compliance with applicable international, regional, and country-specific regulations and standards.\r\nEvaluate regulatory implications of design changes, material changes, labeling changes, packaging changes, and software updates.\r\nIdentify and communicate regulatory and compliance risks throughout development and sustaining activities\r\nStandards & Requirements Management\r\nMaintain awareness of evolving regulations, standards, and industry guidance.\r\nAssess impact of new or revised standards on existing and developing products.\r\nSupport creation and maintenance of\r\nStandards & Compliance Plans (SCPs)\r\nCompliance assessments\r\nMarket-access evaluations\r\nDrive implementation of new regulatory requirements into development processes\r\nProduct Safety & Certification\r\nCoordinate safety and compliance testing activities.\r\nReview and approve test plans and test reports.\r\nSupport certification activities with external laboratories, certification bodies, and approval agencies.\r\nMaintain technical files and compliance evidence supporting regulatory submissions and certifications.\r\nServe as primary contact for country approval and approbation activities where required.\r\nLabeling, Packaging & Environmental Compliance\r\nReview product labeling, packaging, user documentation, and marketing claims for compliance.\r\nEnsure compliance with applicable requirements such as\r\nElectrical Safety\r\nEMC\r\nChemical compliance (RoHS, REACH, POPs, Prop 65, etc.)\r\nBattery regulations\r\nPackaging regulations (including EU PPWR)\r\nEnvironmental sustainability requirements\r\nCountry-specific labeling requirements\r\nApprove regulatory aspects of engineering change orders and product releases.\r\nRisk Management & Issue Resolution\r\nInvestigate safety and compliance issues.\r\nPerform root cause analysis using structured methodologies (e.g., 8D).\r\nSupport corrective and preventive actions.\r\nAssess potential impact of field issues, customer complaints, standards changes, and regulatory findings.\r\nAudits & Quality System Support\r\nSupport internal audits, external audits, regulatory inspections, and certification reviews.\r\nEnsure compliance activities are performed in accordance with Quality Management System requirements.\r\nSupport maintenance of compliance records and technical documentation.\r\nSupport departmental metrics and continuous improvement initiatives.\r\nCross-Functional Collaboration\r\nPartner with\r\nRegulatory Affairs\r\nR&D\r\nSystems Engineering\r\nQuality\r\nManufacturing\r\nProcurement\r\nMarketing\r\nSupply Chain\r\nSustainability teams\r\nProvide regulatory and compliance guidance to project teams and leadership.\r\nSupport project gate reviews and product release decisions.\r\nRequired Qualifications\r\nEducation\r\n* Bachelor's degree in Engineering, Regulatory Affairs, Quality Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or related scientific discipline.\r\nExperience\r\n3–7+ years of experience in product compliance, regulatory affairs, quality, safety engineering, certification, or related fields.\r\nExperience working within regulated product environments.\r\nExperience supporting product development projects from concept through commercialization.\r\nTechnical Knowledge\r\nKnowledge of one or more of\r\nIEC/EN/UL standards\r\nElectrical Safety\r\nEMC\r\nRisk Management\r\nProduct Labeling\r\nChemical Compliance\r\nEnvironmental Compliance\r\nMarket Access Requirements\r\nQuality Management Systems\r\nRegulatory Submission Processes\r\nCertification and Approval Processes\r\nPreferred Qualifications\r\nExperience with Philips Personal Health products.\r\nKnowledge of Oral Healthcare products including power toothbrushes and oral irrigators.\r\nExperience with\r\nSCP development\r\nRMM management\r\nMarket access assessments\r\nSustainability regulations\r\nGlobal packaging and labeling regulations\r\nRegulatory intelligence programs\r\nHow We Work Together\r\nWe believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company's facilities. Field roles are most effectively done outside of the company's main facilities, generally at the customers' or suppliers' locations.\r\nFor this project, you'll be contracted via a Randstad company as a temporary worker/contractor and placed at Philips.\r\nThe hourly pay range for this role is $55.00-60.00\r\nAs a contractor, you'll enjoy cutting-edge challenges and unexpected experiences that make you a more in-demand professional.\r\nEqual Opportunity Employer\r\nRandstad is an equal opportunities employer and does not discriminate against Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.\r\nAt Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact kari.carapella@randstadsourceright.com\r\nJ-18808-Ljbffr","datePosted":"2026-08-14T01:32:57.569Z","dateModified":"2026-08-14T01:32:57.569Z","hiringOrganization":{"@type":"Organization","name":"Socket","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bothell","addressRegion":"WA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"89f2f694dead64cf08aa2ae3"},"url":"https://jobsearcher.com/jobs/89f2f694dead64cf08aa2ae3"}}