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Marousi, Attica, Greece permanent
Regulatory AnalysisPolicy AssessmentRegulatory Strategy DevelopmentRisk ManagementRegulatory ReportingIndustry EngagementRegulatory DocumentationFinancial LicensingExcelPublic Consultation Coordination

One Group | One Energy We are Enerwave, member of HELLENiQ ENERGY and a leader in providing outstanding and innovative energy solutions. We operate with passion, being engaged in heart and mind to wh...

March 4, 2026 View Details
Tokyo, Tokyo, Japan permanent
Regulatory FamiliarityRegulatory WritingProduct KnowledgeEnglish ProficiencyCommunication SkillsLogical ThinkingProblem SolvingNegotiation SkillsAI AwarenessScientific Knowledge

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation...

March 4, 2026 View Details
Greater Noida, UP, India Hybrid permanent
Regulatory AffairsAdministrativeElectronic SubmissionsCustomer ServiceCRM SystemsEnglish ProficiencyRegulatory KnowledgeTechnical SkillsTeamworkDMFs

At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the...

March 3, 2026 View Details
Sunnyvale, CA, United States Hybrid permanent
Regulatory AffairsGlobal ComplianceStrategic PlanningProject LeadershipTechnical DocumentationLead-Time NegotiationsRegulatory StrategyRegulatory FamiliarityRegulatory TrainingQA Metrics

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in r...

March 3, 2026 View Details
Birmingham, AL permanent
Corporate GovernanceRegulatory AffairsMeeting ManagementLegal Research1099 FilingsCommunicationOrganizationTime ManagementMicrosoft OfficeDiligent Board Portal

The work we do has an impact on millions of lives, and you can be a part of it. We help protect our customers against life’s uncertainties. Regardless of where you work within the company, you’ll be h...

March 2, 2026 View Details
Crawley, West Sussex permanent
Regulatory AffairsQuality Management SystemISO 13485FDA QSRMDSAPContinuous ImprovementProduct DevelopmentInternal AuditsSupplier ManagementRegulatory EngagementQuality PrinciplesProduct Documentation

Position title: Senior Director of Regulatory Affairs Reports to: CEO   Position summary: The Head of QA/RA is responsible for the quality and regulatory activities of the organization, including ...

March 3, 2026 View Details
Lima, Peru (Argentina) Hybrid permanent
Regulatory AffairsComplianceGovernment RelationsPolicy DevelopmentCommunicationLeadershipStakeholder ManagementRisk AssessmentPublic Affairs Strategy

We are Kaizen Gaming Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 20 markets. We always aim to leverage cutting-edge technology, provid...

March 3, 2026 View Details
Santiago, Chile (Argentina) Hybrid permanent
Regulatory AffairsPublic AffairsGovernment RelationsPolicy DevelopmentCommunicationLeadershipRisk AssessmentStakeholder ManagementComplianceGovernment Affairs

We are Kaizen Gaming Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 20 markets. We always aim to leverage cutting-edge technology, provid...

March 3, 2026 View Details
Estonia Remote part_time
Regulatory AffairsComplianceHealth ProductsMedical DevicesCompetent Authority InteractionRegulatory StrategyRegulatory DocumentationTranslationBiotechnologyFood Supplements

Freelance opportunity in Estonia! Join our global team as a Local Regulatory Affairs Manager in Estonia. Local Regulatory Affairs Manager will be responsible for ensuring that medicinal and other pro...

March 3, 2026 View Details
Beijing, Beijing, China Hybrid permanent
Regulatory AffairsTechnical ReviewRegulatory ComplianceRegulatory KnowledgeRegulatory CommunicationRegulatory ExamsRegulatory Strategy DevelopmentDrug KnowledgeEnglish ProficiencyComputer Operations

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a ...

March 2, 2026 View Details
Minato City, Tokyo, Japan Hybrid permanent
LeadershipTeam ManagementOrganizational SkillsCommunicationJapanese ProficiencyEnglish Proficiency

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable imp...

March 2, 2026 View Details
North Chicago, IL, United States permanent
Financial PlanningBudget ManagementFinancial AnalysisRegulatory ComplianceGAAPFinancial ReportingProject ManagementTeam LeadershipProcess Improvement

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable imp...

March 2, 2026 View Details
North Chicago, IL, United States Hybrid permanent
Regulatory KnowledgeTeam LeadershipRegulatory ComplianceData AssessmentStrategic PlanningChange ManagementSafety TechniquesRegulatory StrategyTrainingDocumentation

About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a ...

March 2, 2026 View Details
Beijing Yizhuang permanent
Regulatory StrategyLifecycle ManagementRegulatory CoordinationRelationship BuildingRegulatory ExamsProject ManagementEnglish ProficiencyComputer SkillsEthics and Good Practices

Typical Accountabilities • Implement regulatory strategies to achieve in-time and high quality approval and facilitate full speed launch. • Maintain product licenses through timely lifecycle manageme...

March 3, 2026 View Details
Tokyo, Tokyo, Japan Hybrid permanent
Japanese LanguageEnglish CommunicationMedical Device KnowledgeRegulatory AffairsRegulatory StrategyProduct KnowledgeTechnical WritingProject ManagementCommunication SkillsProblem Solving

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation...

March 3, 2026 View Details
Boston, MA (Boston) Hybrid permanent
Regulatory StrategyRegulatory GuidanceCross-functional CollaborationRegulatory Document PreparationRegulatory CommunicationRegulatory Risk ManagementHealth AuthoritiesLifecycle Management

About Formation Bio Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more candidat...

March 2, 2026 View Details
Istanbul permanent
Regulatory ComplianceLifecycle ManagementCMC-related QueriesCard AuthorizationsManufacturing Process DefinitionChange ControlsProduct RegistrationRenewalsAnnual ReportsPQP ParticipationHealth AuthoritiesVeeva Vault

EM&S Turkey Regulatory Affairs Officer • Location: Istanbul About the job Reporting to the EM&S Middle East Quality Manager, the Regulatory Affairs Officer supports regulatory compliance and lifecy...

March 2, 2026 View Details
Hyderabad, Telangana, India permanent
Regulatory StrategyDocumentation ImprovementProduct Phase ManagementDeficiency LettersCMC-related Queriesproject_documentationRegulatory LiaisonProject ManagementProject SupportCommunication

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Associate to join our team. The job responsibiliti...

February 25, 2026 View Details
Hyderabad, Telangana, India permanent
Regulatory AffairsCreative Approval ProcessVariations and ClaimsLife-Cycle ManagementComplianceCross-Functional CollaborationRisk ManagementRegulatory StrategySterile Products

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate wil...

February 25, 2026 View Details
Hyderabad, Telangana, India permanent
Regulatory StrategyDocumentationDeficiency Lettersproject_documentationRegulatory LiaisonProject ManagementTime ManagementCommunicationCMC-related Queries

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Associate to join our team. The job responsibilities for ...

February 25, 2026 View Details
Athens, Attica, Greece permanent
Regulatory AffairsPharmaceuticalsDocumentationProject ManagementCommunicationCollaborationComplianceRisk ManagementMS OfficeTime Management

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Senior Officer to join our team. This position is based i...

February 2, 2026 View Details
Athens, Attica, Greece permanent
Regulatory StrategyDocumentationCMC DocumentationDeficiency LettersCross-functional Collaborationregulatory_standardsRegulatory ComplianceEnglish FluencyMS Office SkillsOrganizational Skills

DEMO SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, is currently looking for a talented Regulatory Affairs CMC Officer to join our team in Athens (Kryoneri). Thi...

November 11, 2025 View Details
Athens, Attica, Greece permanent
Regulatory StrategyDocumentationCMC DocumentationGMP ComplianceCross-Functional CoordinationTeam Liaisonregulatory_standardsMS Office SkillsICH ComplianceDeficiency Letters

DEMO SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, is currently looking for a talented Regulatory Affairs CMC Senior Officer to join our team in Athens (Kryoner...

October 15, 2025 View Details
Athens, Attica, Greece permanent
Regulatory AffairsDocumentationProject ManagementCommunicationMS OfficeOrganization SkillsTime ManagementCustomer ServiceProblem SolvingCompliance

Main duties and responsibilities: • Understanding of Regulatory strategy and documentation requirements • Act as responsible Regulatory Team member for assigned regulatory projects • Prepare regulato...

February 11, 2026 View Details
Boston, Massachusetts, United States Hybrid permanent
Regulatory AffairsU.S. Regulatory SubmissionsCDx DevelopmentBiomedical DevicesPMAGlobal Regulatory RequirementsIVDQ-SubsHealth Authorities

Do you bring a background in Regulatory Affairs, and a passion for driving innovative solutions? Have you contributed to FDA or global regulatory submissions for complex CDx, IVDs or software-based me...

February 2, 2026 View Details
Egypt permanent
Regulatory StrategyOpportunity ShapingIndustry RepresentationInternational Model ApplicationCross-Functional LeadershipRisk ManagementComplianceStakeholder EngagementCapability BuildingExternal Influence

Job Title: Regulatory Affairs Director Introduction to role: Are you ready to shape regulatory strategy and policy to speed access to life-changing medicines? This role puts you at the heart of how ...

March 2, 2026 View Details
Mounds View, Minnesota, United States of America permanent
Regulatory Affairsregulatory_standardsProduct Lifecycle ManagementUS FDA guidelinesClinical Evaluation ReportsU.S. Regulatory SubmissionsQSR ComplianceEU Medical Device RegulationDevice History FilePost-Market Clinical Follow Up

We anticipate the application window for this opening will close on - 7 May 2026   Position Description:        Sr. Regulatory Affairs Specialist for Medtronic, Inc. located in Mounds View, MN. Resp...

March 2, 2026 View Details
Singapore, Singapore, Singapore permanent
Regulatory AffairsProduct RegistrationMedical RegulationsRegulatory AgenciesRegulatory CommunicationProduct TestingClinical RegistersData CollectionTechnology ProjectsCollaborationQuality ManagementISO13485

Job Responsibilities • Product registration: including preparation of registration dossier, design of performance evaluation study and manage execution and communication with CRO (clinical research o...

March 2, 2026 View Details
Hyderabad, Telangana, India permanent
Regulatory AffairsPre-ApprovalRegulatory StrategyGap AnalysisRisk IdentificationCross-Functional CollaborationRegulatory ComplianceProject ManagementChange Proposal Evaluation

At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs Post-Approval Manager to join our team. The candidate wil...

February 25, 2026 View Details
Poland - Warsaw permanent
Project ManagementTime ManagementQuick LearningCultural AwarenessIndependent WorkTeam Collaboration

Turn your curiosity into impact. Join AstraZeneca for a 3 – month hybrid internship starting in July and work with teams pushing the boundaries of science. About the program The Working in Science In...

February 28, 2026 View Details
San Diego, California, United States permanent
Regulatory AffairsFDA RegulationsHardware Product ComplianceISO StandardsRegulatory GuidanceCross-functional CollaborationRegulation UnderstandingProject ManagementDetail-Oriented

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of user...

May 8, 2025 View Details
Alpharetta, Georgia, United States permanent
Regulatory AffairsFDA ComplianceISO StandardsProduct DocumentationAnalytical Testing SalesConformity AssessmentCross-functional CollaborationProject Management

About Us CorDx, a multi-national biotech organization, focused on pushing the limits of innovation and supply in global health. With over 2000 employees across the world serving millions of users in ...

November 18, 2025 View Details
Atlanta, Georgia, United States permanent
Regulatory AffairsFDA ComplianceMedical Device RegulationsISO 13485Product DevelopmentRegulatory DocumentationRegulatory SubmissionsRegulatory MeetingsCross-Functional CollaborationProject Management

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of user...

May 12, 2025 View Details
San Diego, California, United States permanent
Regulatory AffairsFDA ComplianceISO 13485Product DocumentationRegulatory SubmissionRegulatory SupportRegulatory AssessmentChange ManagementRegulatory MeetingsProject Management

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of user...

July 20, 2025 View Details
San Diego, California, United States permanent
Regulatory AffairsDocumentationFDA ComplianceProduct DevelopmentProject ManagementCross-functional CollaborationRegulatory AuditsRegulatory AnalysisRegulatory FilingMicrosoft Office

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of user...

July 20, 2025 View Details
Zürich, Zurich, Switzerland Hybrid permanent
LeadershipRegulatory AffairsLegal StrategyCross-Border ComplianceTeam LeadershipFinancial ServicesRisk ManagementStrategic PlanningClient RelationsIndustry Trends

About Crypto Finance Crypto Finance Group, part of Deutsche Börse Group, provides professional digital asset solutions to institutional clients. The Group comprises Crypto Finance AG, regulated by FI...

February 27, 2026 View Details
Chicago, IL, United States Remote permanent
Regulatory AffairsStrategic PlanningClient CollaborationRegulatory StrategyProduct KnowledgeRisk ManagementRegulatory AuthorisationSubmissionRegulatory ReviewInclusive Culture

At EVERSANA, we are proud to be certified as a Great Place to Work across the globe. We’re fueled by our vision to create a healthier world. How? Our global team of more than 7,000 employees is commit...

February 27, 2026 View Details
Sunnyvale, , United States permanent
Regulatory KnowledgeDocumentationFDAEMACollaborationComplianceTrainingRegulatory IntelligenceSales Cycle SupportSubmission

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in r...

February 27, 2026 View Details
North Chicago, IL, United States Hybrid permanent
Data AnalysisBusiness Process ManagementRisk ManagementData VisualizationProject ManagementCross-functional CollaborationProcess OptimizationRegulatory ComplianceCommunication SkillsCustomer Focus

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable imp...

February 27, 2026 View Details
Boston, Massachusetts Hybrid permanent
Regulatory Strategy DevelopmentRegulatory ImplementationFDA LiaisonRegulatory ReportingRisk ManagementCross-functional CollaborationRegulatory ResearchRegulatoryKnowledgeRegulatory MeetingsRegulatory Precedents

Company Profile:   At Verastem Oncology, we're advancing innovation and addressing the urgent needs of patients living with cancers driven by RAS/MAPK pathway mutations, a key driver of tumor growt...

February 27, 2026 View Details
Giza, El Omraniya, Egypt Hybrid permanent
Regulatory AffairsEU Regulatory FrameworksProduct LabelingCommunication SkillsProject ManagementHealthcare Industry

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are com...

July 23, 2025 View Details
Giza, El Omraniya, Egypt permanent
Regulatory ComplianceProduct RegistrationCompliance MonitoringCross-Functional CollaborationEnglish ProficiencyDetail-oriented

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are com...

February 12, 2026 View Details
Cairo, Al Qāhirah, Egypt permanent
Regulatory ComplianceProduct RegistrationCompliance MonitoringCross-Functional Collaboration

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are com...

July 16, 2025 View Details

Director, Regulatory Affairs Brazil

Ultragenyxpharmaceutical

Sao Paulo City, Brazil (Sao Paulo, Brazil) Hybrid permanent
Regulatory AffairsStrategic PlanningLife Cycle ManagementRegulatory StrategyTeam CollaborationLatin AmericaRegulatory ComplianceBrazilANVISA

Why Join Us? Be a hero for our rare disease patients At Ultragenyx, we fundamentally believe that taking real impactful action to care for the needs of patients and our people is always the right th...

February 27, 2026 View Details
Ljubljana permanent
Regulatory AffairsProject ManagementRisk AssessmentComplianceDocumentation AccuracyAnalytical ThinkingEnglish LanguageCommunication

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief i...

February 27, 2026 View Details
Brampton, Ontario, Canada Hybrid permanent
Regulatory ComplianceRegulatory AffairsRegulatoryKnowledgeProduct ModernizationStrategic PlanningRegulatory MeetingsCompliance MonitoringProduct ApprovalGTS Blocks ManagementRACs Handling

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation...

February 27, 2026 View Details
Petaling Jaya, Selangor permanent
Regulatory AffairsRegulatory StrategyRegulatory Risk ManagementRegulatory ComplianceRegulatory DocumentationRegulatory ReportingRegulatory IntelligenceProject ManagementRegulatory CoordinationRegulatoryKnowledge

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief i...

February 27, 2026 View Details
Reading permanent
Regulatory AffairsProduct RegistrationsRegulatory Project ManagementProject ManagementStrategic InputData QualityRegulatory ProceduresTherapeutic KnowledgeCross-functional CollaborationCustomer Service

Regulatory Affairs Officer • Location: Reading • Hybrid work: 3 days based onsite in Reading About the job As a Regulatory Affairs Officer you will obtain, manage and maintain product Marketing Aut...

February 27, 2026 View Details
Beijing Yizhuang permanent
Regulatory AffairsChina Market ComplianceProject ManagementTeam LeadershipCommunicationRisk AssessmentStakeholder ManagementCollaborationComplianceProblem Solving

RA Associate Director is responsible for managing multiple brands/compounds, to obtain regulatory approval to support various development, manufacturing, sales and marketing activities for the designa...

February 27, 2026 View Details
Peachtree Corners, GA, United States permanent
Regulatory ComplianceMandarin ChineseProject ManagementRegulatory FilingProduct LocalizationRegulatory StrategyRegulatory Strategy DevelopmentRegulatoryKnowledgeRegulatory Project ManagementCross-functional CollaborationRegulatory Audit Support

Primary Function of Position This position will partner with the in-country RA team as well as the Product Localization Engineering (PLE) and other cross-functional supporting teams, make sure the co...

February 26, 2026 View Details