Regulatory Affairs Manager

Role: Regulatory Affairs ManagerLocation: St. Paul, MN - 55117Duration: 6+ Months Shift Timings: 8 AM to 5 PMKey Responsibilities: Leadership & Regulatory Expertise:Lead and manage regulatory submissions for Class III medical devices (IDE, PMA, CE Mark, and clinical trial applications).Develop and execute regulatory strategies to ensure timely approvals in...

Regulatory Affairs ManagerSt. Paul MN6 MonthsRegulatory Affairs Project Manager (Individual Contributor Role)This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. Applies advanced regulatory expertise to guide cross-functional partners and demonstrates strategic thinking and creativity in...

Job Title: Regulatory Affairs ManagerSite/Location: St. Paul, MN 55117 (100% Onsite)Duration: 6 Months Contract on W2 from your start dateShift Time: 08:00 AM - 5:00 PM (Flexible)Pay Rate: $47.00/hr. on W2. Job DescriptionThis position leads project submissions for regulatory approvals and acts independently to identify and resolve problems.Applies advanced...

Title: Regulatory Affairs Project ManagerDuration: 06 monthsLocation: St. Paul, MN 55117 Description:This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. Applies advanced regulatory expertise to guide cross-functional partners and demonstrates strategic thinking and creativity in support of...

Role: Regulatory Affairs ManagerLocation: St. Paul, MNDuration: 06 MonthsShift Timings: 08:00 AM to 05:00 PM Description:Exempt Years’ Experience: 9+ YearsSkills:Demonstrates effective change leadership.Builds strategic partnerships to further departmental and organizational objectives.Develops and executes organizational and operational policies that...

Job DescriptionDetailed Summary:We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will be responsible for performing assigned regulatory activities, including submissions/responses to country authorities.In this role, you will plan and prepare documents for EU MDR...

Job SummaryThis role involves leading project submissions for regulatory approvals and acting independently to identify and resolve problems. The ideal candidate will have advanced regulatory expertise, strategic thinking, and creativity in support of programs.Key ResponsibilitiesLead project submissions for regulatory approvalsApply advanced regulatory...

Job SummaryWe are seeking a highly experienced Regulatory Affairs Manager to lead project submissions for regulatory approvals and drive strategic thinking in support of programs. This role will be responsible for applying advanced regulatory expertise, guiding cross-functional partners, and developing regulatory strategies.About the Role:Leverage extensive...

Beacon Hill Staffing Group, LLC - Director of Regulatory Affairs - Strategy Summary of Position The Director of Regulatory Affairs is responsible for Nuclear Medicine Regulatory Affairs dossiers and associated regulatory affairs activities in the US. Responsibilities include defining and/or authoring compliant content for new and existing dossiers,...

Job SummaryVolt is hiring a Hybrid Regulatory Affairs Coordinator in Maplewood, MN. This role involves investigating and maintaining regulatory product certification claims data, databases, and documentation systems. The ideal candidate will have a technical background and experience in quality assurance.The position requires ensuring accurate data entries,...

Job DescriptionJob DescriptionJob Title: Regulatory Affairs SpecialistLocation: St. Paul, MN 55117Job Type:  100% OnsiteDuration: 6 Months Contract This position leads project submissions for regulatory approvals and acts independently to identify and resolve problems. Applies advanced regulatory expertise to guide cross-functional partners and demonstrates...

**Role Description**The Regulatory Affairs Officer will play a key role in ensuring the health and safety of Minnesota citizens by investigating complaints against licensees and registrants. As a member of the Board of Cosmetologist Examiners, you will be responsible for conducting investigations, collecting evidence, and preparing written reports.**Key...

(Contractor) Regulatory Affairs SpecialistDate: Nov 12, 2024Location: St. Louis, MO, United States About Curium Curium is the world's largest nuclear medicine company with more than a century of industry experience. We develop, manufacture and distribute world-class radiopharmaceutical products to help patients around the globe. Our proven heritage...

Job DescriptionJob Description·         Perform assigned regulatory activities including submissions/responses to country authorities. Daily Responsibilities - Job Description suppliers should use:·         Plan and prepare documents for EU MDR Technical File original submissions or responses to Notified Body for existing Technical Files...

Sumitomo Pharma Director, Regulatory Affairs Saint Paul, Minnesota Apply Now Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology,...

Randstad has an immediate opportunity for a Regulatory Affairs Specialist to work with a global leader in agricultural research. This is a hybrid position located in St. Louis, MO. Local candidates are preferred as relocation cost reimbursement is not available for this postion.What you will do:Manage the state regulatory activities necessary to obtain and...

About Abbott LaboratoriesAbbott Laboratories is a global leader in healthcare, dedicated to improving lives through innovative medical technologies and treatments.Job OverviewWe are seeking a highly skilled Regulatory Operations Specialist I to join our team in St. Paul, MN. As a key member of our Regulatory Affairs department, you will play a critical role...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Collabera. In this role, you will be responsible for performing regulatory activities including submissions/responses to country authorities.

Transforming Global Regulatory StrategySUMITOMO PHARMA America, a global pharmaceutical leader, is seeking an accomplished Director of Regulatory Affairs to spearhead our advanced therapeutic solutions in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With a diverse pipeline of early- to late-stage...

Job Summary">This role involves providing quality and regulatory affairs services, including Drug Master File (DMF) Updates, Health Authority GMP requests, processing customer product complaints; preparing annual product reviews, tracking and trending, and follow-up of Change Control and CAPA programs.">Key Responsibilities:">">Preparation and submission of...