HYBRID - Regulatory Affairs Associate

What are we looking for in our HYBRID - Regulatory Affairs Associate? The Scientific Team at Russell Tobin & Associates is supporting a world-class material science organization that has an opening for aHYBRID Regulatory Affairs Associate near St. Paul, MN! Responsibilities Support global regulatory activities Product compliance and certification...

What are we looking for in our HYBRID - Regulatory Affairs Associate? The Scientific Team at Russell Tobin & Associates is supporting a world-class material science organization that has an opening for a HYBRID Regulatory Affairs Associate near St. Paul, MN!   Responsibilities Support global regulatory activities Product compliance and...

What are we looking for in our HYBRID - Regulatory Affairs Associate? The Scientific Team at Russell Tobin & Associates is supporting a world-class material science organization that has an opening for a HYBRID Regulatory Affairs Associate near St. Paul, MN! ResponsibilitiesSupport global regulatory activitiesProduct compliance and...

In our line of work, life isnt a given - its the ultimate goal. When life takes an unexpected turn, our technology and solutions enable caregivers to make informed diagnostic decisions to improve patient care. This is our shared purpose at Radiomet Regulatory Affairs, Associate, Regulatory, Quality Assurance, Manufacturing, Business Services, Support, Radio

Job DescriptionJob DescriptionThe Scientific Team at Russell Tobin & Associates is supporting a world-class material science organization that has an opening for a HYBRID Regulatory Affairs Associate near St. Paul, MN! ResponsibilitiesSupport global regulatory activitiesProduct compliance and certificationAuthoring and updating Safey Data Sheets and other...

Job OverviewJoin the Scientific Team at RTA US, where we are partnering with a prestigious material science organization seeking a Hybrid Regulatory Affairs Specialist.Key ResponsibilitiesAssist in global regulatory initiativesEnsure product compliance and certificationDraft and revise Safety Data Sheets and other regulatory documentationPerform additional...

**CANDIDATES CURRNETLY WORKING UNDER F1 OPT/F1 OPT STEM/H1-B WILL NOT BE CONSIDERED. W2 CANDIDATES ONLY** Associate MDR/Vigilance Specialist (24 month contract // Hybrid in Mounds View, MN): Mon/Tues on site/in-office, Wed-Fri remote Top 3 things the manager is looking for: Medical Device Reporting experience Previous healthcare experience Medical device...

Recruiter: Spencer Gregory Hale Principal Regulatory Affairs Specialist About the role: The Regulatory Associate is responsible for activities which lead, improve and drive efficiencies across regulatory product approval processes. Acts as a primary Regulatory Affairs representative in Material Controls, Supplier Quality and Medical Electrical Equipment...

Regulatory Affairs Specialist Regulatory Affairs St. Joseph, MO, US Pay Rate Low: 30 | Pay Rate High: 35 + Added - 20/08/2024 Apply for Job **Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Regulatory...

Job Title: Senior Specialist, US Regulatory Affairs OperationsLocation: St, Joseph, MO, 64506 /Athens, GA 30601Duration: 6 months assignmentHybrid: 2-3 days onsiteHourly pay range: $30 to $38/hr. on W2Job Description:Independently perform computerized system testing and proactively suggest improvements in systems and processes. Ensure that all submissions...

Senior Specialist Regulatory AffairsHybrid work schedule: required to be in the office 2-3 days per week$35.00 per hourAnywhere between 8 am to 5 pmMonday-Friday as scheduled and aligned with manager.Location can be St. Joseph, MO or Athens, GAJob Description:Independently perform computerized system testing and proactively suggest improvements in systems...

Job Tittle: Senior Specialist, US Regulatory Affairs OperationsDuration: 18 Months (Possible Extension)Location: St. Joseph, MO (Hybrid)Responsibilities:Independently support data maintenance, archival, and retrieval of regulatory documentation in computerized systems.Assist with preparing high-quality US regulatory submissions required by local and federal...

Our client is a global, research-driven pharmaceutical focusing on treatment options for diseases and conditions for which there is no satisfactory treatment option to date. The company is looking for a Regulatory Affairs Specialist to join the team. This is an amazing opportunity to work on cutting edge treatments and make a difference!Type of Role: 1.5...

Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to: Career development with an international company where you can grow the career you dream of. Free medical coverage for employees* via the Health Investment Plan (HIP) PPO An excellent...

Job Title: - General Quality & Regulatory Affairs Expert 2 Location: St. Louis, MO- Hybrid –(2-3 days on-site) Duration: 12+ Months (possibilities of extension) Job Overview: As a Regulatory Affairs Expert in the Medical Devices sector, you will oversee various regulatory responsibilities with minimal oversight. Your role will involve managing health...

Working at AbbottAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:Career development with an international company where you can grow the career you dream of.Free medical coverage for employees* via the Health Investment Plan (HIP) PPOAn excellent...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.Working at...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.About...

About the Company: Consumer Product Partners is a prominent player in the manufacturing sector, committed to delivering exceptional products to clients globally.Job Title: Regulatory Affairs SpecialistJob Overview:This role focuses on overseeing customer-specific and state agency regulatory compliance data for all products produced across various locations....

Press Tab to Move to Skip to Content Link Select how often (in days) to receive an alert: Select how often (in days) to receive an alert: (Contractor) Senior Manager Regulatory Affairs - Clinical Date: May 3, 2024 Location: St. Louis, MO, United States About Curium Curium is the world’s largest nuclear medicine company with more than a century of industry...