We have other current jobs related to this field that you can find below

  • Regulatory Compliance Specialist

    1 month ago

    St. Paul, United States Murata Electronics Full time

    Regulatory Compliance Specialist Location: US Murata Viosis a global medical device company dedicated to...

  • Senior Digital Content Specialist

    4 weeks ago

    St Paul, United States Genesis10 Full time

    Genesis10 is seeking a highly motivated and detail-oriented Senior Digital Content Specialist with a flair for creativity to complement our current team. Reporting to the Director of Marketing, the Senior Digital Content Specialist will be a key contributor to the success of our marketing campaigns. The ideal candidate has five years of creative writing and...

  • Principal Regulatory Affairs Specialist

    4 weeks ago

    St Paul, United States Boston Scientific Full time

    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...

  • Senior Digital Content Specialist

    3 weeks ago

    St. Paul, United States Genesis10 Full time

    Genesis10 is seeking a highly motivated and detail-oriented Senior Digital Content Specialist with a flair for creativity to complement our current team. Reporting to the Director of Marketing, the Senior Digital Content Specialist will be a key contributor to the success of our marketing campaigns. The ideal candidate has five years of creative writing...

  • Digital Product Specialist

    2 weeks ago

    St Paul, United States Marvin Full time

    Digital Product Specialist - Brand Websites ID 2024-4730 Department Marketing Position Type Regular Location US-MN-Eagan Job Overview Are you passionate about continuously improving users' web experience? Marvin is seeking a Digital Product Specialist to join our Digital Product and...

  • Regulatory Compliance Specialist

    1 month ago

    St Paul, United States AbleNet, Inc. Full time

    POSITION SUMMARY:The Regulatory & Compliance Specialist is responsible for overseeing AbleNet’s organizational compliance with government laws and regulations. Their duties include coordinating with company management to identify potential risks, implementing policies and procedures to uphold laws and regulations and monitoring the company’s adherence to...

  • Sr. Regulatory Specialist

    2 weeks ago

    St Paul, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale Sr. Regulatory Specialist - Electrophysiology Pulsed Field Ablation At Boston Scientific, you'll discover a place where you can have meaningful purpose, improving lives through your life's work. In Rhythm Management (RM) we offer solutions for treating irregular heart rhythms and heart failure and protecting against sudden...

  • Digital Product Specialist

    1 week ago

    St Paul, United States Marvin Full time

    Job Overview: Are you passionate about continuously improving users' web experience? Marvin is seeking a Digital Product Specialist to join our Digital Product and Engineering team. If you're a creative thinker who insists that the user experience can always be improved and enhanced, apply today! The Digital Product Specialist will intake, evaluate and...

  • Regulatory Affairs Specialist

    2 weeks ago

    St Joseph, United States Astrix Full time

    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...

  • Regulatory Compliance Specialist

    1 month ago

    Saint Paul, Minnesota, United States Murata Electronics Full time

    Regulatory Compliance SpecialistLocation:US Murata Viosis a global medical device company dedicated to creating a paradigm shift in the way healthcare is delivered. Through the utilization of our internet-of-things medical-grade sensors and virtual patient care services, we plan to lower the cost of healthcare and improve patient outcomes. Murata Viosis...

  • Regulatory Affairs Associate

    4 weeks ago

    St Paul, United States Redbock - an NES Fircroft company Full time

    **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...

  • Digital Marketing Specialist

    9 hours ago

    St Louis, Missouri, United States Lee Enterprises Full time

    Amplified Digital Activation SpecialistAt Lee Enterprises, we are seeking a skilled Digital Activation Specialist to join our team in the digital marketing department.Key Responsibilities:Analyze orders to identify discrepancies and potential issues, ensuring seamless financial system integrations.Collaborate with cross-functional teams to resolve issues...

  • Regulatory Affairs Specialist

    2 weeks ago

    St Joseph, United States Astrix Full time

    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...

  • Regulatory Affairs Specialist

    4 days ago

    St Joseph, United States Astrix Technology Full time

    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...

  • Senior Digital Content Specialist

    4 weeks ago

    Saint Paul, United States Genesis10 Full time

    Genesis10 is seeking a highly motivated and detail-oriented Senior Digital Content Specialist with a flair for creativity to complement our current team.Reporting to the Director of Marketing, the Senior Digital Content Specialist will be a key contributor to the success of our marketing campaigns. The ideal candidate has five years of creative writing and...

  • Regulatory Affairs Specialist

    2 weeks ago

    St Joseph, United States Compunnel Inc. Full time

    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...

  • Senior Digital Content Specialist

    2 weeks ago

    Saint Paul, Minnesota, United States Genesis10 Full time

    Genesis10 is seeking a highly motivated and detail-oriented Senior Digital Content Specialist with a flair for creativity to complement our current team.Reporting to the Director of Marketing, the Senior Digital Content Specialist will be a key contributor to the success of our marketing campaigns. The ideal candidate has five years of creative writing and...

  • Regulatory Affairs Specialist

    2 weeks ago

    St Joseph, United States RootStaff Full time

    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 Regulatory Affairs Specialist

    1 month ago

    St Paul, United States Abbott Laboratories company Full time

    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...

  • Senior Regulatory Affairs Specialist

    3 months ago

    Saint Paul, United States Collabera Full time

    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...

Regulatory Digital Systems Specialist

2 months ago

St Paul, United States 3M Full time

Job Title: Regulatory Digital Systems Specialist The Impact You’ll Make in this Role: Leads IT systems support and master data management for 3M Medical Device/Cosmetic regulatory requirements (Consumer, Personal Safety, etc) Supports data integrity and master data management Website creation and management Interacts internally and externally to identify and optimize digital solutions to support medical device regulatory Provides regulatory operations support including digital process improvements and other regulatory assignments as required Your Skills and Expertise: Bachelor’s degree or higher from an accredited university completed and verified prior to start Five (5) years of IT systems, regulatory, data analytics, or master data experience, in a private, public, government or military environment Current and valid Driver’s License Additional qualifications that could help you succeed even further in this role include: Master’s degree from an accredited institution Five (5) years of IT, data analytics, or Master data experience in medical device regulatory in a private, public, government or military environment Project management experience Skills include strong attention to detail, flexible, and track-record of execution Interest in supporting a global team Work location: Hybrid Eligible (Job Duties allow for some remote work but require travel to Maplewood, MN at least 2 days per week) Travel: May include up to 5% domestic and international Relocation Assistance: Is not authorized Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status)

#J-18808-Ljbffr