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Senior Project Cargo Jobs in Minnesota (NOW HIRING)

Buyer

Avon, MN · On-site

$60K - $80K/yr

  • Medical

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Senior Project Cargo information

What is a senior project cargo specialist?

Senior Project Cargo specialists are logistics professionals who oversee the transportation and handling of large, heavy, or complex cargo, often for major industrial projects. They are responsible for planning, coordinating, and executing the safe and efficient movement of oversized or high-value items, such as machinery, construction materials, or energy equipment. Their role requires extensive experience in logistics, knowledge of international shipping regulations, and strong project management skills. Senior Project Cargo specialists work closely with clients, carriers, and regulatory authorities to ensure all aspects of the cargo movement comply with safety and legal requirements.

What are some common challenges faced by senior project cargo professionals and how can they be managed effectively?

Senior Project Cargo professionals often encounter challenges such as coordinating complex logistics for oversized or heavy-lift shipments, navigating regulatory requirements across multiple countries, and managing tight project timelines. Effective management involves meticulous planning, proactive risk assessment, and clear communication with stakeholders, including clients, carriers, and customs officials. Leveraging industry relationships and staying updated on the latest transportation regulations can also help mitigate delays and ensure successful project delivery.

What is the difference between Senior Project Cargo vs Project Coordinator?

AspectSenior Project CargoProject Coordinator
CredentialsLogistics certifications, industry experienceProject management certifications, organizational skills
Work EnvironmentHeavy cargo handling, international shippingPlanning, communication, and coordination
Employer & IndustryLogistics companies, freight forwardersConstruction firms, event planning

Senior Project Cargo professionals focus on managing complex logistics and heavy cargo shipments, requiring specialized certifications and extensive experience. Project Coordinators handle planning and communication across various projects, often with less technical specialization. While both roles involve project management skills, Senior Project Cargo roles are more technical and logistics-intensive, whereas Project Coordinators focus on overall project organization.

What are the key skills and qualifications needed to thrive as a senior project cargo specialist?

To thrive as a Senior Project Cargo specialist, you need in-depth knowledge of logistics, freight forwarding, project management, and international trade regulations, often supported by a degree in logistics or supply chain management. Familiarity with transportation management systems (TMS), Incoterms, and specialized cargo handling equipment is typically required. Strong negotiation, problem-solving, and leadership skills help manage complex shipments and coordinate diverse teams. These abilities ensure the safe, timely, and cost-effective movement of oversized or high-value cargo for large-scale projects.

What are the most commonly searched types of Project Cargo jobs in Minnesota?

The most popular types of Project Cargo jobs in Minnesota are:

What are popular job titles related to Senior Project Cargo jobs in Minnesota?

For Senior Project Cargo jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Senior Project Cargo jobs?

Cities in Minnesota with the most Senior Project Cargo job openings:

Senior Regulatory Affairs Specialist - Structural Heart (on-site)

Abbott Laboratories

New Brighton, MN • On-site

$78 - $156/hr

Other

Medical, Retirement

Posted 3 days ago

New


Job description

## Senior Regulatory Affairs Specialist – Structural Heart (on-site)Candidatar-selocations: United States - Minnesota - New Brightontime type: Tempo Integralposted on: Publicado ontemjob requisition id: 31157906Abbott 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 115,000 colleagues serve people in more than 160 countries.Descritivo de Cargo**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* Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.* An excellent retirement savings plan with high employer contribution* Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree* A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune* A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists**Structural Heart Business Mission: why we exist**Our business purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural heart disease.**The Opportunity**We are recruiting for a **Senior Regulatory Affairs Specialist** to join our team on-site in New Brighton, MN. This new team member will be overseeing our innovating Transcatheter Aortic Valve Implantation Franchise within the Abbott Structural Heart Franchise.As an individual contributor, the Senior Regulatory Affairs Specialist will support product development activities to ensure both investigation and commercial regulatory approvals are achieved. In this role, you will provide regulatory input on design and development activities to cross functional teams including software development. Additionally, provide submission authoring and compilation to meet program objectives and timelines.**What You’ll Work On*** Represent Regulatory Affairs on cross functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for Class III medical devices which may include software* Strategic Planning: Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes.* Premarket: Assess the acceptability of quality, preclinical and clinical documentation for submission filing.* Compile, prepare, review and submit regulatory submission to authorities to support both investigational and commercial approval.* Utilize technical regulatory skills to propose strategies on complex issues* Monitor impact of changing regulations on submission strategies. Monitor applications under regulatory review. Monitor and submit applicable reports to regulatory authorities. Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies. Negotiate and interact with regulatory authorities during the development and review process to ensure submission approval.* Postmarket: Maintain annual licenses, registrations, listings and patent information. Assist compliance with product postmarketing approval requirements.* Submit and review change controls to determine the level of change and consequent submission requirements. Analyze the input of cumulative product changes to current product submissions.**Required Qualifications*** Bachelor’s Degree or an equivalent combination of education and experience* 3-4 years’ experience in a regulated industry (e.g., medical products, nutritionals).* 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.* Effectively communicate, prepare, and negotiate both internally and externally with various regulatory agencies. Communicate effectively verbally and in writing.* Ability to work in a highly matrixed and geographically diverse environment.* Has broad knowledge of various technical alternatives and their potential impact on the business.* Exercise good and ethical judgment within policy and regulations.* Use in-depth knowledge of business functions and cross group dependencies/ relationships.* Define regulatory strategy with supervision.* Follow scientific arguments, identify regulatory scientific data needs and with supervision solve regulatory issues.**Preferred Qualifications*** Master’s Degree in Regulatory Affairs preferred and may be used in lieu of direct regulatory experience.* 5+ years’ experience in Medical Device industry* 3 - 5 years of regulatory experience.* Knowledge of software and electrical regulations.* Ability to think analytically and have good problem-solving skills.* PMA or investigational device regulatory submission experience.* Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.)**Apply Now****Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:** www.abbottbenefits.comFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.**The base pay for this position is**$78,000.00 – $156,000.00In specific locations, the pay range may vary from the range posted.Família de CargoRegulatory OperationsDivisãoSH Structural HeartLocalidadeUnited States > Minnesota > St. Paul : 1225 Old Highway 8 NWLocalidades AdicionaisTurno de TrabalhoStandardViagemYes, 5 % of the TimeVigilância médicaNoAtividades de trabalho significativasAwkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO\_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO\_Spanish.pdf #J-18808-Ljbffr