Records Manager Job at Cargill, Wayzata, MN

Z09HRVZ5VklXSUdMelpYMUJtd0xpdGRjaXc9PQ==
  • Cargill
  • Wayzata, MN

Job Description

Cargill’s size and scale allows us to make a positive impact in the world. Our purpose is to nourish the world in a safe, responsible and sustainable way.We are a family company providing food, ingredients, agricultural solutions and industrial products that are vital for living. We connect farmers with markets so they can prosper. We connect customers with ingredients so they can make meals people love. And we connect families with daily essentials — from eggs to edible oils, salt to skincare, feed to alternative fuel. Our 160,000 colleagues, operating in 70 countries, make essential products that touch billions of lives each day. Join us and reach your higher purpose at Cargill. Job Purpose and Impact The Records Manager plays a critical role in supporting and advancing the Global Records & Information Management (RIM) program. As an experienced individual contributor, you will collaborate with the Records & Information Management Center of Expertise (RIM COE) and cross-functional stakeholders to ensure compliance with legal and regulatory recordkeeping requirements. This role will report to the Director of Global Records & Information Management. Key Accountabilities Lead and coordinate the global RIM Network of Records Coordinators, fostering engagement and consistency across regions. Contribute to mergers, acquisitions, divestitures, and joint ventures (MADJV) by providing RIM expertise and support. Develop and maintain global RIM policies, procedures, and best practices, ensuring alignment with legal and business requirements. Design and deliver training programs to build RIM awareness and capability across the organization. Serve as a primary resource for resolving complex RIM-related inquiries in collaboration with internal stakeholders. Monitor and analyze RIM controls, metrics, and reporting to assess program effectiveness and identify opportunities for improvement. Lead and support special projects focused on enhancing records and information management practices. Create and maintain detailed process documentation to support operational consistency and knowledge sharing. Drive continuous improvement initiatives, contributing to the evolution of RIM strategies and systems. Manage complex issues independently, escalating only the most critical matters as needed. Perform additional duties as assigned to support the broader goals of the RIM program. Qualifications Minimum Qualifications Bachelor’s degree in a relevant field or equivalent professional experience. Minimum 4 years of experience in records and information management or a related discipline. Proficiency with records management technologies, including electronic records systems, document management platforms, and enterprise content management (ECM) tools. Experience with tools such as Versatile Enterprise (for physical records) and OpenText (for digital content lifecycle management). Strong understanding of electronic records management practices and experience collaborating with IT teams to implement RIM requirements. Preferred Qualifications Minimum 6 years of experience in a records and information management role, ideally within a large global organization. Certified Records Manager (CRM) or Certified Records Analyst (CRA), or eligibility to sit for certification exams. Exceptional communication and influencing skills, with the ability to engage effectively across all levels of the organization. Demonstrated ability to work independently, exercise sound judgment, and manage multiple priorities. Proven success in team-based environments and project execution. External Applicant Information This position is open to candidates located in the Minneapolis area . The expected salary for this position is approximately $105,000 to $115,000. Compensation varies depending on a wide array of factors including but not limited to the specific location, certifications, education, and level of experience. The disclosed range estimate may be adjusted for any applicable geographic differential associated with the location at which the position may be filled. This position is eligible for a discretionary incentive award. The incentive award amount is dependent upon company performance and your personal. Equal Opportunity Employer, including Disability/Vet. #J-18808-Ljbffr Cargill

Job Tags

Similar Jobs

Uptown Yolk - Southend

Breakfast Cook Job at Uptown Yolk - Southend

 ...**About Uptown Yolk:** Uptown Yolk is a cherished breakfast and brunch spot located between Charlotte's Uptown and Southend neighborhoods...  ...experiences, we are seeking a passionate and dedicated Line Cook to join our dynamic kitchen team. **Role Overview:** As a Line... 

Housekeeper.com

Housekeeper Wanted - Now Hiring Cleaners — $20/Hour Full Time & Part Time Join Our Growing Team! Job at Housekeeper.com

 ...Experience with oven and fridge cleaning is a huge plus! I pay $20.0 per hour and provide flexible working hours.If you take pride in making...  ...how you can help keep my home in top shape. Thank you!Please visit to view full details and to apply. Lots of jobs to choose from!

Latitude Legal

Remote Contract Litigation Attorney: Research & Writing Job at Latitude Legal

 ...A leading legal services company is seeking a Research and Writing Litigation Attorney for a remote contract position, requiring California licensure and a minimum of five years in civil litigation. The role involves drafting legal documents and managing cases flexibly... 

Business Needs Inc

QA tester Job at Business Needs Inc

 ...must live in MA/RI/NH/CT and be available if requested for a F2F interview Duration: 12+ month contract Title: Software QA Tester Any visa is fine, must be local and able to share their passport number as required by state. Requirements: Manual and... 

Cedent

Clinical Research Associate (Dallas, TX) Job at Cedent

The Clinical Research Associate (CRA) position represents an opportunity to grow within an emerging medical device company. Solid knowledge of the processes involved in clinical studies following Good Clinical Practice (GCP)/ICH, and the Code of Federal Regulations is required...