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Manager Internal Audit Risk Management Jobs in Hagerstown, MD

RYAN & WETMORE PC

Audit & Assurance Manager

Frederick, MD · On-site

$95K - $135K/yr

Present audit findings and recommendations to client management or audit committees Process Evaluation and Risk Management * Assess and improve client accounting processes and internal controls

Macy's

Sr. Manager, Asset Protection

Martinsburg, WV

$78K - $130K/yr

Compliance and Risk Management: Maintain standards for compliance with Supply Chain Asset Protection, Macy's Internal Audits, and legal requirements. Analytical Skills and Project Leadership: Review ...

Macy's

Sr. Manager, Asset Protection

Martinsburg, WV · On-site

$78K - $130K/yr

Compliance and Risk Management: Maintain standards for compliance with Supply Chain Asset Protection, Macy's Internal Audits, and legal requirements. Analytical Skills and Project Leadership: Review ...

Walmart

Warehouse Manager

Greencastle, PA · On-site

$65K - $98K/yr

... prepares audit reports for management review Participates in evaluating pollution control and ... risk management practices Assists in the development of company policies practices and procedures ...

Walmart

Distribution Center Manager

Greencastle, PA · On-site

$65K - $98K/yr

... prepares audit reports for management review Participates in evaluating pollution control and ... risk management practices Assists in the development of company policies practices and procedures ...

Walmart

Warehouse Area Manager

Greencastle, PA · On-site

$65K - $98K/yr

... prepares audit reports for management review Participates in evaluating pollution control and ... risk management practices Assists in the development of company policies practices and procedures ...

Walmart

Walmart Warehouse Area Manager

Greencastle, PA · On-site

$65K - $98K/yr

... prepares audit reports for management review Participates in evaluating pollution control and ... risk management practices Assists in the development of company policies practices and procedures ...

Walmart

Distribution Center Area Manager

Greencastle, PA · On-site

$65K - $98K/yr

... prepares audit reports for management review Participates in evaluating pollution control and ... risk management practices Assists in the development of company policies practices and procedures ...

F&M Trust

Loan Servicing Manager

Chambersburg, PA · On-site

Collaborating with lending, compliance, risk management, audit, and other business partners to ... and internal partners. WHY JOIN F&M TRUST? * Lead a critical operational function within a ...

F&M Trust

Loan Servicing Manager

Chambersburg, PA · On-site

Collaborating with lending, compliance, risk management, audit, and other business partners to ... internal partners.WHY JOIN F&M TRUST?Lead a critical operational function within a respected ...

F&M Trust

Loan Servicing Manager

Chambersburg, PA · On-site

Collaborating with lending, compliance, risk management, audit, and other business partners to ... and internal partners. WHY JOIN F&M TRUST? * Lead a critical operational function within a ...

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All JobsInternal Audit Risk Management JobsManager Internal Audit Risk Management JobsManager Internal Audit Risk Management Jobs in Hagerstown, MD

Manager Internal Audit Risk Management information

See Hagerstown, MD salary details

$60.5K

$114.2K

$150.2K

How much do manager internal audit risk management jobs pay per year?

As of Aug 17, 2026, the average yearly pay for manager internal audit risk management in Hagerstown, MD is $114,208.00, according to ZipRecruiter salary data. Most workers in this role earn between $100,100.00 and $132,800.00 per year, depending on experience, location, and employer.

What is the difference between Manager Internal Audit Risk Management vs Internal Auditor?

AspectManager Internal Audit Risk ManagementInternal Auditor
CertificationsCPA, CIA, CISACPA, CIA, CISA
Work EnvironmentOversees audit teams, strategic planningPerforms audits, data analysis
ResponsibilitiesRisk assessment, audit strategy, team managementConducts audits, reports findings
Industry UsageCommon in finance, large corporationsWidespread across industries

The Manager Internal Audit Risk Management typically has broader responsibilities, including overseeing audit teams and developing risk strategies, while the Internal Auditor focuses on executing audits and analyzing data. Both roles require similar certifications and are integral to organizational compliance and risk mitigation.

What are popular job titles related to Manager Internal Audit Risk Management jobs in Hagerstown, MD?

For Manager Internal Audit Risk Management jobs in Hagerstown, MD, the most frequently searched job titles are:

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Regulatory Risk & Quality Manager

CICONIX, LLC

Fort Detrick, MD • On-site

Full-time

Medical, Retirement, PTO

Re-posted 25 days ago

Job description

Regulatory Risk & Quality Manager
About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in business advisory and technical assistance for military health programs. We value exceptional people, unwavering integrity, inclusive collaboration, and enduring impact. 
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Location(s): Fort Detrick, MD
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Position Details:
  • Full-time position
  • Regular weekly hours (0900-1600)
  • No calls, nights, weekends, or holidays!
  • Full benefit program, including: health, PTO, & 401k + contribution
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Requirements:
  • TBD
 
 
Summary:
CICONIX is seeking a Regulatory Risk & Quality Manager to support the Office of Regulated Activities (ORA) in support of the Defense Health Agency Research and Development Medical Research and Development Command (DHA R&D MRDC) team in Fort Detrick, MD.
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About the Role:
  • Provide Knowledge Management and Regulatory Risk and Quality Management support for medical product development within the ORA. Leverage expertise in applicable laws, regulations, and industry best practices to assist the ORA to mitigate regulatory risk and maintain product quality and safety. Ensure compliance with all relevant national and international regulations and standards. Provide expert support to ensure all personnel involved in the conduct of clinical human research are appropriately trained IAW institutional policies, sponsor requirements, and applicable federal regulations, including Good Clinical Practice. The primary objective is to maintain a fully compliant and audit-ready training program that safeguards participant safety and ensures data integrity.
    • Developing and implementing knowledge management strategies to improve information flow and collaboration within the organization.
    • Identifying and mapping critical knowledge within the organization to ensure its preservation and accessibility.
    • Facilitating communities of practice to encourage knowledge sharing and peer-to-peer learning.
    • Implementing and managing knowledge management systems and tools, such as knowledge bases and enterprise search platforms, to centralize and make information easily discoverable.
    • Promoting a culture of knowledge sharing and continuous learning among employees.
    • Ensuring data accuracy and reliability within the knowledge systems.
    • Analyzing knowledge usage and effectiveness to identify areas for improvement and demonstrate the value of knowledge management initiatives.
    • Ensuring regulatory compliance for all medical products (drugs, biologics, and devices), with applicable guidance and regulations.
    • Ensuring Quality Management Systems are developed, implemented and managed IAW relevant standards, such as FDA 21 CFR 820, ISO 13485:2016, and Good Manufacturing Practices.
    • Documentation and Submission preparations, submission and maintenance to include SOPs development and management within ORA.
    • Leading audits and Inspections for internal and external customers, and regulatory audits (e.g., FDA audits).
    • Developing and reviewing CAPAs; Investigating non-conformances, customer complaints, and other quality issues to determine the root cause and implementing CAPAs.
    • Facilitating and documenting risk management activities IAW ORA SOPs, ISO 14971, including risk analysis, evaluation, and control for new and existing medical products.
    • Process risk management to include identifying and mitigating risks associated with manufacturing processes and quality systems.
    • Training Program Management: Maintain a comprehensive training matrix for all research staff, detailing required courses, renewal dates, and role-specific educational needs.
    • Compliance Monitoring: Continuously monitor and track the training compliance of all personnel (including Principal Investigators, Sub-investigators, and Clinical Research Coordinators) engaged in clinical research.
    • Record Keeping and Documentation: Maintain accurate, complete, and up-to-date training records for all research personnel, ensuring they are readily available for internal audits, sponsor monitoring visits, and regulatory inspections.
    • Communication and Reporting: Generate and distribute regular compliance reports. Promptly notify relevant parties of any lapses in required training and oversee remediation.
    • Onboarding and Orientation: Coordinate and document the initial training for all new staff members.
    • Evaluation of Training: Periodically assess the effectiveness of the training program and recommend improvements or additional training modules as needed to address emerging compliance trends or corrective actions.
    • Perform independent reviews and provide reports on documentation, sites, organizations, and facilities to ensure compliance with quality requirements for medical product development and clinical studies as per applicable regulations, standards, and FDA guidance.
    • Provide subject matter expertise and support for the development and implementation of in-house quality systems and procedures, to include the development/writing of new SOPs to support ORA compliance Survey personnel, review procedures, assess facilities, and write SOPs for entities conducting or assisting with non-clinical studies, clinical studies, or manufacturing test articles (Deliverable 60)
    • Upon request and per ORA SOPs provide quality control of deliverables by reviewing work products associated with deliverables in this contract.
    • Provide protocol, project, and procedure specific training to ORA and GDIT staff as well as personnel at clinical sites, CROs, CMOs, and other supported entities, to ensure that work is completed in an acceptable manner.
    • Plan and conduct audits for compliance with applicable regulations for the development and research of FDA regulated medical products to include preparing written audit plans and report(s).
    • Prepare clinical quality assurance management plans IAW Federal Code, guidance documents, including 21 CFR Part 312, 21 CFR Part 812, ICH Good Clinical Practice E6, and ISO 14155, and either Government SOPs or Contractor SOPs that have been reviewed and approved by the Government.
Qualifications:
  • Education:
    • TBD
  • Licensure & Certifications (Current & Unrestricted): 
    • TBD
  • Experience: 
    • TBD
  • Security & Background Check: 
    • U.S. Citizenship and a successful background investigation are required.
    • Ability to obtain and maintain a government security clearance. 
  • Additional Requirements:
    • Willingness to comply with the government vaccination requirements.
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Compensation: TBD
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*This position is contingent and will begin upon contract award.
CICONIX LLC is an Equal Opportunity Employer, including disability/vets. We E-Verify all employees.
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