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Risk Control Manager Jobs in Massachusetts (NOW HIRING)

Loss Control Consultant * Conducts surveys and services accounts by identifying and evaluating ... A.) in Occupational Safety, Risk Management, Insurance or related field preferred * Experience ...

Manager, Quality Control

Bedford, MA · On-site

$122 - $152/hr

Manager, Quality Control Regular Full-Time Bedford, MA, Bedford, MA, US 3 days ago Requisition ID ... risk, or significant business impact. Success in this role requires deep analytical chemistry ...

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Risk Control Manager information

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$37

$66

$87

How much do risk control manager jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for risk control manager in Massachusetts is $66.37, according to ZipRecruiter salary data. Most workers in this role earn between $50.91 and $83.22 per hour, depending on experience, location, and employer.

What does a Risk Control Manager do?

A Risk Control Manager is responsible for identifying, assessing, and mitigating risks that could negatively impact an organization's operations, assets, or reputation. They develop and implement risk management policies, conduct audits, and work closely with various departments to ensure compliance and safety. Their role also includes training staff on risk prevention and preparing reports for senior management. Effective risk control helps prevent losses, legal issues, and enhances the overall resilience of the organization.

What are the key skills and qualifications needed to thrive as a Risk Control Manager?

To thrive as a Risk Control Manager, you need a solid background in risk assessment, loss prevention, and regulatory compliance, often supported by a degree in risk management, business, or a related field. Familiarity with risk management information systems (RMIS), data analysis tools, and certifications such as ARM (Associate in Risk Management) are commonly required. Strong analytical thinking, communication, and leadership skills help you effectively identify risks, collaborate with stakeholders, and implement mitigation strategies. These skills and qualifications are crucial for minimizing organizational losses, ensuring regulatory compliance, and supporting informed decision-making.

How does a Risk Control Manager typically collaborate with other departments to identify and mitigate risks?

A Risk Control Manager works closely with departments such as operations, finance, compliance, and IT to proactively identify potential risks and develop mitigation strategies. This collaboration often involves conducting risk assessments, sharing insights from incident reports, and leading cross-functional meetings to ensure everyone is aligned on risk management protocols. Effective communication and relationship-building are key, as the Risk Control Manager must ensure that risk controls are practical and integrated into daily workflows. By fostering a culture of transparency, they help departments understand their roles in maintaining organizational safety and compliance.

What is the difference between Risk Control Manager vs Risk Analyst?

AspectRisk Control ManagerRisk Analyst
CredentialsCertifications like CRM, ARM, or CPCU often preferredCertifications such as FRM or CRM may be beneficial
Work EnvironmentOversees risk management strategies, collaborates with departmentsAnalyzes data, assesses risks, prepares reports
Industry UsageCommon in insurance, finance, and corporate sectorsWidely used in finance, insurance, and consulting firms

While both roles focus on risk, the Risk Control Manager develops and implements risk mitigation strategies, whereas the Risk Analyst primarily assesses and analyzes risks through data. The manager has a broader strategic role, often supervising teams, while the analyst concentrates on detailed risk evaluation.

Do risk control managers make good money?

Risk control managers typically earn a competitive salary that varies based on experience, industry, and location. They often hold certifications such as CRM or ARM and work in industries like insurance, manufacturing, or finance, with salaries ranging from moderate to high depending on their level of responsibility and expertise.

What are the most commonly searched types of Risk Control jobs in Massachusetts?

The most popular types of Risk Control jobs in Massachusetts are:

What cities in Massachusetts are hiring for Risk Control Manager jobs?

Cities in Massachusetts with the most Risk Control Manager job openings:

Infographic showing various Risk Control Manager job openings in Massachusetts as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $138,041 per year, or $66.4 per hour.

Quality Control Manager / Supervisor - Medical Device Manufacturing || Gardner, MA / Littleton, MA

GD Resources LLC

Gardner, MA • On-site

$90K - $120K/yr

Full-time

Posted 13 days ago


Job description

Quality Control Manager / Supervisor - Medical Device Manufacturing
Location: Gardner, MA / Littleton, MA
Compensation: $90,000-$120,000
Employment Type: Full-Time, Permanent
Job Summary
We are seeking a Quality Control Manager / Supervisor to lead Quality Control activities within a regulated medical device contract manufacturing environment. This position will oversee a team of approximately 4-5 direct reports and be responsible for quality control operations, inspection, calibration, product release, DHR review, nonconforming material controls, and continuous improvement.
The ideal candidate will have strong experience in medical device manufacturing, metrology, calibration systems, and quality control, along with proven supervisory or management experience.
Responsibilities
  • Manage daily Quality Control operations, including inspection, testing, review, and release of materials and finished medical devices.
  • Establish priorities and allocate resources while maintaining production schedules and quality requirements.
  • Develop, implement, and maintain QC procedures, work instructions, inspection methods, and acceptance criteria.
  • Oversee incoming inspection of components, raw materials, labels, packaging materials, and outsourced manufacturing services.
  • Support supplier quality activities and supplier corrective actions.
  • Manage final inspection, product testing, and product acceptance activities.
  • Review quality records supporting final product acceptance.
  • Authorize or oversee final release of finished medical devices.
  • Perform or oversee comprehensive Device History Record (DHR) reviews.
  • Ensure manufacturing and inspection records are complete, accurate, and traceable.
  • Administer and continuously improve the calibration program for inspection, measuring, and test equipment.
  • Coordinate external calibration vendors and service providers.
  • Manage qualification, maintenance, and monitoring of QC equipment.
  • Identify, document, segregate, and control nonconforming materials and products.
  • Participate in MRB activities and support investigations involving nonconformances, complaints, CAPAs, and audits.
  • Lead, coach, mentor, and develop Quality Control Inspectors and Technicians.
  • Conduct training, qualification, and competency assessments.
  • Establish departmental goals and performance metrics.
  • Support internal, customer, supplier, and regulatory audits.
  • Participate in CAPA investigations and process improvement initiatives.
  • Support risk management activities and Quality Management System improvements.
  • Analyze quality metrics and identify opportunities for continuous improvement.
  • Promote a culture of quality, compliance, accountability, and continuous improvement.

Required Qualifications
  • 5+ years of Quality Control, Quality Assurance, or Manufacturing Quality experience within the medical device industry.
  • Minimum 2-3 years of leadership or supervisory experience.
  • Medical device manufacturing experience required.
  • Experience with:
    • Incoming inspection
    • Final product inspection
    • Product release
    • DHR review
    • Calibration management
    • Nonconforming material disposition
    • CAPA participation
    • Internal and external audits
  • Strong knowledge of FDA 21 CFR Part 820 and ISO 13485.
  • Knowledge of metrology and calibration systems.
  • Familiarity with Gage R&R and measurement system analysis.
  • Ability to interpret engineering drawings, specifications, and test methods.
  • Knowledge of statistical sampling plans and inspection techniques.
  • Strong technical writing and documentation skills.
  • Excellent organizational, problem-solving, verbal, and written communication skills.
  • Ability to lead cross-functional teams and influence decision-making.
  • ERP, Electronic QMS, and calibration management system experience preferred.

Education
  • Bachelor's degree in Engineering, Quality, Life Sciences, Manufacturing, or a related technical discipline required.
  • Equivalent combination of education and relevant experience may be considered.

Preferred Qualifications
  • ASQ CQE, CQA, or CQT certification.
  • ISO 13485 Lead Auditor certification.
  • Experience with electronic and paper-based DHR systems.
  • Experience with validation activities, including IQ/OQ/PQ.
  • Contract manufacturing experience preferred.
  • Class II medical device experience or higher preferred.
  • Experience managing calibration and preventative maintenance systems.
  • Experience with supplier management, SCARs, return-to-vendor processes, and final batch release.
  • Ability to read engineering drawings and understand dimensions.