QA Engineer

• Auditing Processes & Data Integrity
• Engage with confidential and sensitive data for learners, faculty, and staff with the highest level of ethics, integrity, and data security
• Audit outcomes of processes to verify accuracy and highlight areas for refinement
• Apply analytical and problem-solving skills to identify, triage, investigate, and escalate process or data integrity concerns
• Perform audits of large data sets from multiple departments to ensure compliance, affirm data quality, and maintain accreditation standards
• Engage in critical analysis and decision-making to evaluate identified inconsistencies, investigate related issues, and assess potential future impacts
• Assist with data collection, pattern identification, and process improvement through embedded collaboration
• Develop subject matter expertise in processes spanning diverse departments
• Remain informed regarding policies and procedures tied to accreditation standards, applicable guidelines, and best practices to help ensure compliance
• Deliver stakeholder support according to SNHU Core Values
• Adjust between multiple projects and tasks, ensuring efficiency and focus
• Other duties and responsibilities as assigned

Quality Assurance Coordinator

• Lead quality engineering guidance and oversight for medical devices and combination products during feasibility, design control, risk management, and lifecycle management.
• Define critical quality characteristics for device components and finished devices in collaboration with the device development team.
• Support internal and external audits as a device or combination product Subject Matter Expert.
• Oversee the quality review and approval of technical documentation, ensuring compliance with regulatory requirements.
• Provide input to process manufacturing design and design transfer for robust product realization.
• Support asset team strategies for regulatory filings, design control, and risk management.
• Lead continuous improvement initiatives for the Quality Management System and lifecycle processes.
• Function as the quality representative on cross-functional initiatives and device development programs.
• Manage quality assurance interfaces with medical device suppliers and testing partners in collaboration with External Quality.

Senior Device Quality Engineering Lead

• Responsible for the life cycle management of R&D and Clinical documents according to company SOPs
• Participate in the implementation of new systems or improvements to existing systems
• Administer the clinical trial documentation system in compliance with regulations and procedures
• Responsible for maintaining and developing training profiles and documentation for Clinical departments

Clinical QA Systems, Documentation Specialist

• Perform a complete review and analysis of transactions as required by all regulatory compliance guidelines
• Manage individual inventory of audit work to meet department quality standards
• Participate in special project work as needed
• Maintain scorecard entries in audit tool accurately and consistently meet all production standards established in departmental protocol
• Share relevant information with the team when received individually through normal work channels

Quality Assurance Analyst

• Analyzes and evaluates complex billing system enhancement projects and testing assignments.
• Possesses and/or assertively obtains the knowledge and experience required to validate complex enhancements to identify and measure process impacts, financial implications, and technical applications.
• Participate in requirement sessions with business operations and IT team to define and document business requirements.
• Troubleshoot system issues for resolution.
• Maintain a log of data tested that displays the number of passes, fails, and defects identified.
• Determine each type of defect along with severity and frequency.
• Create and execute User Acceptance test plans that integrates business, functional, and technical components.
• Confirm requirements based upon the project.
• Conduct end-to-end integration testing and assure software delivered meets requirements and expectations.
• Document test results and review with business end users for approval.
• Create and present Test Strategies and Test Summaries.
• Utilize system tools and resources to conduct data analysis and system validation related to assigned projects.
• Assist with the preparation of user documentation, perform demos and training for system enhancements.
• Propose recommendations which may include compiling, analyzing, and evaluating data.
• Pro-actively identify potential roadblocks, analyze, and propose solutions.
• Collaborate with Business Analyst and Software Developer frequently for requirements and issues clarification.
• Act as a voice for the business users when vetting issues with IT.
• Coordinate tasks associated with large projects involving multiple analysts.
• Create test strategies and test summaries for major system releases.
• Responsible for leading meetings and taking the lead on Release and Status meeting calls in the absence of management.
• Propose recommendations which may include compiling, analyzing, and evaluating data on standardization and protocols of methodology.
• Coordinates the implementation of the new methodologies for large projects/releases across multiple platforms (systems and applications).

User Acceptance Tester, UAT

• Supports the development and execution of QA processes to ensure the effectiveness of IT risk controls, cybersecurity measures, and regulatory compliance frameworks.
• Conducts independent testing and validation of IT risk management policies, standards and controls to ensure alignment with FFIEC, NIST, GLBA, SOX, PCI-DSS, and other industry regulations.
• Performs control testing, improve risk monitoring and foster a culture of continuous improvement in the IT Risk Management space.
• Performs controls testing including walkthroughs, design, and operating effectiveness testing per the Bank’s Enterprise Risk Management (ERM) Management Control Monitoring Program guidelines.
• Assists IT Control owners to obtain issue remediation action plans, track and report status of remediation actions, including maintaining dialogue with the business to ensure timely remediation of issues.
• Compiles, manages, submits and socializes required monthly, quarterly or annual reporting including test results, dashboards and/or testing issue remediation status.
• Assists IT Risk Management with performing root cause analysis on control failures and recommend corrective actions to management.
• Assists with control projects, operational and/or IT risk initiatives, where directed. It is the responsibility of this role to take ownership of all tasks and challenges that they encounter in the operation of their assigned position.

Senior IT Risk QA Analyst

• This job is responsible for testing and delivering complex software requirements to accomplish business outcomes, ensuring the testing strategy and processes are well-defined and continuously improved.
• Key responsibilities include establishing a test and automation strategy, creating common test frameworks, defining and managing test processes including test data generation, defect management and reporting.
• Job expectations include understanding and implementing internal/external mandate, ensuring compliance requirements are met on all levels of test environments, and manages traceability.
• Documents, revises, and maintains all automation program governance standards and routines
• Subject matter expert on all enterprise change management (ECM)
• Facilitator of enterprise toll-gating requirements for the community across Global Markets Tech
• Subject matter expert for automation for application management
• Responsible for tracking of automation program governance health metrics
• Distribute periodic updated metrics and engage with the tech teams to ensure timely correction of data quality issues
• Serve as liaison between the technology delivery leads, for all automation requirement and ensuring all deadlines are met and senior leadership is kept informed of progress
• Drive the management information and visualization tools development
• Capture key project metrics and information for executive level reporting
• Work with globally distributed teams to coordinate various types of information and projects
• Proactively manage risk metrics – focus on “at risk” or “exceeding threshold risks” – work with technology management to address root causes and remediate as required

Quality Engineer – Technology

• Provide overall leadership and direction for Quality Assurance activities across regional manufacturing sites.
• Establish, deploy, and maintain consistent quality standards, policies, and procedures across the region.
• Serve as the primary escalation point for site-level quality issues and systemic risks.
• Oversee the effective operation of the Quality Management System (QMS) across all regional sites.
• Ensure compliance with applicable regulatory, customer, and certification requirements.
• Standardize quality processes including document control, training, change management, deviation management, and corrective and preventive actions.
• Support and lead internal audits, external audits, customer audits, and regulatory inspections.
• Ensure quality expectations are embedded throughout manufacturing operations, from raw material receipt through product release.
• Provide regional oversight of deviation investigations, non-conformances, complaints, and quality incidents.
• Review trends and data to identify systemic issues affecting product quality, reliability, or compliance.
• Partner with site leadership to implement corrective actions that are effective and sustainable.
• Drive continuous improvement initiatives using structured problem-solving and risk-based approaches.
• Identify and proactively mitigate quality and compliance risks across the region.
• Monitor and analyze regional quality performance metrics and establish improvement priorities.
• Support operational excellence initiatives aligned with business objectives.
• Lead, mentor, and develop plant-level Quality Managers and QA teams.
• Ensure consistent training, competency development, and performance expectations across sites.
• Participate in talent planning, succession planning, and performance management for QA staff.
• Promote strong collaboration between Quality and Operations teams.
• Provide quality leadership for new product introductions, process changes, and capital projects.
• Support supplier quality management and material qualification strategies.
• Communicate regional quality performance and risks to senior leadership.

Regional QA Manager

• Provides input to and support of plant and company safety initiatives.
• Manages the development, modification and maintenance of all quality evaluation and control systems in areas of product responsibility, and in compliance with company policies, customer requirements and government regulations.
• Manages and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
• Manages statistical analysis projects to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
• Manages the auditing process of quality systems for deficiency identification and correction, and ensures that corrective action plans are put into place and executed in a timely manner.
• Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with all, customer and regulatory requirements.
• Manages the development of sustainable, repeatable and quantifiable business process improvements. Reports to management as necessary and required on the status of quality assurance programs and practices.
• Manages compliance- all site required agency certifications related to product and process quality. ISO 9001, ISO 13485, QS9000, ISO 14000 and TS16949.
• Manages up front quality planning for new products to ensure appropriate quality systems and processes required to support the introduction are developed and implemented.
• Exchange knowledge and information with other Jabil facilities to ensure best practices are shared throughout the Jabil organization.
• Generate and maintain applicable quality system documentation, as needed. Documents such as Device Master Record (DMR), Design History File (DHF), validation protocols, for example, and other specified documents in support of customer projects.
• Ensure conformity of initial and ongoing validations performed in support of the GMP quality systems.
• Other responsibilities may be assigned from time to time as needed, based on the evolution of the company and the requirements of the department/position.

Site Quality Assurance Manager

• The Manager of Accounting Quality & Compliance supports the organization’s accounting operations by helping ensure adherence to GAAP, maintaining quality standards, and assisting with internal controls and compliance activities.
• Conduct internal reviews of client engagement deliverables to maintain quality and compliance with CSBM standards.
• This role focuses on implementing established policies, performing quality reviews, supporting audits, and providing technical guidance under the direction of senior leadership.
• The manager collaborates with the client teams, helps maintain accurate financial reporting practices, and supports process improvements across CSBM.
• Assist in implementing quality assurance procedures and ensure team members follow established accounting policies and workflows.
• Identify potential issues and recommend improvements to enhance accuracy and consistency.
• Conduct mid-year quality checks, maintaining a high level of professional skepticism, document findings, and suggest corrective actions.
• Assist in developing training materials and help coach staff on best practices, processes, and quality expectations.
• Assist in developing and/or updating standardized templates and procedures.
• Perform routine data analysis to identify potential discrepancies in financial information and ensure accuracy and compliance.
• Stay informed about GAAP updates and help ensure that accounting practices remain compliant.
• Research accounting questions and provide guidance to team members, attain the level of subject matter expert as assigned, and elevate complex issues when necessary.
• Ensure documentation is complete, accurate, and up to date.
• Contribute to developing and maintaining dashboards (Monday) and performance indicators.

Quality Assurance Audit Manager – Finance

• Manage a portfolio of governance and control activities for moderately complex or high-risk business or functional area
• Support the development and execution of the Centralized Governance & Controls (CG&C) AML testing and Quality Assurance (QA) program
• Lead and conduct independent testing and quality assurance reviews to ensure operational risk and compliance requirements are adhered to
• Develop and document a comprehensive inventory of processes and controls

Centralized Governance & Control Specialist – AML Testing, QA Analyst

• Oversee and lead a highly complex and diverse governance and control function for an area of significant risk, complexity or scope
• Manage and oversee the overall discipline and strategy for the respective areas while aligning to the enterprise best practices
• Provides coaching, mentorship and guidance to practitioners, business, executives within area of expertise
• Develop, communicate and implement a holistic governance and control strategy for own specific business function
• Lead partnership with management and respective teams for area of specialization with industry, enterprise, and business awareness
• Ensure an integrated and aggregated view of all related business risk and control activities across the overall function

Senior Manager, Centralized Governance & Control – AML Testing/QA

• Rethinking the vehicle ownership experience through data-driven technology.
• Strengthening client relationships with their customers.
• Managing one of the largest national networks of service providers.

• Serve as a senior advisor and delivery leader on strategic quality and regulatory engagements
• Design and remediate Quality Management Systems (QMS)
• Conduct inspection readiness and mock inspections
• Provide regulatory responses and training
• Manage data integrity, risk management, and compliance transformation
• Oversee investigation responses and submission support
• Lead supplier quality audits and new product introduction development
• Mentor and coach consultants and project Directors within Quality & Regulatory practice
• Collaborate with internal teams for resource alignment and strategy planning

QA/RA Director

• Perform quality activities for Advanced Nuclear projects to ensure compliance with regulatory, customer, and GEH requirements
• Support project execution for procured products
• Work with suppliers to define quality requirements, inspection and verification processes, qualification activities, and test controls
• Provide technical guidance to suppliers to ensure compliance with drawings and specifications
• Resolve supplier quality issues and disposition nonconforming product
• Execute supplier quality surveillance activities for New Reactor programs
• Write and review quality documents, plans, and procedures
• Support corrective action and error prevention efforts

Reactor Project Quality Engineer

• Define and execute tooling management programs aligned with global standards
• Conduct supplier and internal tooling audits and compliance reviews
• Support suppliers in achieving tooling performance and quality targets
• Collaborate across Engineering, Quality, and Supply Chain teams
• Drive tooling validation, monitoring, and continuous improvement efforts
• Lead or support CAPA investigations to prevent recurrence of issues
• Contribute to tooling standardization and tracking system implementation
• Support regional initiatives and capital projects related to tooling

Senior Supplier Quality Engineer – Tooling Design

• Manage technical and scientific professionals responsible for initiation and execution of programs
• Execute quality, food safety, and regulatory programs within Mondelez across their manufacturing, packing, and warehousing partners
• Ensure that Mondelez is consistently producing safe, high-quality products which meet customer expectations and regulatory compliance standards
• Direct seamless execution of source, product, and process to ensure brand protection for all North America Venture Brands
• Facilitate IL6S and the Manufacturing Standards journey at North America Venture Manufacturing Locations
• Develop North America Venture Manufacturer partnerships, including weekly and monthly reviews and joint continuous improvement planning and issue resolution
• Ensure facility continues to meet Mondelēz Quality and Food Safety standards
• Drive continuous improvement in the areas of Quality Assurance and Food Safety.

Manager, Corporate Quality Assurance

• Perform comprehensive TRID quality analysis of Retail and Home Mortgage Direct (HMD) operations
• Validate/review loans for adherence to all regulations
• Review Loan Estimates and Closing Disclosures for accuracy
• Identify and correct clerical or numerical defects
• Provide training to entry-level associates
• Complete complex loan reviews

Post Closing TRID Quality Assurance Analyst – Team Lead

• Author, maintain and implement study-specific Clinical Quality Audit Plan(s) for assigned clinical program(s) and trial(s) to ensure the execution of a phase-appropriate, fit-for-purpose Audit Program
• Represent Quality at cross-functional clinical program meetings and Clinical Study Team meetings and operational activities to provide appropriate Quality guidance on GCP compliance matters to internal departments.
• Identify, mitigate, or escalate clinical quality risks by leveraging GCP knowledge and best practices across all phases of clinical development.
• Maintain program oversight and influence proactive quality management through quality related activities with regard to vendor management, study conduct, and study
• Author and/or review QMS controlled documents which may include standard operating procedures (SOPs) in accordance with applicable regulatory requirements (e.g., ICH E6, FDA, EMA, MHRA, local regulations)
• Oversee the implementation of appropriate and timely Deviation, Investigations and
• Participate in risk review meetings and review study Risk Management
• Conduct QA reviews of essential documents including as applicable Clinical Protocols, Study Plans/Manuals, Investigator Brochures, Investigator’s Brochure, for ensuring quality, accuracy, and completeness
• Collaborate with internal and/or external stakeholders to ensure management of GCP quality issues, CAPAs, and change controls
• Identify process improvements to build compliance into the design and conduct of clinical activities
• Actively support the development and deployment of Inspection Readiness/Management program to support competent authority inspections for sponsor and clinical sites & vendors

Director, Clinical Quality Assurance – CQA

• review calls, correspondence, and database entries to ensure that each team member's performance meets Knowtion Health quality standards
• recommend additional training to Service Delivery when performance review indicates it is needed
• conduct routine and targeted quality audits on RCM tasks such as claim submission, denial management, account resolution, and payment posting
• perform root cause analysis on errors and recurring issues to help reduce rework and improve productivity
• prepare professional review documents analyzing each team member's verbal, written and database proficiency
• demonstrate expertise with Artiva QA review encounters and KTech IQC applications as necessary to review accounts thoroughly
• identify and communicate patterns and trends in team member work to recommend additional training to help the team members meet or exceed quality standards established by Knowtion Health
• provide 1:1 training opportunity to impart knowledge & experience, evaluate skills, guide, mentor, direct, and train internal employees to become confident and proficient in their roles and help them achieve LOB specific certification
• administer current training material and courses

See all jobs on JobTailor

Quality Assurance Coordinator

Senior Device Quality Engineering Lead

Clinical QA Systems, Documentation Specialist

Quality Assurance Analyst

User Acceptance Tester, UAT

Senior IT Risk QA Analyst

Quality Engineer – Technology

Regional QA Manager

Site Quality Assurance Manager

Quality Assurance Audit Manager – Finance

Centralized Governance & Control Specialist – AML Testing, QA Analyst

Senior Manager, Centralized Governance & Control – AML Testing/QA

Quality Assurance Analyst

QA/RA Director

Reactor Project Quality Engineer

Senior Supplier Quality Engineer – Tooling Design

Manager, Corporate Quality Assurance

Post Closing TRID Quality Assurance Analyst – Team Lead

Director, Clinical Quality Assurance – CQA

Specialist I, QA and Learning