Quality Management Systems Engineer Job at NP Aerospace Limited (Coventry)

Principal Quality Engineer (Quality Management Lead)

We are recruiting Principal Quality Engineers (PQEs) to support the Sizewell C (...

Location

United Kingdom , London; Bristol; Suffolk (Sizewell C site); Manchester

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

Background in large, complex and highly regulated environments—ideally in nuclear or similarly regulated sectors—with strong focus on project quality and expertise in a relevant engineering discipline (mechanical, electrical, I&C, fabrication)
Strong understanding of Quality Assurance and Quality Control across engineering, procurement, manufacturing, construction and commissioning
Knowledge of the nuclear sector (preferably new build) and familiarity with Licence Conditions LC6, LC17 and ONR TAG 077 is desirable
Clear understanding of quality management best practice for deployment in large, complex, contract-led organisations
Confident communicator with strong presentation skills, comfortable engaging with individuals, small groups and large audiences
Experience ensuring compliance with national and international standards such as GS‑R‑3, ISO 9001, ISO 19443, ISO 3834 and EN10204
Proven ability to plan and conduct internal and supplier audits
Able to carry out unsupervised inspections to appropriate standards (e.g., pressurised systems)
Experienced in reviewing quality records (e.g., material certification, CFSI) and analysing quality data across an organisation
Experience managing people or leading teams

Job Responsibility

Support development and implementation of QA/QC arrangements across SZC
Identify and conduct supplier audits, and close out findings
Manage quality execution and support supplier technical assessments
Oversee manufacturing and construction surveillance
Manage non-conformances and Quality Release Certificate processes
Drive improvements in quality implementation across the project
Review, accept and monitor Contractors’ Quality Assurance Plans (CQAPs)
Produce and implement Project Quality Control Plans
Ensure deployment of key contractual quality arrangements (GQAS, LTQRs, ITP specifications)
Guide contractors on quality requirements and project-specific arrangements

What we offer

Hybrid Working Opportunity
Flexible working hours – 2/3 days per week in the Bristol office
Market Leading Pension scheme (8% company contribution / 4% personal contribution)
25 days’ paid annual leave + bank holidays + option to buy or sell days
Professional fees reimbursed
Employee referral scheme
Competitive Sick Pay – Support when you need it
Income Protection & 3x Salary Death-in-Service Cover
Free Digital Gym Access – Expert-led fitness classes
24/7 Employee Support Line – Mental health, financial & legal help

Fulltime

Work Management Systems Engineer

Blackbaud is seeking an experienced Azure DevOps & Atlassian Jira Administrator ...

Location

India , Hyderabad

Salary:

Not provided

Blackbaud

Expiration Date

Until further notice

Requirements

2+ years administering Azure DevOps and Atlassian Jira in complex enterprise environments
Strong understanding of Agile, Scrum, Kanban, and scaled Agile frameworks
Experience designing workflows, permission models, project structures, and field configurations
Proficiency with ADO Boards, Repos, Pipelines, and integrations with Git-based source control
Ability to partner with engineering teams to ensure accurate work item hygiene, traceability, and progress reporting
Strong troubleshooting skills across permissions, workflows, automation, and integrations
Experience creating documentation, onboarding content, and user training programs
Ability to manage competing priorities and engage with users at all organizational levels
Able to work flexible hours as required by business priorities
Ability to deliver work which meets all minimum standards of quality, security, and operability

Job Responsibility

Own the administration, configuration, and lifecycle management of Azure DevOps and Atlassian Jira, including projects, boards, workflows, permissions, integrations, and automations
Maintain alignment with established Azure DevOps governance practices and data hygiene expectations, including support for work item hierarchy, backlog structures, and work tracking standards
Define and enforce usage standards, fields, templates, and workflows to ensure consistency and reliable reporting across teams
Partner with product, engineering, and delivery leaders to optimize usage of work management tools in support of Scrum, Kanban, SAFe, and hybrid methodologies
Provide expert guidance on backlog management, user story structures, acceptance criteria alignment, and traceability from ideas to deployments
Ensure integrations between ADO, Jira, Git repos, pipelines, and adjacent systems remain secure, scalable, and well-documented
Build and deliver training, onboarding materials, and documentation to improve team adoption and maturity of work management practices
Support new groups onboarding into ADO and Jira, leveraging best practices and governance guidance established by Azure DevOps Governance teams
Provide hands-on troubleshooting assistance, coaching, and advisory support to users at all levels
Develop dashboards, queries, filters, workflows, and automations to improve transparency and reduce manual work

Fulltime

Senior Supplier Quality Management Engineer

Location

China , Beijing

Salary:

Not provided

BorgWarner

Expiration Date

Until further notice

Requirements

Master's degree preferred
Bachelor's degree or above from a key university
Engineering background required, preferably in Vehicle Engineering, Mechanical Engineering, or related disciplines
Minimum of 5 years of relevant experience in automotive drivetrain systems
Experience in transmission, engine, axle, driveline, or electric drive systems is highly desirable
Strong knowledge of supplier quality management tools and processes, including APQP, PPAP, change management, warranty/claim handling, 8D problem solving, VDA 6.3 process audits, IATF 16949, CQI-9 or other special process audits
Proficient in Six Sigma, Red X problem-solving methodologies, and the application of statistical methods for data-driven decision-making
Excellent communication and negotiation skills
Strong logical thinking and analytical capabilities
high integrity and alignment with corporate values

Job Responsibility

Lead the development and supplier quality management of components for BorgWarner AWD (All-Wheel Drive) systems and Torque Management systems
Drive supplier performance management, continuous improvement initiatives, supplier audits, zero-defect programs, and targeted quality improvement projects
Collaborate closely with Engineering and Purchasing teams to identify cost reduction opportunities in product design and manufacturing processes, and support sustainable cost improvement across the supply base through Lean methodologies
Support fast-paced and rapidly evolving new energy vehicle (NEV) programs and ensure robust supplier readiness for new product launches
Build and maintain a high-performing, competitive, environmentally friendly, and sustainable supply chain aligned with BorgWarner’s quality and sustainability objectives

Fulltime

Quality Systems Engineer

Millennium Space Systems, a part of Boeing Defense, Space and Security (BDS), is...

Location

United States , El Segundo; Los Angeles

Salary:

74800.00 - 131250.00 USD / Year

Boeing

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Physics, or a related STEM discipline
or 4+ years of equivalent Quality Systems Engineering experience in lieu of a degree
3–5 years of experience in aerospace and/or defense manufacturing in a quality systems role
Expert knowledge of QMS requirements and auditing in a complex product environment, with demonstrated experience in one or more of the following standards: AS9100D, ISO 9001:2015
This position requires the ability to obtain a US Security Clearance for which the US Government requires US Citizenship
A final U.S. clearance Post Start is required

Job Responsibility

Develop, lead, and manage the execution of the QMS and its top-level processes, ensuring alignment with AS9100D, ISO 9001, customer, and regulatory requirements
Build and maintain the internal QMS roadmap for tools, capabilities, and processes to match program growth, new product introductions, and customer requirements
Partner with Engineering, Manufacturing, and Global Supply Chain to develop processes, digital tools to meet QMS requirements and advance new quality capabilities
Become a systems expert for QMS tools, processes, and data sets to enable effective quality execution across all programs
Plan, coordinate, and execute the internal & external audit program against AS9100/ISO standards and customer-specific requirements
manage audit scheduling, resource allocation, and results reporting
Support external certification audits and customer audits
interface with third-party registrars and government auditors as required
Measure, analyze, and report quality system and audit metrics to leadership
identify trends and drive systemic corrective actions

What we offer

competitive base pay and variable compensation opportunities
health insurance
flexible spending accounts
health savings accounts
retirement savings plans
life and disability insurance programs
paid and unpaid time away from work
generous company match to your 401(k)
industry-leading tuition assistance program pays your institution directly
fertility, adoption, and surrogacy benefits

Fulltime

Sr Quality Systems Engineer

This is where you make a difference in our patients’ safety. As a member of the ...

Location

Costa Rica , Cartago

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Minimum of 4 years of experience in manufacturing processes, quality systems, regulatory compliance, and GMPs within Baxter or in companies producing healthcare devices
Validated knowledge of ISO 9001, ISO 13485, PMD Law, CMDR, MDSAP, CFR 21 and the Manufacturing Maturity Program (CMMI)
Validated experience in auditing systems and certification as an Internal Auditor
Knowledge and experience in Sterility Assurance
University training in Engineering (Production, Industrial, Chemical, Systems, Electrical, Electronics, Electromechanics) or related career
Equivalent experience in production environments with Quality Systems in the medical device manufacturing industry

Job Responsibility

Own the Complaints, CAPA, Risk Management, Hold and Corrective Actions systems, as well as their critical metrics and participation in local, regional and corporate forums
Implement the Internal Audit Program and follow up on corrective and preventive actions
Assess the regulatory alignment of processes and systems
Ensure they follow applicable directives and standards
Coordinate the system for change oversight, making sure changes stay in sync with regulatory requirements
Ensure evaluations of complaint samples, manufacturing investigations, and coordination with Product Surveillance within defined timeframes
Facilitate root cause analysis and ensure complete documentation in CAPA processes
Implement and maintain the risk system, assessing and controlling risks and leading residual risk
Ensure the accurate execution of the Hold process and the corrective field actions (FCA)
Maintain effective communication with productive areas and lead actions to reduce complaints

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Sr. Quality Systems Engineer

Beacon Technologies is seeking a Sr. Quality Systems Engineer for our client par...

Location

United States , El Segundo

Salary:

Not provided

Beacon Technologies

Expiration Date

Until further notice

Requirements

5+ years of experience in systems engineering on compliance systems, or regulatory technology environments
Bachelor’s degree in Engineering, Computer Science, Information Technology, or related technical field
Understanding of U.S. import compliance requirements related to CPSC, CBP, ACE, and electronic Certificate of Compliance filings are a plus
Experience working with integrated systems such as LIMS, data warehouses, and document management platforms
Trained in Veeva vault configuration and administration is preferred
Proven ability to translate regulatory and business requirements into clear technical specifications
Experience working cross-functionally with IT teams, external partners, and business stakeholders
Strong communication skills, comfortable leading meetings, training sessions, and discussions with both technical and non-technical audiences
Experience supporting external customers or retail partners in compliance-related processes is a plus
Project management experience with system implementations or enhancements

Job Responsibility

Act as the global subject matter expert for Certificate of Conformance (COC) processes related to U.S. imports
Own and continuously improve the end-to-end eCOC workflow, including integrations across Laboratory Information Management Sytem (LIMS), Google Big Query (GBQ), and Veeva
Partner with IT to define business and system requirements for enhancements impacting COC generation, metadata, test report management, and CSV full message set creation
Ensure alignment of system functionality with CPSC Portal and CBP ACE eFiling requirements
Collaborate with laboratories to ensure test reports and supporting documentation are accurately generated and transmitted through the system landscape
Support retailers performing direct import by gathering their eFiling requirements, providing guidance on CSV file creation, and troubleshooting submission issues
Lead business-side project management activities for system implementations, upgrades, and regulatory-driven changes
Oversee configuration, testing, validation, and user acceptance testing for eCOC-related system updates
Support the Organizational Change Management and training team ensuring training are developed and delivered to internal and external users to understand how to download test reports, generate COCs, and create compliant CSV files
Monitor regulatory updates and proactively assess impacts to systems and processes

What we offer

career advancement opportunities
extensive training
excellent benefits including paying for health and dental premiums for salaried employees

Fulltime

Quality Systems Engineer

You don’t see it, but it’s there. Our employees work on the world’s most advance...

Location

United States , Nashua

Salary:

118095.00 - 200762.00 USD / Year

Baesystems

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 4-6 years of related work experience
Strong knowledge and experience with and AS9100 or ISO Quality System
Experience in the use of root cause analysis tools Investigating and resolving customer complaints
Good communication and interpersonal skills
Ability to work independently

Job Responsibility

Support and active engagement with 3rd party AS9100D certification auditors for planning and executing certification audits
Driving prevention activities and Opportunities for Improvement across sites
Leading cross site council responsible for driving Risk Assessments, Lessons Learned and benchmarking
Manage quality training programs
Author and or drive changes to command media that drive optimization, nonconformity prevention aka. mistake proofing, and benchmarking improvements
Engagement with onsite Customer to address nonconformities and present Quality Management System Key Process Indicators (KPIs)

What we offer

health, dental, and vision insurance
health savings accounts
a 401(k) savings plan
disability coverage
life and accident insurance
employee assistance program
legal plan
discounts on things like home, auto, and pet insurance
paid time off
paid holidays

Fulltime

Quality Management Systems Manager

Location

United States , Memphis

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Quality, or a related technical field
Minimum of 5 years managing quality systems within a manufacturing environment
Lean Six Sigma Black Belt or Lean Practitioner certification
Strong knowledge of industry‑specific QMS frameworks
Experience leading audits, developing quality documentation, and training internal teams
Excellent analytical, organizational, and communication skills
Experience using SAP for quality and production data tracking
Familiarity with Microsoft SharePoint for documentation and collaboration
Demonstrated success driving Continuous Improvement and Lean initiatives
Knowledge of APQP, PPAP, FMEA, SPC, or similar quality tools

Job Responsibility

Oversee and maintain the organization’s Quality Management System (QMS), ensuring compliance with all relevant industry standards and regulatory requirements
Manage internal and external audits, including preparation, execution, and corrective follow‑up with customers, registrars, and regulatory agencies
Drive standardization and continuous improvement of quality systems, procedures, and documentation across all departments
Lead cross‑functional process improvement initiatives using Lean Six Sigma methodologies to reduce waste, increase efficiency, and improve product quality
Direct root cause analysis and corrective/preventive action (CAPA) processes to address systemic quality issues
Ensure organization‑wide training, deployment, and adherence to QMS requirements
Support product launches, engineering changes, and manufacturing process modifications to ensure quality system compliance
Maintain and enhance digital quality tools such as document control systems, audit tracking platforms, and corrective action workflows

What we offer

medical, vision, dental, and life and disability insurance
company 401(k) plan

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Quality Management Systems Engineer

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