Quality management system surveillance Job at Airbus (Tianjin)

Senior Director of Quality

HPE is seeking a strategic, customer-focused Senior Director of Quality to lead ...

Location

United States

Salary:

161000.00 - 389500.00 USD / Year

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

Bachelor’s degree in engineering, quality assurance/quality management, or a related field. Master’s degree preferred
10+ years of progressive quality leadership experience, including 5+ years in a senior leadership role managing global teams across hardware, software, and services
Proven experience within complex products and complex supply chains
prior experience in HPC, AI, networking, storage, or comparable high-tech industries encompassing one or more quality management domains is preferred
Proven ability to build and scale QMS and quality programs within complex organizations
Deep knowledge of quality systems, methodologies and tools (Six Sigma, Lean, APQP, FMEA, risk management, root cause analysis). Strong problem-solving and data-driven decision-making skills
Experience with regulatory standards and certification processes (ISO, industry specific)
Experience with supplier quality management, including supplier qualification, audits, and remediation
Proficiency in quality management software and enterprise systems
Strong leadership and people management abilities

Job Responsibility

Define and drive the business unit’s quality strategy, standards, and metrics to ensure product quality, regulatory compliance, and customer excellence
Lead and advance the Quality Management System (QMS), including document control, change control, CAPA, nonconformances, deviation handling, and supplier quality management
Lead, mentor, and develop a high-performing, cross-functional Quality organization by setting clear objectives, tracking performance, developing talent, and fostering a quality-first culture
Collaborate with Product & Engineering leadership to influence design for reliability, testability, manufacturability, and serviceability. Ensure design quality, implement design controls, conduct DFM/DFMEA, participate in design reviews, and develop verification and validation strategies
Ensure compliance with applicable regulations and standards such as FDA, EMA, ISO 9001, ISO 13485, GMP, and GMP-like requirements. Coordinate internal and external audits, inspections, regulatory submissions, and remediation activities
Partner with Supply Chain and Procurement to manage supplier quality, including qualification, performance management, corrective actions, and continuous improvement
Own root cause investigations for systemic quality issues, lead cross-functional corrective actions and verification of effectiveness
Lead risk management activities including FMEA and risk assessments, conduct product safety evaluations, and oversee post-market surveillance to proactively manage risk
Drive continuous improvement initiatives using Lean, Six Sigma, and other methodologies to enhance quality, yield, throughput, and customer satisfaction. Manage quality-focused kaizen events and project portfolios
Prepare and present quality metrics and reports to senior leadership, translating data into actionable insights and strategic recommendations

What we offer

Health & Wellbeing
Personal & Professional Development
Unconditional Inclusion

Fulltime

Quality Manager

Location

Brunei

Salary:

Not provided

Bureau Veritas Certification CZ, s.r.o.

Expiration Date

Until further notice

Requirements

Degree or Diploma in Mechanical, Materials, Quality, or related engineering discipline
ISO 9001 Lead Auditor certification (mandatory)
Minimum 7–10 years experience in QA/QC, inspection, or quality management within the Oil & Gas or critical asset industries
Strong understanding of: ISO 9001 Quality Management Systems, ISO 17020 (Inspection Bodies), ISO 17025 calibration requirements, API/ASME inspection codes and COMPANY quality standards
Familiar with NDT/Advanced NDT competency standards (ISO 9712, SNT-TC-1A, CSWIP, API 570/510/653)
Experience with Vendor Inspection, fabrication surveillance, and document review
Strong analytical, audit, and problem-solving capabilities (NCR, RCA, CAR processes)
Proficient in MS Office, digital inspection systems, and quality management tools
Effective communication and stakeholder management skills to interface with COMPANY representatives
HSSE awareness and required COMPANY training (BOSIET if offshore visits are required)

Job Responsibility

Provide overall leadership and governance of the Contractor Quality Management System (QMS) to ensure full compliance with COMPANY requirements, ISO 9001, and ISO 17020
Oversee all quality functions including: Quality Assurance Engineer, Tools, Materials & Calibration Coordinator, Vendor Third-Party Inspection (VTPI) Coordinator, Quality Engineering Team (Quality Lead, Senior QAQC Engineer, Project QE, QCS Engineer)
Ensure all inspection deliverables, reports, data submissions, workpacks, and documentation meet COMPANY quality standards, procedures, and contractual obligations
Lead the preparation, submission, implementation, and maintenance of the Quality Assurance Plan (QAP), ITPs, Surveillance Plan, and contract-specific quality documentation
Manage and execute internal quality audits, support COMPANY audits, and ensure timely closure of NCRs, CARs, and preventive actions
Ensure calibration compliance of all NDT/Advanced NDT equipment, gauges, EX-rated devices, and inspection tools in accordance with ISO 17025 requirements
Provide quality oversight for Vendor Inspection / TPI activities, including review of Vendor Quality Plans, ITPs, FAT/SAT procedures, and manufacturing surveillance reports
Review and validate inspection data quality, ensuring accuracy, completeness, traceability, and compliance before CIRRAS/SAP submission
Lead quality risk assessments, identify quality gaps, and implement improvements to enhance reliability of inspection execution
Ensure personnel competency and qualification records for inspection/NDT staff are maintained in accordance with contract requirements (ISO 9712, API, CSWIP, ASNT, IRATA)

Regulatory Specialist

At 2San, we are at the forefront of innovation in the global healthcare industry...

Location

United States , Norwood

Salary:

80000.00 USD / Year

2San

Expiration Date

Until further notice

Requirements

Proven regulatory affairs experience within the healthcare sector, with a focus on Class 2 and Class 3 Self-Test IVDs
Deep understanding of regulatory requirements and processes for the US market, including 510(k) management, FDA submissions, and compliance management
Experience with developing, implementing, and managing Quality Management Systems (QMS) in accordance with US and international standards, including familiarity with ISO 13485
Ability to develop and implement regulatory strategies that align with company objectives and product lifecycle
Strong analytical skills for assessing regulatory compliance, interpreting guidelines, and resolving complex issues
Excellent written and verbal communication skills for effective liaising with regulatory bodies, internal teams, and external partners
Proactive in identifying potential regulatory obstacles and developing effective solutions
Meticulous attention to detail with the capability to manage multiple projects and priorities simultaneously
Bachelor’s degree in a relevant scientific discipline (e.g., Biology, Chemistry, Biomedical Engineering) required
advanced degrees or certifications in regulatory affairs or quality assurance preferred

Job Responsibility

Monitoring and management of new and existing 510(k) entries to ensure all product listings are current and compliant with regulatory requirements
Preparing and submitting FDA applications for new product approvals and amendments for existing products, ensuring all submissions are accurate and meet regulatory standards
Maintaining the regulatory tracker to ensure all information is current and in-line with local requirements
Maintaining regular contact with manufacturers for products supplier in US. Ensuring that their conformity assessment is not due to lapse and ensuring that a plan is in place for updated certification. (IVDD to IVDR)
Regularly reviewing and updating the Quality Management System (QMS) to ensure it aligns with both US and international standards, including ISO 13485, and addressing any gaps or non-compliances
Overseeing Complaints Management and Post-Market Surveillance Activities, including the collection, analysis, and reporting of customer feedback and adverse events to regulatory bodies as required. Implementing corrective actions and ensuring continuous product quality and safety monitoring in compliance with regulatory requirements
Collaborating with product development teams to provide regulatory guidance and support from concept through to commercialization, ensuring regulatory considerations are integrated into product lifecycle management
Navigating regulatory pathways to secure product approval and market entry, including strategizing for efficient and compliant product launches
Applying strong analytical skills to assess regulatory compliance, interpret complex regulatory guidelines, and undertake risk assessments for regulatory strategies and submissions
Proactively identifying potential regulatory challenges and obstacles and working collaboratively with cross-functional teams to develop and implement effective solutions

Director of Quality and Regulatory Affairs

The Director of Quality and Regulatory Affairs leads the global QA/RA function a...

Location

United States , Burlington

Salary:

170000.00 - 180000.00 USD / Year

Myomo

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a scientific, technical, or related discipline
advanced degree preferred
8-10+ years of progressive experience in Quality Assurance and Regulatory Affairs within the medical device industry, including significant management experience
5+ years of experience with Class I and/or Class II medical devices
Experience operating within FDA-regulated cGMP environments, including regulatory submissions and agency interactions
Strong knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, EU MDR, ISO 14971, and Design Controls
Experience managing Quality Management Systems (QMS) for medical devices
Experience supporting global regulatory activities (e.g., EU, Canada, APAC preferred)
Demonstrated experience leading QA/RA teams, including talent development and performance management
RAC certification or equivalent is preferred

Job Responsibility

Lead the global QA/RA function and is responsible for execution of the company’s quality and regulatory strategy
Ensure compliance with applicable global regulations and standards (including FDA and ISO requirements) and oversees quality systems across the product lifecycle
Partner cross-functionally to support product development, regulatory submissions, and ongoing compliance activities, while driving continuous improvement in quality processes
Contribute to the development and lead execution of the Quality strategy
Lead departmental planning and budgeting, optimizing resources and operational efficiency
Direct QA/RA staff, including organizational design, talent development and performance management
Develop and continuously improve quality programs, policies, and processes
Ensure Quality Management System (QMS) processes are established, implemented, and maintained
Lead regulatory activities and compliance interactions, serving as the primary liaison with regulatory authorities
Oversee development and execution of global regulatory strategies for product submissions and lifecycle management

Fulltime

Quality Lead II

Join a leading company in the construction industry as a Quality Lead II, where ...

Location

United States , Midland

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, Quality Management, or related field preferred
Minimum 5 years in quality management within the construction industry
Strong understanding of quality management systems in construction
Experience in managing construction scope effectively
Proficient in quality assurance and control processes
Working experience with flow lines, pipelines, wells, and compressors is preferred

Job Responsibility

Provide leadership to implement engineering, procurement, and site quality systems
Ensure services, equipment, and materials meet contract and statutory requirements
Evaluate and monitor Contractor's quality management systems for performance improvement
Oversee development and implementation of Project specific Surveillance Plans and Procedures
Monitor metrics to identify, investigate, and resolve quality issues
Provide direction to discipline inspectors and support the Project Team on quality issues
Promote quality awareness throughout the project

What we offer

Competitive salary based on qualifications and experience

Fulltime

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

Manager, Quality Management System

As the leader of our Quality Management System at Archer, you will play a pivota...

Location

United States , San Jose

Salary:

117500.00 - 155600.00 USD / Year

Archer Aviation

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering (Aerospace, Mechanical, Electrical, or Industrial) with at least 7+ years’ experience leading quality teams within aerospace or other regulated industry
Experience hiring, leading and managing salaried & hourly employees
Experience overseeing and implementing AS9100 certification with an in-depth understanding of AS9102, AS9103, and AS9145
Direct experience establishing and leading CABs and supporting MOR quality reviews with senior leadership
Experience leading all aspects of quality to include: QMS (Quality Management System)
Auditing (Internal & External)
3rd Party Certification, Receiving Inspection
In-Process Inspection
Product Quality Engineering
FMEA (Failure Mode Effects Analysis) implementation

Job Responsibility

Author, maintain, and continuously improve the QMS (Quality Manual, procedures, work instructions) ensuring full compliance with AS9100 and FAA 14 CFR § 21.137 Quality System requirements across all Archer sites
Serve as the primary quality liaison with the FAA during Production Certification, supporting conformity inspections, and airworthiness certificate issuance activities
Establish and govern a unified QMS framework across multiple sites, including standardized audit programs, cross-site corrective action processes, and site-level quality leadership structures
Lead internal and external audits with AS9100 third-party certification body and FAA surveillance audits across all sites
Own the Corrective Action Board (CAB) and Root Cause Corrective Action (RCCA) process to drive systemic resolution of nonconformances across all sites
Define and report KPIs to senior leadership via Monthly Operations Reviews (MOR) and real-time dashboards
Integrate quality into Engineering, Manufacturing, Supply Chain, and Flight Operations processes
Partner with Archer Certification and Safety Department on SMS and Type Certificate obligations
Manage QMS budget and a geographically dispersed quality team

Fulltime

Quality Assurance Engineer

EKFB is seeking to recruit a Quality Assurance Engineer to join the team based i...

Location

United Kingdom , Milton Keynes

Salary:

Not provided

EKFB

Expiration Date

Until further notice

Requirements

Experience working within Quality Assurance in a construction environment
Rail infrastructure experience preferred
Organisational and leadership skills
Ability to understand multiple and conflicting priorities
Good communication and engagement skills
Recognised Quality related qualification desirable
Membership of the CQI (or equivalent profession) desirable
Internal Auditor (ISO 9001 preferred)
Full UK Driving License
CSCS Card Holder (or affiliated scheme)

Job Responsibility

Understand and promote the principles/importance of self assurance within Construction Delivery Team
Understand and promote ownership of Inspection and Test Plans (ITP) and their checklists ensuring quality compliance throughout the construction phases
Collaborate with the Construction Delivery Teams to plan for delivery pre-work processes, ITPs to suit the construction methods/activities, checking records of construction and progressive capture of records
Understand and implement the EKFB Quality requirements to ensure ITP's are compliant and confirm with HS2 requirements and contain the appropriate document references
Support the delivery of all construction phase quality assurance activities/records and be responsible for checking the completeness of the records in accordance with the plans/procedures
Liaise with the Handover and Completion team to ensure the records are adequate for handover
Actively understand quality issues and be instrumental in finding solutions with the Construction Delivery team, the quality team and subject matter experts
Develop and utilise relationships with the Designer’s and Client’s representatives and internal stakeholders to deliver all ITP related aspects of quality and assurance, ensuring seamless information exchange with the Construction Delivery Team
Use relevant IT systems to manage all relevant quality documentation and records and also relevant systems to manage progress of the ITPs between EKFB, Designer and Client representatives
Deliver awareness sessions as part of a wider programme to non-quality professionals and communicate the benefits and knowledge of the Business Management System

What we offer

Competitive salary and benefits

Fulltime

Quality management system surveillance

Airbus

Location:
China , Tianjin

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 22, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Quality management system surveillance

Senior Director of Quality

Quality Manager

Regulatory Specialist

Director of Quality and Regulatory Affairs

Quality Lead II

Principal Quality Engineer (Quality Management Lead)

Manager, Quality Management System

Quality Assurance Engineer

Quality management system surveillance

Airbus

Location:China , Tianjin

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 22, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Quality management system surveillance

Senior Director of Quality

Quality Manager

Regulatory Specialist

Director of Quality and Regulatory Affairs

Quality Lead II

Principal Quality Engineer (Quality Management Lead)

Manager, Quality Management System

Quality Assurance Engineer

Location:
China , Tianjin

Category:
Quality Control

Contract Type:
Not provided

Job Posted:
February 22, 2026