Quality Management System Surveillance Job at Airbus (Tianjin Area)

New

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

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

Supply Chain Quality Manager

The Supply Chain Quality Manager at Flexrotor, you will be responsible to secure...

Location

United States , Bingen

Salary:

86500.00 - 138000.00 USD / Year

Airbus

Expiration Date

February 14, 2026

Requirements

Bachelor’s Degree in aerospace or industrial engineering, logistics management, or an equivalent experience
Minimum eight years (8) years of experience in the aerospace or automotive industry in industrial planning, supply chain management, quality management, and continuous improvement required
Knowledge and expertise in Advanced Product Quality Planning, Risk Management, and Continuous Improvement (Lean Six Sigma)
Experience leading industrial capacity and quality assessments
Demonstrated ability to work effectively in a multi-lingual, multi-cultural environment required
Ability to effectively coordinate the work of others with different technical skills and experiences required
Ability to lead problem definition using a matrix organization and without direct management authority by leveraging communication and interpersonal skills required
Demonstrated capability to adapt and thrive in a high-paced, complex international environment required
High-level of organizational and multi-tasking skills mandatory
Excellent people and stakeholder relationship management is essential

Job Responsibility

Secure part deliveries from suppliers on-time and on-quality
Supporting the supply chain team with operational supplier management and escalation
Responsible for On-Time and On-Quality Delivery of Flexrotor purchased material: Create and manage short-term recovery plans
Responsible for the interface with primary Supplier: Program, Industrial, Supply Chain, and Quality Executives and Senior Management
Responsible for analyzing Supplier's production value stream providing feedback on improvement opportunities to de-risk performance to plan
Assess Lean Manufacturing practices and develop improvement plans
Responsible for supplier quality Approval and Compliance: Secure compliance with AIRBUS Quality Management System (QMS) & industry quality standards
Support internal and external audits: Lead Industrial and Product Assessments & Audits
Responsible for establishing the Supplier surveillance plan and coordinating AIRBUS participation
Responsible for ensuring workable end-to-end industrial planning and regular review of Supplier and its Supply Chains’ Configuration Change Notifications, Multi-Sourcing Strategy, and Transfers of Work

What we offer

Relocation assistance for qualified positions
Comprehensive compensation and benefits package

Fulltime

!

Knowledge and Quality Manager

The Knowledge and Quality Manager supports the effective operation of the firm’s...

Location

United Kingdom , London

Salary:

Not provided

Business Integration Partners

Expiration Date

Until further notice

Requirements

Experience in a knowledge management, quality, operations or PMO-type role within a professional services environment
Strong hands-on experience administering SharePoint and supporting Microsoft 365 collaboration tools
Working knowledge of ISO 9001
familiarity with ISO 14001 desirable
Experience supporting audits and maintaining quality or management system documentation
Clear, concise written communication skills and strong attention to detail
Organised, methodical and dependable
Comfortable enforcing standards and challenging poor practice in a constructive way
Pragmatic, with a strong bias towards clarity, usability and proportionality
Trusted and discreet

Job Responsibility

Act as the day-to-day administrator of the firm’s SharePoint environment, including site structure, permissions, document libraries and metadata
Design and maintain a clear, intuitive information architecture supporting the management system, knowledge base and bid library
Establish, document and enforce good practice for the use of SharePoint, Teams and Outlook
Work with IT to manage access, security settings and tool enhancements
Act as a point of escalation for poor practice, duplication or misuse of collaboration tools
Own and maintain the firm’s knowledge base
Operate document control arrangements
Promote consistent naming conventions, folder structures and document standards across the firm
Maintain the structure and content of the firm’s integrated management system, aligned to ISO 9001 and ISO 14001
Support process owners by ensuring documentation reflects how the firm actually operates

Fulltime

Director, Global Supplier and External Manufacturing Quality

This senior leadership role is responsible for defining and executing the global...

Location

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Chemistry, or Engineering
advanced degree (MBA or comparable) preferred
12+ years in pharmaceutical/CHC quality roles, with at least 2 years in global leadership
Proven experience in external manufacturing and supplier quality management
Proven experience in digital tools and eQMS system for the management of suppliers
Deep knowledge of GMP, QMS, and regulatory frameworks
Strong leadership, negotiation, and stakeholder management skills
Fluent in English
any additional languages a plus
Willingness to travel internationally (30–50%)

Job Responsibility

Develop and implement a global quality strategy for external manufacturing and suppliers aligned with corporate objectives and regulatory standards
Establish governance for supplier qualification, performance monitoring, and lifecycle management
Own the global supplier and CMO Quality Management System (QMS)
Approve and maintain the global supplier/CMO portfolio, including: Qualification and onboarding
Quality agreements
Performance monitoring and scorecards
Periodic business reviews
Ensure timely release of externally manufactured products
Oversee product quality reviews (PQR/APR) and device post‑market surveillance
Ensure adherence to GMP, GDP, ISO standards, and global regulatory requirements (FDA, EMA, ICH, PMDA)

What we offer

competitive salary
comprehensive benefits
extensive opportunities for professional growth and development

Document Controller / Business Support Assistant

This dual-purpose role is to deliver effective management of project documents a...

Location

United Kingdom , South Mimms

Salary:

Not provided

Egis in the UK

Expiration Date

Until further notice

Requirements

Experience working on large complex construction projects or similar
PFI experience advantageous but not essential
Excellent document management skills including experience of using different industry standard and/or bespoke document management software packages including Business Collaborator or other similar packages
Knowledge of administration of Quality Management Systems
Knowledge of administration of IT security policy
Proficient use of MS office including Word, Excel and PowerPoint
Attention to detail including being highly diligent, organized, proactive and able to work on own initiative
Excellent team working skills, ability to build effective relationships at all levels
Good interpersonal and communication skills
Determination to see tasks through to completion, with excellent planning and organisational skills

Job Responsibility

Deliver effective management of project documents and records ensuring they are compliant with all contractual, legal, and Integrated Management System (IMS) requirements
Provide essential business support to the wider team including administrative and general office management activities
Maintain document registers, version control and the timely submission of documents to our client and other relevant stakeholders
Maintain document logs including performance reports for certain workflows including Technical Queries and the Schedule of Submissions
Ensure documents comply with legal, contractual and quality management standards for auditing purposes
Provide support during certified management system surveillance and recertification audits including PAS 99, ISO 44001, ISO 55001, ISO 27001 and PAS 2080
Ensure all submissions follow the correct process and contractual workflow including formal correspondence, review procedure submissions for design and non-design submissions, technical queries and waivers
Manage and update the Schedule of Submissions
Ensure electronic documents are stored securely in the EDRMS and access is restricted for confidential files
Ensure retention periods comply with contractual requirements of Schedule 15

Quality Assurance Manager

We are looking for an experienced Quality Assurance Manager to join our team in ...

Location

United States , Simi Valley

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Minimum of 3 years of experience in quality assurance within a medical device manufacturing environment
Hands-on experience with ISO 13485-compliant Quality Management Systems
Proficiency in Selenium for web browser automation and manual testing
Strong knowledge of quality assurance practices, including testing and regulatory compliance
Demonstrated ability to conduct audits and manage document control processes effectively
Familiarity with complaint handling and post-market surveillance activities
Proven track record of submitting regulatory reports and managing device licenses
Excellent analytical and organizational skills with a focus on data-driven decision-making

Job Responsibility

Serve as the Management Representative, overseeing all aspects of quality system compliance
Coordinate and manage internal and external audits to ensure adherence to regulatory standards
Train staff on quality procedures and regulatory requirements to enhance overall compliance
Handle product recalls, from initiation to closure, while maintaining accurate and compliant recall files
Conduct post-market surveillance activities and maintain Device Master Records to ensure product safety
Submit reportable events promptly in accordance with applicable regulatory guidelines
Renew medical device licenses and registrations for relevant jurisdictions
Prepare management review presentations, analyze quality metrics, and identify trends to support process improvements
Manage the document change order process, ensuring updates to procedures and inspection documents are implemented and recorded accurately

What we offer

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

Quality Management System Surveillance

Airbus

Location:
China , Tianjin Area

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 24, 2026

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Job Description:

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Requirements:

Additional Information:

Job Posted:January 24, 2026

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