Quality Management System Surveillance Job at Airbus (Tianjin Area)

Quality management system surveillance

You will lead and drive the resolution of complex quality issues and continuous ...

Location

China , Tianjin

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Awareness of any potential compliance risks
Commitment to act with integrity

Job Responsibility

Lead and drive the resolution of complex quality issues and continuous improvement projects
Set the measurement standards
Identify/facilitate improvements to increase process performance and product adherence to standards
Increase reliability of processes
Increase repeatability of processes, at initial design phase, before any process changes are made and continuously through the life of a product

What we offer

Support to work, connect and collaborate more easily and flexibly
Fosters flexible working arrangements to stimulate innovative thinking

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

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

Quality System Specialist

As part of the global post market surveillance reporting team, the new colleague...

Location

Hungary , Budapest

Salary:

Not provided

Bio-Rad Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent in a related life science/technical/engineering discipline or equivalent preferred
5+ years experience in a regulated manufacturing industry or equivalent combination of education and experience
Understanding of GMP and quality system standards as they apply to products manufactured by Bio-Rad
Understanding of product post market surveillance requirements for IVD products a plus
Working knowledge of device/drug/biotech manufacturing processes
Detail-oriented and ability to multitask
Problem solving, decision making, time management, organization, communication, leadership, and computer skills
Advanced technical writing and word processing skills
Experience with electronic QMS systems (i.e. Veeva, EtQ, Trackwise) a plus
Fluent English, advanced language knowledge skills in reading and writing

Job Responsibility

Facilitation and generation of product Post Market Surveillance (PMS) and PSUR reports
Analysis of post market data and reviewing completed reports with business partners
Maintaining and supporting databases and systems used for tracking various quality management system (QMS) activities related to post market surveillance
Maintain, archive and completed controlled quality records
Coordinate PMS and post market performance follow-up (PMPF) deliverables with internal business partners
Facilitate and/or chair local/regional PMS Board meetings
Support various QMS and PMS projects (local and global) as needed
Support internal/external audits as needed
Perform other related duties and assignments as needed

What we offer

Life and accident insurance
Private Health Care Services – unlimited examinations, checkups in numerous specialties free of charge
Competitive salary and cafeteria
100% commuting allowance for non Budapest residents
Annual bonus
Annual salary review
Marriage and childbirth allowance
School start allowance
Loyalty award
Employee Referral Program with remarkable referral bonus

Fulltime

Quality System Specialist

As part of the global post market surveillance reporting team, the new colleague...

Location

Hungary , Budapest

Salary:

Not provided

Bio-Rad Laboratories

Expiration Date

Until further notice

Requirements

Bachelor’s degree or equivalent in a related life science/technical/engineering discipline or equivalent preferred
5+ years experience in a regulated manufacturing industry or equivalent combination of education and experience
Understanding of GMP and quality system standards as they apply to products manufactured by Bio-Rad
Understanding of product post market surveillance requirements for IVD products a plus
Working knowledge of device/drug/biotech manufacturing processes
Detail-oriented and ability to multitask
Problem solving, decision making, time management, organization, communication, leadership, and computer skills
Advanced technical writing and word processing skills
Experience with electronic QMS systems (i.e. Veeva, EtQ, Trackwise) a plus
Fluent English, advanced language knowledge skills in reading and writing

Job Responsibility

Facilitation and generation of product Post Market Surveillance (PMS) and PSUR reports
Analysis of post market data and reviewing completed reports with business partners
Maintaining and supporting databases and systems used for tracking various quality management system (QMS) activities related to post market surveillance
Maintain, archive and completed controlled quality records
Coordinate PMS and post market performance follow-up (PMPF) deliverables with internal business partners
Facilitate and/or chair local/regional PMS Board meetings
Support various QMS and PMS projects (local and global) as needed
Support internal/external audits as needed
Perform other related duties and assignments as needed

What we offer

Life and accident insurance
Private Health Care Services – unlimited examinations, checkups in numerous specialties free of charge
Competitive salary and cafeteria
100% commuting allowance for non Budapest residents
Annual bonus
Annual salary review
Marriage and childbirth allowance
School start allowance
Loyalty award
Employee Referral Program with remarkable referral bonus

Fulltime

Quality Conformance Management

Airbus has decided to transfer under a service contract part of the rate of the ...

Location

China , Tianjin

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Bachelor degree in Engineering/Aeronautics major or equivalent
5 year experience in Engineering/Aviation domain
Fluent English both in written and oral speaking is mandatory
Very good technical understanding needed: quality, process, technical aircraft related
Aircraft processes & tools such as SAP, ACPnG, DEMAT, CAPRI, AIRINA...
Fair understanding of configuration management and related tools (CAIR…)
Awareness of any potential compliance risks and a commitment to act with integrity
Ability to work in an international team, with MFT and people from various cultural backgrounds, and across organizational borders
Customer minded with good communication & well developed negotiation skills
Experience on practical problem solving and continuous improvement and general knowledge on corrective tools Reliability: proactive thinking & acting

Job Responsibility

Act as Airbus Plant Quality representative in Tianjin site
Manage Industrial Qualification of special processes
Production Process Verification (PPV) FU.IN.05 process BQM
Produce Constituent Assembly FU.PD.02 process BQM
Manage Operational Surveillance as QCM, Key User of the DeMAT tool and AOS brick owner
Manage staff qualification as unit quality manager, QA administrator and PDR administrator
Manage stamps as stamp administrator
Manage QSR (Quality Survey Report) as QSR Originator and QSR Focal Point
Identify and review quality topics for improvements on the FWD & AFT and ensure proper communication and improvement actions
Manage Events on the FWD & AFT section as Event Operator, Event Manager and Action Plan Leader

Fulltime

Senior Quality Manager – Regulatory Surveillance

We are seeking a self-starting, dynamic Senior Quality Manager to lead regulator...

Location

United States , Boston

Salary:

75.00 - 82.75 USD / Hour

Connexion Systems & Engineering, Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a scientific discipline, operations research, operations management, or related field
Typically 6+ years of relevant experience or equivalent combination of education and experience
Strong facilitation, organization, communication, and influencing skills
In-depth knowledge of global GMP requirements and regulations
Ability to evaluate quality matters and make risk-based decisions
Proven ability to identify and analyze performance indicators
Technical expertise in regulatory compliance, inspections, and quality systems

Job Responsibility

Triage and assess regulatory surveillance items, including new regulations and guidance
Lead cross-functional teams to evaluate the impact of regulations on quality systems and processes
Provide guidance on regulatory expectations, standard industry practices, and implementation options
Support inspection and submission readiness by tracking, reporting, and communicating progress
Present KPIs and metrics to stakeholders to highlight status, risks, and performance

Fulltime

Senior Quality Manager – Regulatory Surveillance

We are seeking a self-starting, dynamic Senior Quality Manager to lead regulator...

Location

United States , Boston

Salary:

75.00 - 82.75 USD / Hour

Connexion Systems & Engineering, Inc

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a scientific discipline, operations research, operations management, or related field
Typically 6+ years of relevant experience or equivalent combination of education and experience
Strong facilitation, organization, communication, and influencing skills
In-depth knowledge of global GMP requirements and regulations
Ability to evaluate quality matters and make risk-based decisions
Proven ability to identify and analyze performance indicators
Technical expertise in regulatory compliance, inspections, and quality systems

Job Responsibility

Triage and assess regulatory surveillance items, including new regulations and guidance
Lead cross-functional teams to evaluate the impact of regulations on quality systems and processes
Provide guidance on regulatory expectations, standard industry practices, and implementation options
Support inspection and submission readiness by tracking, reporting, and communicating progress
Present KPIs and metrics to stakeholders to highlight status, risks, and performance

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Quality Management System Surveillance

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Quality Management System Surveillance

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