Quality Management System Surveillance Job at Airbus (Tianjin Area)

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

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

ISO Quality Compliance Manager

We are seeking an experienced and detail-oriented ISO Quality Compliance Manager...

Location

Pakistan , Rawalpindi

Salary:

Not provided

Translation Empire

Expiration Date

Until further notice

Requirements

Deep understanding of ISO standards (e.g., ISO 9001, ISO 27001, ISO 14001)
Extensive experience in auditing, quality management systems (QMS), and regulatory compliance
Experience in [Insert Industry, e.g., Manufacturing, IT, Healthcare, etc.]
Knowledge of other standards like ISO 45001, GDPR compliance, or sector-specific regulations
Experience with risk management and business continuity planning

Job Responsibility

Manage and ensure ongoing compliance with ISO standards (e.g., ISO 9001, ISO 27001, ISO 14001)
Lead and coordinate ISO certification, surveillance, and recertification audits
Develop, implement, and maintain the company’s Quality Management System (QMS) in alignment with ISO and regulatory requirements
Review and update quality policies, procedures, manuals, and process documentation regularly
Plan, organize, and conduct internal and external audits
ensure timely closure of non-conformities
Identify gaps and areas for improvement
lead corrective and preventive action plans (CAPA)
Deliver ISO standards and compliance-related training and awareness programs to employees
Promote a culture of quality, compliance, and continuous improvement across all departments

Fulltime

New

Logistics Specialist

To ensure complete accuracy, fulfil and comply with Logistics Objectives, QMS an...

Location

United Arab Emirates , Dubai

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Bachelor's in Management/Logistics/Supply Chain/Aviation + 2-3+ years of relevant experience in end to end Warehouse Logistics and Quality Conformance
Proficiency in IT apps - MS Office (Excel, Word, PowerPoint), Gmail, etc.
Experience with logistics software: ERP (SAP), TMS, WMS
Knowledge of shipping software (eg. UPS/FedEx/DHL)
Organizational Skills: Strong planning, time management, and attention to detail
Communication: Excellent verbal & written skills in English
Problem-Solving: Ability to work under pressure, make decisions, adapt
Customer Focus: Service-oriented attitude
Expert in warehouse logistics operations (inbound, inventory handling and outbound) and Quality Conformance
Strong knowledge in order management, logistics management, inventory management, shipping/receiving, warehouse management and Quality Conformance

Job Responsibility

Oversee daily Logistics shopfloor activities to ensure smooth operations and on time delivery of KPIs (daily/weekly/monthly) in line with the agreements
Process Optimization: drive processes, identify bottlenecks, and propose solutions to improve efficiency and optimize costs
Liaise with LSP, suppliers, carriers, Dubai customs and internal teams (sales, production) for seamless operations
Act as a focal point for global to local to global processes (Logistics) coordination, implementation and reporting
Create transparency in the shopfloor operations through timely reporting and escalations
Close collaboration with the Logistics (LSP) WH supervisor and QA team on daily tasks
Coordinate Customs (internal/external) requirements with local/global entities
Participate/Contribute in logistics and QA meetings (Local/Global)
Align with the preparation of rolling shift roaster plans for the QA team
Close monitoring of KPIs, Scraps, Customer claims, Stock Discrepancies and Customer Returns (Red/Blue Channels)

Fulltime

New

Ims / Hseq Coordinator

BMT is a leading global consultancy in design, engineering, science, and risk ma...

Location

Australia , Brisbane; Perth; Melbourne; Adelaide

Salary:

Not provided

BMT

Expiration Date

Until further notice

Requirements

A WHS qualification
Internal lead auditing experience / qualification
Strong auditing knowledge and experience in risk-based audits, compliance, and continuous improvement
Self-motivated, organised, and able to manage time and workload effectively
Experience in preparing for and participating in ISO certifications for ISO 45001, ISO 14001, and ISO 9001
Understanding of WHS and Environmental legislation, quality management systems, risk management principles, and ISO system governance
Sound written and verbal communication skills including presentation skills
Excellent reporting, analytical, and problem-solving skills
Ability to work collaboratively with cross-functional teams and stakeholders
Competence with SharePoint is highly advantageous

Job Responsibility

Maintain and refine HSEQ policies, procedures, and documentation, ensuring accuracy and consistency across platforms
Deliver management system training and communications, simplifying complex requirements for leaders and teams
Develop, maintain, and distribute controlled documents in partnership with Document Owners
Oversee document control and continuous improvement initiatives, maintaining alignment with global and third‑party accreditation requirements
Manage quality assurance, non-conformances, and corrective actions and verify their effectiveness
Prepare the business for external ISO certification and surveillance audits, partnering with operational leaders to ensure readiness and compliance
Plan and deliver risk-based internal audits, manage findings in myOSH (BMT’s online risk management and corrective action platform), and ensure timely close-out of actions. Providing executive summaries of audit results for senior leadership teams
Supporting Health & Safety initiatives such as managing safety training, developing SWMS and JSAs, and supporting with Health & Safety communications

What we offer

Remote, hybrid, and part-time work options
Competitive salary offering
Performance bonuses
Companywide bonuses as part of being an employee benefits trust
Defence Reserve Leave enabling defence reservist employees to undertake ADF obligations without financial disadvantage
24/7 Employee Assistance Program (EAP)
Investment in learning and development

Quality Systems Specialist

Interface with other functions to ensure accurate and timely completion and revi...

Location

United States , Franklin Lakes

Salary:

34.00 - 38.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Knowledge of US and International regulations and standards that apply to the medical device industry including FDA Quality Systems Regulations, ISO 13485, MDD, EU MDR, Canadian MDR, Japan PMDA as well as ANVISA and TGA requirements
In-depth understanding of the application of quality systems to the medical device industry
Experience with Trackwise and SAP
Advanced proficiency in data analysis tools such as Excel, Qlikview and BI report preferred
Bachelors Degree

Job Responsibility

Interface with other functions to ensure accurate and timely completion and review of documents
Collect and Analyze Quality Data to assist with Management Review content development, CER, PMS, Quality Scorecard, etc.
Supports quality system improvement and standardization initiatives within MDS
Support Post Market Surveillance (EU MDR, Canada, etc.) providing data and supporting the preparation of Post Market Surveillance reports and plans for submission to regulatory bodies
Conduct comprehensive literature searches, review of complaints, corrective and preventive actions, and MAUDE database and summarize in a report for medical devices

Fulltime

Analyst 1, Requirements Analysis

The role involves conducting post-market product data analysis, creating necessa...

Location

United States , San Diego

Salary:

Not provided

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Minimum of 2 years of relevant business experience
Experience in data analysis, signal detection, and summarizing data into graphs and statistics
Experience with post-market surveillance, complaints, and service management is preferred
Experience in the medical device industry or an FDA-regulated environment is preferred
Familiarity with Complaint Management Systems and technical documentation is preferred
Excellent written and verbal communication skills
Strong organizational and time management skills
Ability to self-manage in a complex, time-sensitive environment
Intermediate to advanced MS Excel skills (pivot tables, VLOOKUP, formulas)
Ability to effectively collaborate with cross-functional team members

Job Responsibility

Conduct post-market product data analysis and prepare post-market documentation, including surveillance plans and reports
Ensure the adequacy of post-market surveillance documentation, focusing on regulatory compliance and technical/statistical soundness
Collaborate with internal teams such as Medical, R&D, Product Quality, Engineering, and Supplier Quality
regularly interact with executive management
Review and execute post-market surveillance processes continuously, including extracting monthly post-market quality data and updating PMS reports
Perform post-market safety and surveillance activities, including data analysis, tracking/trending, and signal detection
Summarize trends, signals, and escalations
Govern complaint coding schemes and link post-market quality systems to risk management files
Support external and internal audits of post-market surveillance processes
Complete projects and other assigned duties

Fulltime

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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Quality Management System Surveillance

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Location:China , Tianjin Area

Category:Quality Control

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Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 24, 2026

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

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January 24, 2026