Compliance Verification Engineer Job at 2Excel Aviation Ltd (Doncaster)

Compliance Verification Engineer (Electrical / Avionics)

We are seeking a Electrical/Avionics Compliance Verification Engineer to join ou...

Location

United Kingdom , Doncaster

Salary:

60701.00 - 88293.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Extensive knowledge of specialist areas
aircraft Electrical Systems and/or Avionic Systems
Detailed knowledge of Part 21, CS/FAR 23 and 25
Experience of design and integration of complex projects on aircraft under civil or military airworthiness regulations
Ability to compile, technically check and verify compliance of certification programme, compliance checklist, and other certification documentation
Experienced in compliance verification and checking of some or all of: Electrical Load Analyses, Equipment Assessments, EWIS and EZAP analysis, Electromagnetic and Ground Function Test Plans and Reports, system safety assessments and functional hazard assessments, according to technical specialism

What we offer

25 days holiday per year from day one plus bank holidays
6% matched Pension scheme
Group Life Insurance
Health and Wellbeing benefits including Private Health Care and an EAP

Fulltime

Principal Structural Verification Engineer

This unique position involves zero design production. Instead, your sole focus w...

Location

Australia , Adelaide

Salary:

140000.00 - 180000.00 AUD / Year

Randstad

Expiration Date

June 18, 2026

Requirements

15+ years of comprehensive experience in structural engineering design and review across both residential and commercial/industrial sectors
A Bachelor of Engineering (Civil/Structural) or equivalent recognised by Engineers Australia
Chartered Status (CPEng) or listing on the National Engineering Register (NER) is highly desirable
An authoritative knowledge of the National Construction Code (NCC) and Australian Structural Standards (including AS 1170, AS 3600, AS 4100, and AS 2870)
The ability to communicate complex technical compliance issues clearly and diplomatically to external engineers, architects, and internal certifiers

Job Responsibility

Conducting rigorous, high-level reviews of structural drawings, computations, and geotechnical reports for both residential (Class 1 & 10) and commercial (Class 2–9) developments
Reviewing structural designs to ensure alignment with the NCC, providing the critical technical oversight and documentation required to support the firm's building certifiers
Identifying structural design deficiencies or non-compliances, and compiling clear, constructive review reports for external engineering teams to rectify
Acting as the in-house Subject Matter Expert (SME), providing pragmatic, high-level structural advice to the firm’s building certifiers and code consultants to guide their statutory determinations

What we offer

Pure technical focus (no client acquisition targets, no team management pressure, no design delivery deadlines)
True hybrid working (work from home for deep-focus review work, with flexibility to go into Adelaide office for collaboration)
Respected advisory role
Competitive remuneration package

Senior Medical Device Compliance Engineer

The Senior Medical Device Compliance Engineer is responsible for medical device ...

Location

United States

Salary:

130500.00 - 159500.00 USD / Year

SharkNinja

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Engineering (Mechanical, Electrical, Biomedical), Quality, or a related technical discipline
5+ years of experience in design controls, and post-market sustaining of medical devices
Strong experience supporting electromechanical medical devices, preferably within consumer electronics or high-velocity product development environments
Deep expertise in design controls and risk management, including ISO 14971, hazard analysis, DFMEA, requirements management, and verification/validation
Experience supporting post-market design changes, including ECNs, root cause analysis, and lifecycle risk management
Experience working with overseas contract manufacturers and distributors, including qualification, process validation review, and ongoing compliance oversight
Working knowledge of biocompatibility, electrical safety, labeling, and component change impact assessments
Strong communication skills and the ability to operate effectively in a complex, matrixed organization
Pragmatic, detail-oriented mindset suited to fast-paced, innovative-driven environments

Job Responsibility

Drive design control execution for multiple concurrent medical device NPD programs, ensuring high-quality, audit-ready technical documentation
Lead and support the creation, review, and approval of Design History Files (DHFs), including design and development plans, requirements, design reviews, risk management files, verification and validation plans and reports, and traceability, ensuring documentation is complete and submission ready
Translate medical device compliance and regulatory requirements into clear, actionable product and engineering requirements
Ensure risk management activities including hazard analysis, DFMEA, and test planning in alignment with QMS processes
Support post-market design changes by driving and reviewing ECNs, root cause analysis, risk reassessment, and associated verification/validation and documentation updates
Serve as a hands-on QMS Compliance leader within cross-functional teams, influencing execution through expertise, collaboration, and clear decision-making in a matrixed environment
Review supplier qualifications, process validations, and manufacturing documentation from OEMs to ensure compliance with medical device requirements
Support internal audits, supplier audits, and regulatory inspections

What we offer

medical insurance
dental insurance
vision insurance
flexible spending accounts
health savings accounts (HSA) with company contribution
401(k) retirement plan with matching
employee stock purchase program
life insurance
AD&D
short-term disability insurance

Fulltime

ADAS Verification Engineer & Test Lead

We are looking for an experienced ADAS Verification Engineer & Test Lead to join...

Location

Sweden , Gothenburg

Salary:

46667.00 - 66667.00 SEK / Month

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor's or Master's degree in Electrical Engineering, Computer Engineering, Physics, or similar
5–8+ years of experience in system verification engineering
Strong experience in ADAS or autonomous driving systems
Solid understanding of vehicle-level system behavior and automotive standards
Experience with rig (HIL) and vehicle-based testing environments

Job Responsibility

Lead verification activities for ADAS functionalities across system and vehicle levels
Define verification strategies, test plans, and required test environments (rigs and vehicles)
Execute verification activities in lab rigs and real vehicle conditions
Develop and maintain structured test cases based on system requirements
Support certification and compliance-related verification activities
Plan, schedule, and coordinate test activities (vehicles, tracks, drivers, setups)
Analyze test results, identify deviations, and drive corrective actions
Document findings and present clear test results and technical recommendations to stakeholders
Collaborate with cross-functional engineering teams to ensure robust validation setups
Ensure system readiness and quality before release

What we offer

An international community, bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
At Mantu, sustainability is part of everything we do
Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support

Fulltime

Senior Systems Verification Engineer

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent
3+ years of relevant industry experience
Proven organization skills and ability to collaborate with both technical and non-technical personnel
Solid understanding of ISO and/or FDA and other regulatory standards
Knowledge of Design controls, Lifecycle testing processes, MTBF analysis
Applicants must be authorized to work for any employer in the U.S.
Medical device industry experience is preferred

Job Responsibility

Contribute to the planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies)
Engage in test planning during design and development phases
Contribute to the validation efforts for laboratory equipment supporting infusion system testing
Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
Contribute to the development and documentation of system requirements, systems architecture and design
Ensure appropriate traceability between system, subsystem, and software verification
Manage the integration of deliverables from subsystem teams, multi-functional teams and external partners
Resolve competing constraints between interrelated functions
Implement configuration and change management through the complete product life-cycle

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts

Fulltime

Senior Systems Verification Engineer

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent
3+ years of relevant industry experience
Medical device industry experience is preferred
Proven organization skills and ability to collaborate with both technical and non-technical personnel
Solid understanding of ISO and/or FDA and other regulatory standards
Knowledge of Design controls, Lifecycle testing processes, MTBF analysis

Job Responsibility

Contribute to the planning, development and execution of system verification deliverables
Contribute to the validation efforts for laboratory equipment supporting infusion system testing
Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
Contribute to the development and documentation of system requirements, systems architecture and design
Ensure appropriate traceability between system, subsystem, and software verification
Manage the integration of deliverables from subsystem teams, multi-functional teams and external partners
Resolve competing constraints between interrelated functions
Implement configuration and change management through the complete product life-cycle
Build process improvements to streamline testing between system verification, subsystem and software verification

What we offer

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

Senior Systems Verification Engineer

This is where your work saves lives. As a part of Infusion Therapies & Platforms...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent
3+ years of relevant industry experience
Medical device industry experience is preferred
Proven organization skills and ability to collaborate with both technical and non-technical personnel
Solid understanding of ISO and/or FDA and other regulatory standards
Knowledge of Design controls, Lifecycle testing processes, MTBF analysis

Job Responsibility

Contribute to the planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies)
Engage in test planning during design and development phases
Contribute to the validation efforts for laboratory equipment supporting infusion system testing
Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
Contribute to the development and documentation of system requirements, systems architecture and design
Ensure appropriate traceability between system, subsystem, and software verification
Manage the integration of deliverables from subsystem teams, multi-functional teams and external partners
Resolve competing constraints between interrelated functions
Implement configuration and change management through the complete product life-cycle

What we offer

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP) with company matching
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service
family and medical leaves of absence
paid parental leave

Fulltime

Senior Systems Verification Engineer

This is where your work saves lives. As a part of Infusion Therapies & Platforms...

Location

United States , Round Lake

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Mechanical, Electrical, Computer Science, Biomedical Engineering or equivalent
3+ years of relevant industry experience
Proven organization skills and ability to collaborate with both technical and non-technical personnel
Solid understanding of ISO and/or FDA and other regulatory standards
Knowledge of Design controls, Lifecycle testing processes, MTBF analysis
Medical device industry experience is preferred

Job Responsibility

Contribute to the planning, development and execution of system verification deliverables (test plans, test protocols, test cases, test reports, studies)
Engage in test planning during design and development phases
Contribute to the validation efforts for laboratory equipment supporting infusion system testing (e.g., Infuscale, altitude chambers, environmental chambers, and related test systems)
Develop and execute validation protocols, test plans, and reports in alignment with FDA, ISO, and equipment validation best practices
Perform IQ/OQ/PQ activities for lab equipment and ensure complete traceability from requirements through test execution
Contribute to the development and documentation of system requirements, systems architecture and design
Ensure appropriate traceability between system, subsystem, and software verification
Manage the integration of deliverables from subsystem teams, multi-functional teams and external partners
Resolve competing constraints between interrelated functions (Engineering, Risk Management, Compliance, Reliability, Clinical, Human Factors, Regulatory)
Implement configuration and change management through the complete product life-cycle

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

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Compliance Verification Engineer

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