Engineer, Validation Job at Baxter (Stockport)

New

Engineer, Validation

Being an Engineer at Baxter means you play a critical role in helping us achieve...

Location

United Kingdom , Stockport

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Scientific/Engineering Degree or equivalent qualification or the right experience within a validation role
Experience working with Hydrogen peroxide decontamination systems
In depth knowledge of a specific validation/engineering skill set i.e. temperature mapping, airflow and smoke visualization, Biological Indicator application and processing etc
Working knowledge of validation in a pharmaceutical/FMCG/medical devices environment preferably
Experience with Equipment/Process systems, Cleaning Validation, HVAC, QA, QC, or Cleanroom systems would be preferred
Approach tasks with a logical and practical perspective, and have a proactive approach to problem-solving
Display analytical thinking and innovative problem-solving abilities to successfully implement validation strategies
Self-motivated and driven to complete projects/tasks efficiently and effectively
Excellent teamwork skills to contribute effectively as a member of a diverse team and effectively communicate with individuals involved in the project

Job Responsibility

Ensure Site Validation Master Plan (SVMP) is strictly adhered to and that all validation activities are conducted in accordance with established protocols and procedures by executing validation work and a variety of equipment
Develop and implement validation documents and protocols for a variety of processes, equipment, facilities, and systems, with a particular emphasis on aseptic manufacturing
Work closely with the validation team and teams from various departments to assist with the implementation of new processes, products, and equipment at the site
Actively participate in the assessment, review, and approval of changes that may impact the validation status of our facilities, equipment, processes, and systems
Conduct thorough reviews of validation execution and equipment changes carried out by external contractors and internal project team members to ensure compliance with validation requirements
Take ownership of project management and execution for Capital Expenditure and Process Improvement Projects within the EMEA Validation project portfolio
Work with Quality Assurance to react to adhoc validation requirements

What we offer

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Support for Parents
Continuing Education/Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Software Test Engineer / Validation Engineer

To strengthen our testing and validation activities, we are looking for a Softwa...

Location

Italy , Modena

Salary:

Not provided

RE:LAB

Expiration Date

Until further notice

Requirements

Degree in Engineering (Electronics, Computer, Automation, or similar technical fields)
Experience in software testing, verification, and validation for complex systems
Familiarity with requirements-based testing and test case definition
Basic knowledge of electronics, embedded systems, or control units
Experience with test execution, defect analysis, and documentation
Ability to work in structured development and validation processes
Good command of the English language, both written and spoken

Job Responsibility

Contribute to the definition of test procedures and validation strategies for software and electronic systems
Analyze system and software requirements to support test planning and prevent defects early in the development process
Define and execute test cases at functional, integration, and system level
Support the analysis and resolution of software-related issues in collaboration with development teams and suppliers
Participate in verification and validation activities using test benches, simulation environments, or Hardware-in-the-Loop (HIL) setups
Contribute to test documentation, defect tracking, and validation reports
Collaborate with multidisciplinary teams involved in system development, testing, and quality activities

Fulltime

New

Test Engineer – Validation

Love working close to hardware? Join our eShepherd team as a Test Engineer and h...

Location

New Zealand , Hamilton

Salary:

Not provided

Gallagher Group

Expiration Date

July 10, 2026

Requirements

Experience in hardware testing, embedded firmware validation, or mechatronics (not purely software QA)
Familiarity with MCU-based systems (such as ESP32, STM32, Renesas, Arduino)
Working knowledge of C#/C++ and /or Python in embedded or test environments
Experience using lab tools (oscilloscopes, multimeters, soldering tools)
Ability to troubleshoot issues across hardware and firmware
Exposure to manufacturing or production testing / NPI environments
Practical, hands-on problem solver who enjoys working close to hardware
Strong collaboration skills across engineering and production teams
Confluence and Jira documentation experience

Job Responsibility

Validate embedded hardware and firmware to ensure they perform as intended
Validate embedded hardware and firmware performance across the product lifecycle
Work closely with firmware engineers to test and troubleshoot device behaviour on real hardware
Use lab equipment such as oscilloscopes, multimeters, and debugging tools to investigate issues
Support development of test approaches for embedded systems running on microcontrollers
Design and execute test cases to verify firmware features
Contribute to manufacturing test setup and help refine production test processes and SOPs
Work with production and NPI teams to improve reliability and scalability of testing in manufacturing
Help ensure products are robust, reliable, and ready for real-world deployment

What we offer

Competitive salary + performance incentives
The best of both worlds - startup energy backed by Gallagher’s global scale
Real career growth as we scale products globally
Modern tools, tech, and equipment to do your best work
A practical, collaborative engineering team that gets things done
KiwiSaver contributions
Boost App + staff discounts across NZ
Life & Disability Insurance for added peace of mind
Hamilton site perks: free parking, subsidised café, great local eateries nearby
Employee Assistance Programme + wellbeing support

Fulltime

New

Ip Post-Silicon Validation Engineer

WHAT YOU DO AT AMD CHANGES EVERYTHING At AMD, our mission is to build great pro...

Location

Canada , Markham

Salary:

155200.00 - 232800.00 CAD / Year

AMD

Expiration Date

Until further notice

Requirements

Bachelor's or master’s degree majoring in EE, CS or related field
Experience in digital logic design/verification/post-silicon validation
Extensive experience with ASIC debug techniques and methodologies
Knowledge of physical and protocol levels of common high-speed interfaces such as PCIe/CXL/UALINK is an asset
Experience with board/platform-level debug, including clock/power delivery, sequencing, analysis, and optimization
Strong scripting skills (eg. Ruby, Python)
Extensive experience with common lab equipment, including protocol/logic analyzers, oscilloscopes, etc.
In-depth knowledge of PC architectures/PCIe protocol is an asset
Must have excellent written and verbal communication skills
Must excel in a dynamic team working environment

Job Responsibility

Driving the planning, validation, and debug of various hardware IP for forthcoming AMD APU, CPU, Compute and Discrete Graphics SOC programs
Defining, documenting, executing and reporting the overall functional test plan and validation strategy for a set of AMD IP’s
Driving technical innovation to enhance AMD's capabilities in IP validation, including tools and scripts/automation development, technical and procedural methodology enhancement, and various internal and cross-functional technical initiatives
Debugging IP issues found during pre-silicon, bring-up, system validation, and production phases of the SOC programs
Engaging on pre-silicon ‘shift left’ activities with cross-functional teams such as Design Verification (DV), Diagnostics, Emulation and other software/hardware modeling frameworks to ensure readiness for first silicon arrival, enablement of IP functionality, and debug of critical features
Leading collaborative technical discussions to drive resolution of technical issues and roll out technical initiatives
Developing knowledge of system architecture/debug and other internal IP’s
Supporting issues on customer platforms as requested by customer support teams

Fulltime

New

Validation Engineer

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

Location

United Kingdom , Stockport

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Scientific/Engineering Degree or equivalent qualification or the right experience within a validation role
Experience working with Hydrogen peroxide decontamination systems
In depth knowledge of a specific validation/engineering skill set i.e. temperature mapping, airflow and smoke visualization, Biological Indicator application and processing etc
Working knowledge of validation in a pharmaceutical/FMCG/medical devices environment preferably
Experience with Equipment/Process systems, Cleaning Validation, HVAC, QA, QC, or Cleanroom systems would be preferred
Logical and practical perspective
Proactive approach to problem-solving
Analytical thinking and innovative problem-solving abilities
Self-motivated and driven
Excellent teamwork skills

Job Responsibility

Ensure Site Validation Master Plan (SVMP) is strictly adhered to
Develop and implement validation documents and protocols for a variety of processes, equipment, facilities, and systems, with a particular emphasis on aseptic manufacturing
Work closely with the validation team and teams from various departments to assist with the implementation of new processes, products, and equipment at the site
Actively participate in the assessment, review, and approval of changes that may impact the validation status of our facilities, equipment, processes, and systems
Conduct thorough reviews of validation execution and equipment changes carried out by external contractors and internal project team members
Take ownership of project management and execution for Capital Expenditure and Process Improvement Projects within the EMEA Validation project portfolio
Work with Quality Assurance to react to adhoc validation requirements
Support validation activities across all UK Compounding sites

What we offer

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Sr Quality Engineer, Validation

This is where you make a difference in our patients’ safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed. To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity
To collect data & compile summary report for submission to International Regulatory Affairs (IRA) for queries and ANDA

Job Responsibility

Prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
Coordinate with cross functional teams of all departments for execution of all validation activities
Prepare monthly and annual calendars for various periodic qualification/validations
Monitor QMS elements related to validation activity and ensure proper closure of QMS documents
Review scheduled validation activity as per calendar
Ensure samples withdrawal during process validation
Ensure compilation of executed protocols and observation sheets
Coordinate with projects for new equipment installation and prepare protocol
Attend training of each protocol before execution
Collect data & compile summary report for submission to International Regulatory Affairs (IRA)

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Sr Quality Engineer, Validation

This is where you make a difference in our patients' safety. As a member of the ...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed
To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity

Job Responsibility

To prepare, execute, compile and review protocols of equipment, utility, process validation, cleaning validation, and facility qualification
To coordinate with cross functional teams of all departments for execution of all validation activities & inform to Manager regarding any non-conformity from planning and execution
To prepare monthly and annual calendars for various periodic qualification/validations & get it reviewed by Manager and approved by Manager
To monitor the QMS elements like Change Control Management, Corrective and Preventive Action, OOS, non-conformance related to the validation activity and prepare investigation report and ensure proper closure of the QMS documents in Track wise
To review the scheduled validation activity as per calendar and send it to the cross functional & PPA department in advance for execution planning before the scheduled date
To ensure samples withdrawal during process validation & keep Manager updated about any non-conformity
To ensure compilation of executed protocols is done online (as applicable) and observation sheets for process validation and other qualifications are duly filled & signed
To ensure the CFS closure of respective documents
To co-ordinate with projects and other cross functional dept. for prior information on new equipment installation and to prepare the protocol in advance, followed by new equipment qualification and get it reviewed by the Manager
To attend training of each protocol before execution of any validation and qualification activity

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Tech Validation Engineer

Our client are a specialist life science and healthcare company who work with a ...

Location

United Kingdom , Surrey

Salary:

45000.00 - 55000.00 GBP / Year

Network Scientific Recruitment

Expiration Date

Until further notice

Requirements

Scientific graduate and post-graduate qualifications in applied biology, biochemical/biomedical engineering
Understanding of SHE, ensuring compliance with regulatory and legislative requirements
Good understanding of research & pharmaceutical manufacturing regulations – GMP
Membership of relevant professional body
Familiar with Cross contamination control strategies & Quality Risk assessments
Experience in the validation of systems, equipment, and environment
Experience of project delivery
Highly organised and methodical with attention to detail
Able to maintain confidentiality of Company and clients’ information
Experience of working in a Clean Room or Laboratory environment

Job Responsibility

Lead Projects through all stages of design and development
Working with a project team of end users, designers and contractors to deliver high quality projects to timescale
Provide detailed consultancy to project stakeholders in line with regulatory and engineering standards for clean room design and construction
Execution of validation protocols at customer and vendor facilities
Generation of Quality Risk assessments
Lead project meetings including site visits
Generation of Validation Protocols for a full validation life cycle
Producing documentation specific to customer requirements: URS, VMP VP, RTM, DQ, IQ, OQ, & VSR
Responsible for the review, creation and maintenance of project progress reports including internal reports on project progress against budget and costs
Implement continuous improvement suggestions on process, procedures and documentation

Fulltime

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Engineer, Validation

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