About Scrumconnect Consulting: Scrumconnect Consulting is a multi-award-winning digital consultancy, recognised for delivering impactful technology solutions across UK government departments. Our work has positively influenced the lives of over 40 million UK citizens. With a strong commitment to user-centred design and agile delivery, and more to deliver innovative digital services that matter.

Role Description
As a Middle QC Engineer, you will take responsibility for designing and implementing test strategies across cloud-based applications and data services. You will develop automated testing frameworks, support API life cycle validation and ensure quality across CI/CD pipelines. You will work closely with DevOps and development teams to embed quality gates within deployment processes and maintain high standards of reliability across digital services.

Preferred Tech Stack Expertise
Automated testing frameworks, Python or similar Scripting language, API testing tools, CI/CD integration, GitHub, Jira

Responsibilities

• Design and execute comprehensive test plans for cloud-native applications
• Develop and maintain automated regression and integration test suites
• Validate API performance, security and data integrity
• Integrate automated tests within CI/CD pipelines
• Collaborate with architects and engineers to improve testability of solutions
• Support production defect triage and resolution
• Contribute to mentoring junior team members and knowledge transfer initiatives

Diversity & Inclusion

At Scrumconnect Consulting, we believe that diversity drives innovation. We are committed to creating an inclusive environment where every individual is respected, valued, and supported. We welcome applications from candidates of all backgrounds and experiences, and we actively encourage applications from women, people with disabilities, under-represented communities, and those seeking flexible working arrangements

Software Tester role - Global IT Security Software Company

Hybrid working in Horsham, West Sussex

This role will require office attendance multiple times per week.

In this software QA Tester role, you join a testing team responsible for the quality assurance and testing of the company’s IT Security Software. Their platform is built on .Net technologies so we are looking for a software tester with a background with .NET applications and C# testing frameworks.

The Software Tester role requires a professional who balances hands-on testing expertise with growing leadership and process improvement responsibilities.

You will be responsible for designing and executing comprehensive test plans, leading testing efforts for moderately complex features or systems, and ensuring software quality meets the high standards required for mission-critical applications.

In this role you will take ownership of testing activities while mentoring junior team members and contributing to the continuous improvement of QA processes, tools, and documentation.

Role responsibilities will include:

• Design, execute, and maintain comprehensive test plans and test cases

• Run testing efforts for moderately complex features or systems

• Develop and maintain automated test scripts using industry-standard tools

• Collaborate with cross-functional teams to clarify requirements and ensure testability

• Identify, document, and track defects; perform root cause analysis where needed

• Mentor junior testers and support their development through pairing and feedback

• Contribute to continuous improvement of QA processes, tools, and documentation

• Participate in sprint planning, reviews, and retrospectives with a focus on quality

• Work closely with developers to ensure early detection of issues and promote quality-first mindset

• Ensure test coverage aligns with business-critical functionality and user needs

• Support the integration of testing into CI/CD pipelines

• Communicate testing progress, risks, and quality metrics to stakeholders

Skills and Experience:

* Strong proficiency in manual and automated testing techniques

* Experience with test automation tools (e.g., Selenium, Cypress, Postman)

* Solid understanding of software development lifecycle and agile methodologies

* Familiarity with CI/CD pipelines and integration testing

* Strong analytical and problem-solving skills

* Effective communication and collaboration abilities

* Ability to write clear, clean, and documented test cases

* Experience in team working with strong people skills

* Comfortable using version control systems, primarily Git

* Strong attention to detail and commitment to quality

Desirable skills and experience:

* 3 years plus of experience in software testing or quality assurance

* Experience mentoring or coaching junior QA team members

* Exposure to performance, security, or API testing

* ISTQB Advanced Level certification or equivalent

* Experience with .NET applications and C# testing frameworks

* Knowledge of security testing principles and vulnerability assessment

* Experience testing complex enterprise or forensics software

* Familiarity with test management tools (e.g., Jira, TestRail, Azure DevOps)

* Understanding of database testing and SQL

If this job is of interest please apply with your CV

Talentmark is recruiting for a Quality Engineer to join a company in the pharmaceutical industry on a contract basis for 12 months. This is a hybrid role with 50% onsite in Cambridge.

Salary:
Up to £26.69 per hour PAYE or up to £34.54 per hour via umbrella company.

Quality Engineer Role:

Lead design control and risk management activities for combination product development programs.
Support effective risk management activities at external design companies and manufacturing facilities.
Ensure combination product development activities are compliant with all required standards.
Support the generation of all regulatory submission data.Your Background:

Hold a relevant scientific degree or have equivalent working experience.
Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
Experience in design controls and risk management for combination products.
Familiar with device assembly manufacturing processes.
Understand Good Manufacturing Practices (GMP).Company:
Our client is one of the world’s premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines, and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.

Apply:
For more information, or to apply for this Human Factors Quality Engineer please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (phone number removed).

It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check

Quality Engineer, Compliance
Location: Cambridge, UK
Hours: 37 hours per week
Contract: 12 Months
Maximum Supplier Bill Rate: £26.07 per hour

Position Overview
This role sits within the Biotherapeutics Pharmaceutical Research and Development - Devices Centre of Excellence (DCoE).
The Quality Engineer will provide design control and risk management expertise across medical device and combination product development programmes throughout the full product lifecycle. Responsibilities include generating and reviewing Design History File (DHF) and Risk Management File (RMF) components while partnering with cross‑functional teams at all organisational levels.

Key Responsibilities

Lead design control and risk management activities for combination product development programmes, ensuring deliverables are authored, approved, and maintained to support clinical trials and commercial licensure.
Facilitate effective risk management activities at external design and manufacturing partners.
Ensure all development activities comply with internal and external quality and regulatory standards.
Provide input into design validation, including human factors engineering assessments.
Support assessment of external design companies and suppliers regarding quality systems, facilities, and capabilities.
Assist with design and manufacturing investigations for devices used in clinical trials and commercial manufacturing.
Contribute to the creation of regulatory submission data for assigned device projects.
Support internal and external audits of the DCoE Quality Management System.
Education, Skills & Experience Requirements
Education
One of the following is required:

BSc in a relevant science/engineering discipline with minimum 2 years’ experience in pharmaceutical combination product and/or device industries
MSc in a relevant discipline with minimum 2 years’ experience
PhD in a relevant science/engineering disciplineRelevant fields include: chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering, or related areas.
Experience & Knowledge

Demonstrated experience working to ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation.
Proven background in design controls and risk management for combination products.
Familiarity with Human Factors Engineering / Usability Engineering.
Understanding of device assembly and manufacturing processes.
Technical Skills

Working knowledge of:
ISO 9001
ISO 13485
ISO 14971
21 CFR 820
21 CFR 4
EU MDR
Familiarity with:
EN 62366 (Usability Engineering)
EN 60601 (Electrical Medical Equipment)
EN 62304 (Medical Device Software)
Ability to apply established procedures consistently.
Strong attention to detail and accuracy.
Able to prioritise and manage multiple tasks simultaneously.
Capable of working independently with minimal supervision.
Effective communicator with strong interpersonal skills.
Proficiency in standard office software (Word, Excel, PowerPoint).
Understanding of Good Manufacturing Practices (GMP).

Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Morson are working with one of the UK’s leading aerospace manufacturer who are looking for a Quality Lineside Engineer to join their team based at the Filton site in Bristol.

Responsibilities

Perform product inspections according to standards, delegation rules and guarantees attestation of work-orders under his accountability
Performs Clearance of areas, Pre-delivery checks, Duplicate checks of Customer Protection Board items Duplicate checks of Key Risk items
Participates in setting of quality standards and ensures compliance with them in own area of responsibility
Collects and manages Quality issues requiring preventive and corrective actions and contributes to daily workstation Lean activities (e.g. SQCDP, PPS)
Ensures that containment, customer protection board activities and corrective activities are implemented and efficient within dedicated lead-time agreed and communicated within the area
Provides feedback to the Inspection Standard Operations Instruction Owner, to ensure relevant and consistent controls for their update
Ensure the requirements for inspections & controls are cascaded to the shop floor
Support the Quality Conformance Manager in the Set-up of Control Charts and the calculation of capability
Raises non-conformities against design definition, checks reworks, and closes these NCs
Contributes to operators’ qualification and performs surveillance of certified operators and product, according to Quality standards and surveillance plan survey and support
Performs surveillance of processes and process confirmation activities according to Quality standards and surveillance plan. Support risk analysis (FMEA)
Knowledge of the Cost of non-Quality process is required
Ensures that documents to be archived by Quality are completed and gathered in accordance with Quality rules
Essential Skills

Strong communicator with inspection and surveillance experience
Someone who can ensure quality standards are met and able to reacting quickly to customer feedback while working in a fast moving operational environment
Strong problem solver with experience of using PPS techniques
Someone with the ability to successfully lead a multi-functional team to ensure quick problem resolutions
Experience of root cause analysis is also essential
Essential to meet the criteria for this role that you have a good level of engineering, manufacturing, inspection and quality experience and can prove this in your application and experience.
If you are interested in applying for the position then please submit an up to date CV

Your new company

A leading manufacturing organisation in Lisburn is seeking a Quality Engineer to join its expanding team. The business operates in a fast‑paced, high‑precision environment and is committed to delivering products that meet stringent industry standards and customer expectations. With a strong focus on continuous improvement and operational excellence, this is an excellent opportunity to contribute to a growing and forward‑thinking organisation.

Your new role

As a Quality Engineer, you will support the Manufacturing Quality Manager and work closely with production teams to enhance operational performance and ensure consistent product quality. You will play a key role in developing quality standards, driving continuous improvement and supporting problem‑solving activities across the manufacturing and assembly processes.Mon - Thurs 7am - 4.15pm and Fri until 1.15

What you’ll need to succeed

To be successful in this role, you will have:

• A degree in a relevant engineering discipline with at least 1 year’s quality or engineering experience; or an HNC/HND with 2+ years’ relevant experience; or 3+ years’ experience in a Quality Engineering or engineering role.
• Experience using continuous improvement and problem‑solving tools (3C, 8D, A3, PFMEA, APQP, process mapping).
• Strong ability to read and interpret engineering drawings and standards.
• Excellent communication skills, both written and verbal.
• Strong IT skills, particularly in Microsoft Word and Excel.
• A logical, detail‑focused approach and the ability to work independently or as part of a team.
• Ability to work to strict deadlines in a fast‑paced environment.

Desirable:

• 3+ years’ experience as a Quality Engineer in a manufacturing environment.
• Experience in modular manufacturing or construction.
• Strong understanding of ISO 9001:2015 requirements.

What you’ll get in return

You will join a dynamic organisation that values continuous improvement and professional development. Benefits include:

• Competitive salary and benefits package.
• Opportunities for career progression.
• A collaborative and supportive working environment.
• The chance to influence quality standards across high‑profile manufacturing projects.

What you need to do now

If you’re interested in this role, click ‘apply now’ to forward an up-to-date copy of your CV, or call us now.
If this job isn’t quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C’s, Privacy Policy and Disclaimers which can be found at hays.co.uk

ABOUT US

The Guinness Partnership is one of the leading providers of affordable housing in England. We build and manage homes and provide housing services for nearly 160,000 residents nationwide. Our vision is to deliver great service, provide great homes, to be a great business and to be a great place to work. Because everything we do is about our residents, our communities and our people, any profit we make is re-invested in new and existing homes and improving services.

The Guinness Partnership is an equal opportunities employer. We are committed to equality of opportunity for all colleagues, and applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships.

JOB DESCRIPTION

About the role

Are you an experienced Data Quality professional? The Guinness Partnership is seeking a new Data Quality Assurance Analyst to join our Data Assurance Team. This is a full time, 35 hours per week, permanent role based at our Oldham, Bower House office. We are currently working to a hybrid style.

The overall purpose of the role is to undertake relevant, useful, in-depth and complex data analysis to support stakeholders to understand and continuously improve the corporately reported performance information.

What were looking for

We are seeking an individual with proven experience in analysing complex data sets to identify weaknesses in data quality controls, provide clear and actionable recommendations for improvement, and ensure that agreed actions are completed to a high standard.

The role involves working closely with the Head of Data Assurance to develop and enhance our approach to data quality and reporting, as well as collaborating with operational teams to ensure outputs are accurate and reliable.

In this role, you will design and deliver a programme of ongoing data quality testing, providing assurance over the accuracy and integrity of source data and corporate reporting. You will also contribute to targeted projects aimed at improving the quality of key organisational data sets.

The role requires the ability to produce clear and structured work plans to guide analytical activity, while building effective relationships with stakeholders to strengthen the organisations overall approach to reporting and data assurance.

The successful candidate will also have experience in identifying efficiencies and new ways of working, including the use of automation, to enhance the quality, consistency, and reliability of corporate reporting and analysis.

Youll be able to demonstrate

Essential:

• Excellent understanding of the principles of data quality and a track record of driving improvements in them.
• Knowledge of data management practices and data analysis techniques and tools, experience of using them to improve data quality.
• Analytical skills with the ability to collect, organise and analyse large amounts of data and information with attention to detail and accuracy.
• Leading in the identification and presentation of problems and solutions.
• Proven experience of taking a data led approach to analysing and evaluating corporate performance.
• Ability to explain complex information and use findings to influence stakeholders to make improvements.
• Ability to produce robust documentation relating to corporate reporting and benchmarking and analysis and reporting of findings.
• Demonstrates the Guinness Behaviours.

Desirable:

• Awareness of statutory and regulatory requirements relating to Asset Management, Customer Services and Health & Safety.
• Good current knowledge of IT systems used in social housing.
• Ability to understand data tables, SQL and/or system interfaces.

Qualifications

Essential:

• Educated to Level 3 (A level or equivalent) or higher.

Desirable:

• Educated to Level 6 (degree or equivalent) in numerical discipline or modern data related qualification.

If youre interested in finding out more about the key responsibilities of the role and/or to ensure you meet the essential criteria, please review the attached role profile.

REEDTGP

Benefits

• Holidays:We offer 25 27 days holiday a year, plus bank holidays. We will also give you the opportunity to buy up to an additional 5 days. You will also receive additional holiday in line with your length of service (1 extra day per 5 years service, capped at 4 days).
• Competitive Pension Scheme:We will help you save for your retirement through our workplace pension scheme. Guinness match your contribution up to 9%. To help you get the most out of your pension contributions, we operate a salary sacrifice arrangement that means you will pay less National Insurance contributions.
• Benefits Portal:We have a lifestyle benefits scheme, pulling together a range of special offers and great deals. You can make some great savings on everyday shopping from fashion and electronics to travel, leisure and days out and weekly supermarket shopping.
• Performance Pay:Annual Performance Score bonus subject to eligibility
• Life Assurance:For peace of mind Guinness provides three times salary life cover in the event of your death
• Health Plan Options:There are a couple of health care schemes available depending on the post grade
• VDU/DSE:Free eye test vouchers every 2 years with £55 contribution to glasses if requires for VDU work

Additional benefits include:

• Access to the Finance wellbeing portal
• Professional subscription annual payment
• Travel season ticket loan
• Car lease scheme

Up to £39,000

Are you passionate about quality assurance and continuous improvement? Do you enjoy problem-solving, driving process excellence, and making a real impact on manufacturing operations? Yolk Recruitment is excited to support a leading manufacturing company in their search for a skilled Quality Engineer. In this role, you’ll be the key quality contact for designated customers, ensuring top-tier quality assurance of manufactured products. You’ll have the opportunity to influence processes, implement best practices, and contribute directly to the success of a high-performing team.

You’ll work closely with cross-functional teams to identify improvement opportunities, resolve challenges, and help deliver products that consistently exceed customer expectations. If you thrive in a fast-paced, innovative environment and have a strong background in quality standards, this is your chance to take your career to the next level and make a meaningful difference in a growing manufacturing business.

This is what you’ll be doing:

• Serve as the primary quality contact for assigned customers, ensuring their satisfaction by addressing and resolving complaints.
• Participate in Business Improvement / Continuous improvement activities
• Lead and participate in business and process improvement initiatives, applying Six Sigma methodologies to enhance manufacturing processes.
• Provide support during external audits and maintain accreditations ensuring compliance with industry standards.
• Develop and update process FMEA and control plans in collaboration with cross-functional teams to maintain high-quality standards.
• Conduct internal audits in line with the audit schedule.

And this is what you’ll need:

• Experience with Quality Tools & Techniques.
• Experience working within a manufacturing environment.

And this is what you’ll get:

• Competitive salary.
• Private healthcare.
• Early finish on Friday’s.

If you feel you have the skills, experience, and passion to be successful in this Quality Engineer role apply now.

*Please note, whilst we do our best to contact all candidates, due to the high number of applications we receive we cannot guarantee this for every role. If you have not heard anything from us within 7 days of applying - then unfortunately you have been unsuccessful. Please keep an eye on our website for more opportunities.

Your new company
A leading manufacturer based in the heart of Tyrone is seeking a proactive and detail-oriented Quality Engineer to join their growing team. This is an excellent opportunity to work in a fast-paced, quality-driven environment where continuous improvement and customer satisfaction are at the core of operations.

Your new role
As Quality Engineer, you will play a key role in supporting and enhancing product quality through data analysis, customer support, and inspection coordination. You will work closely with customer service, production, and quality teams to ensure compliance, accuracy, and continuous improvement across all processes. Responsibilities include gathering and analysing quality data to identify trends and escalate recurring issues, assisting in the preparation of internal and customer-facing quality reports and providing initial quality support to customer service teams. You will be investigating non-conformances and conducting root cause analysis, coordinating corrective actions and liaising with production to resolve customer issues, performing stock checks and tracking returned items for inspection and monitoring special attention orders to ensure customer specifications are met.You will also be supporting quality audits and ensuring timely closure of customer NCRs.
Mon - Fr - short day Friday.

What you’ll need to succeed

Ideally you will have proven experience in a quality-focused role within a manufacturing environment, strong attention to detail and excellent organisational skills, ability to collaborate effectively across departments and proficiency in Microsoft Excel and report writing. It would be particularly good if you have experience in a manufacturing facility and have familiarity with quality inspection tools or visual inspection systems and knowledge of continuous improvement or lean methodologies.

What you’ll get in return

• Competitive salary and benefits package
• Opportunity to work in a supportive and forward-thinking team
• Career development and training opportunities
• A role where your input directly contributes to product and process excellence

What you need to do now

If you’re interested in this role, click ‘apply now’ to forward an up-to-date copy of your CV, or call us now.
If this job isn’t quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.

Hays Specialist Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job you accept the T&C’s, Privacy Policy and Disclaimers which can be found at hays.co.uk

Astute’s Power team are looking to recruit an Outage QA /QC Engineer in Leeds on a contract basis.

Key skills required for the Outage QA/QC Engineer role

• Perform inspections of boiler pressure parts including membrane walls, superheaters, economisers, headers, drums, and associated pipework.
• Carry out manufacturing surveillance at vendor workshops, including monitoring fabrication activities against ITPs and project requirements.
• Verify welding activities including fit-up, welding parameters, weld mapping, and compliance with approved WPS/PQRs.
• Confirm welder qualifications and ensure consumables and welding processes meet specification requirements.
• Witness and review NDE activities (UT, RT, MT, PT) and confirm acceptance to relevant standards.
• Verify material traceability including heat numbers, MTRs, and PMI requirements where applicable.
• Witness pressure testing/hydrostatic testing and ensure test preparation and documentation is completed correctly.
• Record inspection results, produce reports, and support compilation of QA/QC documentation and turnover packs.
• Raise quality concerns and NCRs, supporting corrective action implementation and close-out.
• Liaise with contractors, site supervision, and client representatives to ensure quality expectations are met.
• Must hold QA/QC inspection experience in heavy industrial environments.
• Must hold Confined Space, Face Fit Testing Certificate, CSCS Card (or equivalent) and CSWIP Welding Inspector Qualification
• Must be prepared to work long hours

Location, day rate and timeframe of the Outage QA/QC Engineer role

• Leeds
• £30.00 per hour
• 2+ Months contract
• April 2026

INDPOW

Astute People are acting as an employment business in relation to this vacancy. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We encourage applications from individuals from all backgrounds but candidates must be able to demonstrate their ability to work in the UK. Astute is also committed to the government’s Disability Confident Employer initiative. We endeavour to get back to everyone, however, if you have not heard anything after 7 days, please consider your application unsuccessful.

(phone number removed) - Monday-Friday + Company benefits + Training + days-based

Telford, Shropshire

Are you an Engineering Graduate looking to kickstart your career in Quality Assurance within a reputable packaging company that has been running for over 25 years who offer full bespoke training and progression opportunities?

This company engineers sustainable packaging solutions tailored for some of the biggest retailers in the UK with a couple being Waitrose, Tesco and Aldi. They have continually grown since establishing in 1998 and are now looking to further grow their engineering team.

In this role you will support 2 other quality engineers and play a key part in maintaining and improving the quality of products and processes through root cause analysis, reviewing quality metrics and using data to drive process improvement.

This varied, technical role would suit a Graduate with an Engineering degree looking for an exciting progressive role with a structured training system allowing you to develop your skills and kickstart your career in Quality Assurance.

The Role

• A mix of desk work and production floor work
• Working alongside production engineers
• Full bespoke training
• Days-based 9am-5pm Monday-Friday

The Person

• Graduate with Engineering degree
• Commute to Telford
• Looking for a mix of desk and production floor work

Training, Graduate, Junior, Quality assurance, QA, QC, Engineer, Telford, CAPA, Root cause analysing, excel, Shifnal, Brockton, sustainability, Bethell

Ref number: BBH24202

If you’re interested in this role, click ‘apply now’ to forward an up-to-date copy of your CV, or call us now.

We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set.

Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C’s, Privacy Policy and Disclaimers which can be found at our website.

(phone number removed) - Monday-Friday + Company benefits + Training + days-based

Telford, Shropshire

Are you a Quality Assurance Engineer or similar looking for a stable, technical role with bespoke training available within a reputable packaging company that has been running for over 25 years?

This company engineers sustainable packaging solutions tailored for some of the biggest retailers in the UK with a couple being Waitrose, Tesco and Aldi. They have continually grown since establishing in 1998 and are now looking to further grow their engineering team.

In this role you and 2 other quality engineers will be responsible for maintaining and improving the quality of products and processes through root cause analysis, reviewing quality metrics and keeping data updated.

This varied, technical role would suit a quality assurance engineer looking, for an exciting, technical role with variety of responsibilities and the opportunity to develop your skills.

The Role

• A mix of desk work and production floor work
• Working alongside production engineers
• Bespoke training
• Days-based 9am-5pm Monday-Friday

The Person

• Quality Assurance Engineer or similar
• Commute to Telford
• Looking for an office based role

Quality assurance , QA, QC, Engineer, Telford, CAPA, Root cause analysing, excel, Shifnal, Brockton, sustainability, Bethell

Ref number: BBH24202

If you’re interested in this role, click ‘apply now’ to forward an up-to-date copy of your CV, or call us now.

We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set.

Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C’s, Privacy Policy and Disclaimers which can be found at our website.

Now is the time to inspire the future of healthcare together.

Our client is a leading global medical technology company with over 170 years of expertise and 18,000 patents. More than 68,000 dedicated colleagues across 70 countries are committed to shaping the future of healthcare. We stand alongside our customers worldwide, supporting them in delivering exceptional care to their patients. Every day, approximately five million patients benefit from our innovative technologies and services in diagnostic and therapeutic imaging, laboratory diagnostics, molecular medicine, digital health, and enterprise services. This commitment is at the heart of everything we do.

Join our client’s team as an IQA Technician within the Point of Care Diagnostics business unit.

Role Overview

The IQA Inspector is responsible for inspecting, controlling, and approving all incoming materials at the Sudbury manufacturing sites. This includes completing all relevant documentation and ensuring traceability in line with applicable quality standards. The IQA Inspector guarantees that all materials used in production meet stringent quality requirements.

Key Responsibilities

• Inspect incoming goods across Sudbury sites using measurement equipment, specifications, and Quality Control Plans (QCPs), ensuring full compliance before assembly.
• Complete all associated documentation and records, adhering to Good Documentation Practises (GDP).
• Contribute to the control and disposition of non-conforming materials, including segregation and documentation, following established procedures.
• Communicate effectively with internal and external suppliers and stakeholders; act as the primary point of contact for part quality enquiries and escalate issues as necessary.
• Complete all assigned training within specified timeframes.
• Support other Quality functions at Sudbury, including in-process testing, inspections, and final product release processes.
• Assist with internal and third-party site audits.
• Participate in SQDIP meetings, provide accurate reports promptly, and take ownership of achieving role-specific KPIs.
• Maintain supplier ‘Quality Approved’ samples for relevant attributes such as colours and finishes.
• Utilise business systems including CATSWEB, CERDAAC, SAP, Documentum, and Learn4U efficiently.

Regulatory Compliance

• Represent the business during customer audits and regulatory inspections, demonstrating compliance with required systems.
• Maintain adherence to Data Integrity Regulations, GAMP standards, 21 CFR Part 11, and other relevant regulatory guidelines.

Environmental, Health and Safety (EHS)

• Ensure compliance with safety, health, and environmental (SHE) legislation.
• Promote a safety-first culture by maintaining a zero-accident environment, preventing accidents, and protecting the facility’s environmental standards.

Teamwork and Quality Assurance

• Collaborate with project teams to support the selection, installation, and commissioning of new equipment.
• Apply knowledge of Quality Management Systems with competence and practical understanding.

Skills and Experience

• Proven ability to manage time effectively, demonstrating a strong drive to succeed.
• Flexible and adaptable approach to varied workloads.
• Self-motivated and reliable, able to work independently and take initiative.
• Effective team player with strong cross-functional communication skills.
• Curious and eager to learn, with excellent written and verbal communication abilities.

Qualifications

• Minimum of five years’ experience in a medical manufacturing environment.
• In-depth knowledge of Quality Management Systems, ISO 13485, and 21 CFR 820.
• Proficient in IT, with strong skills in Microsoft Office applications.
• Familiarity with Good Documentation Practises (GDP) and Good Manufacturing Practises (GMP).

Our client is seeking an experienced Quality Engineer to join their team on a permanent basis in Bristol. This is an exciting opportunity to play a key role in driving quality excellence within a dynamic manufacturing environment.

The Role:

As Quality Engineer, you will take ownership of quality performance across suppliers and internal operations, ensuring robust processes, effective problem resolution, and continuous improvement across the business.

Key Responsibilities:

• Lead and facilitate 8D problem-solving activities for supplier and internal complaints — from initial containment through root cause analysis to verification of corrective actions.
• Support goods-inwards containment activities to ensure non-conforming products are effectively controlled.
• Identify, drive, and implement continuous improvement initiatives to enhance product quality and process capability.
• Support supplier audits and conduct internal audits to ensure compliance and best practice.

About You:

You are a proactive, analytical quality professional with a strong background in manufacturing and a passion for driving standards.

Essential Requirements:

• Degree in Quality, Industrial, Mechanical Engineering, or HNC (or equivalent) in an Engineering discipline.
• Minimum 5 years’ experience within a Quality Engineering or Quality Assurance role in a manufacturing environment.
• Full working knowledge of AS9100 Rev D.
• Experience producing FAIRs to AS9102 Rev C.
• Strong understanding of APQP, PPAP, statistical process control, metrology, inspection methods/equipment, and 8D methodology.
• Excellent analytical, problem-solving, communication, and interpersonal skills.

Desirable:

• ASQ certification.

What’s on Offer:

• Salary up to £50,000 per annum
• Permanent position with long-term career prospects
• A fast-paced, quality-driven environment where your expertise will make a tangible impact
• An inclusive workplace committed to equal opportunities and diversity

Embedded Software QA+Test Engineer
Oxford (3 days a week)
£55,000-£65,000

The RoleMy client is seeking a talented QA + Test Engineer with expertise in Embedded Software to join their team building cutting-edge assurance systems for AI and UAS/UAV/Drone applications.

You will play a crucial role in developing software components that enable safe and reliable operation of AI-enabled robotics and autonomous systems within their product line.

Responsibilities

• Lead the design, development, and implementation of embedded software for SAIF Systems’ Runtime Assurance platform across various hardware architectures and real-time operating systems.
• Ensure compliance with industry standards, regulations, and best practices for safety-critical software development, such as DO-178C, ISO 26262, and IEC 61508.
• Build configuration and pipeline management
• Software-in-the-Loop and Hardware-in-the-Loop including automated deployment across multiple platform
• Integration of different performance testing techniques across multiple types of simulation (gazebo sim, rosbag)

Key Skills and Experience

• Bachelor’s or Master’s degree in Computer Science, Electrical Engineering, or a related field, or equivalent experience, with a strong focus on embedded systems QA, and software development and/or testing.
• Experience with one or more CICD pipeline services (Jenkins, CloudBuild, AWS CodePipeline, etc)
• Experience with infrastructure/Automation techniques (bash, python)
• Knowledge of source control (git)
• Experience with at least one test framework (pytest, gtest)
• Hands-on experience in embedded software testing and QA, with a proven track record in delivering safety-critical systems.

The role comes with generous benefits, is 3 days a week onsite and you must be eligible for UK SC clearance.

No sponsorship is offered for this role.

Please get in touch immediately to be considered!

Up to 70,000 + 20% bonus

London - 3x per week in office

Are you ready to shape a brand-new function and play a pivotal role in a global transformation? Our client, a FTSE 250 organisation, is investing heavily in technology as it moves from a federated model to a centralised global structure. This is your chance to define strategy, build processes, and create a team from the ground up.

As the Test Manager, you will join a newly formed function within the business and have the opportunity to shape and own testing strategy, governance, frameworks, and ways of working. You will define the scope for testing activities, including manual and automated testing, as well as prepare and deliver regular test progress and summary reports.

We are looking for:

• Proven experience in a test management/QA leadership position
• Exposure of working within a large, complex & global organisations
• Experience of working within a green-field testing function, and developing it from the ground up
• Strong knowledge of software testing methodologies, tools (manual and automated), and best practises
• Strong stakeholder engagement skills, including influencing at C-suite level

It would be a bonus if you had:

• Experience within the Hospitality, Travel & Leisure, or Retail industry

If this sounds of interest, please apply today!

Now is our time to inspire the future of healthcare together.

Our client is a leading global medical technology company with over 170 years of heritage and more than 18,000 patents. With over 68,000 dedicated colleagues across more than 70 countries, they are committed to shaping the future of healthcare. We collaborate closely with customers worldwide to support the delivery of high-quality care to patients. Every day, an estimated 5 million patients benefit from our innovative technologies and services in diagnostic and therapeutic imaging, laboratory diagnostics, molecular medicine, digital health, and enterprise services. This is what truly drives us.

We are currently seeking a Quality Engineer to join our client’s team within the Point of Care Diagnostics business line.

The Quality Operations Engineer will be responsible for maintaining, monitoring, and enhancing key elements of the Quality Management System (QMS) at the Sudbury Site. This role will foster a culture of quality through education, mentoring, and leading by example.

Key Responsibilities:

• Provide quality support to the Manufacturing Operations Team.
• Support CAPA and issue resolution to ensure timely and accurate completion.
• Administer and support the deviation process, ensuring timely and precise completion.
• Manage and support the quality notification process for timely and accurate outcomes.
• Prepare for supplier, customer, regulatory, and notified body audits as required.
• Conduct internal and supplier quality audits as necessary.
• Support the change control process.
• Prepare, review, and approve or reject quality-related documentation.
• Deliver training support on key aspects of the Quality Management System.
• Generate quality-related metrics, reports, and KPIs; lead improvement projects and quality initiatives.
• Participate in SQDIP meetings, providing accurate and timely reports; take ownership of achieving target KPIs for the role.
• Utilise business systems such as CATSWEB, CERDAAC, SAP, Documentum, and Learn4U effectively.

Regulatory Requirements

• Represent the business during customer audits and regulatory inspections, demonstrating compliance with systems.
• Maintain compliance with Data Integrity Regulations, GAMP standards, 21 CFR Part 11, and applicable regulatory guidelines.

Environment, Health and Safety (EHS)

• Ensure compliance with safety, health, and environmental (SHE) legislation.
• Promote a safety-first culture, striving for zero accidents; ensure adherence to accident prevention and environmental protection regulations to maintain a safe, productive workplace free from liabilities or defects.

Teamwork and Collaboration

• Engage with project teams to support the selection, installation, and commissioning of new equipment.

Quality Assurance

• Demonstrate competence in the principles and practical application of Quality Management Systems.

Skills and Experience

• Proven ability to manage time effectively with a strong desire to succeed.
• Flexible and adaptable approach to changing workloads.
• Self-motivated, reliable, and capable of working independently.
• Effective team player with excellent communication skills across functions.
• Curious and eager to learn, with strong written and verbal communication skills.

Qualifications

• Minimum of five years’ experience in a medical manufacturing environment.
• Comprehensive knowledge of Quality Management Systems, ISO 13485, and 21 CFR 820.
• Proficient IT skills with strong knowledge of Microsoft Office applications.
• Familiarity with GDP and GMP (Good Documentation Practises and Good Manufacturing Practises).

-------> As a Software Testing & Issue Triaging Engineer, youll be preparing vehicles for testing, planning and executing test activities, and analyzing data to ensure features perform as intended. Youll be hands-on with cutting-edge technology, from functional testing and software validation to exploring real-world scenarios on public roads and proving grounds. This is a hands-on, high-impact role where youll work across embedded systems, vehicle platforms, and global teams to bring new features to life. From debugging in real vehicles to collaborating with architects and engineers across the business, youll play a key role in delivering safe, intelligent, and seamless driving experiences. Your responsibilities: Generate test cases for the features being validated Prepare vehicles and ensure they are ready for all planned test activities Execute test plans in line with defined methods and processes Carry out defect validation and ensure accurate reporting Record test results, update defect logs, and upload data promptly Manage test equipment procurement and create suitable test environments Collaborate closely with validation teams Support cross-functional teams by investigating software issues and providing expert-level technical insight Your Profile Essential skills/knowledge/experience: Bachelors or masters degree in computer science, or related field Technical expertise in test facility and vehicle preparation Proven experience validating driver assistance features at vehicle level (ADAS experience highly desirable) Certification and experience conducting tests on proving grounds Proficiency with data acquisition tools (e.g., CANape, CANalyzer, INCA, Simulink, ADTF) Strong ability to analyze and report test data accurately Skilled in diagnostic fault-finding and interpreting engineering documents, with a structured problem-solving approach Full UK (or EU equivalent) driving license with a clean record Excellent problem-solving skills and attention to detail Ability to lead and work effectively with cross-functional teams Strong communication and leadership skills

Start Date: ASAP

Duration: Permanent with a 6-month probation period.

Contracted Hours: 8am-5pm Monday - Thursday and 8am -1pm Friday

Salary: 45,000 - 50,000

We are seeking a detail-oriented and experienced manufacturing Inspector to join our team. This role is responsible for verifying material certification documents, conducting dimensional inspections, and ensuring compliance with engineering specifications and industry standards, including AS9100 and ISO 9001. The ideal candidate will be proficient in CMM programming and operation, with a strong understanding of FAIR and ISIR documentation requirements. This is a hands-on position that plays a key role in maintaining our commitment to quality and continuous improvement across all stages of production.

Key Responsibilities:

• Review and verify material certification documents to ensure compliance with engineering drawings, specifications, and applicable standards (including AS9100 and ISO 9001).
• Prepare and review ISIR (Initial Sample Inspection Reports) and FAIR (First Article Inspection Reports) in accordance with customer and industry requirements.
• Accurately document inspection findings, including certificate conformity, observations, and any discrepancies.
• Interpret engineering drawings, technical specifications, and material standards to validate documentation.
• Offline program and operate Coordinate Measuring Machines (CMM) to carry out dimensional inspections of components.
• Use a range of additional inspection tools and equipment, such as micrometers, calipers, and gauges.
• Report non-conformances promptly and collaborate with relevant departments to address quality issues.
• Maintain accurate and traceable inspection records in accordance with AS9100 and ISO 9001 quality management system requirements.
• Support continuous improvement initiatives by identifying trends and areas for enhancement in documentation control.
• Participate in audits, internal reviews, and relevant training to uphold and improve inspection standards.

Day-to-day of the role:

• Begin each day by reviewing upcoming jobs and prioritising inspections based on production schedules and customer deadlines.

• Cross-check material certification documents against engineering drawings and specification requirements.

• Offline program and run CMM inspections, ensuring accurate measurement of critical dimensions.

• Carry out manual inspections using handheld tools where applicable, verifying tolerances and surface finishes.

• Prepare and update FAIRs and ISIRs for new product introductions or customer submissions.

• Record all inspection findings in the quality management system and flag any deviations or non-conformances.

• Communicate with all departments and quality teams to resolve issues and support root cause investigations.

• Participate in daily quality stand-up meetings and contribute to continuous improvement discussions.

• Maintain calibration status of inspection equipment and ensure the inspection area remains clean and organised.

• Support audit preparation activities and respond to auditor queries with supporting documentation as needed.

Required Skills & Qualifications:

Essential:

• Proven experience in a quality inspection role within a manufacturing or engineering environment.

• Strong understanding of AS9100 and ISO 9001 quality standards.

• Ability to read and interpret technical drawings, GD&T, and material specifications.

• Proficient in programming and operating CMM equipment.

• Experience with FAIR and ISIR preparation.

• Skilled in the use of precision measuring instruments such as micrometers, calipers, height gauges, and surface testers.

• Excellent attention to detail with strong analytical and documentation skills.

• Confident communicator, able to liaise effectively across departments.

Desirable:

• Formal qualifications in mechanical or manufacturing engineering (e.g., HNC/HND, NVQ, or equivalent).
• Experience supporting internal and external audits.
• Familiarity with customer-specific standards (e.g., Rolls-Royce SABRe).
• Lean or Six Sigma awareness and involvement in continuous improvement activities.

What we are looking for:

We’re looking for someone who brings not just experience, but sound judgment and a steady hand to quality control. You’ll be trusted to work autonomously, make informed decisions, and be a key point of contact when it comes to upholding quality standards. This role suits someone who others naturally turn to for guidance. Would suit someone with a calm, methodical approach, the confidence to handle complex quality challenges and a continuous improvement mindset and the ability to see the bigger picture. Opportunities for progression for the right candidate.

Benefits:

• Competitive salary based on experience.
• Overtime available.
• Friday 1 p.m. finish.
• Life Assurance.
• Cycle to Work Scheme.

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

Stevenage

A phenomenal permanent opportunity has arisen to join the Maritime Weapon System Quality Assurance team supporting projects in the development & production phases of the life cycle at Bristol.

Salary: Circa £50,000 depending on experience

Dynamic (hybrid) working: 2-3 days per week on-site due to workload classification

Security Clearance: British Citizen or a Dual UK national with British citizenship. Restrictions and/or limitations relating to nationality and/or rights to work may apply. As a minimum and after offer stage, all successful candidates will need to undergo HMG Basic Personnel Security Standard checks (BPSS), which are managed by the MBDA Personnel Security Team.

What we can offer you:

• Company bonus: Up to £2,500 (based on company performance and will vary year to year)
• Pension: maximum total (employer and employee) contribution of up to 14%
• Overtime: opportunity for paid overtime
• Flexi Leave: Up to 15 additional days
• Flexible working: We welcome applicants who are looking for flexible working arrangements
• Enhanced parental leave: offers up to 26 weeks for maternity, adoption and shared parental leave -enhancements are available for paternity leave, neonatal leave and fertility testing and treatments
• Facilities: Fantastic site facilities including subsidised meals, free car parking and much more
• Healthcare Cash Plan: The Healthcare Cash Plan benefit provides the option to claim cash back on everyday healthcare expenses such as optical, dental, health and wellbeing and more .

The opportunity:

You will play a pivotal role within an established team with the aim of ensuring all core Quality Assurance activities are met, as well as the potential to work with domestic and international colleagues on projects involving transfer of technology.

This is an outstanding opportunity to network with and see a large variety of MBDA’s functions and activities across all sites. The role will involve working on a multi-national project, as well as with an established Quality network preventing/minimising product non-conformance, supporting smooth equipment delivery, assuring reliable products in Production and continually growing the happiness of our customers.

• Review, give and maintain Project Quality planning documentation.
• Ensure compliance to BMS procedures is maintained.
• Act as Key Point of contact for Design (Project Chief Engineer & CDE) for any Hardware concerns at Bolton.
• Act as External Customer for Product/ Hardware Quality issues/ concerns
• Customer interface for on and off site Product Acceptance activities
• Represent Project at the Op’s NCRP Level 1 & 2
• Act as the Key point of contact for the Project Quality Assurance Manager
• Represent Project QA at the monthly Operations Management
• Report on any escapes to our External Customers
• Ensure product life cycle reviews are planned, carried out and actions handled appropriately.
• Lead product non-conformance and facilitate implementation of non-conformance process.
• Support design and manufacturing defect investigations.
• Provide non-conformance data analysis and summary reports into major equipment and senior management reviews.
• Proactively identify, communicate and mitigate Quality risks and issues to reduce risk and increase customer happiness.
• Participate in process improvement and facilitate local flash audits, providing compliance and process improvement ideas.
• Plan and facilitate quality focused micro training to increase quality process awareness, efficiencies and proficiencies within the Project teams.
• Provide support to the transfer of technology process.

What we’re looking for from you:

• Ideally HNC/HND in Engineering or Quality Assurance is desirable, or equivalent work experience
• Ideally a practitioner of current QA problem solving and improvement methods (8D, RCA, DMAIC, etc.)
• A high degree of self-motivation, autonomy and ability to work proactively, with excellent organisation, communication & social skills
• An ability to inspire change, a respectful great teammate, comfortable working in a matrix organization
• Strong analytical skills; ability to run reports in Excel, use SAP QM system, and document management tools
• Continuous improvement awareness and initiative to deliver improvements
• Ability to understand and respect cultural differences

Our company: Peace is not a given, Freedom is not a given, Sovereignty is not a given

MBDA is a leading defence organisation. We are proud of the role we play in supporting the Armed Forces who protect our nations. We partner with governments to work together towards a common goal, defending our freedom.

We are proud of our employee-led networks, examples include: Gender Equality, Pride, Menopause Matters, Parents and Carers, Armed Forces, Ethnic Diversity, Neurodiversity, Disability and more

We recognise that everyone is unique, and we encourage you to speak to us should you require any advice, support or adjustments throughout our recruitment process.

Follow us on LinkedIn (MBDA), X Instagram (MBDA_UK) and Glassdoor or visit our MBDA Careers website for more information.

QUALITY ASSURANCE ENGINEER NEEDED IN TELFORD (SHROPSHIRE)

We are proud to be working with a long standing FMCG manufacturing business in Telford who are actively seeking a Quality Assurance Engineer to join them on a permanent basis, the working hours with this job are 9am-5pm Monday to Friday (with some slight flexibility on the start and finish time), and the annual salary is paying up to £32,000 per annum (DOE).

The hiring manager would like someone who has some formal qualifications in either the English Language, Mathematics or a Science-based subject, and as the role will involve both office and shop floor duties, we are looking for someone who is proficient with Microsoft Office packages.

Previous experience within the packaging / FMCG / pharmaceutical industry would be highly advantageous, but other industry experience would be considered providing you have the right skill set, the hiring manager would also like someone who has been involved with internal auditing, and a formal qualification in Internal Quality Auditing would be well received.

We are looking for someone who lives within a 25 mile radius of Telford (Shropshire).

Someone who has previously worked as an Internal Auditor, QA Engineer, Quality Auditor, Quality Assurance Technician, Quality Engineer or Compliance Engineer would be a great fit for this role.

What You Will Do:

• Drive quality and product safety improvements across the company, reducing waste and customer complaints.
• Coordinate the timely reporting of customer documentation requirements, including supplier quality questionnaires and non-conformance reports.
• Assist with internal quality system audits, GMP audits, and compliance audits by external accreditation bodies.
• Monitor and ensure compliance with current and changing legislation related to food safety, health and safety, and environmental standards.
• Support waste management and reduction activities, contributing to the company’s environmental goals.
• Provide clear and up-to-date information to other departments, ensuring safe products meet the highest quality standards.

What You Will Bring:

• Formal qualifications in English, mathematics, and a science-based subject, along with an internal quality auditing qualification.
• A Full UK Driving License.
• Experience in Corrective and Preventive Actions (CAPA) and root-cause analysis (RCA).
• Strong communication skills, with the ability to liaise confidently with internal teams, customers, suppliers, and certification bodies.
• Proficiency in Microsoft Office, including Word, Excel, and Outlook, with the ability to produce clear written documentation and analyse numerical data.
• A self-motivated and open-minded attitude, with a willingness to learn and grow within the role.

This company is a leader in its field, specialising in high-quality manufacturing and pioneering innovative techniques that provide environmental and commercial advantages. Joining this team means contributing to a business that values excellence, sustainability, and continuous improvement. This role is your chance to be part of an organisation that works with leading consumer brands and is committed to delivering outstanding results.

Location:

This role is based in Telford (Shropshire).

Interested?:

If you’re ready to take on this fantastic opportunity as a Quality Assurance Engineer, don’t wait. Apply now and take the first step towards an exciting and rewarding career!

Your CV will be forwarded to Jonathan Lee Recruitment, a leading engineering and manufacturing recruitment consultancy established in 1978. The services advertised by Jonathan Lee Recruitment are those of an Employment Agency.
In order for your CV to be processed effectively, please ensure your name, email address, phone number and location (post code OR town OR county, as a minimum) are included.