2,696 Quality jobs in the United Kingdom

Quality Specialist

Curtiss-Wright Corporation

Posted 8 days ago

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Job Description

Curtiss-Wright is looking for a Quality Specialist to join their expanding Corby team. If you are passionate about Quality and interesting in joining a growing global company, we want to hear from you!
**Location: Corby, UK**
**We Take Care of Our People**
Paid Time Off I Retirement with Employer Match I Health and Wellness Benefits I Learning and Development Opportunities I Competitive Pay I Bonus Scheme I Recognition I Employee Stock Purchase Plan ( I Inclusive & Supportive Culture ( *
**Your Challenge:**
+ Monitoring the flow of material through the manufacture/test process and final inspection.
+ Performing data pack and shipping document review.
+ Assisting with the review of inspection/test failure and rejection reports to identify project failure trends and provides recommendations for corrective action.
+ Assisting Quality Engineering and Quality Inspection in the development of inspection plans.
+ Aiding inspection personnel in the identification and resolution of problems encountered during hardware flow to ensure acceptable quality levels are maintained.
+ Assisting with system and process audits as required.
+ Inspection of hardware as required.
+ Other duties as required.
**Your Expertise:**
+ Previous experience in a similar role preferred.
+ Experience in a manufacturing environment preferred.
+ Experience with handheld measuring tools would be desirable.
+ Excellent communication skills.
+ Adaptable and flexible to undertake a range of responsibilities.
+ Team player.
#LI-HP1
_No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our_ **_Talent Acquisition Team ( )_** _and have signed terms in place prior to any submittal. Resumes submitted directly to any Curtiss-Wright employee or affiliate will not qualify for fee payment, and therefore become the property of Curtiss-Wright._
**Compliance Statement**
This position may require exposure to export-controlled information and subject to additional security screening. In the event information provided during the security screening reveals ineligibility to access export-controlled information, any offer of employment may be reconsidered or withdrawn.
Curtiss-Wright values diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition ( ) and we will make all reasonable efforts to accommodate your request.
**Join the WRIGHT Team!**
Over 95 years of growth, Curtiss-Wright is an integrated, market-facing global diversified industrial company and remains a technology leader through this legacy of innovation. Through three well-balanced segments - Aerospace & Industrial, Defense Electronics and Naval & Power, we remain focused on advanced technologies for high performance platforms and critical applications. Diversity, commitment to excellence and dedication to the spirit of pioneering innovation continue to drive the employees of Curtiss-Wright.
**Our Values**
What makes a world-class organization? It all begins with core values that provide a strong foundation for success. Simple in theory, the values of Curtiss-Wright are reflected in every aspect of our operations. To our employees, these are more than words on a wall - we all take these values to heart in our relationships with our customers and each other.
**Leadership**
We lead based on vision and strategic direction, empowering employees to reach goals through thoughtful and decisive action.
**Customer Focus**
We are committed to achieving total quality by meeting our customers' expectations and delivering products and services in a timely fashion.
**Teamwork & Trust**
Working in a spirit of trust and collaboration, we actively encourage employees to contribute their ideas and innovations to keep our company moving forward.
**Respect for People**
We believe that people are our most valuable asset and will always do the right thing in our dealings and interactions with all employees.
**Integrity**
We will act with the highest integrity in all of our business relationships and strategic partnerships.
**What We Offer Our Employees:**
**Opportunity:** As part of the Curtiss-Wright team, you have the opportunity each day to transform the way customers do business, as well as transform your career. Our entrepreneurial environment provides you with excellent experiences that enable you to develop your skills through stretch assignments and the opportunity to work with the best talent in the industry. You will have the opportunity to contribute from day one!
**Challenging Work:** The work we do here is not only challenging, but it is meaningful to our customers, our employees and the communities in which they live and work. You are given the chance to work on some of the most advanced technology projects in the world. Now that something to be proud of!
**Collaborative Environment:** The teamwork among our exceptionally talented people enables us to deliver some of the most advanced solutions to our customers.
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Quality Specialist

DG11 Lochmaben, Scotland Arla Foods Plc

Posted 1 day ago

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Job Description

DG11 1LW

Mon- Fri Days

18months FTC

Looking for an exciting opportunity to make a significant impact in a fast-paced manufacturing company? Due to an internal secondment we are currently seeking an experienced and talented individual to join our Quality, Environmental, Health and Safety (QEHS) team as a key member. As a QEHS Specialist, you will report directly to the Senior QEHS Manager and play a v
Maximise your chances of a successful application to this job by ensuring your CV and skills are a good match.
Please click on the apply button to read the full job description

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Quality Specialist

Lockerbie, Scotland Arla Foods Plc

Posted 1 day ago

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Job Description

temporary

DG11 1LW

Mon- Fri Days

18months FTC

Looking for an exciting opportunity to make a significant impact in a fast-paced manufacturing company? Due to an internal secondment we are currently seeking an experienced and talented individual to join our Quality, Environmental, Health and Safety (QEHS) team as a key member. As a QEHS Specialist, you will report directly to the Senior QEHS Manager and play a v.



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Supplier Quality Specialist

Morgan Ryder Associates

Posted 6 days ago

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Job Description

full time

Supplier Quality Specialist - Multiple Opportunities
Location: Prestwick, Scotland
Salary: up to 50,000
Job Type: Permanent

We're on the hunt for multiple Supplier Quality Specialists to join a business that is entering an exciting new chapter, following a recent change that will strengthen, develop, and expand capabilities like never before. This unique moment in their journey is creating fresh opportunities for the business and for their people, opening doors to growth, innovation, and long-term stability. If you've been considering the next step in your career, there has never been a better time to join this business and be part of shaping future success.

Why jump on board?
Because this isn't just another job, it's a career-launching opportunity packed with growth, challenge, and reward! With ambitious expansion plans fuelling new openings, you'll have the chance to fast-track your development, work on cutting-edge aerostructure projects, and make a real impact in a world-class aerospace environment. Plus, we're offering a strong, competitive salary package that truly values your skills and experience. Whether you're a seasoned pro or ready to take that next big step, we want to hear from you NOW.

Don't miss out, this is where your supplier quality career takes off!

What You'll Do:

  • Lead supplier quality assurance activities to improve and maintain supplier performance.
  • Conduct supplier audits and capability assessments in line with aerospace standards (AS9100, NADCAP).
  • Review and approve supplier quality documentation including PPAP, control plans, and NCRs.
  • Investigate and resolve supplier quality issues using root cause analysis and CAPA.
  • Work closely with procurement, engineering, production, and quality teams to meet business goals.
  • Support supplier onboarding, development, and qualification processes.
  • Deliver regular reporting on supplier quality metrics and improvements.
  • Support the assembly of critical aerostructure components such as spoilers and airbrakes.
  • Drive a culture of continuous improvement and quality excellence throughout the supply chain.

Who We're Looking For:
We are open to candidates at all experience levels , from early-career professionals eager to grow, to seasoned experts wanting to make their mark. The only non-negotiable requirements are:

  • Ability to confidently read and interpret engineering drawings.
  • Proven experience working within a quality function, including performing root cause analysis, and managing CAPA.

Additional strengths include:

  • Knowledge of aerospace quality standards (AS9100, NADCAP) is a strong advantage.
  • Experience conducting supplier audits and quality assessments.
  • Familiarity with quality tools and methodologies such as PPAP, FMEA, 8D problem solving.
  • Strong communication and negotiation skills, with the ability to influence supplier behaviour.
  • Analytical mindset with experience using quality management systems and software (SAP, Minitab preferred).
  • Relevant professional qualifications (CQE, CQA) desirable but not essential.

What's In It for You?

  • Competitive salary and benefits package tailored to your experience.
  • Multiple roles available - plenty of scope for career progression and development.
  • Work in a fast-paced, cutting-edge aerospace manufacturing environment with global impact.
  • Collaborative culture focused on quality, innovation, and continuous improvement.

Ready to Take Off?
If you meet the key experience criteria and want to be part of an exciting growth journey, apply today! Send your CV along with a brief covering letter outlining your relevant experience and why you're interested in these roles.

At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions.

We recruit for companies that operate in the following industries: Defence Equipment, Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy.

Our commitment:

Equal opportunities are important to us. We believe that diversity and inclusion at Morgan Ryder Associates are critical to our success as DE&I positive company, so we want to recruit, develop, and keep the best talent. We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristic.

Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.

This advertiser has chosen not to accept applicants from your region.

Supplier Quality Specialist

South Ayrshire, Scotland £42000 - £50000 Annually Morgan Ryder Associates

Posted 6 days ago

Job Viewed

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Job Description

permanent

Supplier Quality Specialist - Multiple Opportunities
Location: Prestwick, Scotland
Salary: up to 50,000
Job Type: Permanent

We're on the hunt for multiple Supplier Quality Specialists to join a business that is entering an exciting new chapter, following a recent change that will strengthen, develop, and expand capabilities like never before. This unique moment in their journey is creating fresh opportunities for the business and for their people, opening doors to growth, innovation, and long-term stability. If you've been considering the next step in your career, there has never been a better time to join this business and be part of shaping future success.

Why jump on board?
Because this isn't just another job, it's a career-launching opportunity packed with growth, challenge, and reward! With ambitious expansion plans fuelling new openings, you'll have the chance to fast-track your development, work on cutting-edge aerostructure projects, and make a real impact in a world-class aerospace environment. Plus, we're offering a strong, competitive salary package that truly values your skills and experience. Whether you're a seasoned pro or ready to take that next big step, we want to hear from you NOW.

Don't miss out, this is where your supplier quality career takes off!

What You'll Do:

  • Lead supplier quality assurance activities to improve and maintain supplier performance.
  • Conduct supplier audits and capability assessments in line with aerospace standards (AS9100, NADCAP).
  • Review and approve supplier quality documentation including PPAP, control plans, and NCRs.
  • Investigate and resolve supplier quality issues using root cause analysis and CAPA.
  • Work closely with procurement, engineering, production, and quality teams to meet business goals.
  • Support supplier onboarding, development, and qualification processes.
  • Deliver regular reporting on supplier quality metrics and improvements.
  • Support the assembly of critical aerostructure components such as spoilers and airbrakes.
  • Drive a culture of continuous improvement and quality excellence throughout the supply chain.

Who We're Looking For:
We are open to candidates at all experience levels , from early-career professionals eager to grow, to seasoned experts wanting to make their mark. The only non-negotiable requirements are:

  • Ability to confidently read and interpret engineering drawings.
  • Proven experience working within a quality function, including performing root cause analysis, and managing CAPA.

Additional strengths include:

  • Knowledge of aerospace quality standards (AS9100, NADCAP) is a strong advantage.
  • Experience conducting supplier audits and quality assessments.
  • Familiarity with quality tools and methodologies such as PPAP, FMEA, 8D problem solving.
  • Strong communication and negotiation skills, with the ability to influence supplier behaviour.
  • Analytical mindset with experience using quality management systems and software (SAP, Minitab preferred).
  • Relevant professional qualifications (CQE, CQA) desirable but not essential.

What's In It for You?

  • Competitive salary and benefits package tailored to your experience.
  • Multiple roles available - plenty of scope for career progression and development.
  • Work in a fast-paced, cutting-edge aerospace manufacturing environment with global impact.
  • Collaborative culture focused on quality, innovation, and continuous improvement.

Ready to Take Off?
If you meet the key experience criteria and want to be part of an exciting growth journey, apply today! Send your CV along with a brief covering letter outlining your relevant experience and why you're interested in these roles.

At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions.

We recruit for companies that operate in the following industries: Defence Equipment, Food and Drink Manufacturers, FMCG, Packaging, Engineering, Automotive, Aerospace, Warehousing, Logistics, Waste Management, Petro Chemical, Pharmaceutical, Power & Renewable Energy.

Our commitment:

Equal opportunities are important to us. We believe that diversity and inclusion at Morgan Ryder Associates are critical to our success as DE&I positive company, so we want to recruit, develop, and keep the best talent. We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristic.

Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.

This advertiser has chosen not to accept applicants from your region.

Sr Quality Specialist

Zimmer Biomet

Posted 5 days ago

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Job Description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient's mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.
**What You Can Expect**
Under minimal supervision, Maintain Document Control program to ensure compliance to domestic and international medical device regulations.
**How You'll Create Impact**
- Manage Change Control program and coordinate department efforts in processing Quality System change orders. Provide direction and support to Change Analysts.
- Provide leadership to team members in order to support training process and Master Data Management system (SAP).
- Provide support to site LMS Administrators.
- Support standardizing and harmonizing document control processes across sites where applicable.
- Develop and maintain document control procedures and work instructions.
- Provide training on document control system to familiarize users with system. Provide training to new team members.
- Support site assessment process to ensure compliance to external standards and regulations where applicable.
- Develop and execute process improvements when necessary to ensure the Document Control process meets users' needs and requirements.
- Provide local administrator support for implementation and use of integrated electronic document management system.
- Organize and develop an integrated classification and storage system to facilitate access to Quality records including DHRs.
- Coordinate project work related to integration of sites and migration to integrated systems.
- Track and report status of projects managed by Document Control.
- Assist department efforts in aduits, both internal and external, to demonstrate compliance with GMP, ISO, CMDR, MDD and MDR regulations.
**_This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act._**
**What Makes You Stand Out**
+ Knowledge of current Food and Drug Administration (FDA) laws, regulations and practices.
+ Ability to objectively deal with individuals using appropriate tact and diplomacy to establish and maintain a congenial relationship
+ Proficiency in report writing
+ Good word processing and data base skills
+ Outstanding organizational skill
+ High attention to detail.
**Your Background**
+ Bachelor's Degree in life sciences field or equivalent with 3-5 years relevant work experience.
+ Proficient in Enlgish - written and spoken B2.
**Travel Expectations**
+ Up to 5%
EOE/M/F/Vet/Disability
This advertiser has chosen not to accept applicants from your region.

Language Quality Specialist

Reading, South East IQVIA

Posted 8 days ago

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Job Description

As a **Japanese** **Language Quality Specialist** you will work closely with the Head of Quality and Compliance as well as with the Director of Vendor and Language Management. You will help providing continued monitoring over the translation quality of our global pool of suppliers, in order to maintain and improve external freelancers' standards with IQVIA, and ultimately boost overall quality output.
The Language Quality Specialist is a proactive member of the Quality team, contributing to deliver globally an efficient quality management service to internal staff, external resources, and clients.
**RESPONSIBILITIES**
+ Trigger Quality Feedback Reports and improvement plans on selected resources, liaising with all stakeholders (PMs, Quality team, Internal Linguists, External Reviewers, Vendor Managers, etc.).
+ Analyze language quality issues and works on global and local improvement plans with project management and quality teams
+ Support VMs and PMs in anticipating and dealing with quality issues.
+ Flag potential resources for promotion or demotion based on quality results.
+ Run regular analysis on resource and language quality status.
+ Monitor edit distance per language and help to enhance language output.
+ Drive global language quality strategy and establish tools to monitor the quality of outsourced language translations.
+ Work with Terminology Coordinator to make sure language assets are created and updated as needed.
+ Help to build and design a robust and efficient Quality system as well as the creation of SOPs related to this function.
+ Contribute to conceive developments/enhancements and best practices in Language Quality.
**REQUIRED KNOWLEDGE, SKILLS AND ABILITIES**
+ Native level of Japanese language skill (speaking/reading/writing).
+ 3-5 years' experience as a Language Quality Specialist dealing with multilingual projects.
+ Mediation/negotiation skills in working with people from different countries and cultures.
+ Ability to multitask and quickly adapt to change.
+ High level of commitment and motivation is essential.
+ Higher education in translation-related studies, or equivalent experience.
+ Excellent oral, written, and interpersonal communication skills in English.
+ Extensive knowledge of Multilingual Quality Monitoring processes.
+ Proven skills of analysis, time management, organization, and attention to detail.
**PHYSICAL REQUIREMENTS**
+ Extensive use of keyboard requiring repetitive motion of fingers.
+ Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
+ Regular sitting for extended periods of time.
The above information on this description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
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Sr. Quality Specialist

Curtiss-Wright Corporation

Posted 17 days ago

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Job Description

We are looking for a Senior Quality Specialist to join our Christchurch, Dorset team!
As a Senior Quality Specialist, you will be responsible for reviewing inspection/test failure and rejection reports and ensures quality inspection team follows test plans and procedures on a consistent basis. Communicates to Engineering and Manufacturing teams of any unusual or concerning results discovered by the Quality Inspectors.
**Location:** Christchurch UK
**Benefits:** Paid Time Off | Retirement with Employer Match | Health and Wellness Benefits | Learning and Development Opportunities | Competitive Pay | Bonus Scheme | Recognition | Employee Stock Purchase Plan I Inclusive & Supportive Culture
**Your Challenge:**
+ Performs data pack and shipping document reviews / Source Inspections and may perform actual inspection when required.
+ Reviews inspection/test failure and rejection reports and ensures quality inspection team follows test plans and procedures on a consistent basis. Communicates to Engineering and Manufacturing teams of any unusual or concerning results discovered by the Quality Inspectors.
+ Works with Engineering, Manufacturing and Inspection in assessment and resolution. Identifies test/inspection improvements and works with Engineering and Manufacturing teams on acceptable quality levels / improvement implementation.
+ Assist in maintaining QMS and product process documentation as part of a continuous improvement and best practice process.
+ Completes system and process audits.
+ Experienced in the interpretation of engineering drawings, schematics and process plans and assists Quality Engineering, Quality Inspection and Manufacturing in the development of inspection plans.
+ Support in maintaining new supplier evaluation, new parts validation and approval for new projects and resolve problems from supplier parts returned by customer or manufacturing including root cause analysis and problem resolution.
+ Provide follow up to suppliers. Monitor/support suppliers' product/process quality control system improvement by system/process/product audit, supplier training and project management etc.
+ Support the responsible person for site Security Control oversight for the business. Update of Security Procedures, related documents and structure in line with regulatory requirements
**Your Expertise:**
+ Qualified apprentice or recent graduate looking for a development opportunity.
+ BTEC qualifications looking for a wider challenge.
+ Manufacturing / Production experience looking to move into Quality.
+ Communicate well (one2one and in a team).
+ Be computer literate.
+ Be confident in M/S tools use or other associated tools / systems.
+ Be able to take on a task / project and complete it.
+ Have a practical hands-on approach / capability to progress within the business.
+ Being able to read and assess quality data (or have capability to learn how to).
+ Follow instruction but also give instruction over time.
+ Be able manage / lead Quality Projects over time.
+ Be willing to be trained in Quality Regulation, Quality Improvement Tools and Lean Tools over time.
+ Practical experience in a Aerospace company.
+ Awareness of a Quality Regulation standard (AS9100, ISO 9001
**3 - 5 years years experience in either:**
+ A Manufacturing /Production environment.
+ A Technical / Process environment.
+ Quality environment (Quality Assurance, Quality Control, etc).
**Who We Are**
Curtiss-Wright's Defense Solution division is a trusted, proven leader, delivering superior products and services that meet the defense and aerospace industries' toughest challenges with best-in-class value. In 2017, Curtiss-Wright relocated its Avionics, Sensors & Controls and Industrial Business Units into a brand new, purpose-built 160,000 ft2 facility at Bournemouth International Airport.
The state-of-the-art facility has extensive design and manufacturing capabilities as well as in-house environmental stress screening. The facility is committed to quality and excellence in manufacturing for our flight recorder, air data computer, video management systems, computing systems, mission displays and video recorder products.
As the design center of excellence for flight recorders and air data computers, the units had to be lightweight and small - crash survivability requirements exceeding the existing standards for commercial aircraft.
Our Values ( Environmental, Social and Governance
#LI-RF1
_No unsolicited agency submittals please. Agency partners must be invited to participate in a search by our_ **_Talent Acquisition Team ( )_** _and have signed terms in place prior to any submittal. Resumes submitted directly to any Curtiss-Wright employee or affiliate will not qualify for fee payment, and therefore become the property of Curtiss-Wright._
**Compliance Statement**
This position may require exposure to export-controlled information and subject to additional security screening. In the event information provided during the security screening reveals ineligibility to access export-controlled information, any offer of employment may be reconsidered or withdrawn.
Curtiss-Wright is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, sexual orientation, gender identity, physical or mental disability, age, ancestry, legally protected medical condition, family care status, marital status, religion, veteran status, national origin, or any other legally protected status. If you require accommodation during the recruitment process, please contact Talent Acquisition. ( )
**For US Applicants: EEO is The Law - click here for more information. ( you require accommodation due to a disability at any time during the recruitment and/or assessment process, please contact Talent Acquisition ( ) and we will make all reasonable efforts to accommodate your request.
**Join the WRIGHT Team!**
Over 95 years of growth, Curtiss-Wright is an integrated, market-facing global diversified industrial company and remains a technology leader through this legacy of innovation. Through three well-balanced segments - Aerospace & Industrial, Defense Electronics and Naval & Power, we remain focused on advanced technologies for high performance platforms and critical applications. Diversity, commitment to excellence and dedication to the spirit of pioneering innovation continue to drive the employees of Curtiss-Wright.
**Our Values**
What makes a world-class organization? It all begins with core values that provide a strong foundation for success. Simple in theory, the values of Curtiss-Wright are reflected in every aspect of our operations. To our employees, these are more than words on a wall - we all take these values to heart in our relationships with our customers and each other.
**Leadership**
We lead based on vision and strategic direction, empowering employees to reach goals through thoughtful and decisive action.
**Customer Focus**
We are committed to achieving total quality by meeting our customers' expectations and delivering products and services in a timely fashion.
**Teamwork & Trust**
Working in a spirit of trust and collaboration, we actively encourage employees to contribute their ideas and innovations to keep our company moving forward.
**Respect for People**
We believe that people are our most valuable asset and will always do the right thing in our dealings and interactions with all employees.
**Integrity**
We will act with the highest integrity in all of our business relationships and strategic partnerships.
**What We Offer Our Employees:**
**Opportunity:** As part of the Curtiss-Wright team, you have the opportunity each day to transform the way customers do business, as well as transform your career. Our entrepreneurial environment provides you with excellent experiences that enable you to develop your skills through stretch assignments and the opportunity to work with the best talent in the industry. You will have the opportunity to contribute from day one!
**Challenging Work:** The work we do here is not only challenging, but it is meaningful to our customers, our employees and the communities in which they live and work. You are given the chance to work on some of the most advanced technology projects in the world. Now that something to be proud of!
**Collaborative Environment:** The teamwork among our exceptionally talented people enables us to deliver some of the most advanced solutions to our customers.
This advertiser has chosen not to accept applicants from your region.

Supplier Quality Specialist

Prestwick, Scotland Morgan Ryder

Posted 1 day ago

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Job Description

Supplier Quality Specialist – Multiple Opportunities

Prestwick, Scotland

up to £50,000

Permanent - Global Travel


We’re on the hunt for multiple Supplier Quality Specialists to join a business that is entering an exciting new chapter, following a recent change that will strengthen, develop, and expand capabilities like never before. This unique moment in their journey is creating fresh opportunities for the business and for their people, opening doors to growth, innovation, and long-term stability. If you’ve been considering the next step in your career, there has never been a better time to join this business and be part of shaping future success.


Why jump on board?

Because this isn’t just another job, it’s a career-launching opportunity packed with growth, challenge, and reward! With ambitious expansion plans fuelling new openings, you’ll have the chance to fast-track your development, work on cutting-edge aerostructure projects, and make a real impact in a world-class aerospace environment. Plus, we’re offering a strong, competitive salary package that truly values your skills and experience. Whether you’re a seasoned pro or ready to take that next big step, we want to hear from you NOW.

Don’t miss out, this is where your supplier quality career takes off!


What You’ll Do:

  • Lead supplier quality assurance activities to improve and maintain supplier performance.
  • Conduct supplier audits and capability assessments in line with aerospace standards (AS9100, NADCAP).
  • Review and approve supplier quality documentation including PPAP, control plans, and NCRs.
  • Investigate and resolve supplier quality issues using root cause analysis and CAPA.
  • Work closely with procurement, engineering, production, and quality teams to meet business goals.
  • Support supplier onboarding, development, and qualification processes.
  • Deliver regular reporting on supplier quality metrics and improvements.
  • Support the assembly of critical aerostructure components such as spoilers and airbrakes.
  • Drive a culture of continuous improvement and quality excellence throughout the supply chain.


Who We’re Looking For:

We are open to candidates at all experience levels , from early-career professionals eager to grow, to seasoned experts wanting to make their mark. The only non-negotiable requirements are:

  • Ability to confidently read and interpret engineering drawings.
  • Proven experience working within a quality function, including performing root cause analysis, and managing CAPA.

Additional strengths include:

  • Knowledge of aerospace quality standards (AS9100, NADCAP) is a strong advantage.
  • Experience conducting supplier audits and quality assessments.
  • Familiarity with quality tools and methodologies such as PPAP, FMEA, 8D problem solving.
  • Strong communication and negotiation skills, with the ability to influence supplier behaviour.
  • Analytical mindset with experience using quality management systems and software (SAP, Minitab preferred).
  • Relevant professional qualifications (CQE, CQA) desirable but not essential.


What’s In It for You?

  • Competitive salary and benefits package tailored to your experience.
  • Multiple roles available – plenty of scope for career progression and development.
  • Work in a fast-paced, cutting-edge aerospace manufacturing environment with global impact.
  • Collaborative culture focused on quality, innovation, and continuous improvement.


Ready to Take Off?

If you meet the key experience criteria and want to be part of an exciting growth journey, apply today! Send your CV along with a brief covering letter outlining your relevant experience and why you’re interested in these roles.

This advertiser has chosen not to accept applicants from your region.

Quality Specialist/ Artwork Manager

EC1 London, London Room at the Top Recruitment

Posted 6 days ago

Job Viewed

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Job Description

contract

We have an opportunity to work for our global animal health pharmaceutical client as a fully remote Quality Specialist – Artwork Manager. The role is a full-time PAYE temporary contract position initially signed off for 12 months with a possible extension and offers an hourly rate of £27.76 - £47.20 per hour, depending on experience, plus 25 days holiday pro rata and other benefits.

The purpose of the position is to manage the operational implementation of artwork changes for several small and large molecule external Contract Manufacturing Organizations (CMO’s) in the EU covering finished product packaging and quality as well as supply chain related adaptations. 

Due to the new Veterinary Regulation (EU) 2019/6 which became effective 28 January 2022 it is required to adapt the Summary of product characteristics (SPC) and subsequently the related artwork components to the new QRD 9.0 template to be finalized by 28 January 2027.

The job holder will be reporting to the External Manufacturing Quality (EMQ) EMEA Lead and being part of the multifunctional QRD team as a point of contact for products packaged at CMO’s and in close contact with the responsible project contact at the CMO.  Candidates should have a minimum of 3 years’ experience working within a similar Artwork Quality/GMP or Regulatory environment.

Role Functions & Responsibilities:

  • Be the EMQ Site Point of Contact (SPOC) for the QRD 9.0 project
  • li>Be in close contact with central Reliance QRD SPOC and in close contact with global Artwork department (GRA Operations)
  • Be in close contact with the responsible project contact at the CMO
  • Be the change task owner in Reliance (quality management system for change controls)
    • Take part in stakeholder meetings
    • Execution and timely closure of identified task
    • If applicable develop new technical specification with follow up actions
    • Execute the Quality Representative role
  • Develop an artwork switch plan together with the global artwork department, the QRD Reliance Manager, the Global Supplier Management (GSM) contact and the project contact at the CMO for the impacted products 
  • li>Escalate challenges and risks with respect to project timelines and resources to CMO Governance

Experience, Knowledge & Skills:

  • Solid knowledge of the Good Manufacturing Practices (GMPs) in pharmaceutical industry.
  • 3 Years’ experience in Quality/GMP or Regulatory environment.
  • < i>Solid knowledge about compliance requirements for change management and change control
  • You are at ease with transversal projects
  • Enjoy working in a dynamic & multicultural environment
  • Enjoy working in a cross functional team and interact with various departments
  • You speak English fluently
  • Have good adaptability and integration skills
  • Results oriented
  • Experience with artwork management

Qualifications:

  • Bachelor’s degree in science (Pharmacist, Engineer or equivalent) or something similar 
  • Solid knowledge of the Good Manufacturing Practices (GMPs) in pharmaceutical industry
  • Solid knowledge about compliance, regulatory or quality requirements in the pharmaceutical industry
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