940 Quality Director jobs in the United Kingdom

Ready to elevate your career with a top-tier steel fabrication leader?

We're expanding our team in Thirsk and looking for a skilled QA/QC Engineer to help drive excellence across major industries like Petrochemical, Pharmaceutical, and Nuclear. Join us on our exciting journey of growth and innovation, where you'll benefit from robust career development opportunities, clear progression paths , and the chance to shape the future of engineering excellence.

Who this job suits:

This role is ideal for an experienced Quality Engineer with a meticulous eye for detail, analytical skills, and prior exposure to large, complex, multi-disciplined projects in regulated environments. Your knowledge of Welding, ISO 3834 & EN 1090 will be high advantageous.

Key Responsibilities:

• Liaise with internal and external stakeholders to ensure project inspections and technical requirements are met.
• Ensure compliance to ISO 3834, EN 1090, ISO 9001.
• Collate and analyse data, support audits, and liaise with clients.
• Utilize extensive hands-on experience in Quality Management Systems and Principles.
• Interpret and accept contract NDT reports on behalf of the business.

Skills and Experience:

• CSWIP 3.1 certified
• Auditor certified
• PCN Level 2 certified
• Time-served apprenticeship, HNC, HND or equivalent
• Knowledge of ISO 3834 (welding inspection) and/or EN 1090 advantageous
• Experience with LTQRs advantageous

Location : Thirsk

Contract: 12 month FTC - Fixed Term Contract

Salary: circa £40k - £45k (dependent on experience)

Hours: 37.5 hours per week. 07.45 – 16:45 Monday - Thursday, 7.30 - 12:00 Friday.

Benefits: Pension, Medical Cover, 25 days + BH, Cycle to Work, Save as you earn scheme, Counselling & Support, further Benefit schemes.

APPLY NOW!

Contact Jacob Golding for further details – –

We are seeking an accomplished Director of Quality Assurance to lead the Quality function within a rapidly growing, high-technology company in the semiconductor industry. This strategic position will oversee the company’s Quality Management System (QMS), supplier and subcontractor performance, product reliability, and customer quality support — ensuring world-class standards are achieved and maintained across all operations.

Key Responsibilities

• Provide strategic direction and leadership for all Quality Assurance activities across manufacturing, supplier management, and customer support.
• Oversee and continuously improve the company’s Quality Management System, ensuring compliance with ISO 9001 and relevant industry standards (JEDEC, AEC).
• Drive product reliability initiatives and implement robust quality processes across design, development, and production.
• Manage supplier and subcontractor performance, establishing strong partnerships and accountability for quality and delivery.
• Lead internal and external audits, and act as the primary contact for customer quality escalations and certifications.
• Chair Health & Safety meetings, conduct inspections, and ensure all regulatory and safety policies are effectively implemented.
• Use data-driven insights to identify root causes, implement corrective actions, and enhance process capability.
• Promote a culture of quality, safety, and continuous improvement across all levels of the organisation.

About You

• Proven track record in senior Quality leadership within the semiconductor or electronics manufacturing sectors.
• Deep knowledge of JEDEC, AEC, and ISO 9001 quality standards and regulatory frameworks.
• Strong background in supplier quality management, product reliability, and customer quality support.
• Experienced in driving data-driven decision-making and leading cross-functional quality initiatives.
• Lean Six Sigma (Green or Black Belt) certification strongly preferred.
• Excellent leadership, communication, and stakeholder management skills, with the ability to influence at executive level.

Apply now for more information!

Are you looking for some further experience in Pharmaceutical QC? Do you have prior experience with GC & HPLC in a cGMP environment?

A Global Pharmaceutical Manufacturer are seeking a QC Analyst to join the team at their site in Kirklees. This is a 6 month FTC and would be ideal if you are immediately available and looking to add to your existing experience in Pharmaceutical QC.

Role Overview

• Full Time , 6 month Fixed term Contract. Day Shifts. £27,000pa.
• Analysis of Raw Materials and Finished Products to SOPs.
• Utilise analytical equipment , predominantly HPLC & GC.
• Interpretation and checking of Analytical Data.
• Monitoring, Calibration and occasional basic troubleshooting/maintenance of instruments and analytical equipment.
• Preparation of all relevant documentation in line with applicable standards.

Requirements

• Prior working experience in a cGMP environment using HPLC and GC is essential.
• Degree or equivalent in relevant scientific discipline (or equivalent working experience) is essential.
• Ability to work independently in time pressured environment.
• Excellent communication skills and attention to detail.

In return

This 6 month FTC is an excellent opportunity to add some additional experience to your CV, working alongside industry leaders in a well renowned pharmaceutical organisation.

For more information, please contact Louis Williams

If this QC Analyst job is not quite right for you, but you’re interested in similar opportunities, please take a look at our other Jobs in the Pharmaceutical Sector. Network Scientific is a multi-award-winning recruitment agency dedicated to connecting top talent with opportunities across the scientific and technical sectors. We specialise in temporary, permanent, and contract placements, and pride ourselves on being an ethical and knowledgeable consultancy with a strong focus on candidate care.

Please note that all applicants for this role should be able to prove that they are legally entitled to work in the country specified. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

A Quality Inspector (Weld & NDT) role is pivotal in upholding quality standards and compliance within manufacturing environments. Responsible for inspections and documentation review, this position fosters a culture of operational satisfaction and adherence to project requirements.

Who this job would suit:

Ideal for CSWIP 3.1 & PCN Level 2 certified QA/QC professionals with meticulous attention to detail and excellent communication skills. Suitable for those experienced in welding procedures and quality assurance protocols, who thrive in collaborative environments.

Key Responsibilities:

• Complete inspections to ensure material at goods inwards meet the required standards.
• Liaise with sub-contractors and treatment works to carry out inspections of sites.
• Visit suppliers and produce relevant inspection reports.
• Utilise your Welding inspection and NDT knowledge to ensure work is completed to a safe and high standard in compliance with company and ISO standards are followed.

Requirements:

• CSWIP 3.1 certified is essential.
• PCN Level 2 in MPI & DPI essential
• Experience within Nuclear, MOD or Heavy Fabrication is highly advantageous.

Permanent

Pay rate: £24.11 per hour (47k basic) + Overtime at premium rates + Bonus! (OTE circa £55k+)

Location: Deeside

Working Hours: 37.5 hrs (Mon-Thurs), (Fri)

Contact Details:

For inquiries or to apply, please contact Jacob on or

The Role:

Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.

As an employee, you'll be part of a continually growing organization, working alongside exceptional colleagues and strategic partners worldwide, contributing to global health initiatives.

Moderna's commitment to advancing the technological frontier of mRNA medicines ensures a challenging and rewarding career experience, with the potential to make a significant impact on patients' lives worldwide.

Moderna's mission is to establish a leading-edge research, development, and manufacturing facility at Harwell, as part of a long-term commitment to onshore mRNA vaccine production for respiratory diseases. This initiative will create a multitude of highly skilled jobs and foster collaboration with academic, NHS and government partners across the UK. We're looking for global experts eager to join us in this endeavour, contributing to a future where access to life-saving vaccines is a reality for all.

This position, reporting to the Associate Director, Quality Control, is an essential part of the Harwell QC team focused on GMP-compliant stability and analytical chemistry testing. As a key contributor, you will support critical release and stability testing operations and play a major role in the management of global stability programs. You will operate and maintain a suite of sophisticated instrumentation, manage cGMP documentation, and support the timely delivery of results across the QC chemistry function. The role offers direct involvement with cutting-edge analytical techniques, stability data management, and regulatory compliance frameworks — as well as exposure to Generative AI tools and digital platforms enhancing Moderna's QC infrastructure.

Here's What You'll Do :

Your key responsibilities will be:

• Execute routine analytical chemistry and stability testing using HPLC, UPLC, GC, UV, Karl Fischer, particle size analysis (DLS), and other analytical techniques.
• Support testing across raw materials, components, in-process and drug substance samples.
• Complete all cGMP documentation for analytical work in full compliance with applicable guidelines.
• Perform LIMS (LabVantage) data entry and complete electronic assay forms for traceability and review.
• Carry out HPLC (AEX) and NaOH plate-reader assays in support of manufacturing stat testing.
• Provide general laboratory support: reagent preparation, inventory management, equipment maintenance, and housekeeping.
• Ensure safe laboratory operations, actively contributing to EHS compliance.
• Participate in procurement and stock management of lab consumables and supplies.

Your responsibilities will also include:

• Conduct stability program operations: set down, pull, labeling, verification, inventory updates, and disposal.
• Author, review, and revise stability protocols, SOPs, and technical reports.
• Maintain and trend stability data, performing statistical analyses and ensuring real-time visibility of study progress.
• Interface with external labs for sample shipment and testing data coordination, and update internal databases and binders accordingly.
• Support regulatory submissions by contributing to stability sections and ensuring alignment with FDA, EU, and ICH guidelines.
• Assist with troubleshooting analytical methods and instrumentation as required.
• Support training and mentorship of junior staff as needed.
• Contribute to quality systems documentation including investigations, deviations, CAPAs, and change controls.
• Promote a positive, inclusive, and collaborative culture in line with Moderna's values.
• Ensure strict adherence to GDP, data integrity, and internal SOPs across all executed tasks.
• Complete all required training and qualifications in accordance with assigned learning plans.

The key Moderna Mindsets you'll need to succeed in the role:

• We obsess over learning. We don't have to be the smartest—we have to learn the fastest.
  
  In this highly technical and regulated environment, your ability to absorb evolving regulatory guidance, apply new analytical tools, and quickly learn from experimental data will be critical to your effectiveness.
• We digitize everywhere possible using the power of code to maximize our impact on patients.
  
  With increasing use of Generative AI tools and digital systems like LIMS at the core of Moderna's QC infrastructure, your comfort with digital platforms and data-driven execution will allow you to unlock greater speed, accuracy, and compliance.

Here's What You'll Need :

• Education: BA/BSc in Chemistry or Biology (preferred) or other relevant scientific discipline
• Experience: At least 5-7 years in Quality Control Laboratory of a Pharmaceutical Company
• Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations (specify GMP, GLP, GCP, GVP or other applicable standards)
• This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.
• As part of Moderna's commitment to workplace safety, this role may require an enhanced pre-employment check.

At Moderna, we believe that when you feel your best, you can do your best work. That's why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between.

• Quality healthcare and insurance benefits
• Lifestyle Spending Accounts to create your own pathway to well-being
• Free premium access to fitness, nutrition, and mindfulness classes
• Family planning and adoption benefits
• Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
• Savings and investments
• Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply

Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at .