216 Field Inspector jobs in the United Kingdom

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 .

Who Are We?

Tanpopo Japanese Food are a well-established food manufacturing business specialising in Japanese Food based in Feltham who have been operating for over 25 years. We are currently seeking a detail-oriented and dedicated Quality Control and Labelling Assistant (Night Shift, 00:00-08:00) to join our food production team.

As a Quality Control Assistant, you will play a critical role in ensuring that our products meet the highest standards of quality and safety. You will be responsible for conducting inspections, monitoring processes, and maintaining accurate records in accordance with our quality control procedures.

We do not offer sponsorships

Main Responsibilities Will Include:

• Perform quality control checks in the production area to ensure compliance with company standards and regulatory requirements.
• Record and monitor probe temperatures during work in progress (WIP) to ensure proper handling and storage of products.
• Maintain defrosting records, including in-code checks, defrosting methods, and temperature records.
• Conduct product sanitisation and chlorine concentration checks for high-risk items, along with regular test strip checks.
• Supervise and manage the cleaning schedules in the production area to uphold cleanliness and hygiene standards.
• Check products for metal detection by running them through the metal detector.
• Weigh and verify products as part of daily production specification weight control reports.
• Maintain records of dressing quantities used during production.
• Monitor and record fridge and freezer temperatures regularly.
• Cross-check all production documents and submit weekly reports to the QA department.
• Report any food safety and hygiene issues to QA Supervisors and Production Managers promptly.
• Provide monthly updates on internal product rejection rates.
• Keep track of short-dated and expired raw material stock and inform relevant departments for necessary actions.
• Perform weekly calibration of internal scales, probes, air temperatures, and dishwasher probes, and document the results – taking corrective actions as required based on calibration results.
• Handle printing of labels for the entire shift and ensure proper stock count and consumption label updates.
• Coordinate maintenance for all printers and perform regular cleaning of the printers.
• Execute label changeovers and update label racks in the production area and the label room.
• Transfer labels from the label room to the printer room as needed.

What Are We Looking For?

• Proven experience in a quality control or food production role, preferably in a food manufacturing or processing environment.
• Knowledge of food safety regulations, quality control standards, and industry best practices.
• Excellent attention to detail and a strong commitment to maintaining high-quality standards.
• Proficient in record-keeping and documentation, with strong organisational skills.
• Effective communication skills to collaborate with cross-functional teams and report any issues promptly.
• Ability to work independently with minimal supervision and function well as part of a team.
• Strong problem-solving and decision-making abilities to address quality control challenges effectively.
• Flexibility to work in shifts and adapt to changing production demands.
• Ability to work in a fast-paced and physically demanding environment.
• Basic computer skills, including proficiency in MS Office applications.
• Food safety certifications (e.g., HACCP, SQF, ServSafe) are a plus.

Benefits:

• Company pension
• Discounted or free food
• Employee discount
• Free parking
• On-site parking
• Referral programme

Pay: £12.50 per hour

Ability to commute/relocate:

• Feltham TW14 0RB: reliably commute or plan to relocate before starting work (required)

We do not offer sponsorships

Join Our Dynamic Onsite Technical Team at IPL Inchture

We are thrilled to announce an exciting opportunity for a Quality Control Inspector to become a vital part of our onsite Technical Team at our Potato site in Inchture. If you are passionate about Quality and are eager to contribute to a dynamic team, this role is perfect for you

Position Details:

• Schedule: Monday - Friday, 7:30am - 4:00pm

• Location: IPL, Inchture - Site Based Role

• Contract Type: Permanent

Key Responsibilities:

• Effectively and efficiently manage the quality of stock from arrival at the site to despatch

• Make decisions on the most effective and efficient use of the product

• Provide the Senior Product Manager with accurate and timely information to communicate to the grower

• Investigate all rejections for their product

• Ensure all reports are completed, scrutinised and progressed on a daily basis

• Interaction with the Packhouse to maintain ASDA Specification and Compliance

• Complete internal audits

What are we looking for?

• Educated to GCSE Level A, B or C (or equivalent) in English and Maths

• Basic knowledge of Microsoft Office programmes such as Word and Excel

• Experience of working in a food manufacturing environment

• Basic knowledge of BRC Auditing

• Basic Food Hygiene Certificate

• Working Knowledge of the PR2 data system

• Assertive (Willing and able to challenge the norm)

• Self-disciplined, Systematic and Precise

What's in it for you?

At IPL, Forza, and Kober , we're dynamic businesses, dedicated to fostering the development of our colleagues and creating an exceptional work environment. We believe in the power of teamwork and collaboration to drive our success. To continue our growth, we're seeking individuals who embody our values, culture, and commitment.

In return, we offer opportunities for professional development, a competitive salary, and a comprehensive benefits package, including:

15% Asda In-store Discount

Paid Annual Leave Allowance – varies depending on shift pattern

Enhanced pension scheme

Life Assurance - All our colleagues benefit from life assurance of 4 x their annual base salary

- Free, direct access to health and wellbeing support service, including unlimited video consultations with a UK-based GP 24/7, physiotherapy, and mental health support

Grocery Aid - We've partnered with Grocery Aid to provide our colleagues and their families with a wide range of emotional, practical, and financial support services

Electric Vehicle Scheme*

Asda Mobile Discount - 30% off a wide range of Asda Mobile bundles and add-ons for our colleagues and one of their family members

Discounted health assessments - We have exclusively negotiated rates on Self-Pay BUPA Health Assessments for you and members of your household

Asda Pet Insurance discount – Up to 10% Discount

Mortgage Advice Bureau (MAB) - MAB can provide fee-free*, no-obligation mortgage and protection advice

Exclusive Exchange Rates via Asda Money - our colleagues can get a better exchange rate for their travel money when buying currency through Asda Travel Money (TravelEx)

Ride-to-work scheme - We work with Evans to provide our colleagues with great savings across their range of bikes, clothing, and equipment

Care Concierge - The Care Experts. Talk to us - we're listening - Legal & General's Care Concierge resource

Plus, lots more Depending on job band, other fantastic benefits are also available including private healthcare, car allowances, and long-term incentive schemes.

Like what you've read? Then do your research, update your CV, and once you're ready, hit the apply button. Don't delay, apply today

Our purpose here at IPL, Forza & Kober is simple, we are one team who creates exceptional value for our customers and our mission is to support Asda on their journey to becoming #2 in the marketplace.

Through our people we live and breathe our values and we play to our strengths, but we also support each other's development. We are a community of passionate individuals who possess a wide variety of skills and expertise, who work collectively to form a high performing team and a company to be proud of.

We are committed to a fully inclusive business that is representative of our customers, locations and the communities we serve. We recognise the value in diversity and welcome applications from all candidates regardless of sex, age, race, religion, gender or sexual identity and socio-economic background. We are committed to making IPL, Forza and Kober a place where everyone can enjoy a successful career and have systems in place to support all our colleagues. We are seeking applications from candidates who share our values, culture and celebrate diversity in all its forms.

Our culture is our people and our people are our culture

ECQA is
currently seeking experienced inspectors in England to support our quality control operations for "Diffuser and Candle" products.

Location: Warminster, England, United Kingdom

Type: Freelance / Part-time Inspector

Industry:
Diffuser and Candle

Experience: Prior inspection experience is preferred

Scope of Work:

On-site inspection at warehouse/factory

Check product packaging and labeling

Measure product dimensions

Conduct visual quality checks

Take clear photos

Fill out standard inspection report (template provided)

Requirements:

Based in or near
Warminster, England

Familiar with product quality control procedures

Knowledge of AQL standards

Responsible, detail-oriented, and punctual

Able to follow inspection protocols and meet reporting deadlines

CV submission deadline: September 22, 2025

Interested or know someone suitable?

Please send your CV to

Let's connect and collaborate

Requisition ID: 60790

Position Type: FT Fixed Term

Workplace Arrangement: #LI-Onsite

Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.

This is a fixed-term, onsite position based in Portadown, Northern Ireland, running until the end of August 2026, with the potential for extension.

The site specialises in the production of cheese blocks, sliced cheese, and grated cheese bags.

As a Quality Control Specialist, you will support the technical team by conducting routine inspections, monitoring production processes, and ensuring compliance with food safety standards. You'll assist with audits, equipment calibrations, data reporting, and documentation management. The role also involves cross-functional collaboration to uphold site standards and contribute to quality improvement initiatives.

As a Quality Control Specialist, you will:

• Play a key role in maintaining product integrity and food safety standards
• Conduct routine inspections and monitor production processes
• Support the technical team with problem-solving on the factory floor
• Assist with equipment calibrations and preparation for external audits
• Carry out internal audits including glass & perspex, pest control, and temperature checks
• Trend and report data, including results from the daily Taste Panel
• Manage samples, traceability documentation, and ensure technical records are audit-ready
• Collaborate with all departments to uphold site standards
• Contribute to ongoing quality improvement initiatives across the site
• Perform other day-to-day tasks as requested to support quality and technical operations

• Experience in a food manufacturing or quality control environment
• Solid understanding of food safety standards and regulatory compliance
• Familiarity with laboratory testing methods and equipment
• Competence in using Microsoft Office and quality management systems (e.g., SAP, QMS)

• 25 days annual leave (excluding bank holidays)
• Matched pension scheme
• Access to our employee development platform and Udemy learning resources
• Benefits platform offering discounts and cashback at major retailers
• A collaborative and inclusive work environment with opportunities for career growth

Kerry is an Equal Opportunities Employer. Consistent with our policy of providing equality of opportunity for all, we are required to seek particular information from applicants. As part of your application you will be asked to answer a short number of questions. This information will be held separate to your application and treated in the strictest of confidence.

Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a "starter kit," investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.

Recruiter: #LI-MU1

Posting Type: LI

At OSI Electronics UK, we deliver end-to-end electronic manufacturing services—from design and prototyping to PCB assembly and full box builds. Serving both domestic and international markets, we pride ourselves on producing high-quality, reliable products with outstanding customer support and timely delivery.

Role Summary

We are seeking a proactive and experienced Quality Engineer to strengthen our site’s quality function. This role is key to driving continuous improvement across quality standards and ISO systems.

You will be responsible for developing, implementing, and maintaining robust quality assurance and control systems. This includes defining standards, inspection methods, and procedures to ensure the precision, accuracy, and reliability of our products.

Key Responsibilities

• Lead quality initiatives to support continuous improvement and ISO compliance.
• Define and implement inspection, testing, and evaluation procedures.
• Review engineering designs to incorporate quality requirements.
• Act as the primary contact for shop floor quality issues (mechanical fit, process quality, component specifications).
• Conduct investigations and enforce rapid containment and long-term corrective actions.
• Compile and present regular quality reports to the Quality Manager and relevant teams.
• Analyse production data and develop key quality metrics.
• Support production teams with technical guidance to meet quality standards.
• Communicate quality-related information across internal and external stakeholders.
• Complete First Article Inspection Reports (FAIRs) per customer specifications.
• Liaise with suppliers to ensure incoming goods meet quality standards.
• Manage customer, supplier, and internal quality concerns using 8D corrective action reports.
• Conduct internal and external audits.

Candidate Profile

• HNC qualification or equivalent.
• Minimum 5 years’ experience in electronics manufacturing.
• Solid understanding of ISO9001, ISO14001, ISO13485, and Lean Manufacturing principles.
• Strong IT skills and data analysis capabilities.

QC Engineer

Hinkley Point C, HPC

With a track record of 50 years in the nuclear energy sector, Boccard is ideally placed to serve this new era of nuclear as a leading specialist in engineering, manufacturing, construction and maintenance across the energy industry.

To support our continued growth, Boccard are looking for a qualified QC Engineer to work onsite at HPC. The QC Engineer is responsible for carrying out inspections and surveillance in accordance with the Project Quality Plan. To develop, foster and promote a culture with the client of operational satisfaction. They will support QC Inspectors with daily tasks and create lifetime records, while playing a key role to develop, foster and promote a culture with our client of operational satisfaction.

Key responsibilities

1. Ensure that the Project Quality Plan / Inspection Test Plan is written in-line with the project requirements and is being effectively implemented and shared with relevant managers.
2. Review of all documentation, LTRs & final certification packages are in accordance with contract requirements
3. Review calibration and test equipment are in full compliance with company & contract requirements.
4. Ensure weld procedures comply with relevant code & contract requirements.
5. Carry out any Quality Awareness Training.
6. Analyse non-conformance reports
7. Final review of all fabrication and assembly documentation before submission to the client
8. Maintain the approved suppliers listing and requesting any documentation that may have expired.
9. Liaising with Suppliers, Subcontractors, clients etc and attend meetings where appropriate.
10. Issue of any Quality Documents required by client to Document Control for approval/review.
11. Liaise with sub-contractor and ensure all documentation runs concurrently with the project requirements.
12. Liaise with client representatives relating to QA/ QC operation
13. Conducting Audits of the Works and Projects Quality System, including Sub-contractors and Supplier systems where appropriate. Issuing NCRs where applicable and ensure that they are addressed in a timely manner
14. Review and recording of all Quality Questionnaires and supporting documents for additional Suppliers and Subcontractors wishing to be added to the HPSL ‘Approved Supplier Listing’
15. Colette and keep upto date SQEP Files for HPSL Personnel – issue to client if required by Contract/Client.
16. To carry out any other reasonable duties within the overall function of the role.
17. To be fully aware and comply with Boccard UK Ltd’s policy on Equality & Diversity

Qualifications and Experience

• Advanced knowledge of modern welding procedures
• Excellent communication skills with a good eye for detail
• Significant experience in working on pipe spooling contracts
• Knowledge of RCCM manufacturing specifications
• Computer literate and willing to train on internal digital plat
• forms
• Previous Nuclear experience preferred
• CSWIP 3.1 minimum
• PCN Level 2 MPI – Preferred
• PCN Level 2 UT– Preferred
• PCN Level 2 Radiographic Interpretation– Preferred

Compensation and Remuneration

• A highly competitive salary
• Pension scheme
• 25 days annual leave
• On-going investment in your training and development
• Life Assurance x4 salary
• Employee Assistance Programme

Role: Quality Control Reviewer

Business Unit: Bioscript Regulatory Writing

Location: Macclesfield / London (Hybrid or remote - UK)

About Us

Established in 2005, Bioscript Group is formed from multiple, specialist businesses to support our global pharmaceutical clients; we draw on their multidisciplinary expertise to help navigate critical decisions at key points in the product lifecycle.

Our scientific and strategic expertise helps our clients make better decisions. We provide medical communication services, market access consulting and regulatory writing support with deep domain expertise to effectively navigate complex disease areas.

The Opportunity

The role of the Quality Control Reviewer is to conduct quality control (QC) and other supportive activities to support delivery of accurate, compliant and submission-ready documents prepared by writers in Bioscript Regulatory Writing (including internal and external writers), or by clients.

Key Responsibilities

• Perform QC review and manage QC projects in accordance with agreed upon timelines.
• Verify accuracy of document content using source documents including, but not limited to, clinical regulatory documents (e.g. protocols, clinical study reports, CIOMS reports, clinical summaries/overviews), statistical analysis plans and data tables, figures, and listings.
• Verify internal consistency within a document and across related documents.
• Verify uniformity and compliance of documents with internal or client standards (e.g. document templates, style guide, publishing requirements).
• Record QC findings and identify appropriate corrections to address findings.
• Collaborate with document authors and other team members (as needed) to resolve QC findings.
• Proactively share knowledge and experience to support transfer of knowledge across the team.
• Take responsibility for ensuring optimum use of own time. Flag capacity or bottlenecks to the QC Manager so that resource can be allocated most efficiently. Efficiently manage competing projects, proactively flagging potential issues to the QC Manager.
• Support the Project Management team by monitoring the progress of all assigned projects against the agreed QC schedule and QC budget specification.
• Support the regulatory writing team (eg, supporting other QC Reviewers, editorial support for writers (eg, populating tables, drafting narratives etc).
• Understand QC and publishing processes and strategy, client procedures, and best practice for projects.
• Proofread, edit, compile, and publish regulatory documents according to BRW or client conventions and applicable regulatory and industry guidance.
• Ensure adherence to agreed client/Bioscript standard operating procedures.

About You

• Previous experience working as a QC Reviewer / Regulatory Writer within an agency or pharmaceutical setting
• Previous experience of document publishing preferred
• Attention to detail to ensure accuracy and quality in all deliverables
• Ability to take initiative and manage multiple tasks independently
• Strong communication skills

Our people are at the heart of our business

We are focused not just on delivering the exceptional for our clients, but for our teams too. We understand everyone is different and believe in treating everyone as an individual with opportunities to develop your skills and career around our disciplines.

Our benefits include:

• Salary which aligns with your experience and skillset
• 25 days holiday + bank holidays + winter shutdown + holiday purchase scheme
• Enhanced sick and compassionate leave
• Enhanced maternity, paternity & adoption leave
• Birthday charity donation to a charity of your choice
• Bonus Day off to be spent giving back to the community
• Life Insurance and Critical Illness cover
• Private Medical (Vitality for UK based colleagues)
• Health cash plan or wellbeing allowance
• International Employee Assistance Program

We are committed to creating an inclusive and diverse workplace. We encourage applications from all individuals who meet the minimum requirements of the role. If you require any reasonable adjustments during the application or interview process, please contact us via or by calling .