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We are looking for a motivated Laboratory Specialist to support Quality Assurance activities within a regulated laboratory environment. This role will involve assisting with HPLC-based analysis, stability studies, and routine laboratory testing, while ensuring work is completed in line with quality standards and procedures.\n\nYou will work closely with cross-functional teams including Microbiology, Quality, and Manufacturing, gaining valuable experience in a highly collaborative setting.\n\nKey Responsibilities\n\n * Support analytical chemistry testing using HPLC, chromatography, and other laboratory techniques.\n\n * Assist with method development, validation, and transfer activities under supervision.\n\n * Contribute to stability studies and shelf-life assessments.\n\n * Carry out routine analysis and support release testing for manufacturing.\n\n * Maintain accurate documentation in line with cGMP and data integrity requirements.\n\n * Help review analytical data and identify trends.\n\n * Support investigations into out-of-specification (OOS) results and contribute to root cause analysis and CAPA activities.\n\n * Assist with troubleshooting analytical methods and laboratory instrumentation.\n\n * Work collaboratively with colleagues across Quality, Manufacturing, and Microbiology.\n\n * Contribute to continuous improvement of laboratory processes and workflows.\n\nRequirements\n\n * Degree in Chemistry, Analytical Chemistry, or a related scientific field.\n\n * Placement year, internship, or some laboratory experience in an analytical, QC, or QA environment is desirable.\n\n * Basic understanding of HPLC and analytical laboratory instrumentation.\n\n * Awareness of method validation and stability studies is beneficial.\n\n * Understanding of cGMP, quality systems, or regulated environments would be an advantage.\n\nSkills\n\n * Good data analysis and interpretation skills.\n\n * Strong attention to detail and a willingness to learn.\n\n * Good problem-solving and organisational skills.\n\n * Clear written and verbal communication skills.\n\n * Ability to work effectively as part of a team.\n\nCareer Development\n\nThis role provides structured training and mentorship, offering an excellent opportunity to develop skills in quality assurance, Chemistry, laboratory validation, and regulatory compliance within the life sciences industry

Quality Engineer to join a UK-based, multi-billion pound specialist chemicals company with subsidiaries in 101 countries and over 300 manufacturing sites. The company supplies bonding, sealing, waterproofing, and structural solutions for the construction and industrial sectors. This permanent, days-based Quality Engineer role will lead continuous improvement projects, investigate batch issues and complaints, and foster a quality-focused culture across the business.\n\nSalary & Benefits:\n\n£37,000 - £42,300 (DOE)\nPermanent, days-based\nLocated on site in Leeds\n8.00-16.30 Mon-Fri (1-hour lunch)\n25-28 days holiday plus bank holidays\nPension up to 10%, private healthcare, group life cover 6x salary, Global Income Protection\nEnhanced maternity/paternity pay, product discounts\nOccasional lab shift cover (approx. twice a year) and weekend overtime (Sat 1.5x, Sun 2x) \n\nKey Responsibilities of the Quality Engineer:\n\nLead continuous improvement projects and recommend enhancements\nCover laboratory technicians on a flexible basis\nReport on measurement KPIs\nThe Quality Engineer will promote a compliant culture across all business areas\nConduct investigations to resolve batch issues and customer complaints\nDemonstrate strong experience in a relevant function, R&D, or as a process chemist (degree qualified)\nConduct thorough investigations establishing root cause and corrective actions \n\nRequirements of the Quality Engineer:\n\nProven experience leading continuous improvement projects - ESSENTIAL\nExperience with Lean and Six Sigma problem-solving approaches\nSAP experience\nTrack record of managing projects and delivering to schedule\nExperience with MS Office and statistical software\nPrevious work in QC/R&D laboratories\nEither a HND, HNC, or Degree in Chemistry, Chemical or Process Engineering, or equivalent OR strong, time-served industry experience in an equivalent role\nBackground in Manufacturing - Chemical, or Process would be desired\nInternal auditing training (desirable)\nExperience or knowledge of databases and Python (desirable) \n\nThis Quality Engineer role offers the chance to join a reputable company known for its collaborative culture, technical expertise, and development opportunities.\n\nApply now for this Quality Engineer position

PLEASE NOTE THIS IS A PERMANENT STAFF ROLE AND NOT CONTRACT\n\nONLY UK RESIDENTS WITH FULL RIGHT TO WORK IN THE UK WILL BE CONSIDERED\n\nWelding Inspector / Coordinator (CSWIP Qualified) Leeds\n\nAbout the Role\n\nWe are seeking an experienced and proactive Welding Inspector / Coordinator to join our team. The successful candidate will play a key role in ensuring welding activities meet the highest standards of quality, safety, and compliance across all project phases.\n\nKey Responsibilities\n\nConduct visual inspections of welds in accordance with relevant codes, standards, and client specifications.\nCoordinate welding activities and support production teams to ensure best practices are followed.\nReview and interpret welding procedures, WPS, PQRs, and welder qualifications.\nComplete and maintain detailed inspection reports, NCRs, and quality documentation.\nMonitor and verify consumables, materials, heat treatment cycles, and traceability.\nLiaise with project managers, QA/QC teams, and external auditors.\nEnsure compliance with HSE policies and promote a strong safety culture.\n\nSkills & Experience\n\nCSWIP 3.1/3.2 certification (essential).\nProven experience in welding inspection within [fabrication / heavy industry / oil & gas / construction].\nStrong working knowledge of industry codes (e.g., ISO, EN, ASME).\nAbility to read and interpret technical drawings and specifications.\nExcellent communication skills and attention to detail.\nAbility to work independently and manage multiple tasks simultaneously.\n\nBenefits\n\nCompetitive salary and benefits package.\nOpportunity for career development and further certification.\nSupportive team environment with long-term project stability

HV Project Engineer\nLeeds (Hybrid)\n£65 an hour - Outside IR35\n12 Month Contract\n\nEssential Skillset:\n\nEnd-to-end delivery of HV renewable/grid projects (400kV)\nCoordination of civil, electrical, P&C, SCADA, and OEM interfaces\nStrong DNO/TNO /Grid Operator experience\nDevelopment and control of ITPs, QA/QC, and commissioning documentation\nOversight of subcontractors and multi-disciplinary delivery teams\nPreparation and completion of full O&M and handover documentation packs\nSupport to procurement, FAT witnessing, and technical compliance checks\nRisk management across design, construction, and commissioning phases\nStrong understanding of CDM, Grid Code, G99/G100, BS EN standards\nProven experience in renewable energy / utility-scale infrastructure delivery \n\nIf this role is of interest to you, please get in touch with Daisy Black at JAM Recruitment as soon as possible

Quality Engineer for leading Chemical and Materials Manufacturer - West Yorkshire\nDo you have a QA/QC background with a desire to develop your career. If YES this is the opportunity for you!\nCompany: Progressive multinational Chemical and Materials manufacturer with excellent reputation in the marketplace. The company has a passion for new technology development, continuous improvement and sustainability.\nHours of work: Monday to Friday, 37.5 hours per week (typically 8am to 4.30pm, but can be flexible around this).\nWhy join? :\n * Career development and learning opportunities.\n * Excellent salary and benefits.\n * 25 days holiday (rises with service) + Bank holidays\n * Service awards and other generous benefits.\n * Life insurance and income protection schemes.\nLocation: West Yorkshire\nDuration: Permanent position.\nSalary: Up to £42k (depending on your skills and experience)\nYou will be involved in:\n * Quality investigations (RCA, CAPA).\n * Provide plant support with Non-conformances and working with R&D to find appropriate solutions.\n * Reporting quality measurements against KPIs and internal auditing.\n * Collating and reviewing data to make improvements to site operations and quality.\n * Look at and implementing continuous improvement activities across the site, running your own projects.\nWhat do you need to be considered?\nYou will need\n * Science or engineering qualification ideally to degree level or equivalent experience.\n * Experience of Quality systems (CAPA, NCR, RCA, internal auditing).\n * Excellent team working experience.\n * Knowledge of Continuous improvement - lean & six sigma principles in relation to problem solving.\n * Excellent verbal and written communication skills.\nWhat to do next...\nInterested?\nIf you are looking for a role which offers variety, personal and professional development; run your own projects, and the opportunity to put your passion for quality in to action, then this is the role for you!\nDon't delay!\nApply now to avoid disappointment, as the company is looking to interview in the next 2 weeks.\nNB - The company is unable to provide sponsorship for this role, so you must be able to work full time, permanently in the UK without restrictions

Associate Analyst QC – Pharmaceutical Microbiologist – 18m FTC We Are Rosemont For over 50 years, Rosemont Pharmaceuticals has been a trusted name in the development and manufacture of oral liquid medicines. With a portfolio of over 130 products - including 70 licensed medicines - we’re proud to support healthcare professionals and patients, especially those with swallowing difficulties. Our purpose is clear: to improve patient outcomes through innovation in liquid formulations. We’re highly respected across the pharmaceutical industry and have played a key role in establishing best practices for dysphagia care. Our mission is to create a globally connected, people-focused organisation where every individual is empowered to thrive and achieve their best. If you're passionate about making a meaningful impact to patients across the world and want to be part of a company with a strong heritage and ambitious vision, we’d love to hear from you. About the Role As an Associate Analyst in our Quality Control – Microbiology team, you’ll play a vital role in ensuring the safety, quality and compliance of our raw materials and finished products. Working in accordance with cGMP standards, you’ll perform microbiological testing, support investigations, ensure accurate documentation and contribute to our continuous improvement culture. This is an excellent opportunity for someone with analytical laboratory experience who is looking to develop deeper technical expertise in a fast‑paced pharmaceutical QC environment. This role is an 18 Month Fixed Term Contract. Key Responsibilities • Conduct visual inspections and microbiological TVC/PET testing to USP, EP and BP monographs., • Ensure laboratory cleanliness, safety compliance and high standards of housekeeping., • Review internal and contract laboratory data to ensure regulatory compliance and accuracy., • Participate in OOS, OOT, aberrant result and failure investigations; recommend corrective actions., • Troubleshoot equipment issues and conduct routine calibrations according to SOPs and work instructions., • Write, revise and maintain QC SOPs, work instructions and technical reports., • Support key QC systems such as stability studies, RM risk assessments, reference standards and environmental monitoring., • Collate QC data for regulatory submissions and support method transfer documentation., • Uphold QC best practices, company values, safety standards and good documentation practices. About You We’re looking for someone who brings: Experience & Knowledge • 2–4 years’ experience in a GMP analytical laboratory., • Previous experience with TVC/PET (AET) testing is essential., • Bachelor’s degree in a relevant scientific discipline or A-level / scientific background with extensive analytical laboratory experience., • Proficiency in microbiology techniques., • Experience with GMP documentation and QC laboratory processes. Skills & Competencies • Strong problem-solving skills and attention to detail., • Effective communication and the ability to work collaboratively within a team., • Ability to investigate quality events and support root-cause analysis., • Good business awareness and customer service mindset., • Flexibility to support business needs, including occasional out-of-hours work. Benefits At Rosemont, we believe great benefits go beyond salary. That’s why our offering is shaped by what our people truly value: 🏆 Annual Bonus – Recognising your contribution to Rosemont. 🏥 Healthcare Cash Plan or Private Medical Cover – Personal cover to support your health and wellbeing 💰 3% Employee / 5% Company Pension Contribution – Helping you plan for the future 🌴 26 Days Annual Leave + Bank Holidays 📅 Flexible Working – Including hybrid and flexible working hours available 🚗 Free On-Site Parking – Convenient access to our Leeds facility 🎉 Rosemont Rewards Platform – Discounts, free perks, and wellbeing tools for all employees We are committed to fostering an environment of enablement where our people can grow, develop their talents, and pursue meaningful career paths. By placing patients and customers at the heart of everything we do, we drive high performance through accountability, consistency, and a strong governance structure. We champion inclusion, community, and a rewarding employee experience - creating a culture that supports development, celebrates achievement, and empowers individuals to thrive. Diversity & Inclusion is integral to our culture and reflecting the patients we serve. At Rosemont, we believe equal opportunity for all is fundamental to our company's values and all our applicants can expect fairness and transparency in our recruitment process. If this sounds like the perfect next step in your QC career, we’d love to hear from you - apply today and help us shape the future of patient-focused medicines!

Associate Mechanical Engineer (Management Role) About the Role: As an Associate Mechanical Engineer, you will work across a range of projects throughout EMEA while acting as a key member of the management team. This role requires a proactive problem-solver who can apply current technologies and make independent technical decisions in a fast-paced environment. You will be an experienced engineer with strong commercial awareness, collaborating with colleagues to ensure high standards in design processes and engineering delivery. About You: • Hybrid working arrangement based in UK or Ireland, with office attendance as required, • Honours degree in Mechanical Engineering (Chartership advantageous but not essential), • 10+ years’ experience within mechanical engineering, ideally in data centres, industrial, high-tech, or commercial sectors, • 3+ years’ experience managing multidisciplinary teams, • 3+ years’ project management experience across mechanical and electrical projects, • Strong communication, presentation, and organisational skills, • Ability to engage effectively with stakeholders at all levels, • Passion for innovation and adoption of emerging technologies, • Review technical designs to ensure scope and intent are fully understood, • Optimise project functionality and cost efficiency, • Ensure effective collaboration between mechanical and electrical disciplines, • Lead and develop a high-performing team, ensuring QA/QC and delivery targets are met, • Monitor project costs and identify opportunities for savings, • Support resource planning, including outsourcing where required, • Interpret contracts and ensure compliance with terms and conditions, • Engage with senior leadership on industry trends and new technologies, • Support business development and new project acquisition, • Build and maintain strong relationships with clients, suppliers, and partners, • Contribute to internal quality assurance standards and processes, • Oversee delivery of multiple large-scale projects, • Conduct team development through regular reviews and mentoring, • Support training and performance improvement initiatives, • Modern office environment designed for collaboration and wellbeing, • Strong focus on professional development and career progression, • Flexible working hours, • Annual leave increasing with service, • Pension scheme, • Travel expense support, • Cycle-to-work or travel schemes, • Ongoing training and education support, • Chartership support, • Private healthcare contribution, • Professional membership fees covered, • Paid statutory leave, • Health screenings and vaccinations, • Gym or fitness support, • Referral bonus scheme, • Active social and wellbeing programme

Quality Control (QC) Software Tester (Remote Working Opportunity) Are you a Warehouse "Super-User"? Why not Become our Quality Control (QC) Expert. Ever wished you could Stop just using WMS software - Start breaking it, Fixing it, and Building it? We have the perfect opportunity for you. At Helm, we don’t build code for the sake of it. We build outcomes for high-volume shippers moving 100+ orders a day. To do that, we need someone who knows what a "perfect shipping day" actually looks like. The Despatch Company delivers industry-leading Warehouse Management Systems, powering thousands of e-commerce, 3PL, and logistics operations worldwide. Our flagship products, provide advanced inventory, fulfilment, and warehouse automation capabilities. Learn more at helmwms.com. We are not looking for a corporate software tester. We are looking for the Warehouse Supervisor, Ops Lead, or "Go-To" Floor Person who is tired of fighting clunky systems and ready to build a better one. Real world, hands-on, warehousing experience having ideally worked in an e-commerce business using a WMS system will fit right in. If you have worked for a 3PL, or in the client setup space, even better. We are expanding our Quality Assurance department, bringing together a dedicated testing team with a natural leader, who can drive automated testing, strengthen release reliability, and ensure our WMS platforms are robust, scalable, and ready for real-world warehouse environments. Is this you? • The Floor Legend: You are the person everyone asks for help when the WMS acts up, the labels won't print, or a new e-commerce client needs to be onboarded., • E-commerce DNA: You’ve lived the pick-pack-ship grind. You know that in high-volume e-commerce, a "small glitch" at 3pm is a disaster., • Sharp & Tech-Literate: You are not a coder, but you are "techy." You have probably used YouTube or AI to solve problems before. You are curious, fast, and bored of just packing boxes., • 3PL Experience (Nice to have): If you have handled client setups or multi-tenant warehousing, you’ll fit right in. The Role: Your job is to be the final gatekeeper. Before a feature reaches our customers, it has to pass you. • Real-World Testing: You will put new features through the ringer. If a workflow is slow, confusing, or "doesn't work like a warehouse actually works," you send it back to the Developers., • Master the Tools: We will train you on the technical side. Using modern AI and testing platforms, we will show you how to turn your warehouse knowledge into professional software QC., • Outcome Obsessed: Our customers pay for a service, not code. You will ensure the "service" is bulletproof. Why make the jump? • Trade the High-Vis for High-Tech: Move into a career in software without losing the expertise you have spent years building., • Work with a Sharp Team: Join a crew that values shipping efficiency over "coding for the sake of it.", • Build the Future: Help us create the WMS you always wished you had when you were on the floor. If you’ve got the warehouse brains, we have got the tools………let’s build. What We Offer • Opportunity to work on market-leading WMS platforms used globally., • The chance to influence how real users experience our products., • A role that values judgement, common sense, and user empathy., • Exposure to multiple products across different stages of development., • A collaborative, remote working environment that really pulls together., • This a full-time, permanent position., • Salary (DOE)

End-to-end delivery of HV renewable/grid projects (400kV).Coordination of civil, electrical, P&C, SCADA, and OEM interfaces.Strong DNO/TNO /Grid Operator experience.Development and control of ITPs, QA/QC, and commissioning documentation.Oversight of subcontractors and multi-disciplinary delivery tea

Senior Project Engineer – Pharmaceutical Utilities & Facilities (Permanent) Location: West Yorkshire Salary: £50-£60k The Role We’re looking for a Senior Project Engineer with a Chemical or Mechanical Engineering degree to lead CAPEX improvement projects in utilities and facilities within the pharmaceutical sector. If you’ve successfully delivered projects in HVAC, Boiler, and Water systems and thrive in a regulated, GMP environment, you’ll play a pivotal role in upgrading and optimizing critical plant infrastructure. Key Responsibilities Lead and manage CAPEX projects across HVAC, Boiler, and Water processes from concept to completion. Define project scope, technical specifications, budgets, and schedules. Collaborate with operations, maintenance, QA/QC, and regulatory teams to ensure seamless project delivery. Ensure projects meet GMP, safety, and environmental standards. Identify opportunities for process optimization and cost efficiencies. Support commissioning, qualification, and handover of new or upgraded systems. Mentor junior engineers and provide technical leadership across projects. What We’re Looking For Degree in Chemical or Mechanical Engineering. Proven experience delivering CAPEX projects in pharmaceutical utilities/facilities. Strong hands-on experience with HVAC, Boiler, and Water treatment systems. Knowledge of GMP and regulatory compliance. Excellent project management, problem-solving, and communication skills. Ability to lead projects autonomously while collaborating across teams. Why Join Take ownership of high-impact infrastructure projects in a leading pharmaceutical environment. Work in a collaborative and innovative team. Career growth and professional development opportunities. Competitive salary and benefits package. Apply Now: Submit your CV and cover letter to

Job Title: HV Commissioning Engineer. You will play a key role at the construction-to-commissioning interface, ensuring systems are delivered safely, compliantly and ready for operational handover. QA/QC, commissioning and client teams.

A leading engineering firm in the UK is seeking a Field Inspection Engineer to provide quality surveillance services.

A prominent UK commercial law firm in Leeds is seeking a junior solicitor to join their dynamic Corporate team. This role involves engaging in corporate M&A transactions, providing early responsibility with direct client contact and significant exposure to high-profile private equity deals.

A leading Medical Device Company based near Leeds is seeking a Quality Control Technician to ensure the quality, safety, and compliance of life-saving products. The role involves operating vision systems, performing quality control activities, and assisting with internal audits.

A prominent legal firm in Leeds seeks an experienced lawyer for commercial contract matters.

Known for its strength in delivering complex, cross-border work, the firm offers an environment where lawyers are encouraged to think commercially, work internationally, and play a meaningful role in shaping client outcomes. For those at Senior Associate level, experience supervising or mentoring ju

You'll assist with calibration, operate CMM equipment, and support documentation processes for new products.

Associate Analyst QC – Pharmaceutical Microbiologist – 18m FTC.

An exciting opportunity has arisen to join a client of ours, a leading Medical Device Company based on the outskirts of Leeds currently looking to recruit a detail‑driven Quality Control Technician to join their team. This role is essential in ensuring the consistent quality, safety, and compliance of life saving products (Heart Valves) through inspection, documentation, and support of key systems used in the manufacturing processes. You will play a key part in operating vision systems, supporting product release activities, and assisting with internal audits - helping maintain exceptional standards across the production environment. Starting Salary - £27,360 Large amount of training and progression for the ideal candidate. Working hours are Monday to Thursday 7am to 3.30pm and Friday 7am - 1.30pm Job Description * Operate Vivtro and BDC vision systems to support valve processing and inspection. * Complete routine maintenance and asset‑care tasks aligned with the vision systems’ maintenance schedules. * Perform Quality Control activities including inspection and release of labels, WIP materials, and final packaging components. * Conduct incoming inspections for components and raw materials against established specifications. * Support preparation activities for internal audits and regulatory facility inspections. * Assist with document and record administration, including reviewing and completing DHRs. * Support final valve inspection, testing, and product release processes. * Contribute to additional quality‑related projects as assigned by the QC Team Leader or Quality Engineering Manager. Qualifications / Skills * Strong initiative with the ability to follow detailed manufacturing instructions. * Excellent collaboration skills with cross‑functional teams. * High attention to detail, especially with product inspection and documentation processes within cleanroom environments. * Confident with standard MS Office applications (Word, Excel) and basic electronic equipment such as printers and scanners. * Strong written and verbal communication skills, including accurate spelling and grammar. * Ability to multitask effectively while maintaining accuracy and quality. * GCSEs, A‑Levels, or equivalent high‑school level qualifications. * Minimum 5 years’ experience in a manufacturing environment—preferably within the medical device or pharmaceutical sectors. * Prior experience in Quality Control within manufacturing is highly desirable. * Experience working with electronic document management systems is an advantage. Note: this vacancy is being advertised by Ingenuity Employment Solutions ltd acting as an employment agency

Senior Project Engineer Smart4Sciences West Yorkshire, England, United Kingdom (On-site) Senior Project Engineer - Pharmaceutical Utilities & Facilities (Permanent) Location: West Yorkshire Salary: £50-£60k The Role We're looking for a Senior Project Engineer with a Chemical or Mechanical Engineering degree to lead CAPEX improvement projects in utilities and facilities within the pharmaceutical sector. If you've successfully delivered projects in HVAC, Boiler, and Water systems and thrive in a regulated, GMP environment, you'll play a pivotal role in upgrading and optimising critical plant infrastructure. Key Responsibilities Lead and manage CAPEX projects across HVAC, Boiler, and Water processes from concept to completion. Define project scope, technical specifications, budgets, and schedules. Collaborate with operations, maintenance, QA/QC, and regulatory teams to ensure seamless project delivery. Ensure projects meet GMP, safety, and environmental standards. Identify opportunities for process optimization and cost efficiencies. Support commissioning, qualification, and handover of new or upgraded systems. Mentor junior engineers and provide technical leadership across projects. What We're Looking For Degree in Chemical or Mechanical Engineering. Proven experience delivering CAPEX projects in pharmaceutical utilities/facilities. Strong hands-on experience with HVAC, Boiler, and Water treatment systems. Knowledge of GMP and regulatory compliance. Excellent project management, problem-solving, and communication skills. Ability to lead projects autonomously while collaborating across teams.Why Join Take ownership of high-impact infrastructure projects in a leading pharmaceutical environment. Work in a collaborative and innovative team. Career growth and professional development opportunities. Competitive salary and benefits package. Apply Now: Submit your CV and cover letter

PLEASE NOTE THIS IS A PERMANENT STAFF ROLE AND NOT CONTRACT ONLY UK RESIDENTS WITH FULL RIGHT TO WORK IN THE UK WILL BE CONSIDERED Welding Inspector / Coordinator (CSWIP Qualified) Leeds About the Role We are seeking an experienced and proactive Welding Inspector / Coordinator to join our team. The successful candidate will play a key role in ensuring welding activities meet the highest standards of quality, safety, and compliance across all project phases. Key Responsibilities Conduct visual inspections of welds in accordance with relevant codes, standards, and client specifications. Coordinate welding activities and support production teams to ensure best practices are followed. Review and interpret welding procedures, WPS, PQRs, and welder qualifications. Complete and maintain detailed inspection reports, NCRs, and quality documentation. Monitor and verify consumables, materials, heat treatment cycles, and traceability. Liaise with project managers, QA/QC teams, and external auditors. Ensure compliance with HSE policies and promote a strong safety culture. Skills & Experience CSWIP 3.1/3.2 certification (essential). Proven experience in welding inspection within [fabrication / heavy industry / oil & gas / construction]. Strong working knowledge of industry codes (e.g., ISO, EN, ASME). Ability to read and interpret technical drawings and specifications. Excellent communication skills and attention to detail. Ability to work independently and manage multiple tasks simultaneously. Benefits Competitive salary and benefits package. Opportunity for career development and further certification. Supportive team environment with long-term project stability

A recruitment agency in the UK is seeking candidates for night shifts with an immediate start.The role involves washing, cutting, and bagging goods for dispatch along with quality checking products to ensure they meet high standards.Applicants must have recent experience in a warehouse or food produ

Zelfstandig) beoordelen van het verkregen resultaat en bij afwijkingen rapporteren aan Supervisor Biochemistry of Manager QC.

The successful candidate will oversee all aspects of new client onboarding and periodic EDD reviews, manage complex and ad-hoc escalations, and perform Quality Control (QC) reviews of EDD assessments. Overseeing and guiding the team to deliver reviews to a high standard and within agreed timelines;

Carry out regular QC checks (product deemed high risk as well as regular product).

As a QA/QC Engineer you will, as part of a dedicated site quality and inspection team, be expected to co‑coordinate the establishment and implementation of the Project quality plan, site inspection and test procedures of the subcontracted installation. The QA /QC Engineer will be an exemplar ambas

Review and discuss garment quality inspection scenarios with the model, and verify whether model reasoning aligns with real factory QC practices. Ready to turn your garment manufacturing QC expertise into the knowledge base for tomorrow’s AI? Apply today. Project Title: Garment Manufacturing QC Sp

An established industry player is seeking dedicated individuals for assembly line roles.In this position, you will be responsible for assembling components, operating factory machinery, and ensuring quality control of finished products.The role offers a structured schedule with both day and evening

A leading biotechnology firm in the UK seeks a QC Analytical Scientist to oversee testing of gene therapy products, adhering to EU and FDA GMP requirements.

A leading analytical compliance company in the United Kingdom is seeking a Lab Analyst to join their Compliance team.This role involves high-quality analytical testing using laboratory equipment like GC-MS and HPLC, with responsibilities including collaboration across teams, maintenance of accurate

Welding QA/QC Engineer - Submarines. We are now recruiting for the exciting role of a Welding QA/QC Engineer, to be involved in an industry leading, cutting-edge project supporting the Royal Navy and its state-of-the-art nuclear powered submarine fleet.

A leading contract research organization is seeking an experienced chromatography wizard to join their QC/Analytical team in Essex, UK.

The QC Analytical Scientist is responsible for the testing of gene therapy products and associated materials used for manufacturing to EU and FDA GMP requirements. Maintain QC facilities to meet GMP requirements, conduct necessary checks to support any health authority, customer/stakeholder site vis

A leading chemicals company in West Yorkshire is seeking a temporary QC Analyst to join their team.

A leading international law firm is seeking a Senior Lawyer to play a crucial role in delivering high-value Financial Services M&A transactions.The ideal candidate will have at least 7 years PQE, strong experience in M&A, and the ability to manage transactions independently.This position offers a co

This role performs hands‑on QC tasks, supports QC Technicians as needed, and works closely with QC leadership and weekday QC teams to maintain continuity, productivity, and accuracy in deliverables. The QC Technician is responsible for executing Quality Control operations, ensuring that digital me

Support and report to the Site QA/QC Manager on all quality matters. QA/QC for Power Plants, HVDC or O&G projects.

A biotechnology firm in Greater London is looking for a Quality Control Validation Specialist who will ensure that analytical methods for gene therapy products meet EU and FDA GMP standards.This role involves creating validation protocols, maintaining compliance, and supporting the Quality Managemen

A leading UK railway company in Greater London is seeking a Vehicle Builder Engineer to join their team in Selhurst Depot.The role involves vehicle preparation, fabrication, and quality control while ensuring compliance with safety procedures.Candidates must have at least two and a half years of rel

Lead the QA/QC function for all Modular Services projects, ensuring compliance with ISO 9001 and relevant industry standards. Strong background in QA/QC within modular construction, LV/MV electrical systems, switchgear, Power pods/E house and Modular services. We are seeking an experienced QA/QC Lea

A highly successful manufacturing business are seeking 2 temporary QC Technicians to join their QC Lab. If this Chemicals QC Technician Job is not quite right for you but you're interested in other opportunities, take a look at our other science jobs. Are you immediately available and looking to gai

A leading construction firm in London is seeking a Lead QAQC Engineer to oversee quality assurance and control activities on a high-profile site. Candidates should possess extensive knowledge of QA/QC procedures and health and safety systems.

This role performs hands‑on QC tasks, supports QC Technicians as needed, and works closely with QC leadership and weekday QC teams to maintain continuity, productivity, and accuracy in deliverables. Participate in client supervised sessions as needed to provide technical QC input and answer questi

If you have the Quality Control background to be successful in this QC Technician role, we would love to hear from you. We are excited to offer a fantastic opportunity for an experienced QC Technician to join a well-established manufacturing company on the Wirral. Previous experience within a QC lab

A recruitment agency is seeking a Production Operative in Exeter, UK.You will ensure products meet quality standards while operating machinery efficiently.Key responsibilities include conducting quality checks and maintaining a clean workspace.Ideal candidates should have experience in a production

A leading fashion company in the East Midlands is seeking an experienced Mid QC to ensure quality standards for luxury T-shirts. The ideal candidate has QC experience, strong attention to detail, and a passion for fashion.

Candidates should possess a degree in Microbiology and extensive experience in a pharmaceutical QC setting, along with strong leadership and technical writing skills.

A UK-based recruitment agency seeks an experienced CMM Programmer in Poole.The position offers a four-day working week and structured core hours in a quality-driven precision engineering environment.Responsibilities include programming Aberlink CMMs and conducting inspections on CNC machined compone