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Logistics Administrator • Hourly Rate: £13.50, • Location: Basingstoke, • Job Type: Full-time Temp with a possibility of the role going Temp to Permanent, • Hours: 08:30-17:30 Monday to Friday Join the team as a Logistics Administrator in our state of the art warehouse in Basingstoke. This role is ideal for someone with prior logistics administration experience, looking to further their career in a dynamic and modern environment. Day to day of the role: • Coordinate and monitor supply chain operations., • Ensure premises, assets, and communication ways are used effectively., • Utilize logistics IT systems to optimize procedures., • Recruit and coordinate logistics staff according to availabilities and requirements., • Supervise orders and arrange stocking of raw materials and equipment to ensure they meet needs., • Communicate with suppliers, retailers, customers, etc. to achieve profitable deals and mutual satisfaction., • Plan and track the shipment of final products according to customer requirements., • Keep logs and records of warehouse stock, executed orders, etc., • Prepare accurate reports for upper management. Required Skills & Qualifications: • Proven experience as a logistics administrator., • Experience in customer service will be appreciated., • Knowledge of laws, regulations, and ISO requirements., • Ability to work with little supervision and track multiple processes., • Computer-savvy with a working knowledge of logistics software (ERP)., • Outstanding organizational and coordination abilities., • Excellent communication and interpersonal skills. Benefits: • Competitive salary., • Opportunities for professional development., • Dynamic and modern working environment.

Quality Engineer \n\nLocation: Remote (Occasional in-person meetings in Basingstoke)\nContract Length: 9 months\nHourly Rate: £27.00\nWorking Pattern: Full Time (40 hours/week)\n\nAre you ready to make a meaningful impact in the Life Sciences industry? Our client is seeking a dedicated Quality Engineer to join their high-performing team! This is an exciting opportunity to advance your career while contributing to solutions that make the world healthier, cleaner, and safer.\n\nWhat You'll Do:\nAs a Quality Engineer, you will play a crucial role in ensuring quality compliance across operations. Your responsibilities will include:\n\nQuality Oversight: Conduct detailed documentation reviews and monitor processes to uphold the highest standards.\nCompliance Maintenance: Support and maintain compliance with GMP/GxP, ISO, and other regulatory requirements.\nIssue Investigation: Lead root cause analysis efforts to investigate quality issues effectively.\nChange Management: Manage and support change control activities while assisting in internal and external audits and inspections.\nDocumentation: Author and review quality documentation such as SOPs and investigation reports.\nData Analysis: Perform data analysis, trending, and reporting of quality metrics.\nCollaboration: Work closely with cross-functional teams to drive corrective and preventive actions.\nContinuous Improvement: Support initiatives aimed at enhancing quality systems and processes. \n\nWho You Are:\nTo thrive in this role, you should possess:\n\nA Bachelor's degree in Life Sciences, Engineering, Chemistry, Biology, or a related technical field, with 5+ years of experience in quality assurance/control (or an advanced degree with 3+ years of relevant experience).\nExperience in regulated industries (pharmaceutical, medical device, or biotech preferred).\nProficiency with quality management systems (MasterControl, Document Control Systems) and CAPA processes.\nDemonstrated expertise in root cause analysis, investigation techniques, and implementing corrective actions.\nStrong knowledge of GMP/GxP regulations, ISO standards (9001/13485), and quality system requirements.\nExcellent problem-solving skills and attention to detail.\nStrong verbal and written communication skills with the ability to collaborate across various functions. \n\nHow to Apply:\nIf you're excited about the opportunity to contribute to life-changing products and work with a talented team, we want to hear from you! Apply today to join our client's mission in making the world a better place.\n\nDon't miss out on this chance to be a part of something meaningful. Let's make a difference together!\n\nAdecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.\n\nAdecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser

Electrical Control & Engineering Specialist\nSalary: £55,000-£66,000\nLocations: Ashford (Kent), Basingstoke, Birmingham, Bootle, Bristol, Cardiff, Chelmsford, Crewe, Edinburgh, Glasgow, Leeds, Milton Keynes, Newcastle upon Tyne, Norwich and Sheffield\nHybrid Working: 3 Days Per Week On Site\n \nWe are supporting a major regulatory organisation in the search for Electrical Control & Engineering Specialists to join a specialist team focused on electrical safety, control systems integrity, risk management and legal compliance across high hazard industries.\n \nThis is an excellent opportunity for experienced Electrical, Controls, E&I or ICSS Engineers looking to apply their technical expertise in a role centred on investigation, assurance, governance and improving safety standards. \n \nYou will apply your experience and knowledge of Electrical Distribution Systems and Complex control systems to identify risk and underlying issues on site across a wide range of industries (often from first principles).\n \nYou will be: \n\nInvestigating serious electrical and control systems incidents and identifying root causes\nInspecting industrial sites and assessing the effectiveness of risk management and safety controls\nProducing technical reports and providing specialist support during legal proceedings and investigations\nInfluencing organisations to improve compliance, reduce risk and enhance electrical and control systems safety \nRequirements\n\nDistribution and use of electricity at both high and low voltage, including safe systems of work and where applicable, compliance with BS7671\nElectrical, electronic, programmable and safety-related control systems as applied to process control equipment and machinery, including risk assessment, design, installation, testing, maintenance and modification with application of ISO 13849, IEC 62061 and IEC(phone number removed) where relevant\nExperienced with PLC-based automation and industrial controls in industries such as utilities, power, oil and gas, chemicals, manufacturing or other major hazard environments\nChartered Engineer status is preferred. Candidates with an appropriate engineering degree and the ability to achieve Chartered status within one year are also encouraged to apply.\nA full UK driving licence is essential. \nApplicants must have the right to work in the UK. Sponsorship is not available for this position.\n \nBenefits:\nCivil Service pension with 28.97% employer contribution, hybrid working, 25-30 days annual leave, professional development and flexible working.\n \nElectus Recruitment Solutions provides specialist engineering and technical recruitment solutions to a number of high technology industries. We thank you for your interest in this vacancy. If you do not hear from us within seven working days, please presume your application has been unsuccessful on this occasion. You are free to resubmit your CV or details in the future, and we shall assess your suitability then.\n \nThis is a permanent role

Calibration Technician\nBasingstoke\n\nOn-site, Full Time\n£27k - £30k depending on experience\n\nAbout the Role:\n\nWe are looking for a Calibration Technician to join our client’s calibration laboratory near Basingstoke. This role is focused on the accurate and timely calibration of customer equipment, ensuring results are valid, traceable and issued in line with agreed lead times.\n\nWorking as part of the team you will support the delivery of high-quality calibration services in accordance with ISO 17025 standards, using approved procedures, appropriate measuring equipment and controlled environmental conditions. The role will involve calibrating a range of instrumentation, including pressure and torque equipment, and contributing to the smooth operation of the laboratory.\n\nKey Responsibilities:\n\n Perform calibrations in line with recognised and approved procedures\n\n Carry out pressure and torque calibrations using approved methods and reference standards\n\n Process calibration orders within the lab to agreed lead times\n\n Ensure the timely release of calibration results and reports\n\n Maintain traceability to national and international standards\n\n Ensure the validity and accuracy of calibration results and certificates\n\n Carry out interim checks on reference equipment, including pressure and torque standards, in accordance with defined processes\n\n Ensure standards and measuring equipment are functioning correctly and fit for purpose\n\n Handle and process customer equipment safely and correctly\n\n Provide technical support to order fulfilment and internal sales teams when required\n\nWhat We’re Looking For:\n\n Experience working within calibration or a metrology laboratory environment, including exposure to pressure and torque instrumentation\n\n Understanding of calibration procedures, traceability and measurement uncertainty\n\n Strong attention to detail and commitment to quality\n\n Ability to work to defined procedures and meet deadlines\n\n Good communication skills and a team-focused approach\n\n Willingness to support on-site calibration when required\n\nBenefits:\n\n Free onsite parking\n\n 37.5-hour working week\n\n Pension scheme, life insurance and income protection (subject to successful probation)\n\n 22 days holiday + 3 additional days at Christmas + bank holidays\n\nApply now if you are a Calibration Technician or technically minded professional looking to develop your career within a structured, ISO 17025-accredited laboratory environment

Quality and Regulatory Labelling Program Manager\n\nLocation: Basingstoke (Remote with monthly meetings)\nContract Type: Temporary (9 months)\nHourly Rate: £27.00\n\nWorking Pattern: Full Time (40 hours/week)\n\nAre you ready to make a significant impact in the Life Sciences industry? Join our dynamic team as a Quality and Regulatory Labelling Program Manager! We are seeking an enthusiastic individual who will lead our enterprise-wide labelling initiatives, ensuring compliance and accuracy across regulated markets. If you have a passion for quality and a knack for project management, this is the role for you!\n\nWhat You'll Do:\n\nLead Initiatives: Take charge of labelling quality and regulatory initiatives, ensuring globally harmonised product labelling.\nCollaborate: Work closely with diverse teams-Regulatory Affairs, Quality Assurance, Supply Chain, and Marketing-to design and implement innovative solutions.\nManage Programs: Oversee program planning, budgeting, and execution while coordinating cross-functional teams.\nEnsure Compliance: Drive timely implementation of labelling changes, regulatory submissions, and market-specific obligations.\nCommunicate Strategically: Deliver presentations to senior leadership on compliance risks, implementation progress, and operational impacts. \n\nWhat You Bring:\n\nA Bachelor's or Master's degree in Quality, Regulatory Affairs, Life Sciences, Engineering, or related fields (MBA preferred).\nExperience: 7+ years managing complex programs within Life Sciences or highly regulated industries.\nProject Management Skills: Expertise in program methodologies, risk management, and change control.\nKnowledge: Strong understanding of global labelling regulations (FDA, EU MDR/IVDR, ISO, GMP). \n\nReady to Make a Difference?\n\nIf you're excited about leading strategic labelling initiatives and driving compliance, we want to hear from you! Apply today and embark on this journey with us.\n\nJoin us in ensuring the highest quality and regulatory standards in the Life Sciences industry. Your expertise could be the key to our success!\n\nAdecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.\n\nAdecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser

Join Our Client as a Quality Systems PMO Program Manager!\n\nAre you ready to take the lead in transforming quality management systems within the life sciences industry? Our client is seeking a dynamic and experienced Quality Systems PMO Program Manager to spearhead enterprise-wide QMS initiatives. This is a temporary full-time position offering an hourly rate of £27.00 for an initial contract length of 9 months. Embrace the opportunity to work remotely with just a monthly meeting commitment!\n\nWhy This Role Matters:\nAs a key player in our client's mission, you will lead the charge in ensuring consistent, compliant, and efficient quality processes across global operations. Your expertise will shape the future of quality management, and you will partner with cross-functional teams to implement scalable solutions that enhance governance and operational integration.\n\nKey Responsibilities:\n\nDefine program deliverables, timelines, and success metrics for QMS harmonisation initiatives.\nLead global QMS integration programs to standardise quality processes across divisions.\nFacilitate alignment among Supplier Quality, Commercial Quality, and Manufacturing Quality teams.\nDrive the integration of Distribution Centres into enterprise QMS frameworks.\nManage program planning, governance, and risk management activities.\nOversee the implementation of standardised quality processes across sites and suppliers.\nCommunicate program progress and risks effectively to stakeholders. \n\nWhat You Bring:\n\nExperience: 7+ years in managing global Quality Systems, PMO, or enterprise transformation programs, preferably within life sciences.\nKnowledge: Strong understanding of QMS, quality regulations (FDA, ISO 13485, GMP), and continuous improvement methodologies (Lean, Six Sigma).\nSkills: Excellent stakeholder management, analytical thinking, and organisational abilities. Proven track record in developing governance frameworks and executive reporting structures.\nLeadership: Ability to influence cross-functional teams and promote a culture of quality and accountability.Ready to Make an Impact?\nOur client is eager to welcome a passionate and driven professional to their team. If you are looking for a role that challenges you and allows you to contribute to meaningful change within the life sciences field, we want to hear from you!\n\nApply Now!\nDon't miss your chance to be part of this exciting journey. Submit your application today and take the next step towards a rewarding career with our client. \n\nJoin us in shaping the future of quality management. Your journey starts here!\n\nAdecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.\n\nAdecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser

Are you an experienced leader who wants to take ownership of our Quality, Health & Safety and Environmental function? Managing a small QSHE team, you will help us implement better departmental structure whilst building our QMS and HSE systems processes. We are a Multi-site FMCG operation in Basingstoke. Please apply to learn more. \n \nBASIC SALARY: Up to £45,000 dependant on your relevant experience. \n \nBENEFITS: \n· 22 Days Holiday \n· Pension \n \nLOCATION: Basingstoke, Hampshire \n \nCOMMUTABLE LOCATIONS: Hook, Fleet, Farnham, Aldershot, Farnborough, Frimley, Camberley, Alton, Andover, Thatcham, Newbury, Reading, Wokingham. \n \nWhy you should join us: \n \n· This is a brand new role - take on responsibility for the QSHE department, own it, and develop it with your knowledge and expertise \n· We are growing quickly in headcount and turnover, so it is an exciting time to join us and develop your career \n \nJOB DESCRIPTION: QSHE Manager - FMCG, Food Manufacturing \n \nAs QSHE Manager you will be responsible for leading, developing and implementing our Quality, Safety, Health, Environmental and Compliance systems across both operational sites. \n \nYou'll oversee all compliance activities with initially two direct reports to ensure effective day-to-day quality, food safety and compliance. \n \nA significant part of this role will involve establishing and embedding processes, procedures, assessments and management systems across the business, supporting the company's progression towards ISO certification and FSSC 22000 / ISO 22000 accreditation. \n \nThis is a hands-on leadership role requiring both strategic system development and operational management capability within a fast-paced manufacturing environment. \n \nKEY RESPONSIBILITIES: QSHE Manager - FMCG, Food Manufacturing \n \n· Team Leadership and Management \n· ISO & Food Safety Certification \n· QHSE management systems implementation and development \n· Health & Safety and risk assessments \n· Environmental and Operational compliance \n· Auditing & Governance \n \nYOUR BACKGROUND: QSHE Manager - FMCG, Food Manufacturing \n \nEssential experience: \n \n· Experience in a Senior level QSHE, Technical or Compliance Management role within manufacturing, food production, beverage or an FMCG environment. \n· Experience managing or supervising compliance / quality personnel. \n· Experience implementing a QMS, procedures and compliance frameworks or at least heavily influencing and modifying. \n· Working knowledge of HACCP, GMP, Health & Safety and food safety standards. \n· Experience preparing businesses for external audits and certification. \n· Strong organisational, leadership and communication skills. \n· Ability to manage priorities across multiple operational sites. \n· Practical, hands-on and solutions-focused approach. \n \nDesirable experience: \n \n· Experience implementing ISO systems and/or FSSC 22000 / ISO 22000. \n· NEBOSH, IOSH or equivalent qualification. \n· HACCP Level 3 or above. \n· Lead Auditor qualification. \n· Experience within co-packing or fast-paced manufacturing environments. \n \nTHE COMPANY:\n\nWe are a multi-site FMCG operation and support our customers with a range of services including storage, eCommerce fulfilment, contract packing, shrink sleeving, pick & pack, and distribution - letting you focus on selling, scaling, and being shelf ready.\n\nWe already work with businesses of all sizes, from start up brands to global FMCG players, delivering tailored, no-fuss logistics solutions.\n\nPROSPECTS:\n\nWith business growth comes opportunity, people who work here wear many hats, but as the business expands, your opportunities are endless - potential for progressions as well as your own personal development. To create something to look back at and say, "we did that". It will be difficult, but the rewards are there to be had.\n\nIt is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services: QHSE, Quality, Health & Safety, Environmental - FMCG, food, beverage, manufacturing, co-packing, fulfilment, compliance, ISO, HACCP. \n \nINTERESTED? Please click apply. You will receive an acknowledgement of your application. \n \nWallace Hind Selection, alongside our client embrace diversity, champion equality, and foster inclusion to create a work environment where everyone belongs and thrives. \n \nPlease Note: Wallace Hind Selection have been chosen as the retained recruitment partner of our client and therefore any direct applications to our client from candidates or agencies will be forwarded on to us direct. \n \nREF: JAC18480, Wallace Hind Selection

Quality Control InspectorLocation: Basingstoke\n Contract: Temporary ( 6 months)\n\nWorking Hours: Monday to Thursday: 7:30am - 4:00pm & Friday: 7:30am - 1:30pm\n\nHourly Pay rate: £18-£22\n\nStart date: 6th July 2026\n\nMake Quality Count - From Day One\n\nWe are seeking a detail‑driven Quality Control Inspector to play a vital role in our manufacturing operation. This position focuses on incoming inspection of parts and machines, ensuring quality standards are met before production even begins.\n\nYou'll be at the heart of quality excellence-capturing accurate inspection data, supporting strong supplier performance, and helping maintain smooth, efficient workshop operations.\n\nIf you take pride in precision and want your work to have a real impact on product quality, this could be the perfect opportunity for you.\n\nKey Responsibilities\n\nCarry out incoming inspections on parts and machinery to confirm compliance with specifications\nAccurately capture, measure, and record quality data within the workshop\nMaintain and support quality systems to ensure effective process control\nSupport supplier quality assurance, including identifying and escalating non‑conformances\nConduct and document First Article Inspections (FAI)\nIdentify, quarantine, and report non‑conforming materials to prevent production disruption\nWork closely with suppliers, purchasing, and manufacturing teams to resolve quality issues efficientlyTechnical Skills & Experience\n\nConfident using measurement equipment such as calipers, micrometres, height gauges, test meters, and scanners\nStrong ability to read and interpret engineering drawings and technical schematics\nKnowledge of GD&T (Geometric Dimensioning & Tolerancing) - desirable\nUnderstanding of quality standards (e.g. ISO) and health & safety regulations\nComfortable using SAP or inventory systems and Microsoft Office applications \n\n Skills and Qualifications\n\nExceptional attention to detail, with a keen eye for defects or specification issues\nStrong documentation and record‑keeping skills (inspection records, certificates of conformance)\nClear, confident communication skills, able to work cross‑functionally\nA proactive, problem‑solving mindset to minimise delays and maintain production flow\nExperience in a manufacturing, engineering, or supply chain environment is highly desirable\nCommitment to health & safety complianceWhat We Offer\n\nContinuous support from Adecco\nSubsidised canteen & free refreshments all day, every day\nFree car parking and excellent public transport links\nFull training and ongoing investment in your development\nClear career progression opportunities\nFull PPE\nGym access\nIf you are interested, please submit your CV and we will be in touch with you to discuss the role!\nAdecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explaining how we will use your information is available on our website

Q&RA Engineer\n\nLocation: Remote (Monthly meetings in Basingstoke)\nContract Type: Temporary (9 months)\nHourly Rate: £23.50\nHours: Full Time (40 hours per week)\nStart Date: ASAP\n\nAre you ready to make a meaningful impact in the Life Sciences industry? Join our client's dynamic team as a Q&RA Engineer and be part of a mission that aims to make the world healthier, cleaner, and safer!\n\nIn this exciting role, you will ensure quality compliance across operations while collaborating with talented professionals who share your commitment to excellence. This is your chance to contribute to groundbreaking solutions that tackle some of the world's toughest challenges!\n\nPosition Overview:\nAs a Q&RA Engineer, you'll be at the forefront of quality assurance, providing essential oversight through documentation reviews and process monitoring. You will work collaboratively with cross-functional teams to deliver life-changing products to customers.\n\nWhat You'll Do:\n\nSupport Compliance: Help maintain compliance with GMP/GxP, ISO standards, and regulatory requirements.\nInvestigate Quality Issues: Lead root cause analysis efforts and manage change control activities.\nConduct Audits: Support internal and external audits and regulatory inspections.\nDocument Quality: Author and review SOPs, investigation reports, and other critical quality documentation.\nAnalyse Data: Perform data analysis, trending, and reporting of quality metrics.\nDrive Improvements: Collaborate with teams to implement corrective and preventive actions and support continuous improvement initiatives. \n\nWho You Are:\n\nEducation: Bachelor's degree in Life Sciences, Engineering, Chemistry, Biology, or a related technical field with 5+ years of relevant experience (or an advanced degree with 3+ years).\nExperience: Background in regulated industries (pharmaceutical, medical device, or biotech preferred) with proficiency in quality management systems and CAPA processes.\nSkills: Strong knowledge of GMP/GxP regulations, ISO standards, and excellent technical writing abilities.\nProblem Solver: Advanced problem-solving skills with a keen attention to detail.\nTeam Player: Exceptional interpersonal skills that enable collaboration across functions and levels. \n\nReady to Make a Difference?\nIf you are enthusiastic about quality assurance and ready to embark on a fulfilling journey in the Life Sciences sector, we want to hear from you!\n\nJoin our client's team and be a part of something bigger! Together, we can make a difference.\n\nAdecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.\n\nAdecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.\n\nBy applying for this role your details will be submitted to Adecco. Our Candidate Privacy Information Statement explains how we will use your information - please copy and paste the following link in to your browser

Job Title: Quality Engineer Location: Hellaby, England, United Kingdom Workplace type : on-site Employment: Permanent Come build something that matters. Job Summary: The Quality Engineer is responsible for ensuring the quality and reliability of products throughout the production process. This role involves developing and implementing quality control procedures, conducting inspections and tests, analysing data, and collaborating with cross-functional teams to identify and resolve quality issues. The Quality Engineer plays a critical role in maintaining high standards of product quality and driving continuous improvement initiatives. Qualifications • Bachelor's degree in engineering or a related field., • Proven experience in quality engineering or a similar role, preferably in a manufacturing environment., • Strong knowledge of quality control principles, methodologies, and tools, including PPAP (Production Part Approval Process) and Control Plans., • Familiarity with quality management systems, such as ISO 9001. Proficient in statistical analysis and data interpretation., • Excellent problem-solving and analytical skills. Detail-oriented with a strong focus on accuracy and precision., • Effective communication and interpersonal skills to collaborate with cross-functional teams., • Ability to work independently and prioritize tasks in a fast-paced environment., • ISO auditor trained, with experience in conducting internal audits for ISO 9001, ISO 14001, and ISO 45001 standards. Responsibilities • Development, implementation, and updating of quality control procedures and documentation (PPAP, Control Plan, FMEA)., • Execution of inspections and tests on materials, components, and finished products to identify defects, with proper documentation of results., • Collaboration with cross-functional teams to resolve quality issues and implement corrective actions, documenting the activities carried out., • Analysis of quality data to identify areas for improvement and define strategies to reduce defects., • Monitoring of production processes to ensure compliance with quality standards and regulatory requirements., • Technical support to production teams to resolve quality issues and improve process efficiency., • Root cause analysis of problems and implementation of preventive measures., • Management and updating of quality documentation, ensuring accessibility and accuracy., • Management of non-conforming materials, both internal and supplied, and collaboration with suppliers to resolve issues., • Supervision and support of quality control personnel., • Conducting internal audits to verify compliance with ISO 9001, ISO 14001, and ISO 45001 standards. The Details: You’ll receive a competitive salary and a great benefits plan, including: • Medical, dental, life, vision, paid time off, benefits in support of your well-being., • Discounts on Stanley Black & Decker tools and other partner programs. And More: We want our company to be a place you’ll want to be – and stay. Being part of our team means you’ll get to: • Grow: Be part of our global company with 20+ brands to grow and develop your skills along multiple career paths., • Learn: Have access to a wealth of learning resources, including our digital learning portal., • Belong: Experience an awesome place to work, where we have mutual respect and a great appreciation for a wide range of perspectives and experiences., • Give Back: Help us continue to make positive changes locally and globally through volunteerism, giving back, and sustainable business practices. What’s more, you’ll get that pride that comes from empowering makers, doers, protectors, and everyday heroes all over the world. We’re more than the #1 tools company. More than a driving force in outdoor power equipment. More than a global leader in industrial. We’re visionaries and innovators. As successful as we’ve been in the past, we have so much further to go. That’s where you come in. Join us!

Q&RA Engineer Location: Basingstoke, with occasional on-site attendance required (approximately once per month for meetings) Pay Rate: £27 per hour We are currently recruiting for a Q&RA Engineer to support quality assurance and regulatory activities within a highly regulated environment. As a Quality Engineer, you will provide essential quality oversight through detailed documentation review, process monitoring, and collaboration with cross-functional teams. You will help maintain compliance, investigate quality events, and drive continuous improvement initiatives within a collaborative and quality-focused environment. This is a 9-Month contract with the posibility of an extension. Key Responsibilities • Support and maintain compliance with GMP/GxP, ISO, and regulatory requirements, • Investigate quality issues and lead root cause analysis activities, • Manage and support change control activities, • Conduct and support internal and external audits and regulatory inspections, • Author and review quality documentation including SOPs and investigation reports, • Perform data analysis, trending, and reporting of quality metrics, • Collaborate with cross-functional teams to drive corrective and preventive actions (CAPA), • Support continuous improvement initiatives and quality system enhancements

The role offers a basic salary of up to £45,000, alongside a range of benefits including 22 days holiday and a pension. This hands-on leadership role requires experience in the FMCG sector, a strong understanding of ISO certification, and the capability to influence compliance and quality measures.

Quality Systems PMO Program Manager Location: Basingstoke, with occasional on-site attendance required (approximately once per month for meetings) Pay Rate: £27 per hour We are currently recruiting for a Quality Systems PMO Program Manager to support enterprise-wide Quality Management System (QMS) transformation and harmonisation initiatives within a highly regulated environment. This role will focus on driving consistent, compliant, and efficient quality processes across global operations while supporting operational excellence and continuous improvement initiatives. This is a 9-month temporary contract with the possibility of an extension. Key Responsibilities: Lead programme management and execution of enterprise QMS transformation and harmonisation initiatives Define programme deliverables, governance structures, timelines, and success metrics Support global QMS integration projects focused on standardising quality processes, governance models, and compliance frameworks Collaborate with cross-functional teams across Quality, Operations, Manufacturing, Distribution, Supplier Quality, Commercial, Regulatory, and IT functions Drive integration of distribution and operational quality processes into enterprise QMS frameworks Oversee implementation of standardised quality processes and harmonised operating models across sites and business units Lead remediation and quality transformation initiatives supporting inspection readiness and compliance improvements Develop communication plans, governance reporting, and executive updates relating to programme progress, risks, and milestones Identify and manage programme risks including compliance gaps, operational disruption risks, supplier quality concerns, and integration challenges Coordinate reporting activities including KPI dashboards, governance reporting, and quality metrics visibility Support development and execution of enterprise quality roadmaps and transformation strategies Drive continuous improvement initiatives focused on process simplification, standardisation, efficiency, and scalability Ensure harmonised QMS processes comply with applicable regulations and standards including FDA, ISO 13485, GMP, GDP, and regional regulatory requirements Technical Responsibilities: Apply structured PMO and project management methodologies across enterprise quality transformation initiatives Track completion of harmonisation milestones, remediation activities, system integrations, CAPAs, and compliance deliverables Facilitate governance meetings, steering committee sessions, quality councils, audit readiness activities, and executive reporting Manage integrated project plans including schedules, budgets, resource allocation, dependencies, risks, and implementation timelines Support issue resolution and proactively mitigate operational, compliance, and integration risks Maintain centralised governance documentation, action trackers, controlled records, and reporting repositories Partner with IT and Digital Quality teams to support implementation and optimisation of enterprise QMS platforms and workflow solutions Support harmonisation of quality processes including CAPA, Change Control, Document Control, Training Management, Audit Management, Supplier Quality, Complaint Handling, and Distribution Quality processes Support regulatory inspections and internal audits related to enterprise QMS effectiveness and operational compliance Utilise Lean, Six Sigma, and continuous improvement methodologies to support sustainable operational improvements Leadership Responsibilities: Lead and coordinate global, cross-functional, geographically distributed teams Influence stakeholders across Quality, Operations, Distribution, Supplier Quality, Commercial, Regulatory, IT, and leadership functions Drive alignment and adoption of harmonised QMS standards and operating models across business units Facilitate decision-making and prioritisation through structured governance and data-driven insights Promote a culture of quality, compliance, accountability, and continuous improvement Coach teams on PMO governance, risk management, change leadership, and transformation execution Collaborate with senior leadership to establish strategic roadmaps, governance frameworks, and enterprise quality priorities Experience: Minimum 7 years' experience managing complex Quality Systems, PMO, or enterprise transformation programmes Experience within Life Sciences, Medical Devices, Diagnostics, Biotechnology, Pharmaceutical, or other regulated industries preferred Strong experience with enterprise QMS harmonisation, quality systems integration, and operational transformation initiatives Experience integrating Supplier Quality, Manufacturing Quality, Commercial Quality, and Distribution Quality processes Experience supporting regulatory inspections, remediation programmes, audit readiness, and compliance transformation activities Strong understanding of global quality regulations and standards including FDA, ISO 13485, GMP, GDP, and related quality system requirements Experience with enterprise quality systems, digital quality platforms, and governance frameworks preferred Experience with Lean, Six Sigma, or continuous improvement methodologies beneficial Knowledge, Skills & Abilities: Strong understanding of Quality Management Systems and enterprise quality governance models Deep understanding of quality processes including CAPA, change control, audits, supplier quality, training, and document management Strong programme and stakeholder management capabilities within matrix organisations Excellent communication, analytical, organisational, and problem-solving skills Experience developing governance frameworks, dashboards, KPIs, and executive reporting structures Ability to drive cross-functional alignment across geographically distributed teams Familiarity with enterprise QMS software platforms and digital quality tools Strong change management and organisational transformation capabilities Ability to manage competing priorities within fast-paced regulated environments Brook Street NMR is acting as an Employment Business in relation to this vacancy. 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Quality and Regulatory Labelling Program Manager Location: Basingstoke, with occasional on-site attendance required (approximately once per month for meetings) Pay Rate: £27 per hour We are currently recruiting for a Quality and Regulatory Labelling Program Manager to support global labelling quality and regulatory initiatives within a highly regulated environment. This role will focus on ensuring compliant, accurate, and globally harmonised product labelling across international markets while driving continuous improvement and operational effectiveness. This is a 9-month contract with the possibility of an extension. Key Responsibilities: Lead the planning, coordination, and execution of global labelling quality and regulatory initiatives Support compliant implementation of labelling changes, artwork updates, UDI requirements, IFUs, translations, and market-specific labelling obligations Collaborate with cross-functional teams including Regulatory Affairs, Quality, Manufacturing, Packaging, Supply Chain, and Commercial functions Manage program governance, timelines, deliverables, budgeting, risk assessments, and reporting activities Lead labelling remediation projects, artwork harmonisation initiatives, and compliance transformation activities Coordinate implementation of product labelling changes related to regulatory updates, product modifications, safety notices, recalls, or market expansion activities Support inspection readiness activities and coordinate responses to regulatory observations and internal audit findings Track commitments, corrective actions, and implementation milestones to ensure timely completion and sustained compliance Drive continuous improvement initiatives focused on labelling accuracy, standardisation, compliance, and operational efficiency Ensure labelling processes comply with applicable regulations and standards including FDA, EU MDR/IVDR, ISO, GMP, UDI, and regional market requirements Technical Responsibilities: Apply structured program and project management methodologies to regulatory and labelling initiatives Manage integrated project plans including schedules, resources, dependencies, budgets, and implementation activities Monitor completion of labelling change controls, artwork approvals, remediation activities, and compliance actions Facilitate governance meetings, review boards, audit sessions, and executive reporting activities Maintain audit records, artwork approvals, and version-controlled documentation in accordance with regulatory requirements Support implementation and optimisation of labelling systems, artwork management tools, and compliance reporting platforms Coordinate UDI implementation, product traceability initiatives, multilingual labelling requirements, and IFU updates Identify and mitigate compliance, operational, and supply chain risks associated with labelling activities Leadership Responsibilities: Lead and coordinate cross-functional and geographically distributed teams Build strong working relationships across Quality, Regulatory, Operations, Engineering, Procurement, and Commercial functions Support stakeholders in prioritising activities and managing resource constraints Deliver presentations and updates to senior leadership regarding programme status, compliance risks, and implementation progress Promote a culture of quality, compliance, accountability, and continuous improvement Coach and support project teams on programme management best practices and change management principles Education: Bachelor's and/or Master's degree in Quality, Regulatory Affairs, Life Sciences, Engineering, Business, or related field required MBA or advanced degree preferred PMP or equivalent Project Management certification preferred ASQ certifications (CQE, CQA, CMQ/OE) or RAC certification preferred Lean Six Sigma certification preferred Experience: Minimum 7 years' experience managing complex programmes and strategic initiatives Experience within Life Sciences, Medical Devices, Diagnostics, Biotechnology, Pharmaceutical, or other regulated industries preferred Experience with labelling operations, artwork management, change control, audit management, and remediation programmes preferred Strong understanding of product labelling lifecycle management including IFUs, packaging artwork, UDI, translations, and market-specific labelling requirements Experience supporting regulatory inspection readiness and cross-functional transformation initiatives Strong understanding of global labelling regulations and quality standards including FDA, EU MDR/IVDR, ISO, and GMP requirements Experience with process improvement methodologies such as Lean or Six Sigma beneficial Knowledge, Skills & Abilities: Strong programme and project management capabilities including governance, scheduling, reporting, and risk management Strong understanding of labelling operations, regulatory frameworks, and compliance processes Familiarity with labelling systems, artwork management platforms, and electronic document management systems Excellent analytical, problem-solving, and critical thinking skills Strong communication and presentation skills with the ability to engage stakeholders at all levels Proficient in MS Office applications including MS Project, Excel, and PowerPoint Ability to independently manage strategic initiatives within complex matrix organisations Ability to work collaboratively across multiple teams, functions, sites, and regions Strong organisational skills with the ability to manage multiple priorities and deadlines effectively Ability to travel up to 10-30% annually depending on business requirements Brook Street NMR is acting as an Employment Business in relation to this vacancy. 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Are you an experienced leader who wants to take ownership of our Quality, Health & Safety and Environmental function? Managing a small QSHE team, you will help us implement better departmental structure whilst building our QMS and HSE systems processes. We are a Multi-site FMCG operation in Basingstoke. Please apply to learn more. BASIC SALARY: Up to £45,000 dependant on your relevant experience. BENEFITS: · 22 Days Holiday · Pension LOCATION: Basingstoke, Hampshire COMMUTABLE LOCATIONS: Hook, Fleet, Farnham, Aldershot, Farnborough, Frimley, Camberley, Alton, Andover, Thatcham, Newbury, Reading, Wokingham. Why you should join us: · This is a brand new role - take on responsibility for the QSHE department, own it, and develop it with your knowledge and expertise · We are growing quickly in headcount and turnover, so it is an exciting time to join us and develop your career JOB DESCRIPTION: QSHE Manager - FMCG, Food Manufacturing As QSHE Manager you will be responsible for leading, developing and implementing our Quality, Safety, Health, Environmental and Compliance systems across both operational sites. You'll oversee all compliance activities with initially two direct reports to ensure effective day-to-day quality, food safety and compliance. A significant part of this role will involve establishing and embedding processes, procedures, assessments and management systems across the business, supporting the company's progression towards ISO certification and FSSC 22000 / ISO 22000 accreditation. This is a hands-on leadership role requiring both strategic system development and operational management capability within a fast-paced manufacturing environment. KEY RESPONSIBILITIES: QSHE Manager - FMCG, Food Manufacturing · Team Leadership and Management · ISO & Food Safety Certification · QHSE management systems implementation and development · Health & Safety and risk assessments · Environmental and Operational compliance · Auditing & Governance YOUR BACKGROUND: QSHE Manager - FMCG, Food Manufacturing Essential experience: · Experience in a Senior level QSHE, Technical or Compliance Management role within manufacturing, food production, beverage or an FMCG environment. · Experience managing or supervising compliance / quality personnel. · Experience implementing a QMS, procedures and compliance frameworks or at least heavily influencing and modifying. · Working knowledge of HACCP, GMP, Health & Safety and food safety standards. · Experience preparing businesses for external audits and certification. · Strong organisational, leadership and communication skills. · Ability to manage priorities across multiple operational sites. · Practical, hands-on and solutions-focused approach. Desirable experience: · Experience implementing ISO systems and/or FSSC 22000 / ISO 22000. · NEBOSH, IOSH or equivalent qualification. · HACCP Level 3 or above. · Lead Auditor qualification. · Experience within co-packing or fast-paced manufacturing environments. THE COMPANY: We are a multi-site FMCG operation and support our customers with a range of services including storage, eCommerce fulfilment, contract packing, shrink sleeving, pick & pack, and distribution - letting you focus on selling, scaling, and being shelf ready. We already work with businesses of all sizes, from start up brands to global FMCG players, delivering tailored, no-fuss logistics solutions. PROSPECTS: With business growth comes opportunity, people who work here wear many hats, but as the business expands, your opportunities are endless - potential for progressions as well as your own personal development. To create something to look back at and say, "we did that". It will be difficult, but the rewards are there to be had. It is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services: QHSE, Quality, Health & Safety, Environmental - FMCG, food, beverage, manufacturing, co-packing, fulfilment, compliance, ISO, HACCP. INTERESTED? Please click apply. You will receive an acknowledgement of your application. Wallace Hind Selection, alongside our client embrace diversity, champion equality, and foster inclusion to create a work environment where everyone belongs and thrives. Please Note: Wallace Hind Selection have been chosen as the retained recruitment partner of our client and therefore any direct applications to our client from candidates or agencies will be forwarded on to us direct. REF: JAC18480, Wallace Hind Selection TPBN1_UKTJ

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Working knowledge of international standards for quality management systems (AS9100, ISO9001).

Act as the primary liaison with UK regulatory authorities, including HMRC, DBT and ECJU, regarding licence applications, approvals and compliance enquiries.

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