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Fully Qualified Science Teacher – Secondary Schools Location: Liverpool Contract Type: Full-Time / Permanent About the Role We are currently seeking a passionate and fully qualified Science Teacher to join a range of well-established secondary schools across Liverpool. This is a fantastic opportunity for an enthusiastic educator to inspire students and contribute to high-quality science education within dynamic and inclusive school environments. The successful candidate will deliver engaging lessons across Key Stages 3 and 4, with opportunities to teach Key Stage 5 depending on specialism and experience. You will play a key role in fostering curiosity, critical thinking, and a strong understanding of scientific principles among students of all abilities. Key Responsibilities • Plan and deliver engaging, practical, and well-structured Science lessons in line with the national curriculum, • Teach across KS3 and KS4 (KS5 teaching available depending on specialism), • Specialise in one or more disciplines: Biology, Chemistry, or Physics, • Assess and monitor student progress, providing clear and constructive feedback, • Differentiate teaching to support all learners, including SEN and high-achieving students, • Create a safe, inclusive, and stimulating classroom and laboratory environment, • Support students in achieving strong GCSE (and A-Level where applicable) results, • Work collaboratively with colleagues to develop schemes of work and share best practice, • Participate in school activities, parents’ evenings, and continuous professional developmentRequirements, • Qualified Teacher Status (QTS) or equivalent, • Degree in Science or a related discipline (Biology, Chemistry, Physics, or similar), • Experience teaching Science within a UK secondary school setting, • Strong subject knowledge and a passion for science education, • Excellent classroom management and organisational skills, • Strong communication and interpersonal abilities, • Commitment to safeguarding and promoting the welfare of pupils, • Ability to inspire, motivate, and challenge students of all abilitiesDesirable (Not Essential), • Experience teaching GCSE and/or A-Level Science, • Specialism in Biology, Chemistry, or Physics at KS5, • Familiarity with schools in Liverpool or the local education landscape, • Experience delivering practical science lessons and maintaining lab safety standards, • Use of innovative teaching methods or technologyWhat We Offer, • Opportunities to work in a variety of supportive and high-performing secondary schools across Liverpool, • Competitive salary aligned with MPS/UPS, • Ongoing professional development and training opportunities, • Supportive leadership teams and collaborative working environments Applications will be reviewed on a rolling basis, and early applications are encouraged. All applicants will require the appropriate qualifications and training for this role. Please see the FAQ’s on the Teaching Personnel website for details.All pay rates quoted will be inclusive of 12.07% statutory holiday pay. This advert is for a temporary position. In some cases, the option to make this role permanent may become available at a later date.Teaching Personnel is committed to safeguarding and promoting the welfare of children. We undertake safeguarding checks on all workers in accordance with DfE statutory guidance ‘Keeping Children Safe in Education’ this may also include an online search as part of our due diligence on shortlisted applicants.We offer all our registered candidates FREE child protection and prevent duty training. All candidates must undertake or have undertaken a valid enhanced Disclosure and Barring Service (DBS) check. Full assistance provided.For details of our privacy policy, please visit the Teaching Personnel website.

Qualified Person – North West England – Competitive Package BioTalent are currently representing a growing pharmaceutical manufacturer based in the North West in their search for an experienced Qualified Person. You will be integral to the Quality department supporting on the week to week release activities alongside other major QA projects for the site. This position requires individuals to have prior experience working on a license and preferably with terminally sterilised products. Key requirements – • Review and evaluate batch records and authorise batch disposition., • Manage the site QMS, monitor compliance with GMP and drive quality improvements., • To review and approve deviations and laboratory investigations in compliance with GMP., • To investigate and respond to complaints., • Highly collaborative, regular interaction with senior management, Regulatory groups, QPPV, Supply chain, site-based QA, distributors, testing labs, warehouses, sales departments, customers and regulators., • Ability to work independently with limited supervision, self-driven, responsive and results orientated. Duties: • The successful candidate will be qualified to degree level (as a minimum) in a relevant scientific discipline., • The candidate must be eligible to act as a Qualified Person for medicinal products (as defined in EU Directive 2001/83/EC) and have been named on a UK MIA., • Robust technical knowledge of EU GMP, regulations and guidelines. Experienced in the operation of an EU regulatory approved QMS., • At least 5 years’ experience in a GMP QA role within the pharmaceutical industry and experience of managing quality systems., • Ability to work independently with limited supervision, self-driven, responsive and results orientated. This is an excellent opportunity for an individual who is looking to work in a fast paced, dynamic environment supported by a wider QA team. Shortlisting for this role has begun with a view to holding first stage interviews over the next couple of weeks. For further information please contact Sarah Pawar on 0203 9115 888 or email a copy of your CV to

🚀 Quality Assurance Manager – North Merseyside 💰 Up to £50,000 🏭 Pharma / Life Sciences Manufacturing We’re supporting a specialist life sciences manufacturer as they grow their QA function. If you’re detail‑driven, GMP‑savvy and ready for a role where quality genuinely matters, this is one to explore. Full time | Permanent | On site This is a brilliant opportunity to step into a senior QA role within a global life sciences leader. You’ll take ownership of the Quality Management System, lead a small team, and ensure the site continues to meet ISO, GMP, MHRA and FDA requirements. Perfect for someone who thrives in a hands‑on environment where quality is truly valued. 🔍 What You’ll Be Doing You’ll lead and continuously improve the site’s Quality Management System, including: • Leading, controlling and improving the ISO 9001 QMS, • Managing GMP activities and delivering GMP training, • Writing, revising and approving SOPs, • Performing internal audits, supplier audits and hosting customer audits, • Managing complaints, NCRs and CAPAs, • Acting as the departmental SME for quality activities, • Supporting FDA‑related systems for the CTS laboratory, • Supervising the QA Assistant and QC Assistant, • Preparing monthly quality metrics and management information 🎓 What You’ll Bring • Experience in a senior QA role within an ISO/GMP‑regulated environment, • Strong understanding of ISO standards, quality systems and audit practices, • Excellent communication skills with the ability to train and influence, • High attention to detail, strong organisational skills and a proactive mindset, • A BSc/MSc in a scientific discipline 💼 Why It’s a Great Move • Join a respected, specialist life sciences manufacturer with a strong quality culture, • Lead and shape the site’s QA function with real autonomy 📩 Interested? Reach out to Nexus Life Sciences for a confidential chat or send your CV directly. #QualityAssurance #GMP #LifeSciencesJobs #PharmaCareers

QA/RA Assistant/Manager– £35,000- £45,000– Central Tech, L3 5LJ The Role Are you highly organised with a sharp eye for detail in regulated environments? Ready to build your career in quality and regulatory affairs while helping shape standards in a growing laboratory setting? This is an exciting opportunity for a QA/RA Assistant/Manager to join Guilford Street Laboratories and play an important role in maintaining and improving the Integrated Management System (IMS). As a QA/RA Assistant/Manager, you will support quality, regulatory and information security processes while helping ensure compliance across laboratory operations. This role offers the chance to work closely with technical teams, strengthen your expertise and develop your career within diagnostics, healthcare and laboratory quality systems. If you are ready to take the next step in your career and join a forward-thinking laboratory team, apply today and help shape quality excellence at Guilford Street Laboratories. Key Responsibilities: • Support the maintenance and continuous improvement of the IMS, • Assist with compliance across ISO 15189, ISO 13485, ISO 27001, UKCA, CE, and relevant FDA/IVDR requirements, • Manage controlled documentation, including SOPs, policies, and laboratory procedures, • Support internal and external audits, including CAPA tracking, • Work alongside laboratory teams to maintain quality standards across testing and data integrity, • Assist with supplier, reagent, and service provider approvals, • Support risk management, nonconformance, and change control processes, • Maintain training and competency records, • Provide administrative support to the Quality and Regulatory department The Company Guilford Street Laboratories is committed to reshaping the future of diagnostics. We apply cutting-edge machine learning to unlock better ways to detect, stratify, and monitor disease. Our values—innovation, accuracy, collaboration, empowerment, and service—guide everything we do. At Guilford Street Laboratories, your work will directly support healthcare professionals in delivering earlier and more accurate diagnoses for patients worldwide. Benefits: • Salary of £35,000–£45,000, • Full-time position, 35 hours per week, • Career development within a regulated scientific environment, • Exposure to leading laboratory and regulatory standards, • Supportive and collaborative team culture, • Valuable hands-on experience across quality and regulatory systems The Person We are looking for a QA/RA Assistant/Manager who has: • A degree in Biomedical Sciences, Life Sciences, Laboratory Sciences, Quality Management, Regulatory Affairs, or similar, • Previous experience within a laboratory, IVD, diagnostics, or regulated healthcare setting, • Strong knowledge of laboratory quality systems, • Excellent organisational and communication skills, • Confidence working with controlled documentation, • A real interest in diagnostics, laboratory quality, and regulatory compliance

SENIOR FOOD TECHNOLOGIST — R&D Chalice Supplements | L36, Liverpool | On-Site | Full-Time | PhD-Level Preferred ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ ABOUT CHALICE SUPPLEMENTS Chalice Supplements is a privately owned, family business laser-focused on one thing: gummies. We believe gummy delivery is the future of the supplements industry — the fastest-growing format in the market and the one with the greatest potential to make health products people actually want to take. That conviction sits at the heart of everything we do. We have recently made a significant investment in that future — substantially expanding our factory, production capacity, and output to establish ourselves as a leading gummy contract manufacturer in the UK. This is a business with serious ambition, real momentum, and a clear direction of travel. But beyond the science and the scale, we are driven by something more meaningful: the belief that well-formulated, efficacious supplements can genuinely improve people's lives. Every product that leaves our facility has the potential to help someone sleep better, manage stress, navigate menopause, support their mood, or address a health challenge that has been quietly affecting their quality of life. That is not something we take lightly — and neither should you. ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ THE ROLE This is a fully on-site, hands-on senior role based at our production facility in L36, Liverpool. You will be on the factory floor, in the lab, and at the heart of our manufacturing operation — not behind a desk all day. This is not a remote or hybrid position; we need someone present, engaged, and embedded in the day-to-day reality of gummy production. As our primary technical lead on gummy formulation and product development, you will own projects from concept through to commercial launch. You will work directly and closely with our CEO, as well as our operations, quality, and commercial teams, playing a central role in shaping how we develop and scale products across our client base. We are looking for someone who brings exceptional technical ability and is equally driven by purpose. Someone who genuinely cares about the end consumer — who is as motivated by the person taking the product as they are by the formulation itself. Someone who gets a genuine thrill seeing a product they formulated on the shelf at Boots or Holland & Barrett, or in a TV advert reaching millions of people. If you want your work to matter at scale, and you believe that great science can change lives, this role was built for you. ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ KEY RESPONSIBILITIES FORMULATION & TEXTURE DEVELOPMENT • Lead end-to-end formulation development for gummy products across active ingredient categories including vitamins, minerals, adaptogens, and functional blends, • Systematically adapt ingredient ratios — gelling agents, humectants, sugars, polyols, and co-solvents — to engineer distinct gummy textures including firm, soft, chewy, and jellied profiles, • Work across pectin, starch, and alternative plant-based gelling systems to understand how each interacts with active ingredients, pH, and processing conditions to influence final texture, • Develop and document formulation matrices that map ingredient variables to sensory and physical outcomes, building institutional knowledge around what levers drive texture change, • Manage ingredient compatibility, dosage levels, and regulatory constraints across a broad formulation portfolio CURING & PROCESS CONDITIONS • Design and run structured curing trials to determine optimal temperature, humidity, airflow, and time conditions for each gummy formulation, • Investigate how variations in curing parameters influence texture development, moisture loss, surface finish, and long-term stability, • Establish curing protocols for new products and document critical process parameters to enable consistent reproduction at scale, • Work with production teams to translate lab and pilot curing conditions into commercially viable manufacturing processes SHELF LIFE & STABILITY • Design and execute shelf life studies (real-time and accelerated) across product lines, with particular attention to how texture evolves over time, • Interpret and act on stability data to refine formulations and packaging specifications — including moisture barrier requirements, • Build robust stability protocols that support regulatory submissions and customer product claims, • Maintain deep working knowledge of water activity, hygroscopicity, and moisture migration in confectionery systems and how they drive textural degradation MANUFACTURING SCALE-UP & PROCESS OPTIMISATION • Translate bench and pilot formulations into scalable manufacturing processes on commercial gummy lines, • Collaborate closely with production teams to troubleshoot process variability and optimise yields, • Define critical control points and in-process parameters for new product launches, • Drive continuous improvement of existing product formulations from a cost, quality, and process efficiency standpoint HEALTH INNOVATION & CONSUMER IMPACT • Develop formulations targeting specific health outcomes — including sleep, stress and anxiety, women's health and menopause, energy, immunity, and cognitive performance, • Stay current with clinical research, emerging ingredients, and consumer health trends to identify where new product innovation can have the greatest impact, • Champion the consumer internally — ensuring efficacy, bioavailability, and active delivery are never compromised in pursuit of cost or speed, • Bring proactive ideas for new product concepts based on emerging health needs, novel ingredients, or unmet gaps in the current market, • Approach every brief with genuine enthusiasm — treating each formulation as an opportunity to create something that makes a meaningful difference in someone's life TECHNICAL & CROSS-FUNCTIONAL LEADERSHIP • Act as the internal technical authority on gummy technology, food science, and ingredient functionality, • Partner with commercial and client-facing teams to translate briefs into technically viable product concepts, • Provide technical input into raw material sourcing decisions and supplier evaluation, • Support documentation requirements including specifications, SOPs, and technical dossiers ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ WHO WE ARE LOOKING FOR ESSENTIAL • PhD in Food Science, Food Technology, Nutrition, Chemistry, or a closely related discipline — or equivalent demonstrable expertise at senior level, • Proven track record in food or supplement product development, with hands-on formulation experience, • Deep technical understanding of gummy or confectionery systems (gelling agents, humectants, active stabilisation), • Strong experience designing and interpreting shelf life and accelerated stability studies, • Ability to operate across bench-scale development and commercial manufacturing environments, • Exceptional analytical rigour, attention to detail, and scientific problem-solving ability, • Clear communicator — able to translate complex technical information for non-technical stakeholders, • Genuine passion for health, wellness, and the potential of well-formulated supplements to improve people's lives — this is not just a job, it is a mission, • The kind of person who gets a real buzz seeing a product they formulated on a supermarket shelf, in a TV advert, or in the hands of a customer — and who uses that as fuel to make the next one even better HIGHLY DESIRABLE • Experience in a contract manufacturing or multi-client product development environment, • Familiarity with UK and EU food supplement regulatory frameworks (FSA, EFSA), • Knowledge of health categories such as sleep, stress, menopause, or cognitive performance and the evidence base behind key actives, • Knowledge of clean-label, vegan, or free-from formulation challenges, • Experience with gummy-specific manufacturing equipment and process parameters, • Publication record or demonstrable contribution to applied food or nutritional science, • Proficient in the use of laboratory testing equipment and analytical techniques — including HPLC, rheometry, texture analysis, water activity measurement, and related instrumentation used in food and supplement quality assessment ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ WHAT WE OFFER • A senior, hands-on role with real ownership across the gummy product development function, • Competitive base salary commensurate with experience, with a performance bonus structure built around mutually agreed targets — your effort and results will be recognised and rewarded accordingly, • Direct access to and a close working relationship with the CEO — your voice will be heard and your contributions will matter, • A fast-paced, entrepreneurial environment where decisions are made quickly and great work is celebrated, • Participation in our Employee Ownership Scheme — as we scale, we believe the people who help build this business should share in what it becomes. A meaningful equity stake in Chalice will be allocated to the team that helps us reach our long-term ambitions. This is a genuine opportunity to build something, and to be rewarded not just for your time, but for your contribution to the journey ━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━━ To apply or learn more, please contact us directly. Chalice Supplements is an equal opportunities employer.

About the Role: The Phlebotomist is an essential member of the healthcare team, responsible for collecting and preparing blood and other specimens for laboratory testing. This role requires skillful venipuncture techniques, attention to detail, and the ability to provide a calm, professional experience for patients. The Phlebotomist ensures all samples are accurately labeled, handled, and processed in accordance with regulatory and safety standards. Client Information: This healthcare provider offers essential laboratory services, focusing on accurate specimen collection and preparation for medical testing. They are dedicated to patient care and regulatory compliance. Responsibilities: • Perform venipuncture using straight and butterfly needles for blood specimen collection • Label, centrifuge, package, and store specimens according to established procedures • Greet patients professionally and clearly explain the collection process to ease anxiety • Ensure proper identification and matching of requisition forms with specimen tubes • Maintain compliance with OSHA, DEP, and laboratory safety regulations • Accurately document patient information, specimen data, and test requisitions • Respond to phone inquiries and communicate lab results as appropriate • Maintain cleanliness and safety of work environment and equipment • Attend required annual department training sessions • Perform other duties as assigned by supervisors or management Qualification: • Associate's Degree Required Skills: • Must have at least 2 years of recent experience in the specialty within the past 2 years. • Proficient in specimen collection procedures and blood draw techniques • Knowledge of lab protocols, safety regulations, and compliance standards • Ability to interact with patients professionally, calmly, and compassionately • Detail-oriented with strong organizational and documentation skills Preferred Skills: • Prior experience in a high-volume or hospital-based lab setting is a plus • Familiarity with electronic medical records (EMR) systems

Medical Field Service Engineer Biomedical & Critical Care Equipment Critical Care & Life Support, Ventilation, Patient Monitoring and all other associated equipment North West based, covering Greater Manchester, Liverpool, Merseyside, Lancashire & Cheshire £40K - £41K + Car + Excellent benefits package including Healthcare, Contributory Pension Scheme and Full and Comprehensive Manufacturers based Product Training An excellent opportunity for an experienced Biomedical Engineer, EBME Engineer, Medical Field Service Engineer, or ex HM Forces Engineer (RAF, Navy or REME), to join a market leader in sophisticated Biomedical and Critical Care Equipment, offering first class product training and opportunities for career development The Company - Medical Field Service Engineer, Biomedical & Critical Care My client is a leading manufacturer of medical systems. This organisation’s impressive portfolio of products and fully integrated medical systems incorporates many aspects of the healthcare equipment sector and includes medical imaging diagnostics and critical care equipment. Offering 'best in class' solutions across a wide range of equipment modalities, their success is based upon a commitment to world leading manufacturing facilities, outstanding product innovation, excellent customer care and the recruitment and development of good people. They employ thousands of people globally and are an integral part of an instantly recognisable worldwide technology group. The Role - Medical Field Service Engineer, Biomedical & Critical Care Following expansion, they seek to recruit a customer focused and technically motivated Medical Field Service Engineer, responsible for the service, repair, breakdown and maintenance of their range of highly advanced critical care and life support equipment product portfolio, based at hospital and healthcare centres throughout the North West Region. Your Background - Medical Field Service Engineer, Biomedical & Critical Care To be considered for this exciting role, you must be able to demonstrate a strong background working in a high value electronic capital equipment environment. You should be qualified to a minimum ONC or HNC level or above in electronics or another relevant technical discipline. Applications are encouraged from Service Engineers from a wide range of electronic sectors, including biomedical device, medical equipment, laboratory device, print press, semi-conductor, ex Armed Forces (Radar / Weapons Systems and Biomedical Engineers), industrial / commercial imaging or other areas of electronic capital equipment. You must have impeccable customer service skills to show you can remain professional in customer facing environments. The Benefits - Medical Field Service Engineer, Biomedical & Critical Care In return, the successful applicant will benefit from first class product training, recognised by the industry, which will run on an ongoing basis as new products are introduced. A generous remuneration package is also guaranteed, including competitive salary, company car, healthcare, contributory pension scheme, phone and laptop, along with the opportunity to progress your career within a market-leading organisation. This vacancy is being advertised by TRS Consulting Services Limited. The services advertised by TRS Consulting Services Limited are those of an employment agency and / or employment business.

Graduate Geologist\n\nLiverpool\n\n£26000 to £32000 per Annum plus Benefits\n\nPermanent Role\n\nI am actively searching for a Graduate Geologist to join an established environmental consultancy delivering ground investigation and contaminated land services from its Liverpool office.\n\nThis is an excellent opportunity for a recent graduate to begin a technical career within a practical, project-driven environment.\n\nAs a Graduate Geologist, you will work alongside experienced engineers and scientists on a wide range of site investigation projects. Based in Liverpool, the role combines office-based reporting with regular site work, giving you early exposure to the full project lifecycle. You will assist with data collection, soil and groundwater logging, laboratory coordination, and the preparation of interpretive reports.\n\nThe role will suit a Graduate Geologist who is keen to develop strong technical foundations while learning how environmental risks are assessed and managed. Projects will vary in size and complexity, including residential, commercial, and infrastructure schemes across London and surrounding areas, while being supported from Liverpool by a collaborative and approachable team.\n\nGraduate Geologist, Candidate Requirements:\n\nA degree in geology, environmental science, geotechnical engineering, or a related subject\nFull UK Driving Licence\nLive within a commutable distance of Liverpool\nFull Right to Work in the UK permanentlyCompany Benefits:\n\nFlexible working\nFirst class training and development scheme\nClear progression plan \n\nInterested in this or other roles in Geotechnical or Geo-Environmental, please do not hesitate to contact William Lisle. We have many more vacancies available on our website.\n\nThis is a permanent role. Penguin Recruitment is operating as a Recruitment Agency in respect to this position

About Plessey We’re building the hardware foundation for next-era computing. Plessey is a world-leading technology company driving the next generation of photonic devices and systems. With over 70 years of innovation, we combine research, materials science, process engineering, and manufacturing under one roof. We’re recognised as a global authority in microLED displays, optical computing, and optical interconnects. Join us to work on breakthrough technologies shaping the future of light-based technology and computing. Lead We don’t follow industry trends; we create them, pushing boundaries and setting standards others aspire to. Every team member has the power to make decisions, drive change, and deliver excellence. We support each other, challenge one another for the best solutions, and lead by example. Together, we build industries and technologies that shape the future and scale toward our vision of the next era of computing. Grow We expand our capabilities every day — deepening our expertise, improving how we work, and pushing the boundaries of what’s possible. Curiosity fuels us: we question assumptions, explore new ideas, and innovate with light-based technologies. By investing in and empowering our people, we strengthen Plessey’s impact and help shape the future of optical technology. Trust We operate like a family—honest, reliable, and supportive. We have each other’s backs, own our actions, and uphold the highest standards of integrity and safety. We trust each other to deliver, our customers to challenge us, and our expertise to guide the way. Together, trust enables the collaboration essential for breakthrough innovation and lasting impact. Location Located at our head office and state-of-the-art fabrication facility in Plymouth. About the Role We are looking for a Senior Software Engineer to support the development of automated reliability and characterisation test systems for MicroLED devices. The role combines test software development, instrument control, and data analysis, supporting both the execution of reliability campaigns and the analysis of device performance and degradation. The engineer will work closely with hardware engineers and test engineers to develop software tools that control laboratory equipment, automate test procedures, and analyse large datasets generated during device testing. Key Responsibilities • Develop and maintain automated test software for reliability and characterisation systems., • Interface with laboratory instruments and test hardware using LabVIEW, C++, and Python., • Support the execution of device reliability campaigns and engineering experiments., • Develop tools for data collection, processing, and analysis., • Work with engineering teams to interpret results and identify device behaviour trends., • Contribute to improving the automation and robustness of internal test platforms. Skills, Knowledge and Expertise • Master’s degree in Physics, Electronic Engineering, or a related discipline., • Proficiency in LabVIEW and C++., • Working knowledge of Python for data processing and analysis., • Hands-on experience with communication protocols such as SPI and I²C., • Experience working with laboratory bench instruments such as power supply units (PSUs), oscilloscopes, pattern generators and multimeters., • Strong analytical mindset with attention to detail., • Ability to work independently with minimal supervision. Advantage • Experience with NI TestStand for automated test environments., • Background or practical experience in semiconductor device testing., • Experience analysing large datasets and developing mathematical models for device behaviour and degradation., • Familiarity with reliability testing methodologies (e.g., lifetime or stress testing).

About the client Our client is a confidential leading international integrated energy company with a strong global project engineering capability, currently driving an ambitious energy transition programme spanning CCS/CCUS, renewables, and hydrogen alongside its traditional oil and gas portfolio. The Basingstoke engineering office is a fully integrated project execution hub delivering multi-discipline engineering across all phases of complex projects worldwide, with a dedicated Subsea Systems department at its core. Project scope The assignment is based within the client's Basingstoke Subsea Systems department, providing Flow Assurance technical leadership across multiple concurrent international oil and gas projects — from feasibility and concept development through FEED, detailed engineering, and handover to operations. The role also extends to CCUS projects, covering CO₂ transportation system assessment and thermo-hydraulic studies specific to CO₂ transport. The Senior Engineer will operate as both a technical lead and a Discipline Project Lead (PDL), accountable for Flow Assurance deliverables across assigned projects and responsible for mentoring junior engineers within the discipline. The client operates a hybrid working policy: up to 12 working days per month from home are available, enabling approximately 60% remote working. Role overview To provide senior Flow Assurance technical leadership across the full project lifecycle — from conceptual studies through FEED, tendering, detailed engineering, and operations support — ensuring technical rigour, cross-discipline integration, and compliance with applicable standards across the client's international oil and gas and CCUS projects. Reporting line: You will report to the Flow Assurance Coordinator and the Chief of Subsea Systems, and work in daily coordination with discipline engineers, interface disciplines (Pipelines/Subsea, Process/Facilities, Operations), contractors, and reservoir and laboratory teams. Key responsibilities Technical delivery • Prepare all Flow Assurance technical documentation across project phases: conceptual study, FEED, tendering, contract package preparation, detailed engineering, and operations, • Review and approve FEED, tender, and detailed engineering deliverables prepared by contractors for the Flow Assurance discipline, • Identify, define, and analyse complex multiphase hydrocarbon transportation schemes, • Assess CO₂ transportation systems, evaluate operating envelopes, and support thermo-hydraulic studies for CCUS projects, • Provide technical support to interface disciplines — Pipelines/Subsea, Process/Facilities, Operations — ensuring integrated solutions across all project phases, • Support operations and troubleshoot start-up and commissioning issues as required Procurement & contractor management • Follow up supplier calls for tender and selection processes: qualifications, clarifications, and technical recommendations for the Flow Assurance discipline, • Manage interfaces with reservoir engineering and laboratory teams throughout the project lifecycle Project leadership & PDL duties • Act as Discipline Project Lead (PDL) on assigned complex projects: perform technical and administrative PDL functions, • Proactively identify and report manhour and schedule variations due to scope changes; escalate to the Flow Assurance Coordinator and Chief of Subsea Systems, • Support the Flow Assurance Coordinator and Chief of Subsea Systems in preparing manhour estimates for new proposals, • Liaise with engineering disciplines throughout the project execution phase; coordinate and manage cross-discipline interfaces Standards, mentoring & continuous improvement • Ensure awareness of and compliance with international standards and codes applicable to Flow Assurance, • Advise on correct interpretation and application of company internal standards and HSEQ policies; develop new standards as required, • Mentor engineers within the Flow Assurance team; contribute to knowledge sharing and continuous improvement across the discipline, • Support technical and safety reviews: HAZOP, HAZID, risk assessments, design and safety reviews Key deliverables • Flow Assurance technical documentation delivered on schedule and to the required quality standard across all assigned project phases, • Contractor and FEED deliverables reviewed and approved within defined timescales, • Manhour estimates and variation forecasts provided accurately and proactively, • PDL functions performed rigorously across assigned complex projects, • Junior engineers mentored with structured guidance and discipline knowledge transfer Requirements Education • Degree in Engineering with graduate-level knowledge of thermodynamics and fluid dynamics — petroleum, chemical, mechanical, or related discipline Experience Must-have: • Extensive experience as a Flow Assurance Engineer across the full project development lifecycle — from concept development through FEED, detailed engineering, and handover to operations, • Proven capability in identifying, defining, and analysing complex multiphase hydrocarbon transportation schemes, • Experience performing technical review of Flow Assurance documentation produced by team members and contractors, • Experience with Technical Audit and Design & Safety Reviews — HAZOP, HAZID, Risk Assessment, • Ability to manage complex and diverse assignments with a high degree of independent technical judgement Nice-to-have: • Operational experience (commissioning, start-up, or production support), • Experience on CCUS projects — CO₂ transportation system assessment and thermo-hydraulic modelling Technical skills • Proficient with Flow Assurance simulation software: OLGA, PVTSim, Multiflash, Pipenet, Pipesim, Hysys, Unisim, • Familiarity with programming languages (Matlab, C++, Python) — an advantage, • Strong understanding of international codes and standards applicable to Flow Assurance and subsea systems, • Knowledge of HSE and technical risk integration into engineering and project solutions Soft skills • Strong technical leadership and engineering judgement — able to operate independently at senior level, • Effective communicator across disciplines, stakeholder levels, and cultures — both laterally and vertically within the organisation, • Collaborative and multidisciplinary approach to project delivery, • Structured task prioritisation and ability to manage concurrent workstreams under pressure, • Fluent English — mandatory

Job Title: Armis Security Specialist Job Summary We are looking for an Armis Security Specialist to support and optimize security operations across laboratory, OT, and IoT environments. The role focuses on Armis platform management, asset visibility, risk identification, incident monitoring, and implementation of security policies within R&D lab environments. Key Responsibilities • Manage and support daily operations of the Armis platform for lab and OT/IoT environments, • Monitor, analyze, and investigate security alerts, vulnerabilities, and anomalous activities, • Maintain asset inventory, device classifications, and risk scoring using Armis, • Develop and implement security policies, procedures, SOPs, and remediation plans, • Collaborate with IT, cybersecurity, and R&D teams to improve lab security posture, • Support incident response, reporting, and compliance with frameworks like ISO 27001, NIST, and GxP, • Hands-on experience with Armis or similar OT/IoT security platforms, • Strong understanding of TCP/IP, VLANs, routing, switching, firewalls, and NAC, • Experience in cybersecurity, network security, or OT/IoT security, • Knowledge of vulnerability management, incident response, and security monitoring, • Experience in pharmaceutical, biotech, or R&D lab environments, • Exposure to SIEM, CMDB, and vulnerability management tools, • Certifications such as Security+, CISSP, GSEC, or GICSP preferred

The successful candidate will be responsible for the management of the Tradebe CWR site Laboratory. Maintenance of all laboratory equipment, supplies and service agreements.

Walker Cole International is searching for a Quality Director to join a well-established pharmaceutical manufacturing business with on-site operations in the UK. As the Quality Director, you will lead the site Quality function, providing strategic and operational oversight across both Quality Assurance and Quality Control teams while ensuring the site operates in full compliance with GxP requirements. Your responsibilities will include: • Providing strategic leadership across the site QA and QC functions, ensuring compliance with cGMP and EU GMP requirements., • Leading and developing Quality teams while embedding a strong quality culture across manufacturing and laboratory operations., • Overseeing key Quality Systems including deviations, CAPAs, investigations, change controls, and batch disposition activities., • Acting as the senior Quality representative during regulatory inspections, customer audits, and internal compliance reviews., • Partnering closely with Manufacturing, Engineering, and Supply Chain teams to support operational performance and continuous improvement initiatives. The successful candidate will demonstrate the following: • Extensive Quality leadership experience within a pharmaceutical manufacturing environment., • Proven experience managing both QA and QC teams within a regulated GMP facility., • Strong understanding of pharmaceutical manufacturing operations, investigations, and regulatory compliance expectations., • Eligibility to act as a Qualified Person (QP) on a Manufacturing Authorisation licence would be highly desirable, though not essential., • A collaborative and pragmatic leadership style with the ability to influence stakeholders across all levels of the organisation. Quality Assurance | Quality Control | QA | QC | QP | Qualified Person | GMP | cGMP | Pharmaceutical Manufacturing | CAPA | Deviations | OOS | Batch Release | Audit | Head of Quality | Quality Director | MHRA | EU GMP

Graduate Geoenvironmental Engineer Location: Aberdeen Salary: £26,000-£30,000 Are you a recent graduate eager to begin your career in geoenvironmental engineering? An exciting opportunity has arisen to join a well-established environmental consultancy delivering innovative solutions across contaminated land, geotechnical, and environmental projects throughout the UK. You will become part of a knowledgeable and supportive team, gaining hands-on experience across a broad range of residential, commercial, and infrastructure developments while building strong technical and professional skills. What's on Offer: Competitive salary package Structured graduate training and mentoring Generous annual leave entitlement Pension scheme Flexible working opportunities Exposure to a wide variety of technically challenging projects Friendly and collaborative working environment Clear opportunities for long-term career progressionKey Responsibilities: Assisting with Phase 1 Preliminary Risk Assessments and Desk Studies Supporting and carrying out Phase 2 intrusive ground investigations Soil and rock logging, sampling, and groundwater/gas monitoring Coordinating environmental and geotechnical laboratory testing Interpreting site investigation data and assisting with risk assessments Supporting remediation strategies and earthworks assessments Preparing factual and interpretative technical reports Maintaining health & sa...

What will you do? Make an impact! The successful candidate will be responsible for the management of the Tradebe CWR site Laboratory. Their tasks will include: • The management and performance of sample analysis in line with BMS procedures for: pre-acceptance, trade effluent discharge, solvent routing, external treatment, flow meter, regulatory and general requirements., • Maintenance of all laboratory equipment, supplies and service agreements., • Support the Technical Manager with associated Site Chemist duties when required., • Provision of technical support to business projects as appropriate when required., • General administrative duties. Organise the time of the lab chemist and ensure sufficient lab cover at all times., • Support wider Tradebe group to deliver projects, develop the lab network and other tasks that may be assigned from time to time. Do you have what it takes? • Essential - Educated to HNC standard in Chemistry or closely associated discipline., • Essential - Experienced in Lab Operations., • Essential - IT skills (Excel/Word)., • Desirable - Experience in Waste Analysis. What's in it for you? • Competitive salary and bonus - up to £35,600 (dependent on experience), • Contributory Pension, • Flexible benefits (access to our benefits platform for discounts and cash back ...

You’ll work alongside experienced technicians and gain practical, industry‑recognised skills in a professional laboratory environment. A strong interest in healthcare, science, design or hands‑on work. You will complete a recognised Dental Laboratory Technician Apprenticeship alongside your ro

NHS is seeking an enthusiastic and reliable Salaried GP for 6 sessions per week in Liverpool. The role focuses on providing high-quality clinical care, including consultations and managing laboratory results. The position requires GMC registration and a commitment to patient-centered care.

A dental laboratory in Liverpool is searching for a Dental Lab Technician to join their empathetic team specializing in innovative dental solutions. You will work closely with a small team, ensuring timely production while reporting to the lab supervisor.

Prysmian Group is seeking an Oceania R&D Laboratory Intern in Liverpool for a 12-month fixed-term contract. The intern will support the lab manager, participate in improvement projects, and perform various tasks as required.

Liverpool University Hospitals NHS Foundation Trust is seeking a HCPC registered Specialist Biomedical Scientist for its Virology department.In this role, you'll assess patient needs, perform routine and advanced laboratory work, and ensure accurate reporting of test results while adhering to health

The Liverpool School of Tropical Medicine is seeking a Registered Biomedical Scientist for their Clinical Diagnostic Parasitology Laboratory in Liverpool.

The Laboratory Manager will provide professional, strategic and operational leadership for the Production Laboratory at Liverpool University Dental Hospital. Act as an expert professional advisor on dental laboratory matters to clinical teams, senior leaders and service managers. The Laboratory Mana

We are inviting applications for two Band 3 Medical Laboratory Assistant positions in Cellular Pathology:. A substantive position in the Histology Laboratory. Both roles support daily laboratory operations, equipment maintenance, digital scanning systems and IMS databases, and routine tasks such as

The Liverpool School of Tropical Medicine is hiring a Postdoctoral Research Associate in Medicinal Chemistry to join the Burrows Laboratory. This role focuses on synthetic organic and medicinal chemistry for global health, including developing new methodologies and integrating AI approaches.

Support the Technical Manager with associated Site Chemist duties when required. The successful candidate will be responsible for the management of the Tradebe CWR site Laboratory. Maintenance of all laboratory equipment, supplies and service agreements.

Then Scientific Laboratory Supplies (SLS) is the right fit for you. SLS are the UK’s largest independent supplier of laboratory equipment, chemicals and consumables.

We are pleased to invite applications for two Band 3 Medical Laboratory Assistant positions within Cellular Pathology. The successful candidates will be responsible for participating in routine activities associated with a Cellular Pathology Medical Laboratory Assistant role, including:. The post h

A leading NHS Trust in England is seeking a Haematology Consultant to cover both clinical and laboratory duties.

Liverpool University Hospitals NHS Foundation Trust is seeking a Laboratory Manager to oversee the Production Laboratory at Liverpool University Dental Hospital. This role demands strong leadership abilities, a commitment to quality management, and the drive to implement digital innovations like CAD

The haematology service covers both clinical and laboratory haematology with six consultants. High level experience in clinical and laboratory haematology.

Part‑time Research Assistant – Laboratory based project on the geoarchaeology of the Neanderthal "Flower Burials" at Shanidar Cave, Iraq.Analyse sediments – sediment granulometry, geochemistry.Record and enter laboratory results; data entry and interpretation.Assist in drafting internal report

The Laboratory Manager will provide professional, strategic and operational leadership for the Production Laboratory at Liverpool University Dental Hospital. As a senior technical authority, the post holder will transform and professionalise laboratory services to ensure the delivery of safe, high��

Eurofins Scientific SE is looking for a Development Scientist in Liverpool. This role involves supporting the development of new product formulations and managing laboratory logistics.

Medical Field Service Engineer (Pathology Laboratory Diagnostics). Pathology Laboratory Diagnostics). The service, installation, breakdown, repair and calibration of a wide range of sophisticated medical laboratory diagnostics systems, utilised within pathology departments, NHS laboratories and clin

QC Technician Temporary initially but could lead to a permanent position Pay Rate - £13 p/h Hours - 8am-4pm or 9am-5pm About the Role We are currently recruiting for a QC Technician to join a busy quality team within a manufacturing environment. This role would suit someone with strong attention to detail, good organisational skills, and previous experience within a quality or manufacturing environment. The successful candidate will be responsible for carrying out quality control inspections, testing materials and finished products, maintaining accurate records, and supporting the Quality Assurance team to ensure compliance with company procedures and GMP standards. Key Responsibilities Carry out quality control checks on incoming materials and finished products Confirm the identity and condition of incoming materials Sample and test incoming materials in line with raw material specifications Record and maintain accurate quality control documentation and test results Ensure all materials are correctly status-labelled and identified Disposition and status-label returned or non-conforming materials Support environmental monitoring activities and sample collection procedures Maintain and update supplier and quality control databases Assist with periodic material retesting where required Work closely with QA and production teams to ensure quality standards are maintained Identify and escalate quality concerns in line with company procedures Maintain high levels of accuracy and attention to detail in all tasks Requirements Previous experience within a quality control or manufacturing environment Good understanding of GMP standards and quality procedures Strong attention to detail and organisational skills Good verbal and written communication skills Confident using computer systems and databases Ability to work independently and as part of a team Good numeracy and record-keeping skills Ability to prioritise workload and meet deadlines Qualifications & Experience Good general education including GCSE Maths and English (or equivalent) Previous experience within a quality or manufacturing role Keywords: QC Technician, Quality Control Technician, Quality Technician, QA Technician, GMP, Manufacturing Quality, Laboratory Technician, Quality Inspector, Production Quality Control, Medical Devices, Quality Assurance Support. Winsearch acts as an employment agency for permanent staff. We recruit for roles based in Engineering & Manufacturing, Food & Drinks, Pharmaceutical, Supply Chain & Procurement and Professional Services. View our latest jobs today on our website (url removed) and follow us on LinkedIn. Our clients and their customers come from diverse backgrounds and so do we. We hire our people from various walks of life, each of whom make our company stronger with their talent, uniqueness, and expertise. This is what makes our company special; if you want to help us grow and take this ethos to our clients, then we cannot wait to collaborate with you! The UK has now left the European Union. Any EU, EEA or Swiss citizens living in the UK that wish to remain in the UK post Brexit need to apply to the EU Settlement Scheme. Although the closing date for applications was 30th Jun 2021, if you have not yet applied but believe that you would qualify under the EU Settlement Scheme, the Home Office have confirmed that they will consider late applications. For further information please see (url removed) /> Many Thanks

QC Technician (Nights) Birkenhead, Wirral £32,990+ excellent benefits incl Bonus Hours - 10:00pm - 8:00am Monday to Thursday only A brand-new opportunity for 1 additional experienced QC Technician working on a Night shift rota to join a well-established, growing manufacturing business on the Wirral. With strong plans for 2026, this is a great time to join a respected company with long-term stability. The role includes: Incoming goods and finished product QC • Chemical analysis of raw materials and concentrates • Completing batch records and QC documentation • Identifying and reporting quality issues • Calibration and monitoring of lab equipment About you: Previous QC laboratory experience • Educated to HNC level minimum in a Chemistry related subject would be preferred however candidates with relevant QC testing experience in a manufacturing laboratory setting will also be considered • Ideally familiar with raw materials, packaging and blend testing • Detail-focused, organised and quality-driven • Experience in viscometry, density meter testing and GC would be advantageous however training will be provided What's on offer: Competitive salary, generous holiday allowance, bonus scheme, pension, healthcare benefits and free parking. Apply now to find out more. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us

QC Technician (Nights) – Temporary (Up to 16 Months) | Monday–Thursday, 10:00pm–8:00am | Salary: £32,990 Ready to join a forward-thinking manufacturing business that’s growing rapidly and investing heavily in its future? At Hydrokem Aerosols, we’re looking for a QC Technician to join our night shift team on a temporary basis (up to 16 months). This is a great opportunity to play a key role in ensuring product quality and compliance within a fast-paced production environment—while enjoying a long weekend every week. The QC Technician Role Working within the Quality Control function, you’ll be responsible for ensuring all raw materials and finished products meet required standards through inspection, testing, and accurate documentation. What You’ll Be Doing Conducting incoming goods quality inspections Performing finished product quality control checks Carrying out chemical analysis of raw materials and product concentrates Ensuring all quality documentation (including Batch Manufacturing Records) is completed accurately and on time Reporting quality issues to Production and Quality Assurance teams Managing the segregation of non-conforming items and supporting corrective actions Calibrating, verifying, and monitoring laboratory measuring equipment What We’re Looking For Previous experience in a QC laboratory within a manufacturing environment Knowledge of testing packaging, components, raw materials, and blend analysis Experience with in-line sampling of finished products Familiarity with producing Certificates of Analysis and Certificates of Conformance A meticulous, highly organised approach with strong attention to detail What’s in It for You? 25 days holiday (pro rata) + Christmas shutdown Holiday purchase scheme Company bonus scheme Pension Sick pay (after qualifying period) Simplyhealth cash plan Accident insurance & life assurance Bike2Work scheme Free weekly fruit Free onsite parking £1,000 employee referral bonus Working Pattern Night shifts: Monday to Thursday, 10:00pm – 8:00am Enjoy a three-day weekend every week Apply Now If you’re a detail-driven QC professional looking for your next opportunity in a supportive and growing business, we’d love to hear from you. APPLY NOW for immediate consideration

If so, perhaps working as an Apprentice Laboratory Technician for our Surfacing business is your career call. Achieving a Modern Apprenticeship in Technical Laboratory Skills. As an Apprentice Laboratory Technician:.

Customers: Pharmaceutical & Cosmetic, Food & Beverage, Water & Environmental and Contract Laboratory Testing sectors. The role is primarily field-based for visiting customers, generating sales leads, attending promotional events, exhibitions, and technical conferences and continuously exploring micr

Supply Chain Assurance Specialist with proven expertise in Public Procurement and Supplier Assurance.This is an exceptional opportunity to join the global authority in.National Timing Centre (NTC) programme.Coordinate and deliver supply chain assurance activity across relevant suppliers, pr

Production Shift Laboratory Technicians - Hampshire, UK – Healthcare. This is a varied, hands-on role combining laboratory, production, and quality responsibilities. Assist with calibration, preventative maintenance, and upkeep of laboratory equipment.

More recently, the laboratory became one of the founding businesses within a wider specialist laboratory group, creating an exciting new chapter of investment, collaboration and shared expertise. Reporting directly to the COO, you will hold full site leadership responsibility for this Dover-based la

Element has an excellent opportunity for a Laboratory Technician in our busy Preparation Laboratory based in Deeside. Working in the laboratory assisting in the preparation of soil/water samples. Reporting of results using LIMS (Laboratory Information Management System).

Strong organizational skills, with the ability to manage time effectively and support multiple aspects of laboratory and project activity. Knowledge of supporting laboratory operations, including inventory management, ordering, and health and safety documentation. This role offers the chance to gain

National Physical Laboratory is seeking a Quantum Measurement Programme Manager to lead high-impact initiatives within the UK's quantum portfolio.

Experience of managing, working in a supervisory capacity or in an organising role in a laboratory or research facility is desirable, as well as close familiarity with laboratory chemical safety hazards and controls. Molecular-Beam Epitaxy (MBE) Laboratory Manager. In addition, they will manage and

The successful candidate will be taught to identify asbestos in building material samples within our busy UKAS accredited laboratory. The role also requires commitment to study and laboratory skill development to pass written and practical exams. A laboratory or scientific background and microscope