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Job Title: R&D Scientist Location: Slough, UK (Onsite) Duration: 12 months contract Job Description • Ambr250, • Degree: BSc or MSc, • Field: Life science, Biotechnology, Biochemistry, Molecular Biology, • Adhere to EHS policy, LSO profile and other site guidance to be an employee, • Recording data in electronic notebook, • Write study plan and execute experiments, • Buffer and medium preparation, filteration and storage, • Perform and develop non standard assay and procedure for project work, • CHO cell culture in deep well plate, shake flask, roller bottles, ambr250 vessel, bioreactor up to 5 liters, • Daily monitoring of culture station for cell growth , viability, metabolites and various process parameters, • Work as part of a team, • Completing housekeeping activities to maintain workplace standards., • Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind., • Lab chores as assigned

Job Title: R&D Scientist Location: Slough, UK (Onsite) Duration: 12 months contract Job Description • Ambr250 operator, • Degree: BSc or MSc, • Field: Life science, Biotechnology, Biochemistry, Molecular Biology, • Adhere to EHS policy, LSO profile and other site guidance to be an employee, • Recording data in electronic notebook, • Write study plan and execute experiments, • Buffer and medium preparation, filteration and storage, • Perform and develop non standard assay and procedure for project work, • CHO cell culture in deep well plate, shake flask, roller bottles, ambr250 vessel, bioreactor up to 5 liters, • Daily monitoring of culture station for cell growth , viability, metabolites and various process parameters, • Work as part of a team, • Completing housekeeping activities to maintain workplace standards., • Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind., • Lab chores as assigned

Title: Senior Administrative Assistant Location: Maidenhead | Hybrid (3 days on site) Length: 19/05/2026 - 18/11/2026 (6 months possibility to extend) Hour Rate: £15.38 PAYE + Holiday Pay Our client is looking for an Administrative Professional to support a busy Commercial Operations function within a globally recognised organisation within the biotechnology and healthcare sector. Responsibilites • Provide day-to-day administrative and PA support to senior leadership, including diary management and meeting coordination, • Organise internal and external meetings, including agendas, logistics, catering, venues, transportation, and action tracking, • Support leadership team meetings and wider business alignment meetings, • Process expenses through Concur, • Create and manage purchase orders through SAP, including goods receipting and invoice schedule tracking, • Coordinate contracts and agreements using systems including DocuSign and internal contract management tools, • Assist with the creation, formatting, and management of presentations, contracts, tender submissions, and other commercial documentation, • Maintain team distribution lists, organisational charts, calendars, and internal communication channels, • Manage and update Microsoft Teams channels, permissions, notifications, and shared documents, • Support mandatory training reporting and follow up with teams on completion deadlines, • Organise conferences and HCP meetings, including bookings, logistics, and promotional materials, • Prepare and quality-check compliance documentation for approval and archiving processes, • Support HCP and HCO disclosure reporting and data collection activities, • Arrange both domestic and international travel, accommodation, transfers, and itineraries Qualifications • Previous experience in an Administrative Assistant, PA, Executive Assistant, or Office Support role, • Strong diary management and meeting coordination experience, • Experience managing purchase orders and administrative processes, • Confident using Microsoft Office applications including PowerPoint, Outlook, Excel, and Teams, • Strong organisational skills with the ability to multitask and prioritise effectively, • Excellent written and verbal communication skills, • Comfortable working across multiple teams and stakeholders, • High attention to detail and ability to manage sensitive documentation, • Team-oriented with strong interpersonal and relationship-building skills, • Experience with systems such as SAP, Concur, DocuSign, or similar is beneficial This role is ideal for someone with strong PA, office support, and coordination experience who enjoys managing multiple priorities and keeping teams organised and running efficiently. If this sounds like you, please apply!

Our client, a global biotechnology company that researches, develops, manufactures, and markets biotherapies and vaccines to treat serious medical conditions are looking for a Trade Compliance Specialist EMEA to join their team and offices in the Maidenhead, Berkshire area. Main Purpose of the Role: As the Trade Compliance Specialist EMEA within Global Trade Compliance Team, you will play a pivotal role in driving the execution and continuous enhancement of the companies world-class import and export compliance program across the EMEA region. On Offer: • Two specialist roles offering real ownership: one focused on Export Control, one focused on Customs Compliance & Classification, • Standalone positions with direct visibility and influence, reporting straight to the Head of Department, • Hybrid balance with structure: work 3 days per week on‑site in Maidenhead, with flexibility as long as one day is a Monday or Friday, • Strong salary potential: £50K–£70K DOE, with the upper range reserved for high‑calibre specialists, • Immediate start for candidates ready to step into a pivotal compliance function, • Opportunity to shape processes in a growing, compliance‑focused environment Duties and Responsibilities of the Trade Compliance Specialist: • Implementing company Global Trade Compliance policies, guidelines, develop and deploy regional and local procedures., • Overseeing day-to-day EMEA import and export operations to ensure compliance with customs regulations, export controls, free trade agreements, and pharmaceutical-specific government requirements., • Monitoring regional key industry developments, legislative and regulatory changes affecting company businesses, assessing impact, and translate into processes and controls., • Developing and managing import/export data, duty spend and savings metric monthly reports., • Managing customs brokers and other outsourcing vendors in the region, including KPIs, broker SOPs, adherence to contract obligations, performance, reporting of export and import data as per company requirements, POAs., • Leading transition and implementation to new selected brokers., • Supporting origin and preference determination, including LTSD process, customs value, duties and VAT for imports and duty program utilization as per company Policies., • Support non-commercial shipments import and export process, including HS classification, customs valuations determination and license/permit determination/application/application etc., • Supporting government audits and Customs certifications, Internal Corporate audits., • Identifying duty and VAT cross-border mitigation opportunities, analysing cost benefits, and leading the implementation of duty savings initiatives., • Managing SAP GTS and master data activities including denied party screening, trade embargo blocks, and other GTS-related upgrades and projects. To Be Considered: • Bachelor’s degree required, • Experience in pharmaceutical industry or other highly regulated, multi-location environments such as Aerospace, Healthcare, FMCG, • Experience in SAP GTS System, • Proven experience in managing complex Customs and trade operations, • Experience with special Customs programs (inc. FTAs, Value Reconciliation, IPR, OPR, Tariff Suspensions, bonded Warehouse etc.), • Strong knowledge of Customs and Export controls regulations, HS and Explanatory Notes, binding rulings, and Customs Valuation rules, as well as a thorough knowledge of entry processing, international freight industry standards and practices, and INCOTERMS., • Excellent skills in organization, prioritization, and negotiation; able to perform under pressure, • Self-motivated, goal oriented, and able to work independently in delivering results, • Strong analytical skills with the ability to leverage data to drive decisions and priorities, • Excellent communication skills and able to influence and challenge senior leaders and peer groups For more details, please contact Willis Global – a leading Recruitment Consultancy for the Supply chain & Logistics industry

Job Description Check below to see if you have what is needed for this opportunity, and if so, make an application asap. Job Title: R&D Scientist Location: Slough, UK (Onsite) Duration: 12 months contract Job Description • Ambr250, • Degree: BSc or MSc, • Field: Life science, Biotechnology, Biochemistry, Molecular Biology, • Adhere to EHS policy, LSO profile and other site guidance to be an employee, • Recording data in electronic notebook, • Write study plan and execute experiments, • Buffer and medium preparation, filteration and storage, • Perform and develop non standard assay and procedure for project work, • CHO cell culture in deep well plate, shake flask, roller bottles, ambr250 vessel, bioreactor up to 5 liters, • Daily monitoring of culture station for cell growth , viability, metabolites and various process parameters, • Work as part of a team, • Completing housekeeping activities to maintain workplace standards. xrnqpay, • Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind., • Lab chores as assigned

A global biotechnology company is seeking a Trade Compliance Specialist EMEA to enhance their import/export compliance program. Responsibilities include overseeing compliance operations, managing customs brokers, and supporting audits.

Senior Clinical Research Associate (SCRA). Previous experience as a Clinical Research Associate within a CRO, pharmaceutical, or biotechnology organisation. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes

Your new company You'll be joining a global biopharma company who are expanding their research teams to focus on advancing preclinical discovery through innovative, translational in-vitro technologies, such as organoid culture. You'll work in a highly collaborative environment supporting immunology and inflammation programs across early discovery and development. Your new role As a senior scientist in the R&D team you'll be working alongside an experienced team, carrying out complex in-vitro modelling for drug discovery and development programmes. You will play a key role in developing and applying advanced translational systems to support preclinical evaluation of therapeutic candidates. This is initially a 12 month contract that has the potential to extend and is a lab based role. Key duties include: Designing, developing, and optimising organoid‑based disease models, particularly for immunology and inflammation Implementing and refining complex in vitro assays using single‑ and multi‑organ‑on‑chip platforms and related systems Carrying out a broad range of analytical assays including FACS, MSD, ELISA, and qPCR Troubleshooting technical challenges in assay performance and model development Collaborating with project and functional teams to deliver high‑quality data to timelines Authoring protocols, SOPs, and technical documentation aligned with internal standards Preparing and presenting results/data both in team meetings and for internal reports and scientific communications What you'll need to succeed You should have: An MSc / PhD (or equivalent experience) within biochemistry, biotechnology, cell / molecular biology or similar, with good hands-on experience in organoid culture and/or organ‑on‑chip model development Proven expertise with FACS, MSD, ELISA, and qPCR‑based assays A strong knowledge of multiple in-vitro techniques and assays used within drug discovery and/or development Ideally the ability to troubleshoot complex in-vitro systems Strong communication skills. as presenting results / data and liaising with a wide range of stakeholders is essential for this role Experience with advanced imaging (e.g. confocal microscopy, IHC, imaging mass cytometry) is an advantage Prior work in immunology, autoimmune or inflammatory disease models is strongly preferred ALL candidates must hold the right to work in the UK without sponsorship until at least June 2027. No sponsorship is available for this role. What you'll get in return You'll get the chance to amke a significant impact on the company's protfolio and R&D projects within drug dsicoveyr and development, as well as working in a highly collaborative atmosphere with a number of opportunities for personal & professional development. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Keywords: Organoid, In‑vitro, Scientist, R&D, Research, Pharmaceutical, Drug, Immunology, Inflammation, Preclinical, Models, Disease, Organ on a chip, OOC, Assay, FACS, ELISA, qPCR, MSD, Imaging, Confocal, IHC, Bioprinting, Cellular, Translational, Discovery, Development, Biology, Autoimmune, Analytics, Validation, Systems

Job title: R&D Scientist Location: Slough Contract Length: 12 months Working Hours: 37.5 hours/week Pay Rate: £17.96/hour About the Role We are currently looking for a Scientist to join our Bioprocess Analytics and Automation group within R&D Protein and Process Analytics. This team is responsible for delivering high-value technical innovation, both via specialist analytical projects and as part of wider collaborative project teams. As a Scientist, you will be responsible for planning and execution of scientific/ experimental work for target projects, including elements of laboratory work, scientific writing and review, testing of new technologies, method development and optimization. This position requires experience in analytical separation and characterization of biotherapeutics proteins, and with analysis of relevant protein CQAs/ PTMs, as charge/ size variant analysis, purity and glycosylation profile. Key Responsibilities: Planning and execution of scientific activities for target projects, including elements of laboratory work, scientific writing and review, testing of new technologies and method development Performing a range of analysis using purification techniques, impurity testing and others. Training will be provided to the right candidate. Analysis and interpretation of complex data and presentation to internal stakeholders Execution and reporting analytical studies, and communication with the project team Key requirements: BSc or MSc in life sciences or equivalent. Preferred area of study: Biochemistry/ Biology/ Biotechnology Previous practical industry and/or academic experience in an analytical laboratory Experience with liquid handling instruments is a bonus Knowledge and practical expertise in chromatography (RP, HILIC, SEC, IEX), capillary electrophoresis (CE-SDS, icIEF) and other relevant techniques for protein analysis Research focused, with a keen interest in innovation within the biologics area A good general background in established analytical methods in the industry, and understanding of the state-of-the-art technologies and their applications in the area of analytical characterization of biotherapeutics Good communication and interpersonal skills Proven ability to deliver innovative solutions to scientific challengesGuidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy

Our client, a global biotechnology company that researches, develops, manufactures, and markets biotherapies and vaccines to treat serious medical conditions are looking for a Trade Compliance Specialist EMEA to join their team and offices in the Maidenhead, Berkshire area. Main Purpose of the Role: As the Trade Compliance Specialist EMEA within Global Trade Compliance Team, you will play a pivotal role in driving the execution and continuous enhancement of the companies world-class import and export compliance program across the EMEA region. On Offer: * Two specialist roles offering real ownership: one focused on Export Control, one focused on Customs Compliance & Classification * Standalone positions with direct visibility and influence, reporting straight to the Head of Department * Hybrid balance with structure: work 3 days per week on‑site in Maidenhead, with flexibility as long as one day is a Monday or Friday * Strong salary potential: £50K–£70K DOE, with the upper range reserved for high‑calibre specialists * Immediate start for candidates ready to step into a pivotal compliance function * Opportunity to shape processes in a growing, compliance‑focused environment Duties and Responsibilities of the Trade Compliance Specialist: * Implementing company Global Trade Compliance policies, guidelines, develop and deploy regional and local procedures. * Overseeing day-to-day EMEA import and export operations to ensure compliance with customs regulations, export controls, free trade agreements, and pharmaceutical-specific government requirements. * Monitoring regional key industry developments, legislative and regulatory changes affecting company businesses, assessing impact, and translate into processes and controls. * Developing and managing import/export data, duty spend and savings metric monthly reports. * Managing customs brokers and other outsourcing vendors in the region, including KPIs, broker SOPs, adherence to contract obligations, performance, reporting of export and import data as per company requirements, POAs. * Leading transition and implementation to new selected brokers. * Supporting origin and preference determination, including LTSD process, customs value, duties and VAT for imports and duty program utilization as per company Policies. * Support non-commercial shipments import and export process, including HS classification, customs valuations determination and license/permit determination/application/application etc. * Supporting government audits and Customs certifications, Internal Corporate audits. * Identifying duty and VAT cross-border mitigation opportunities, analysing cost benefits, and leading the implementation of duty savings initiatives. * Managing SAP GTS and master data activities including denied party screening, trade embargo blocks, and other GTS-related upgrades and projects. To be Considered: * Bachelor’s degree required * Experience in pharmaceutical industry or other highly regulated, multi-location environments such as Aerospace, Healthcare, FMCG * Experience in SAP GTS System * Proven experience in managing complex Customs and trade operations * Experience with special Customs programs (inc. FTAs, Value Reconciliation, IPR, OPR, Tariff Suspensions, bonded Warehouse etc.) * Strong knowledge of Customs and Export controls regulations, HS and Explanatory Notes, binding rulings, and Customs Valuation rules, as well as a thorough knowledge of entry processing, international freight industry standards and practices, and INCOTERMS. * Excellent skills in organization, prioritization, and negotiation; able to perform under pressure * Self-motivated, goal oriented, and able to work independently in delivering results * Strong analytical skills with the ability to leverage data to drive decisions and priorities * Excellent communication skills and able to influence and challenge senior leaders and peer groups For more details, please contact Willis Global – a leading Recruitment Consultancy for the Supply chain & Logistics industry

Serve as a subject matter specialist on matters related to how European life sciences regulatory agencies regulate pharmaceuticals, biopharmaceuticals, biotechnology products, biosimilars, generic drugs, and nonprescription products. Advanced-level (and preferably expert-level) knowledge of European

The Biotech team supports some of the world’s leading biotechnology companies across the full spectrum of biotechnologies from diagnostics to therapeutics including platform and manufacturing technologies. Experience of and willingness to work in a broad spectrum of biotechnology work.

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally.At Getinge we exist to make life‑saving technology accessible for more people.To make a true difference for our customers – and to save more lives, we need team players, forward

An exceptional academic track record in biotechnology.

A leading biotechnology company is seeking a Field Service Engineer to support their Life Sciences service team in the South of England.

An exceptional academic track record in biotechnology.

As a Systems Project Manager, you will become an integral part of a fast‑paced and collaborative IT team.The primary focus of the role is the delivery of MLL’s CRM and ITSM platforms, including associated system migrations, while also overseeing a range of smaller internal initiatives.Responsibi

There’s never been a better time to join our award winning Programme Management Unit.Our transformation programme continues to change how we work, shaping a dynamic, adaptable and outward looking organisation that works more effectively with our partners to make a lasting difference to quality of

This is a casual, part-time role offering flexible working.As a Bank Activities Coordinator at a Barchester care home, you'll help to create a stimulating environment that enables us to deliver exceptional all-round care and support for our residents.Our ethos is all about celebrating life, so you'l

We're currently looking for individuals across the country to take part in remote paid market research, including online focus groups, product trials, and consumer studies.Earn up to £700 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing

At Barchester, we are offering a rare opportunity for an experienced IT Project Manager to join us in a new permanent position.In this role, you will be responsible for managing the full lifecycle of IT projectsensuring delivery on time, within budget, and to a high-quality standard.You will work cl

We're currently looking for individuals across the country to take part in remote paid research, including remote focus groups, product trials, and consumer studies.Earn up to £700 a week in your free time by providing feedback on everyday products and services.If you're comfortable sharing your op

This is a casual, part-time role offering flexible working.As a Bank Kitchen Assistant at a Barchester care home, you'll help to provide the first-class food and hospitality that enable us to give our residents exceptional all-round care and support.A healthy, nutritious diet is vital to ensuring ou

As a Bank Laundry Assistant at a Barchester care home, you'll help to make sure our residents receive quality care and support in the best possible surroundings.By making sure each resident has clean clothing and bedding, you'll be playing your own part in helping everyone to feel comfortable and at

We are seeking a motivated and detail-oriented Junior Research Assistant to support research projects and data collection activities.In this role, you will assist with literature reviews, data gathering, analysis, and documentation while ensuring accuracy and adherence to research protocols.This is

Senior Care Assistant (Nights) - Tarring Manor, Worthing - £14.Bedded Nursing, Dementia and Residential Care Home.Shifts include alternate weekends.At Caring Homes, we're not just about providing care; we're about creating a warm and welcoming home for our residents and our xrnqpay incredible team

Job Description Project Manager (Engineering) Near Reading We are seeking an experienced Project Manager to lead the delivery of engineering projects across their full lifecycle.This role involves managing programme timelines, resources, and budgets while ensuring technical compliance and quality

Job Description We are currently recruiting for Warehouse Operatives for one of our busy client based in Thame.Due to the nature of the business this role would be best suited to a candidate with previous warehouse experience.Candidates MUST have a experience of using an Electric Pallet Pump Truck.

Job Description An exciting new Warehouse Operative opportunity at DX! * This is a Backshift / Afternoons vacancy* About Us DX are a market leading provider of a wide range of delivery services, including parcel freight, secure, courier and logistics services.We provide a wide range of speci

Job Description We are currently looking for a Project Manager in the Beaconsfield area to join our team on a full-time, long-term basis, working closely with our installation teams and customers to deliver high-quality bathroom projects.This opportunity is with a respected and growing company with

Mechanical Project Manager Wokingham Up to £75,000 Car Allowance We are working in partnership with a leading engineering and facilities services provider to recruit a Mechanical Project Manager for a high-profile, state-of-the-art commercial site in Wokingham.This is a fantastic opportunity to jo

Senior Scientist/Engineer (Time & Frequency) Job Type: Permanent Start date: Subject to clearance Salary: £51,000-£60,000 per annum Benefits Location: Richmond Upon Thames, London Hours of work: 40 Hours Per Week / Hybrid Working 3/2 Split between Site & Working From Home The Role: As the

Reablement Care Assistant – We are recruiting across East Hertfordshire .Bishops Stortford – Havers, Birchanger, Hockerill, Thorley].Guaranteed hours available for the right candidates – giving you the security of regular work.We believe great work deserves great pay!.Reablement care is about

Fire & Security Project Manager Leicester / East Midlands £50,000 £65,000 package Pertemps is currently working with a well-established Fire & Security contractor who is looking to appoint a Fire & Security Project Manager to join their growing team.This is a key role within the busin

Mechanical Project Manager | M&E Building Services | West London.This is a fantastic opportunity for an experienced Mechanical Project Manager to join a well-established construction and building services contractor delivering a varied portfolio of projects typically ranging from £100k to £1m.

Please note that unfortunately we cannot provide sp0ns0rship*.Full UK driving license / Access to own vehicle is essential*.Are you wanting to join one of the .We pride ourselves in providing the highest level of care to our clients and ensuring each clients induvial needs our met.Here at All Care

Our client is a well funded and fast growing proteomics start up who are welcoming an exceptional Protein Biochemist to join their ambitious and energetic team.You will be working on technology that doesnt exist anywhere else and joining at a key inflection point as the business moves through develo

Female Care Assistants – Extra Care (Brighton).Full-Time hours, Part-Time hours, Guaranteed hours contract hours weekends and Nights .Female Care Assistants – Extra Care (Brighton).Patching Lodge Extra Care, BN2 0AQ.Day shifts and waking nights available.Fixed‑location care within modern Extr

Care Assistant Nights Whiteley Village, Hersham, Walton-on-Thames KT12 4ES 36hrs Permanent - Breaks are paid NIGHTS - £13.Public Transport is poor, so a driver is preferable if you are not local.SPONSORSHIP IS NOT AVAILABLE Roles available - FULL TIME NIGHTS 36hrs hour per week - £13.Breaks Pai

All Care (GB) Limited — Caring With Compassion, Every Day.At All Care (GB) Limited, we know that exceptional care is built on kindness, connection, and genuine human moments.Our carers don’t just support people — they brighten days, build trust, and help individuals live safely and independent

Our client based near Colnbrook is looking for a Temporary Warehouse Forklift Operative - Nights 7pm to 7am to join their team.Duties: Palletise goods appropriately and efficiently Ability to build and break down pallets Accurate order fulfilment and labelling Operate counterbala

Care Assistant ( Windsor and Maidenhead ).Please note that unfortunately we cannot provide sp0ns0rship*.Full UK driving license / Access to own vehicle is essential*.Are you wanting to join one of the .Windsor and Maidenhead area? If so.We pride ourselves in providing the highest level of care to o

Due to promotion of the current job holder, this worldwide market leading manufacturer of packaging machinery supplying the pharmaceutical market is looking to recruit an experienced Project Manager who is a qualified Engineer, and who has experience of a similar role working with the pharmaceutical

Flexible/Agency - offered based on your availability.Holiday pay is separate, NOT inclusive of your hourly pay.As a Senior Care Assistant, you'll work closely with Management to deliver high standards o.

Job Description Care And Support Worker - Competitive Salary - £13.Per Hour Make a real difference every day as a Care and Support Worker, supporting people in their own homes across the community.Join the Altogether Care team in Yeovil , where your compassion and reliability will be valued and sup