Trabajos pharmaceuticals en Reino Unido

Join one of London's leading M&A practices and work on some of the market's most complex and high-profile transactions. Our client's M&A team advises on sophisticated cross-border public and private M&A matters for listed companies, multinational organisations and financial sponsors across sectors including technology, financial services, fintech, pharmaceuticals, media and industrials. The firm is seeking an Associate with 2-4 years' post-qualification experience to join the London team. You will advise on complex domestic and international transactions, working closely with leading practitioners and high-profile clients. Key Requirements: • 2-4 years' relevant UK PQE., • Strong experience in public and private M&A transactions., • Proven ability to manage complex cross-border deals from inception to completion., • Experience gained at a leading corporate/M&A practice., • Commercially minded with strong client relationship skills., • Strong academic credentials and commitment to high-quality work. About you: You are proactive, collaborative and thrive in a fast-paced environment. This is an excellent opportunity to join a market-leading team known for its high-quality work, strong culture and collaborative approach. For a confidential chat about this, or other roles which we are handling, please contact Laura Klass. Please note that where a level of preferred experience or qualification is indicated, this is a guideline only and does not preclude applications from candidates with more or less experience. Our consultants will review your application and assess your suitability. We endeavour to respond to all applications within 72 hours, however due to the volume of applications we receive we may not be able to respond to every candidate individually and would advise that if you do not hear from us you should assume you are not successful in your application. Jameson Legal acts as an employment business for temporary recruitment and as an employment agency for fixed term contract and permanent recruitment.

Employment Senior Associate | Top 100 Firm, Legal 500 & Chambers ranked \n \nI am currently working with a highly regarded national law firm on an exciting Employment Senior Associate opportunity in NW London. This is a firm that has built an excellent reputation for combining high quality legal work with a genuinely supportive and collaborative culture. They offer the scale, resources and client base of a major national practice whilst maintaining a friendly, approachable environment where lawyers are trusted, valued and given the flexibility to thrive. \n \nFor employment lawyers seeking a role that offers interesting work, strong career prospects and a healthy work life balance, this is an opportunity well worth exploring. \n \nThe Firm \n \nThis is a Top 100 UK law firm with a strong reputation for both the quality of its work and the quality of its people. \n \nThe firm offers a full service legal practice with offices across England and has cultivated a culture centred on collaboration, authenticity and long term career development. Lawyers are encouraged to build lasting client relationships, develop their expertise and contribute to a supportive working environment. \n \nFlexible and hybrid working is firmly embedded within the firm's culture, with team members typically attending the Watford office two to three days per week. Individual requirements can be discussed as part of the recruitment process. \n \nThe firm is committed to fostering an inclusive workplace where individuals from all backgrounds can achieve their full potential. \n \n \nThe Opportunity \n \nAn opportunity has arisen for an experienced Employment Senior Associate to join a Legal 500 recognised employment team. \n \nThe team advises an impressive and diverse client base across sectors including manufacturing, financial services, recruitment, pharmaceuticals, energy and education. Clients range from regional businesses through to national and international organisations, ensuring a varied and engaging workload. \n \nThis position offers the opportunity to play a significant role within a close knit local team whilst also benefiting from the support, expertise and resources of a highly successful national employment practice. \n \nThe work will cover a broad range of employment matters including: \n \n• Day to day employment law advisory work \n \n• Employment contracts and workplace documentation \n \n• TUPE matters \n \n• Respondent employment tribunal litigation \n \n• Complex contentious employment issues \n \n• Exposure to a small amount of high value claimant work \n \nThe role is highly collaborative, with regular interaction across multiple offices and practice areas to deliver a seamless service to clients. \n \nThe Candidate \n \nApplications are welcomed from employment lawyers with solid post qualification experience gained within private practice. \n \nThe successful candidate will have: \n \n• Experience across both contentious and non-contentious employment matters \n \n• Strong technical employment law knowledge \n \n• Excellent client relationship and communication skills \n \n• A collaborative and team focused approach \n \n• A genuine enthusiasm for employment law and business development \n \nAdvocacy experience would be advantageous but is not essential. \n \nThe firm is open to considering candidates from a variety of backgrounds, whether currently working within a local practice, regional firm or larger national organisation. \n \n \nBenefits \n \n• 25+ days annual leave \n \n• Private healthcare \n \n• Life assurance \n \n• Bonus scheme \n \n• Health insurance \n \n• Cycle to work scheme \n \n• Season ticket loans \n \n• Referral bonus scheme \n \n• Eye care support \n \n• Additional employee discounts and benefits \n \n \nFor a confidential discussion about this Employment Senior Associate opportunity, please do reach out \n \n\n

Commercial Administrator Location: Park Royal area, North West London — Office-Based 5 days. Salary: Circa £40,000 per annum Contract: Permanent, Full Time Please kindly note this is an ON SITE role, and this is non-negotiable at this time. We will be unable to proceed with applicants who request flexibility in next stages. We appreciate your understanding! About the Company Our client is a growing healthcare organisation providing specialist pharmaceutical services to hospitals and healthcare providers across the UK. Operating within a highly regulated environment, the business plays an important role in supporting patient care through quality, safety, and reliable service delivery. As the organisation continues to grow, they are looking to strengthen their Commercial team with the addition of a dedicated Commercial Administrator. The Opportunity This is a newly created role providing dedicated administrative support to the Commercial team. Working closely with Key Account Managers and senior commercial stakeholders, you will act as a central point of coordination for commercial activity, helping to ensure customer information, contracts, documentation, reporting, and internal processes are managed accurately and efficiently. About You We are looking for a highly organised individual who enjoys working in a fast-paced environment and takes pride in delivering accurate, high-quality work. You will ideally have: • Previous experience in an administrative, commercial support, sales support, or business support role within a healthcare/pharma setting., • Salesforce.com experience is a must., • Excellent organisational skills and strong attention to detail., • The ability to prioritise workloads and manage multiple tasks simultaneously., • Strong written and verbal communication skills., • Proficiency with Microsoft Office, including Excel, Word, Outlook, and PowerPoint., • Experience maintaining records, reports, and business documentation., • A proactive and solutions-focused approach., • Confidence working independently while supporting multiple stakeholders., • Experience within healthcare, pharmaceuticals, manufacturing, or another regulated industry would be advantageous but is not essential. What’s on Offer • Salary of circa £40,000 per annum + benefits., • Opportunity to join a growing healthcare organisation., • Supportive and collaborative working environment., • Exposure to a busy, commercially focused team., • Opportunities for professional development and growth.

Engagement Manager – Commercial Due Diligence | Healthcare & Life Sciences We're working with a leading specialist strategy and due diligence consultancy focused exclusively on healthcare, life sciences, pharmaceuticals, medtech, and healthcare services. Due to continued growth and a strong pipeline of transaction activity, the firm is looking to appoint an Engagement Manager to lead commercial due diligence projects for private equity investors, venture capital funds, lenders, and corporate clients. This is an excellent opportunity for an experienced consultant looking to take on greater responsibility, manage client relationships, and lead project teams within a highly respected healthcare-focused advisory business. The role: • Leading commercial due diligence engagements from project kick-off through to final recommendations, • Managing day-to-day client interactions and acting as a trusted advisor throughout the transaction process, • Overseeing market assessments, competitor analysis, customer research, and growth opportunity evaluations, • Synthesising complex data into clear investment recommendations and executive-level presentations, • Managing and developing consultants and analysts, • Supporting business development initiatives and contributing to proposal development Ideal background: • 4–8 years' experience within strategy consulting, commercial due diligence, healthcare consulting, or a related advisory environment, • Experience leading workstreams or managing projects within transaction-focused engagements, • Strong analytical and problem-solving capabilities, • Excellent client management and stakeholder engagement skills, • Healthcare, life sciences, pharma, medtech, or healthcare services experience is highly desirable, • Advanced degree (MBA, PhD, MSc, MD, or equivalent) advantageous but not essential What's on offer: • Exposure to high-profile healthcare and life sciences transactions, • Direct interaction with private equity investors and senior industry executives, • Significant responsibility and client-facing exposure from day one, • Clear progression path towards Associate Partner and Partner, • Collaborative, intellectually rigorous, and entrepreneurial culture If you're interested in discussing this opportunity confidentially, please reach out directly.

QC Analyst – Pharmaceuticals Location: South London (Fully Site-Based) Employment Type: Full-Time About the Role: We are seeking a highly skilled and motivated Quality Control Analyst to join a pharmaceutical team in South London. This is a fully site-based role, ideal for someone with a strong background in analytical chemistry and a passion for maintaining high standards in a GMP-regulated environment. Key Responsibilities: • Perform routine and non-routine analysis of raw materials and finished pharmaceutical products using HPLC (essential), GC, UV, and FTIR techniques (preferred)., • Demonstrate advanced troubleshooting skills with HPLC systems and lead Out of Specification (OOS) investigations., • Ensure all testing is conducted in compliance with GMP standards and internal SOPs., • Accurately document results and maintain laboratory records in accordance with regulatory requirements., • Support method development and validation activities as needed., • Collaborate with cross-functional teams to resolve quality issues and improve laboratory practices. Requirements: • Proven experience in a GMP-compliant pharmaceutical QC laboratory., • Strong proficiency in HPLC is essential, including troubleshooting and OOS investigations., • Experience with GC, UV, and FTIR techniques is highly desirable., • Excellent attention to detail and ability to work independently in a fast-paced environment., • Strong communication and documentation skills. What’s on Offer: • Competitive salary and benefits package., • Opportunity to work in a dynamic and supportive team., • Career development and training opportunities. Key Words: QC, quality control, analyst, analytical scientist, chemistry, chemist, chromatography, HPLC, GC, TLC, FTIR, UV Vis, techniques, GMP, Good Manufacturing Practice, laboratory technician, pharmaceutical, healthcare, supplement, medical.

Interim Global Senior Procurement Specialist London (Hybrid) The Opportunity An exciting opportunity for an experienced procurement professional to join a rapidly growing biopharma organisation during a critical period of transformation. This is a hands-on interim role requiring someone who can quickly add value, bring structure to a fast-paced environment, and support the evolution of the procurement function. A key focus of the role will be leveraging Power BI to enhance procurement reporting, spend visibility, and business intelligence as the organisation transitions to a more data-driven approach. Key Responsibilities • Lead procurement activities across R&D, clinical development, manufacturing, and supply chain categories., • Manage sourcing, supplier negotiations, contracts, and supplier performance., • Support procurement activities relating to raw materials, clinical trial supplies, CROs, CDMOs, and specialist service providers., • Develop and maintain procurement dashboards, reporting, and spend analytics using Power BI., • Deliver cost-saving initiatives, improve supplier performance, and mitigate supply chain risks., • Support procurement governance within GMP, GDP, and GCP-regulated environments. About You • Proven procurement experience within biopharma, pharmaceuticals, biotechnology, or another highly regulated industry., • Experience sourcing raw materials, manufacturing categories, clinical services, and supplier partnerships., • Strong understanding of procurement across R&D, pre-clinical, Phase I–III clinical development, and manufacturing operations., • Advanced Power BI experience is essential., • Able to hit the ground running, manage ambiguity, and thrive in a changing environment., • Strong commercial, analytical, stakeholder management, and negotiation skills. Why Apply? • Immediate opportunity to make a visible impact., • Play a key role in procurement transformation and reporting improvement., • Work closely with senior stakeholders across a growing global organisation., • Hybrid working with flexibility and autonomy. Please contact Ethan Allen on ethan.allen@arguilesearch.com for more details

Associate Scientist – Upstream Process Development Roles: Full-time, permanent Location: Harrow, London (5 days per week on site) Salary: Competitive + bonus + benefits Candidates must have the legal right to work in the UK - we cannot offer any form of sponsorship for this role The Role: As we develop our new ‘Biopharma’ business unit at Accord, we’re seeking a proactive and methodical Research Scientist / Research Associate to join our growing Upstream Process Development team. You will support our cell culture operations (revival, subculture, cryopreservation, cell culture media preparation), optimising mammalian cell culture parameters through our Ambr250 bioreactors and other advanced process development equipment. Working across the clone lifecycle in the bioreactors, you’ll perform inoculation till harvest including daily monitoring activities and associated data analysis in-line with all quality and safety requirements. To ensure the best results, you’ll undertake regular data analysis (such as cell density, viability parameters, metabolite analysis, etc.) from advanced process development equipment and troubleshoot technical activities. To support the smooth running of the department, you will complete COSHH, risk assessment and peer review lab documentation and maintain equipment-specific SOPs. Design of Experiments will be routinely performed for process development activities, producing data summary and progress reports, along with participating in safety inspections, stock checks and maintaining our ‘state of the art’ machines. In this exciting role, you’ll get the opportunity to learn and work collaboratively with the different workstream teams (in the UK and with our colleagues abroad from our established Biopharma unit at Intas Pharmaceuticals) and to grow with the team to support our ambitious growth plans. The Person: • Experience in a similar Research Scientist / Research Associate role within the biopharma / biotech / contract research labs sector, with good technical experience in automated bioreactors for mammalian cell culture (e.g. ambr250/small scale bioreactors)., • Conduct upstream process development activities including seed train expansion, production bioreactor operations (shake flask, spinner flask, Ambr250, benchtop bioreactors)., • Prepare and document media, feeds, buffers, and supplements accurately and in a timely manner., • Monitor batch performance by regularly recording parameters (VCD, viability, metabolites, pH, DO, etc.) and responding to deviations or unexpected trends., • Set up, operate, clean, and maintain cell culture equipment including incubators, bioreactors, and analytical tools., • Able to execute cell culture activities such as media/ feed preparations, Ambr/ Bioreactor maintenance, daily monitoring independently, • Proficient in mammalian cell culture techniques (e.g., CHO, HEK) in shake flasks, Ambr250, and small-scale bioreactors., • Experience in daily monitoring and primary recovery of bioreactors., • Good knowledge of GLP and understanding of GMP requirements., • Good understanding of therapeutic antibody / protein quality attributes., • Good IT and data analysis skills, including use of Microsoft Office (i.e. Excel, Word, PowerPoint) and biopharma analysis software (e.g. Biopat process insights, MFCS, DoE software etc.), • Excellent communication skills (written and spoken English), confident working with colleagues of all seniority levels and able to navigate cultural differences with ease., • Proactive and agile team player, but equally comfortable working on own initiative., • Strong organisation skills, able to manage conflicting tasks to meet deadlines and to solve problems on your feet, even in a busy and changeable work environment., • Degree / Masters / PhD level qualification in a Biological Science or technical scientific discipline. The Rewards: In return, we offer a competitive salary package (with bonus, holiday and pension scheme), and a range of other benefits to support our team. Not to mention the opportunity to be part of a new department within a progressive and expanding business with increasing global reach, and the support of ongoing training and development. How to Apply If you possess the experience, passion and ability to make this role a success then we would like to hear from you. Please complete your Candidate Profile on our careers site to apply for this role. For more information, you can contact us on: careers@accord-healthcare.com

We are seeking a Regulatory Affairs Manager to join our global team based in Hampshire, UK. The Regulatory Affairs Manager role offers you an exciting opportunity to join our highly motivated Product Development – Injectables team, a patient-centric, fast paced environment focused on rare diseases. This position operates within Alimera Sciences Limited, a subsidiary of ANI Pharmaceuticals, with a 3 day per week in office expectation. If you are a regulatory professional with European experience who is looking to expand and grow in their career, then this could be an excellent opportunity for your development! It is a global role, with a primary focus on our international (non-US) markets, which will provide opportunity for you to expand your international and US regulatory experience across a wide breadth of projects and submissions. The successful candidate will be responsible for leading regulatory activities for international projects, providing regulatory guidance and liaising with external partners including regulatory authorities. This role is a key member of a highly visible team and provides prominent exposure across multiple business units and with leadership. As a dynamic growing company, this role values accountability, adaptability and a proactive mindset to support the company’s expansion. TASKS / RESPONSIBILITIES • End to end management of complex global projects and submissions, from developing strategies through to the filing of applications and post-approval implementation., • Oversee and support licensing partners in international regions (including Middle East, Asia, Australia)., • Responsible for a range of submissions from initial authorisation applications, variations/supplements, annual reports through to clinical trials and educational materials., • Regulatory point of contact for key projects, collaborating closely with multiple cross-functional areas including PV, Quality, Manufacturing, Supply, Medical and Marketing., • Understand, interpret and advise on regulatory legislation and guidance., • Interact with regulatory authorities to facilitate successful submissions and approvals., • Author high quality Common Technical Dossier (CTD) modules and regulatory technical documents., • Input into cross-functional submission documents, e.g. clinical protocols, PSUR, DSUR, PADER, educational materials, quality/manufacturing reports., • Management of regulatory labelling texts, including coordination of translations. PROFESSIONAL QUALIFICATIONS/EXPERIENCE • Degree in life sciences, engineering, pharmacy or higher, • Minimum of 5 years experience in European Medicinal Regulatory Affairs., • Proven ability to accurately assess regulatory impact, develop effective strategies and deliver submissions. Prior experience with European MRP/DCP is required., • Excellent written and verbal communication skills in English., • Experienced at authoring regulatory technical and submission documents., • Proven track record with navigating post-approval CMC changes, including ability to identify regulatory impact, data requirements and achieve successful filings., • Sound performer in interacting with and influencing regulatory authorities., • Prior US medicinal regulatory affairs experience and familiarity with global regulations, including US, is beneficial but not required. Knowledge of medical devices and drug-led combination products is desirable. SKILLS AND COMPETENCIES • Effective and influential communicator – you have strong verbal and written skills, able to clearly convey regulatory positions and persuade internal and external stakeholders., • Broad knowledge of European regulatory systems, including relevant current and upcoming legislation, • You can understand and interpret regulatory legislation and guidance documents., • Self-motivated, self-reliant and able to work independently in a fast-paced, deadline driven environment., • Effective networker and team worker – you are able to build effective working relationships with colleagues, external partners and regulatory authorities., • Strong analytical thinking and problem-solving skills, with a high attention to detail. Proven ability to deliver well thought-through and evaluated solutions., • Sound project management and organizational skills – you are able to effectively plan time and prioritize to achieve goals., • Flexible approach – able and eager to learn new things, think creatively and laterally, and think outside the box. Willingness to roll up your sleeves and get things done.

EHS & Sustainability Senior Specialist, 12-month contract Vertex Pharmaceuticals Type of Role: Contract position, Inside IR35 Contract length: 12 months Location: Hybrid, 3x days in Paddington, London (W2 6BD), plus international travel. Department: Environmental Health Safety & Sustainability Looking for opportunities with purpose, impact and possibilities? Our client, Vertex, is a global biotechnology company that invests in scientific innovation. As they grow their pipeline at pace, they are strengthening their reputation for creating transformative medicines for people with serious diseases. General Summary: The Environmental, Health, Safety and Sustainability (EHSS) Senior Specialist will contribute to the effective management of the environmental, health and safety (EHS) program. The role will apply technical knowledge to identify areas for improvement and implement changes in a collaborative manner. The role requires good knowledge in multiple EHS disciplines (e.g. environmental and safety permitting, chemical safety, biosafety, radiation safety and other physical agents, laboratory safety, fire safety, ergonomics, facilities safety, sustainability, auditing and inspection). Key Duties and Responsibilities: • Supports EHSS activities / programs at International HQ and International Offices., • Maintains site EHS programs including record keeping., • Develops and reviews site policies and procedures., • Conducts internal audits and inspections., • Completes and reviews risk assessments., • Ensures accident investigations are undertaken by managers, providing support where necessary and ensuring improvement strategies are recommended and actioned., • Provides EHS guidance and training to new team members., • Attends Safety Committee meetings and other cross-functional team meetings., • Manages regulatory licenses including environmental permits and regulated chemical licenses., • Supports EHS sub-team projects., • Assists with Global EHS programs and collaborations across sites., • Participates in the site emergency response teams Knowledge, Skills and Education: • Possesses expanded knowledge of federal, national and local environmental, health and safety regulations with a practical approach to implementation., • Ability to explain complex safety information clearly and concisely., • Proficient computer and documentation management skills., • Ability to solve problems and meet project goals., • EH&S experience in Pharmaceutical/Biotechnology research., • Trainings that may be required depending on the role: HAZWOPER, RCRA, DOT/IATA, • Bachelor's degree in Chemistry, Biology or Life Science related discipline., • Environmental, Health or Safety qualification e.g. NEBOSH certificate, IOSH, ASP. Vertex is partnering with Talent Works to manage their international temporary job openings. If you are successful in your application, you will be employed by Talent Works to work on a temporary assignment at Vertex.

Production Technician 📍 Wimbledon, Surrey 🕒 Monday to Friday | 6:30am – 3:00pm Are you an experienced Production professional looking for your next opportunity within a quality-focused manufacturing environment? We are recruiting for a Production Operator to join a well-established and growing business in Wimbledon. This role would suit someone with previous experience working under GMP regulations who enjoys hands-on manufacturing work and takes pride in maintaining high standards of quality and compliance. The Role As part of the production team, you will play a key role in ensuring products are manufactured safely, efficiently, and in line with company procedures and quality requirements. Key Duties • Carry out production activities in accordance with GMP and company procedures, • Operate manufacturing and processing equipment safely and effectively, • Follow detailed work instructions and standard operating procedures (SOPs), • Complete production documentation and batch records accurately, • Conduct routine weighing, mixing, packing, assembly, or processing tasks, • Maintain high standards of housekeeping, cleanliness, and workplace safety, • Support quality, compliance, and continuous improvement initiatives About You We are keen to speak with candidates who have: • Previous experience within a production, assembly or manufacturing environment, • Exposure to industries such as pharmaceuticals, food production, cosmetics, medical devices, or chemicals, • Experience operating production or packaging machinery, • A reliable and positive attitude with good team-working skills What's in It for You? • Regular day shifts with no weekend working, • Stable Monday to Friday schedule, • Full training and ongoing development support, • Friendly, collaborative working environment, • Opportunity to join a growing manufacturing business, • Long-term career prospects within a regulated production setting If you have manufacturing experience and are looking to join a company that values quality, teamwork, and continuous improvement, we'd love to hear from you. Apply now to find out more.

My client is seeking a Consultant to join their Healthcare & Life Sciences Consulting team in London. This is an opportunity to work on high-impact strategic projects across healthcare, pharmaceuticals, life sciences, medtech, and healthcare services. Their clients include investors, healthcare providers, life sciences companies, and public sector organisations. As a consultant, you will play a key role in project delivery, combining rigorous analysis with strategic thinking to help clients make informed business and investment decisions. Responsibilities • Work as an integral member of client project teams, supporting project leadership and mentoring junior colleagues., • Conduct market, company, and industry research using both primary and secondary research methodologies., • Analyse complex datasets and develop insights that inform strategic recommendations., • Build market models, forecasts, and commercial assessments., • Translate findings into clear, compelling, client-ready presentations and reports., • Take ownership of workstreams and contribute to the successful delivery of engagements., • Develop hypotheses, test assumptions, and support strategic decision-making for clients. Requirements • Minimum 3 years of professional experience, ideally within strategy consulting, healthcare consulting, life sciences consulting, or a related field, with extensive focus on commercial due dilligence., • Experience working within a leading consulting firm is advantageous., • Strong analytical and problem-solving capabilities., • Proven experience conducting market research and analysing quantitative and qualitative data., • Advanced Excel and PowerPoint skills., • Excellent written and verbal communication skills., • Demonstrated ability to manage work independently while collaborating effectively within teams., • Advanced degree in a STEM discipline preferred; MSc, PhD, MD, or equivalent qualifications are advantageous., • Strong interest in healthcare, life sciences, and the broader healthcare ecosystem. What We Offer • Competitive compensation and performance-based bonus., • Early responsibility and direct client exposure., • Fast-paced learning and professional development., • Hybrid working model with flexibility and autonomy., • Opportunity to work on a diverse range of healthcare and life sciences projects., • Collaborative, entrepreneurial, and intellectually stimulating environment. If you are passionate about healthcare and life sciences and enjoy solving complex strategic challenges, we would welcome your application.

MEP Quantity Surveyor Bath £65,000 - £85,000 + Travel Allowance + Bonus + Pension + Holidays + Private Medical Insurance + Career Progression + Immediate Start An exciting opportunity has arisen for a Quantity Surveyor to join a leading construction contractor working on large-scale projects across multiple sectors. If you're an experienced QS looking to take the next step in your career with a company that offers clear progression pathways, this role is for you! You'll be working with a company known for delivering high-quality construction solutions across various industries, including data centres, pharmaceuticals, and advanced manufacturing. This is a fantastic opportunity to work with an industry leader, delivering cutting-edge projects while advancing your career to the next level. If you're ready for the challenge, apply today! The Role As A Quantity Surveyor Will Include: • Managing commercial aspects of the project, ensuring cost efficiency and value for money., • Ensuring accurate and timely reporting of project finances., • Working closely with site teams to mitigate financial and contractual risks. As A Quantity Surveyor You Will Need: • A degree in Quantity Surveying or equivalent experience., • Strong commercial acumen with experience managing large-scale construction projects., • Background in commercial project delivery with values around £50m., • Good understanding of MEP works within the construction sector - either electrically or mechanically biased Keywords: Quantity Surveyor, Senior QS, Construction QS, MEP Quantity Surveyor, Commercial Construction, Cost Management, Procurement, Contract Negotiation, Project Cost Control, UK Construction, Hull, Yorkshire, Commercial Projects, United Kingdom, Data Centres, Warehouse, Pharmaceutical, Engineering, Construction, Bristol, London, Somerset, Somerton, Yeovil, Kent, Bath, Oxford, Reading

Project Controls Manager Soben is an award-winning construction consultancy with bold ambitions and a clear trajectory for growth. Since launching in 2011, we’ve built a reputation for technical excellence, client focus, and delivery certainty. Now, we’re entering a transformative new chapter. In March 2025, Soben became part of Accenture’s Infrastructure and Capital Projects practice, within its Industry X division. This strategic acquisition combines our deep expertise in cost and commercial management with Accenture’s global scale and digital innovation. For our team, this unlocks a wealth of opportunity: 🌐 Access to world-class resources and technology, enhancing how we deliver capital projects 🏗️ Involvement in high-profile programmes across sectors such as data centres, energy, and pharmaceuticals 📈 Career development at scale, with exposure to international clients and cutting-edge project environments 💡 A platform for innovation, as we continue to challenge traditional consultancy models and lead digital transformation About the opportunity We are looking for a Project Controls Manager to join our team. The successful candidate will provide leadership and coordinate all aspects of Project Controls including reporting, cost control, progress measurement, schedule development, and schedule control. In this role you will: • Responsible for developing and maintaining the baseline and monthly schedules, cost reports, portfolio reports, and customer reports (when applicable) for custom projects, • During Execution, produce weekly / monthly reports in line with the project reporting calendar, providing details on progress, actuals, forecast, and explanation of variances, • Motivated to support an industry-leading regional project planning team capable of managing internal/external customer projects including EPCs, within both the office and construction site environments, • Use planning IT systems and work processes to provide reliable and consistent reporting and analysis to ensure that we can meet the project, regional/global project portfolio, and business requirements, • Collaborate with the Product Line and Project Execution teams to develop and deliver competitive project schedules aligned to the execution scope and strategy during the bid phase through award and execution, promoting the growth of the client’s businesses while consistently delivering on project commitments in terms of cost and schedule, • Develop and maintain accurate progress & earned value measurement systems for engineering, procurement, manufacturing, construction, and commissioning to provide credible control throughout the project execution phase, • Help maintain and improve the capabilities of the regional team to support the business needs across the broad portfolio of offerings, • Provide close collaboration with and support across the other regional and global teams to ensure effective resource sharing, lessons learned, best practices, and the development of appropriate work processes and procedures across the global execution teams, • Lead a project controls team when assigned to a mega project, • Follows client’s established standard processes, procedures, and formats required for corporate reporting and deliverables, • Perform additional duties as assigned About you • Bachelor's degree or equivalent, • Minimum -10 years’ project planning experience, ideally with 2 years in Nuclear Decommissioning, • A recognised Degree in Quantity Surveying, Construction Management, or Engineering, • Sound knowledge, proven skills, and competencies in the application of project planning principles, methodologies, and tools, • Support all phases of project execution, particularly around schedule development, progress measurement/reporting, and earned value, within a large project-oriented EPC or Owner Organization, • Must have a track record of delivering accurate schedule information, reporting, and guidance to senior management, • Organised and detail-oriented About life at Soben We’re on a mission to rewrite the rules. We’re a diverse team of professionals who consider our work a vocation, not just a job. This sense of purpose and affinity for what we do is what fuels our ambition, driving us to keep learning and seeking new challenges. Inclusion is at the heart of our company’s culture. We’re proud of our unique personality, and we know that our diverse team brings a wealth of perspectives that enrich our work. Grow with us Our people are our greatest asset, so you’ll get ongoing training and personal development to help you flourish, building a long-term and successful career with us. We’re small but mighty – you’ll have opportunities to progress quickly and be trusted with responsibilities you could only dream of in a larger organization, including the chance to work on some of the industry's most exciting projects Our Leadership Principles Soben’s Leadership Principles are at the heart of our culture. They guide how we engage with each other and with our clients, and how we help our talented employees flourish in their careers. • We always deliver on our promises, no matter how small, • We are driven to solve our clients’ problems as if paying our rent or mortgage depends on it, • We have a bias for action. Actions make things happen, • We employ the best people who are ambitious, hardworking, humble, and open to feedback. We empower them to “proceed until apprehended”, • We have a business owner mentality to cost management, • We are open, honest, and direct in our communications, • We have a growth mindset, • We reinvest our profits to create a sustainable business for the long term About us Soben is an award-winning construction consultancy with bold ambitions and a clear trajectory for growth. Since launching in 2011, we’ve built a reputation for technical excellence, client focus, and delivery certainty. Now, we’re entering a transformative new chapter. If you’re ready to play a key role in delivering exceptional consultancy services across the EMEA region, and want to grow your career in a supportive, dynamic, and high-impact environment, we’d love to hear from you.

Overview: We are seeking a highly motivated and analytical individual to join our investment banking team in London. As an Investment Banking Associate, you will play a crucial role in assisting with financial analysis, deal execution, and client interactions within the healthcare industry. This position offers an opportunity to work closely with senior bankers, clients, and industry experts to facilitate strategic transactions and provide insightful financial solutions. Key Responsibilities: • Financial Analysis: Conduct comprehensive financial analyses, including financial modeling, valuation assessments, and financial statement analysis, to evaluate potential investment opportunities in the healthcare sector. Analyze industry trends, market dynamics, and competitive landscapes to assess the financial performance and growth prospects of healthcare companies. • Deal Execution: Support in the execution of mergers and acquisitions, capital raising, and strategic advisory transactions for healthcare clients. Assist in drafting transaction-related materials, including pitch books, offering memorandums, management presentations, and other deal documentation. Coordinate due diligence efforts, liaising with internal and external teams to ensure timely and accurate information exchange. • Client Engagement: Develop and maintain relationships with healthcare clients and other stakeholders. Assist in client meetings and presentations, helping to articulate the firm's capabilities and insights related to the healthcare industry. • Industry Research: Stay informed about industry developments, regulatory changes, and emerging trends affecting the healthcare sector. Contribute to the creation of thought leadership pieces and reports regarding healthcare market dynamics, innovations, and investment opportunities. • Team Collaboration: Collaborate with cross-functional teams, including legal, compliance, and operations, to ensure successful deal execution and adherence to regulatory requirements. Assist senior team members in various tasks and projects as needed, supporting a seamless workflow and efficient operations within the team. Qualifications: • Bachelor's degree in finance, economics, business administration, or related field; Master's degree in business administration (MBA) is a plus., • Previous experience in investment banking, finance, or healthcare industry is preferred., • Strong financial modeling and analytical skills, including proficiency in Excel and financial modeling software., • Excellent verbal and written communication skills with the ability to present complex information in a clear and concise manner., • Demonstrated ability to work in a fast-paced environment, manage multiple tasks, and meet deadlines effectively., • Passion for the healthcare industry and understanding of its dynamics, including healthcare providers, pharmaceuticals, biotechnology, medical devices, and related sectors., • Strong work ethic, attention to detail, and a proactive, team-oriented approach.

About Artemis Legal Recruitment We recruit legal professionals for leading international law firms, from associate to partner. We also specialise in niche legal operations roles. The Client A leading US law firm with a fantastic client base and a well established London office. The Competition team in London & Brussels is comprised of five partners providing advice on the full spectrum of EU and UK competition law matters, foreign direct investment controls and competition disputes. They work on complex UK merger control cases and many high-profile, cross-border deals requiring regulatory approval in Brussels and worldwide. The firm has strengths in many sectors, but specifically in pharmaceuticals, tech & retail. Qualifications • The client is seeking associates with top quality experience gained from a leading UK or Brussels based Competition team., • The client is looking for a qualified associate with between one to two years of experience.

Our client, a leading global strategy consultancy, is seeking a senior manager with pricing strategy and data analytics experience to join its highly focused Pricing team, which sits within the broader Strategy arm of their organisation. Their Strategy function team serves a number of sectors including retail, consumer goods, healthcare, pharmaceuticals, transport and industrial manufacturing sectors serving UK, European and international clients. They work with C-level executives to identify, structure and solve their most critical strategic issues related to deal strategy, and growth strategy. Their Pricing team focuses on solving pricing and revenue optimisation problems for its clients using data and analytics techniques to deliver a sustainable solution which can deliver both short- and long-term margin improvements. As a team, they are a group of bright committed individuals who are passionate about delivering fantastic client work, solving complex data related problems, investing their time in acquiring new analytical skills, and having fun both inside and outside of work. Experience and responsibilities: • Lead teams, lead multi-disciplinary and complex projects under difficult circumstances and has delivered substantive, measurable operational improvements in complex businesses., • Able to operate across the full value chain of the sale - identify opportunity, shape it with client, develop proposal, commercials, scope etc and then close the deal., • Able to work alongside a client counterpart to scope, plan, mobilise and manage the progress of a project., • Capable of holding ultimate responsibility for the final output of a complex and multi-disciplinary project, including budgets, risk files and other relevant documentation., • Build strong, trusted adviser relationships with senior management and mid-level executives., • Supported / been involved in client pitches, bid managing sales efforts, having initial conversations with prospects (potentially supported by partners and directors) to shape ideas and opportunities., • Ability to review and assess large volumes of technical data and distil the key strategic insights., • Ability to evaluate complex challenges and deliver insightful recommendations that can be practically executed., • Strong numerical capabilities combined with sound commercial acumen., • Able to provide constructive and robust challenge to the work of colleagues to ensure the highest delivery standards., • Sound understanding of risk management in professional services environment., • Strong interpersonal/social /coaching skills and team-players, right cultural fit and attitude, highly motivated. Qualifications: • Experience of pricing strategy consulting, ideally from either a boutique pricing strategy consulting firm, or experience in the pricing department in a corporate environment., • Ideally some experience in deal environment in pre or post deal margin improvement work., • Track record of working closely with large corporate clients and/or private equity to deliver high impact recommendations., • Detailed understanding of the pricing commercial knowledge across industries to need to make a real impact with our clients, and you can build the networks to make the role a success., • Considerable experience of leading and managing complex projects., • Experience of managing or supporting high value business development activities with senior stakeholders., • Extensive consulting experience including sales and business development skills., • Evidence of strong problem-solving and analytical capabilities., • Has had good exposure to managing senior / board room clients – able to manage and secure buy-in from senior stakeholders during the project., • Ability to work with other teams within a business to identify the most suitable combination of skills to deliver high impact for clients., • Excellent English written and oral communication skills., • A first class or 2.1 degree in quantitative/analytical studies such as economics, maths, statistics, engineering or equivalent experience. Successful applicants will be contacted within 24 hours to discuss futher. Cambridge Credentials adding people....adding value

Part Qualified Patent Attorney – Biotechnology London | Hybrid Working | Market-Leading Salary & Benefits Our client is one of the UK's premier intellectual property firms, recognised for advising some of the world's most innovative companies, research institutions and emerging life sciences businesses. Renowned for its outstanding training, collaborative culture and long-term career development, the firm offers exposure to a truly international client base and some of the highest quality work available in the market. Due to continued growth, an opportunity has arisen for a Part Qualified Biotechnology Patent Attorney to join its highly regarded Life Sciences team. Working alongside leading practitioners in the field, you will advise clients across a broad range of cutting-edge technologies, including biotechnology, pharmaceuticals, biologics, cell and gene therapies, diagnostics and medical innovations. This is an ideal opportunity for someone looking to accelerate their career within a firm that offers genuine progression and a market-leading remuneration package. Key Responsibilities • Drafting and prosecuting UK, European and international patent applications., • Advising clients on patentability, freedom to operate and infringement matters., • Managing a diverse portfolio of biotechnology and life sciences clients., • Assisting with EPO opposition and appeal proceedings., • Working closely with overseas associates on international filing strategies., • Building and developing strong client relationships through direct contact., • Supporting business development and contributing to the continued growth of the practice. Requirements • Part Qualified Patent Attorney working towards UK and European qualification., • Academic background in Biotechnology, Molecular Biology, Genetics, Biochemistry or a related Life Sciences discipline (PhD highly advantageous)., • Previous experience within private practice or an in-house patent environment., • Excellent written and verbal communication skills., • Strong commercial awareness and an interest in developing client relationships., • Ability to manage a varied workload and thrive in a collaborative team environment. What's on Offer • Market-leading salary package., • Industry-leading bonus and benefits scheme., • Hybrid and flexible working arrangements., • High-quality international client base., • Exposure to complex and commercially significant life sciences work., • Outstanding training and mentoring from leading practitioners., • Clear and transparent career progression pathway., • Supportive, collaborative culture with an excellent work/life balance. This is a rare opportunity to join one of the market's leading Life Sciences patent teams, offering the chance to work on cutting-edge technologies while building a long-term career within a firm that genuinely invests in its people.

Senior Technical Manager – Data Centre / Mission Critical Services - OTE £100,000 ++ c£85,000/£90,000 + Car or Allowance + Bonus upto 20% + Mgmt Benefits. Overview A leading global provider of integrated facilities and corporate real estate management is actively recruiting for multiple critical roles: Senior Technical Manager to join their Data Centre Operations and Critical Engineering division. These are exceptional opportunities for experienced professionals who bring deep technical expertise, a proactive mindset, and a passion for operational excellence in mission-critical environments. The Role The successful candidates will demonstrate strong technical leadership with a risk-based approach to operations. Both roles are central to the management and delivery of technical excellence across a campus portfolio of data centres and critical environments. Working closely with the technical team and reporting to senior leadership, you will be a key point of contact for technical queries, compliance, and high-performance service delivery. Your focus will be on maintaining robust technical standards while ensuring the safety, reliability, and integrity of the site's critical infrastructure. Core Responsibilities • Lead technical operations to ensure optimal performance and compliance across all critical services., • Act as a technical authority for permits, risk assessments, and method statements., • Ensure all personnel under your direction operate safely, professionally, and in line with industry best practices., • Conduct investigations and produce reports for any incidents, breaches, or safety concerns., • Lead or attend client meetings as the technical representative., • Oversee and support the training and development of engineering staff, ensuring competency in all aspects of critical systems., • Approve and maintain high standards of technical documentation, including safety programs, switching schedules, SOPs, MOPs, and EOPs., • Manage and review site-specific technical training programs., • Take part in succession planning through mentoring and upskilling of junior engineers., • Act as a Senior Authorised Person (or work towards this designation) for HV/LV systems and confined spaces., • Support audit readiness and compliance across critical systems., • Provide guidance on technical improvements and drive innovation in operational delivery., • Escalate urgent issues and provide technical solutions swiftly and effectively. What We’re Looking For • Experience in mission-critical environments such as data centres, power generation, pharmaceutical, manufacturing, nuclear, or military engineering., • Ideally electrically biased with a broad understanding of mechanical, air conditioning, and building services systems., • Strong leadership capabilities with the ability to manage teams and influence across multiple levels., • Familiarity with compliance and health & safety frameworks in critical environments., • Experience with technical reporting, process creation, and training management., • Able to lead and embed a culture of safety, excellence, and continuous improvement., • Technically confident with a solution-oriented mindset and a focus on risk mitigation. Why Join? • Be part of a globally respected organisation delivering cutting-edge solutions in the data centre sector., • Work within a supportive, forward-thinking technical leadership team., • Play a key role in shaping the future of critical infrastructure operations., • Benefit from a competitive package, ongoing training, and long-term career opportunities in a growing industry. Ideal for ex-forces or professionals from high-reliability industries such as pharmaceuticals, nuclear, manufacturing, or power generation.

Job Title: Head of Architecture Location: Watford Salary: £65,000 Job Type: Permanent, Full-Time Job Ref: 40764 About Them? I am working with a well-established multidisciplinary consultancy specialising in the design and delivery of complex scientific, research, and advanced manufacturing facilities. Working across sectors including pharmaceuticals, biotechnology, higher education, and industry, they provide integrated design, project management, and construction management services. Their collaborative approach enables them to deliver innovative, tailored solutions for technically demanding projects. About You? The ideal candidate will be an experienced architect with over 10 years industry experience, with a proven track record of heading up a busy architectural team. This position is a client facing role, where applicants should be confident in early stage conversations around complex build projects. In this role, you will provide leadership across the architectural function while working closely with senior stakeholders. The ideal candidate will also have the potential to support the wider engineering leadership team and collaborate with the Head of Engineering, combining strong technical expertise with leadership and commercial awareness. If you're ready for a change then please do get in touch. Molly.McGuire@mustardjobs.co.uk About Us? At mustard, we don’t just recruit we connect people with careers that matter. As a certified B Corp, we’re committed to doing business the right way: balancing profit with purpose, and always putting people and the planet first. That means treating candidates with respect, being upfront about roles, and never wasting your time. With deep roots in the design sectors, we know what makes an agency tick and more importantly, what makes a role right for you. You’ll get honest advice, behind the scenes insight, and full support throughout the process. No fluff. No false promises. Just solid recruitment with a conscience.

Mechanical Design Engineer Slough Up to £50,000 DOEA leading engineering and technology organisation is seeking a Mechanical Design Engineer to join its multidisciplinary team based in Slough. This is an exciting opportunity to work on innovative, environmentally focused solutions used across a wide range of global industries.The Company Our client is an established and internationally recognised organisation specialising in advanced sustainable technologies. With decades of innovation behind them, they develop cutting-edge solutions used in sectors such as food & beverage, pharmaceuticals, electronics, and water treatment.They offer a collaborative, forward-thinking environment where individuals are encouraged to contribute ideas, take ownership, and develop their careers within a growing global group.----------------------------------------The Role As a Mechanical Design Engineer, you will take ownership of product design from concept through to production. Youll translate customer requirements into practical, manufacturable solutions and ensure products perform reliably in real-world environments.Key Responsibilities Deliver mechanical design solutions for customer-focused projectsDevelop robust designs from concept through to productionProduce and maintain 2D/3D CAD drawings (Inventor or similar)Apply best practice engineering standards across the product lifecycleValidate designs through analysis, prototyping, and testingDesign for manufacture, assembly, and cost efficiencyDrive modularisation and standardisation initiativesManage and maintain accurate product data within ERP systemsTroubleshoot issues, identify root causes, and implement solutionsCollaborate with operations to ensure right-first-time manufacturingInterpret and challenge customer specifications where appropriate----------------------------------------About You Degree (or equivalent experience) in a relevant STEM disciplineProven experience in mechanical design from concept to productionStrong 3D CAD skills and technical drawing capabilitySolid understanding of GD&T and engineering drawing standardsExperience with design for manufacture and material selectionAnalytical, hands-on problem solver with a proactive mindset----------------------------------------Whats on Offer Opportunity to work on innovative, sustainable technologiesCollaborative and supportive team environmentClear development and progression pathwaysExposure to global projects and leading industry clientsApply now or reach out to Ellie at Orion Electrotech for further detailsINDKATPBN1_UKTJ

You will support the Quality function in maintaining and improving the Quality Management System (QMS), ensuring ongoing compliance with GDP standards, ISO requirements, and client expectations. This is a key role focused on driving quality administration efficiency, supporting audits, and promoting a strong compliance culture across internal teams and suppliers.Location: East Midlands (occasional travel to Birmingham)Working Hours: 40 hours per week, Monday to FridayThe RoleYou will support the Quality function in maintaining and improving the Quality Management System (QMS), ensuring ongoing compliance with GDP standards, ISO requirements, and client expectations. This is a key role focused on driving quality administration efficiency, supporting audits, and promoting a strong compliance culture across internal teams and suppliers.Key ResponsibilitiesProvide QA support to internal departments to ensure activities are carried out in line with GDP standards and company proceduresOffer guidance and advice to operational teams to support compliance and best practiceManage and maintain change controls, deviations, and CAPA records, ensuring timely completion and effectivenessSupport the scheduling and coordination of supplier audits, internal audits, and annual reviewsCollate and analyse data for reports, investigations, KPIs, and quality metricsAssist in the self-inspection audit programme and support QA management activitiesPrepare documentation and support client audits and regulatory inspections, ensuring audit readinessSupport supplier management activities, including verification, audit actions, and performance monitoringContribute to the ongoing development and compliance of the QMS in line with GDP, ISO 9001, and ISO 13485Build strong working relationships with internal and external stakeholders to support QMS activities and compliance initiativesSupport client onboarding processes, including validation, SAP testing, and process walkthroughsAssist with global quality reporting, including KPI submission to the wider QA functionSupport product quality, complaints, and investigation processesReview inbound documentation, returns paperwork, and temperature monitoring data, ensuring compliance with ALCOA principles and archiving standardsAbout YouYou will be highly organised, detail-oriented, and comfortable managing a varied workload. Strong communication skills are essential, along with the ability to build relationships across different levels of the business.You will ideally have experience in:Quality administration, including document control, mailbox management, and audit schedulingSupporting QMS activities such as investigations, CAPAs, change controls, and audit readinessWorking with GDP standards, ISO 9001, and ISO 13485 (or similar regulated environments)Using systems such as SAP, electronic QMS platforms, and temperature monitoring toolsMicrosoft Office applications (Excel, Word, Visio, etc.)Previous experience in healthcare, pharmaceuticals, or medical devices is advantageous but not essential.What's on Offer25 days annual leave plus 8 bank holidays, with the option to purchase up to 5 additional daysPension schemeLife assurance (4x salary)Employee Assistance ProgrammeEmployee discount schemeRobert Walters Operations Limited is an employment business and employment agency and welcomes applications from all candidatesTPBN1_UKTJ

Executive Associate / Learning & Development Project Associate\nLondon | Hybrid Working\nAre you a highly organised, commercially aware professional who thrives in a fast-paced environment supporting senior leadership and delivering exceptional client experiences?\nWe are seeking an ambitious Executive Associate / Learning & Development Project Associate to join a growing, entrepreneurial business that works with global clients across leadership development, coaching, consulting and learning programmes.\nThis is not a traditional Executive Assistant role. It offers a unique blend of executive support, project coordination, client relationship management, learning and development administration, and business operations.\nWorking closely with the Managing Director, you will become a trusted extension of the leadership team, helping to deliver a premium service to clients while ensuring the smooth running of key business operations.\nThe Opportunity\nThis is an exciting role for someone who enjoys variety, responsibility and autonomy. You will be involved in everything from coordinating global workshops and managing client projects to supporting executive-level stakeholders and driving operational excellence.\nThe successful candidate will thrive in a high-performance culture where accountability, initiative and results matter more than hours worked.\nKey Responsibilities\n Providing executive support, diary management and stakeholder coordination for the Managing Director.\n Coordinating training programmes, coaching engagements and consulting projects.\n Managing workshop, conference and virtual event logistics.\n Acting as a key point of contact for clients, consultants and external partners.\n Preparing contracts, proposals, reports and client documentation.\n Managing invoicing, reporting and business administration activities.\n Supporting property and operational administration where required.\n Ensuring exceptional client service and maintaining high standards across all deliverables.\nAbout You\nYou will be a proactive and highly capable professional who enjoys taking ownership and building trusted relationships with senior stakeholders.\nIdeal Background\nWe are particularly interested in candidates from:\n Professional Services\n Legal Services\n Financial Services\n Investment Banking\n Insurance\n Technology or SaaS\n FinTech\n Pharmaceuticals\n Management Consultancy\n Executive Search\n Corporate Learning & Development\nPersonal Attributes\nThe successful candidate will demonstrate:\n Executive presence and professionalism.\n Intellectual curiosity and the ability to learn quickly.\n A growth mindset and willingness to take on new challenges.\n Exceptional organisation and prioritisation skills.\n Strong relationship-building capabilities.\n Resilience and adaptability in a dynamic environment.\n A proactive approach to problem solving.\n Commercial awareness and understanding of client service excellence.\n Ownership, accountability and a commitment to follow-through.\nWhy Join?\nThis is an opportunity to join a growing business where your contribution will have genuine impact. You will work closely with senior leadership, engage with international clients and consultants, and play a key role in supporting the continued growth and success of the organisation.\nIf you are an intelligent, driven and highly organised professional looking for a role that offers variety, responsibility and long-term development, we would love to hear from you

Senior QA Officer\n\nWe are exclusively supporting one of our longest standing clients in a significant expansion through the course of 2026.\n\nAs part of this, they are appointing a new position of Senior Quality Assurance Officer within their operational quality team on site in South London.\n\nThis person will strike the balance in hands on quality activities, as well as performing a deputy in absence of the Team Leader. As well as the usual operational quality activities such as batch release, deviation management and change control implementation, this person will need to take a lead on process ownership of investigation management and risk assessments.\n\nIf you enjoy working in a flat structured team, with broad responsibilities and a genuine opportunity for development, this could be the ideal career move.\n\nThis is a fully site based role in South London.\n\nFor further details, please contact Mark Bux-Ryan.\n\nWhat you need to bring:\n\n Established QA experience within a GMP setting – ideally pharmaceuticals, although food manufacturing will be considered.\n\n Evidenced experienced of independent process ownership within QA activities – ideally investigation and risk assessment management\n\n Excellent stakeholder management skills\n\n Flexible and adaptable approach\n\nQuality, QA, officer, investigation, risk, deviation, management, CAPA, change, control, batch, review, release, GMP, manufacturing, food, supplement, pharmaceutical, nutraceutical, SOP, senior, specialist, system, operation

Job Title: Sustainability Lead\n\nLocation: Hayes, London\n\nSalary: £50,000 – £65,000 + 10% Car Allowance + Package\n\nWorking Pattern: Full-Time, Site Based\n\nAbout the Company\n\nTSL Projects is a leading engineering and construction contractor delivering complex projects across Data Centres, Advanced Manufacturing, Pharmaceuticals, Logistics and Food Production sectors throughout the UK and Europe.\n\nDue to continued growth, we are seeking an experienced Sustainability Lead to join a major advanced manufacturing project in Hayes. This is an opportunity to take ownership of sustainability delivery on a highprofile construction programme, supporting project teams to achieve ambitious environmental, carbon and certification objectives.\n\nThe Role\n\nAs Sustainability Lead, you will act as the project's sustainability subject matter expert, providing technical guidance and leadership throughout the project lifecycle.\n\nWorking closely with operational teams, clients, consultants and subcontractors, you will lead sustainability initiatives, manage certification requirements and ensure compliance with project sustainability commitments.\n\nThe successful candidate will be a visible presence on site, supporting project delivery teams and driving best practice across all sustainability and environmental activities. Sustainability Leads typically oversee sustainability strategies, certification processes, site assessments and carbon reduction initiatives throughout construction projects.\n\nSustainability Lead - Key Responsibilities\n\n Lead sustainability delivery across a major construction project.\n\n Manage BREEAM certification requirements from design through to project completion.\n\n Maintain sustainability trackers, evidence registers and compliance documentation.\n\n Undertake site sustainability inspections and audits.\n\n Support project teams in achieving environmental and sustainability objectives.\n\nRequirements\n\n Degree qualified in Sustainability, Environmental Management, ESG, Construction or a related discipline.\n\n Minimum 3 years' experience within a sustainability role in construction or the built environment.\n\n Demonstrable BREEAM delivery experience (essential).\n\n Experience managing sustainability compliance and certification requirements.\n\n Full UK driving licence.\n\n Ability to work full-time on site.\n\nDesirable\n\n BREEAM AP qualification.\n\n LEED AP accreditation.\n\n OneClick LCA experience.\n\n PAS 2080 experience.\n\n ISO 14001 Internal Auditor qualifications\n\nWhat's on Offer\n\n £50,000 – £65,000 salary.\n\n 10% car allowance.\n\n Comprehensive benefits package.\n\n Long-term career progression opportunities.\n\n Exposure to major industrial and advanced manufacturing projects.\n\n Opportunity to play a key role in delivering sustainability objectives on complex construction programmes.\n\nApply:\n\nIf you have strong contractor-side sustainability experience, proven BREEAM delivery capability and are looking to progress your career with a leading international contractor. We welcome you to apply

Customer Success Manager - ERP Software - Remote / Midlands(ERP, Customer Success, Account Management, Software, Remote) - Build meaningful client relationships with a fast-growing ERP software company! A Customer Success Manager(ERP, Customer Success, Account Management, Software, Remote) is required by a leading ERP software provider with a 29-year track record of delivering cutting-edge solutions to merchants, wholesalers, distributors, and retailers. Their modern cloud-based ERP suite is trusted across sectors such as food & drink, builders' merchants, and pharmaceuticals. With a high-performing technical team and regular software updates every two weeks, they are revolutionising how businesses manage operations. You will need: Experience in customer-facing account management, customer success, or client service roles. Strong empathy and top-tier communication skills. Background managing or supporting smaller commercial accounts. Exposure to software or tech-enabled services is an advantage. Midlands-based and happy to travel to Southampton once a month. Join a business that values personal development and empathy. You'll work remotely, supported by a collaborative and knowledgeable team. You'll have exposure to a rapidly evolving ERP product and a clear path for progression into senior customer success or account management roles. Day to day, you'll: Collaborate with a close-knit team to support and retain smaller commercial clients. Speak to customers daily, understanding challenges and resolving them with internal support. Deliver exceptional service, focusing on satisfaction over sales. Strengthen long-term client relationships, driving engagement and loyalty. Why Apply? 100% remote with only monthly travel to Southampton Emphasis on empathy, service, and long-term client value Modern, agile ERP product with bi-weekly feature releases Clear progression opportunities into senior roles Supportive, expert team culture please apply!

About Avery Dennison Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We are Making Possible™ products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, advance sustainability, circularity and transparency, and better connect brands and consumers. We design and develop labeling and functional materials, radio-frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information that improves the customer experience. Serving industries worldwide — including home and personal care, apparel, general retail, e-commerce, logistics, food and grocery, pharmaceuticals and automotive — we employ approximately 35,000 employees in more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at _. Avery Dennison is an equal opportunity employer. Please let us know if we can support you with reasonable accommodations throughout the application process by contacting our team via _. We do not accept unsolicited referrals or resumes from any source other than directly from candidates. We are unable to offer sponsorship or relocation for this role This role is subject to right-to-work checks as per UK Employment Law What we can offer you! - Your Role: In this is very versatile, home-based role as Technical Sales Specialist / Representative - UK / Ireland (_) we are looking for a fresh mind to join our high performing team in Cramlington with direct reporting line to our Country Sales Manager. Your Mission: • While travelling extensive within UK and Ireland you will be the first point of contact for technical support and advice to our customers in the printing and converting industry, regarding applications, and/or conversion., • To ensure a reliable and strong partnership with your customers you will analyse, troubleshoot, and quickly resolve our customers' issues when it comes to printing, adhesives, conversion, or label application., • But it is not only technical advisory, and solution selling; you will also show all advantages of our new products, applications and technical developments to your community, e.g. through product training sessions at our locations and our customers’ sites., • Thus, opting for our technical sales job certainly means going all out for an exciting, dynamic and multi-faceted opportunity, offering new and insightful challenges each day. What we expect from you! - Your Expertise: • University Degree or equivalent, • Previous work experience of 3+ years in a technical support, research and development or (technical) sales position within a manufacturing organisation is important, • Experience in printing, converting, and/or packaging/labeling technology market, as well as knowledge of label / packaging industry, printing technologies and/or labeling solutions is beneficial, • Creativity and innovation, entrepreneurial spirit for growing a sustainable business to set your career at Avery Dennison, • Valid driving license Location: Cramlington Hours: 37.5 hours per week What we can offer: • 25 days annual leave plus usual bank holidays (or equivalent shifts), • Company Car, • Bonus opportunity, • Private Medical Insurance, • Health benefit cash plan, • Pension with up to 10% Employer contributions, • Life assurance 4 x basic salary, • Employee Assistance scheme including life & legal advice., • Free on-site Parking, • Structured learning and development / Mentoring program, • International environment, • Events such as International Women’s Day, Earth Day, etc., • A growing, and welcoming team with a good spirit! Who we are! - Our Story: Each of us, Every day!_. One Team! Being open to every voice, every day, brings our value of diversity to life and makes Avery Dennison a vibrant and engaging place to be. We understand diversity and equal opportunities as enrichment for our future-oriented work. Across our diverse, global team, every voice makes us stronger. When we listen to and learn from each other, there is no limit to what we can achieve together. Each of us is unique, and we appreciate bringing together different personalities and talents. Avery Dennison is an equal-opportunity employer. In the EMEA region, we have these Employee Resource Groups: • EmpoWer - focusing on the engagement, mentoring, and promotion of women, • Mental Health - striving to provide a safe space for employees to discuss mental health issues in the workplace, • Unite - supporting the LGBTQI+ and ally community in the EMEA region To find out more about all our employee resources groups globally as well as our Diversity, Equity & Inclusion approach, please go to our Diversity and Inclusion pages in the About Us section of our website: _ At Avery Dennison, we do what we love, and we love what we do - Just click here, and get to know us better: Life @ Avery Dennison (_)

NB - this role is working for an automation manufacturer that supplies to automation products and parts to specialist sectors like Pharma/Life Science *. Life Science and pharmaceuticals. Do you possess a proven track record of driving business development in the life science and pharmaceutical sect

Maintain a strong understanding of blood cancer research developments and the evolving needs of people affected by blood cancer ensuring relevance in partnership work. Were the UKs specialist blood cancer charity and our vision is clear: were here to beat blood cancer. We fund world-class research;

Solutions Engineer. London area (hybrid). Circa £65,000 (OTE up to £150,000) + benefits. Founded in 2016 by Engineers from Stanford and MIT, and having received £27million in funding, my client is a truly impressive organisation who are breaking boundaries in the scientific world and are on a mission to accelerate industrial R&D. As a high-growth startup now employing 130 talented professionals, they have developed an AI driven R&D platform, used by the world’s leading Chemists, Material Scientists and Biologists, to dramatically accelerate how new products are discovered, developed and brought to market. My client works with an enviable selection of R&D clients across chemicals, pharmaceuticals, advanced materials and food and beverages. Their pre-sales team was formally established two years ago, so you’re getting in early to shape how this function operations, as the company scales. Due to continued, fast and strategic expansion, an opportunity has now arisen for a Solutions Engineer to join their fast-paced pre-sales team in London. Does this sound like the engaging and exciting next step of your career? The key responsibilities for your new role as Solutions Engineer are as follows: Owning the full technical pre-sales process – from first demo through business value case development, technical evaluation positioning and pilot execution. Architect and build custom demonstrations...

Job Title: Sustainability Lead Location: Hayes, London Salary: £50,000 £65,000 + 10% Car Allowance + Package Working Pattern: Full-Time, Site Based About the Company TSL Projects is a leading engineering and construction contractor delivering complex projects across Data Centres, Advanced Manufacturing, Pharmaceuticals, Logistics and Food Production sectors throughout the UK and Europe. Due to continued growth, we are seeking an experienced Sustainability Lead to join a major advanced manufacturing project in Hayes. This is an opportunity to take ownership of sustainability delivery on a high-profile construction programme, supporting project teams to achieve ambitious environmental, carbon and certification objectives. The Role -Sustainability Lead As Sustainability Lead, you will act as the project's sustainability subject matter expert, providing technical guidance and leadership throughout the project lifecycle. Working closely with operational teams, clients, consultants and subcontractors, you will lead sustainability initiatives, manage certification requirements and ensure compliance with project sustainability commitments. The successful candidate ...

PE-Backed Scientific Services Group Remote / Hybrid | UK-Wide Newly Created Role Due to Continued Growth Our client is a rapidly growing, private equity-backed scientific services group operating across highly regulated sectors including healthcare, pharmaceuticals, law enforcement, government and

Scientific Implementation Associate. My client works with an enviable selection of R&D clients across chemicals, pharmaceuticals, advanced materials and food and beverages and their high-velocity implementation team has been pivotal to their success – with individuals taking ownership of custo

Join to apply for the Controls and Automation Manager role at Dechra Join to apply for the Controls and Automation Manager role at Dechra Direct message the job poster from Dechra Talent Acquisition Partner - Talent Management, Executive Search Why Dechra? Thank you for checking out our vacancy, we're delighted you want to learn more about joining Dechra. A career at Dechra is different. Sure, we're a growing global company with a presence in 27 countries but our purpose is simple - to achieve the sustainable improvement of animal health and welfare globally. If you want to be part of a team that invests in your future and ensures you have the support to reach your full potential and thrive, please read on. The Opportunity The Controls and Automation Manager is responsible for overseeing the design, development, and maintenance of automated systems and control processes across manufacturing operations. This role ensures compliance with regulatory standards, optimizes production efficiency, and guarantees the safe, reliable, and effective operation of automated systems used in pharmaceutical manufacturing. As a key leader in the engineering team, the Controls and Automation Manager will collaborate with cross-functional teams, including production, quality assurance, IT, and compliance, to drive continuous improvement in automation technologies while ensuring alignment with industry best practices and regulatory requirements (such as cGMP, FDA, and EMA standards). Role Responsibility So, what will you be doing? This role has a broad and varied remit and the successful candidate will have responsibility for duties including: Lead the implementation and maintenance of automation and control systems in manufacturing environments. Oversee the integration of new automation systems and upgrades to existing systems, ensuring minimum downtime during transitions. Manage and mentor a team of controls engineers, automation technicians, and other relevant staff.Collaborate with other departments (production, quality, engineering, IT, etc.) to resolve automation-related challenges and drive process optimization. Foster a culture of continuous improvement and innovation, encouraging staff development and knowledge sharing. Create and manage project timelines, resources, and budgets, ensuring adherence to internal and external timelines. Develop risk assessments and mitigate potential issues associated with new automation initiatives. Design, develop, and optimize control systems (PLC, SCADA, DCS, etc.) for various pharmaceutical manufacturing processes. Evaluate and implement new technologies to improve system performance, energy efficiency, and safety. Conduct troubleshooting and root cause analysis for automation-related issues, ensuring minimal impact on production. Participate in regulatory inspections and audits, providing technical support and ensuring adherence to compliance standards Prepare and review documentation related to automation systems, including SOPs, protocols, and reports. Promote a culture of safety by ensuring that all automation systems are designed and maintained to meet safety standards and risk management guidelines. Develop and enforce safe working practices related to automation equipment and control systems. The Candidate Here at Dechra we pride ourselves on being an inclusive employer. We know that individuals' unique background and experience can bring a wealth of variety and expertise to our global workforce. For this role, we're particularly keen to hear from those who have/are: Minimum of 5 years in automation/controls management within a regulated manufacturing environment, ideally within the pharmaceutical, biotech, or life sciences industries. Strong knowledge of PLC, SCADA, DCS, HMI, and other control systems. Experience with automated systems in pharmaceutical manufacturing, including process control, packaging, and laboratory automation. Familiarity with pharmaceutical regulatory requirements (e.g., FDA, cGMP). Proven experience leading cross-functional teams and managing complex projects from concept to implementation. Proficient in automation software (e.g., Siemens, Allen Bradley, Rockwell), and strong understanding of industrial networking protocols. Strong analytical and troubleshooting skills for diagnosing and resolving complex technical issues in control and automation systems. Additional Information: Occasional global travel may be required with this role. This role is based in the UK / remote. What we can offer you: 33 days annual (inclusive of Bank Holidays) Employee Assistance Program Life Assurance Enhanced Family Leave Bonus (discretionary) Car or car allowance (discretionary) Discounted Pet Food About the Company If a career at Dechra has piqued your interest, find out more at Dechra Careers. Dechra is a growing, global specialist in veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide. All applications received are reviewed by our internal talent acquisition team and we will get in touch if your skills and experience match what we're looking for. Should you not hear back from us within 28 days please don't be too disappointed - we may keep your CV on our database for any future vacancies which could be suitable, and we encourage you to keep an eye on our career site. We value diversity within our global workforce and encourage an inclusive culture. Any questions or queries, please contact us. Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Engineering and Management Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Dechra by 2x Get notified about new Automation Specialist jobs in England, United Kingdom. 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Senior Project Manager vacancy in Southwest, UK (151CM) Overview Our client is seeking an experienced Senior Project Manager to support the delivery of complex, fast‑track construction projects across sectors including data centres, pharmaceuticals, logistics, and advanced manufacturing. Working closely with a Project Director, you will play a central role in driving delivery across multidisciplinary teams, subcontractors, and stakeholders while ensuring programme, quality, and commercial objectives are achieved. This role is ideal for experienced professionals who thrive in fast‑paced project environments and are comfortable taking ownership within high-performance teams. The Role You will support project delivery from pre‑construction through to completion and handover. Responsibilities Oversee day‑to‑day project delivery activities Manage programme, budget, and quality performance Support MEP coordination and technical delivery Coordinate subcontractors and supply chain partners Maintain project schedules and delivery milestones Manage project risks and early warning processes Build and maintain strong client relationships Ensure project controls and delivery standards are consistently achieved What We’re Looking For Strong experience delivering projects within complex construction environments Ability to manage multidisciplinary teams and supply chains Understanding of commercial and contractual responsibilities Strong organisational and stakeholder management skills Proactive and delivery-focused mindset Experience within fast-track or technically complex projects would be advantageous Ideal Backgrounds Ex‑military officers or senior NCO candidates with experience managing complex operations, engineering activities, or large teams from construction and infrastructure delivery environments, engineering or technical project management backgrounds, defence or operational delivery programmes The Environment You will be working in a high-performance environment where delivery pace, accountability, and collaboration are key. The client delivers projects at speed while maintaining strong standards across quality and safety. The Opportunity Exposure to major industrial and mission‑critical developments Career progression within a growing delivery environment Opportunity to work on technically complex, high-value projects * Strong package and long-term development opportunities #J-18808-Ljbffr

Scientific Implementation Associate. London area (hybrid). From £50,000 + excellent benefits. Founded in 2016 by Engineers from Stanford and MIT, and having received £27million in funding, my client is a truly impressive organisation who are breaking boundaries in the scientific world and are on a mission to accelerate industrial R&D. As a high-growth startup now employing 130 talented professionals, they have developed an AI driven R&D platform, used by the worlds leading Chemists, Material Scientists and Biologists, to dramatically accelerate how new products are discovered, developed and brought to market. My client works with an enviable selection of R&D clients across chemicals, pharmaceuticals, advanced materials and food and beverages and their high-velocity implementation team has been pivotal to their success with individuals taking ownership of customer projects, within six months. The company provides a proven internal career path, with Scientific Implementation Associates frequently advancing into leadership roles. Due to continued, fast and strategic expansion, an opportunity has now arisen for a Scientific Implementation Associate to join...

Key Account Manager | Unlicensed Medicines (Hospital Pharmacy)LondonThis is an exciting opportunity to join a growing, specialist pharmaceutical organisation operating within the Unlicensed Medicines (ULM) space. This Key Account Manager role will suit a highly commercial individual with strong NHS hospital pharmacy relationships, looking to take ownership of a key London territory while making a direct impact on patient access to critical medicines. Company Overview:Our client is a well-established and ambitious organisation specialising in the supply of Unlicensed Medicines to NHS hospitals, supporting continuity of care where licensed alternatives are unavailable. They are recognised for their reliability, responsiveness, and ability to deliver high-quality solutions in a complex and regulated environment.Strong presence within the NHS hospital pharmacy and procurement spaceHigh-growth area with significant investment and expansion plansCollaborative culture with close alignment across commercial, procurement, and regulatory teamsOpportunity to build strategic relationships with senior NHS stakeholdersFlexible, field-based role with autonomy and progression opportunities Job Overview:As a Key Account Manager, you will be responsible for driving sales and developing strategic partnerships across NHS hospital accounts, with a particular focus on London.You will work closely with Chief Pharmacists, Medicines Management teams, and Procurement Pharmacists, positioning the business as a trusted partner for Unlicensed Medicines supply.This is a highly commercial role where you will combine account management and business development to grow market share and deliver against revenue targets.Key Responsibilities:Manage and grow key NHS hospital accounts within LondonDeliver against sales and margin targets across the Unlicensed Medicines portfolioBuild and maintain strong relationships with pharmacists, procurement teams, and key stakeholdersDevelop and implement account plans aligned to business objectivesIdentify and convert new business opportunities within NHS TrustsProvide insight into market activity, demand trends, and competitor landscapeWork cross-functionally with internal teams to ensure compliant, high-quality supply solutionsRepresent the business at NHS meetings, conferences, and industry events To be successful:We are looking for a commercially driven Key Account Manager with strong experience selling into NHS hospital pharmacy environmentsProven background in pharmaceuticals, Specials, or Unlicensed MedicinesStrong network across hospital pharmacists, procurement pharmacists, and medicines management teamsSolid understanding of NHS structures, procurement processes, and regulatory frameworksTrack record of achieving or exceeding sales targets within a regulated healthcare settingStrategic thinker with strong account planning and stakeholder engagement skillsSelf-motivated, proactive, and comfortable working in a field-based role across LondonFull UK driving licence How to apply:If you’re a commercially minded Key Account Manager with experience working with NHS pharmacists and an interest in the Unlicensed Medicines / Specials market, we would love to hear from you.Apply now or contact Alice Smith for a confidential discussion.

Jazz Pharmaceuticals is looking for an Associate Director of Drug Product Development who will oversee drug product aspects from formulation to commercialization.

What you’ll bring: Advanced degree (MSc) in Business Administration, Human Resources, Organizational Psychology, Instructional Design, or a related field 5+ years of relevant post‑collegiate client facing job experience in consulting or project management within organisational design * Stron

PARDGROUP SPA LONDON, United Kingdom Design Hybrid Company Description Pardgroup, a leading company in integrated services for retail and large-scale distribution, is looking for a new Senior Designer to join our UK team in London.Position The new colleague will carry out the following activities: *

Overview GFIC recruits for a Global Food Ingredients company: Sales Manager Nutritional, Cosmetical and Functional Food Ingredients Area UK and Ireland Important is you have selling experience of Supplements to Food-, Cosmetic and Pharmaceuticals Clients in the UK You have experience of selling

We have an exciting opportunity for an Executive Office Assistant role for a Pharmaceuticals company based in London.

Vertex Pharmaceuticals is seeking an International Tax Analyst in Greater London.

Ability to travel to external vendors/CMOs sites nationally and international as and when required Knowledge and Qualifications Masters Degree (or equivalent) in Pharmacy Knowledge of Clinical Trials regulations gained through pharmacy or equivalent on work experience * Knowledge of the processe

Recursion Pharmaceuticals in Greater London is seeking a dedicated team member to develop project strategies and collaborate across disciplines to bring new therapeutics to patients.

The ideal candidate should possess extensive experience within complex project environments and a proactive approach to delivery. Ex-Mill Recruitment Ltd is looking for a Senior Project Manager to oversee the delivery of complex construction projects, including data centres and pharmaceuticals, in H

The Team You’ll Join Our group is a bold, agile, interdisciplinary collective of biological, computational, drug discovery, and machine learning scientists deeply focused on the singular goal of bringing new therapeutics to patients at an accelerated pace.You will develop project strategy and exec

Idorsia Ltd is reaching out for more – We have more ideas, we see more opportunities and we want to help more patients.In order to achieve this, we will develop Idorsia into a leading biopharmaceutical company, with a strong scientific core.Headquartered near Basel, Switzerland – a European biot

More About Recursion Recursion is a clinical stage TechBio company leading the space by decoding biology to industrialize drug discovery. Recursion is headquartered in Salt Lake City, where it is a founding member of BioHive, the Utah life sciences industry collective. We are an application-oriented