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At Hologic, we are dedicated to enabling healthier lives everywhere, every day, by advancing women’s health through innovative gynecological solutions. Guided by The Science of Sure, we strive to provide clinicians with precise, reliable technologies that support minimally invasive management of abnormal uterine bleeding, fibroids and other benign gynecological conditions. Our Gynecological Surgical Solutions portfolio, including NovaSure endometrial ablation, MyoSure tissue removal systems and related hysteroscopic technologies, is designed to enhance clinical outcomes, reduce the need for more invasive procedures and improve quality of life for women around the world. Hologic is now looking for an International Scientific Affairs Manager focused on our Gynecological Surgical Solutions portfolio. In this role, you will act as a scientific and clinical expert for the product range, driving the generation, interpretation and communication of high-quality evidence to support safe, effective and evidence-based use of our technologies across international markets. As a key ambassador for Hologic, you will engage with international KOLs, support advisory boards and investigator-initiated research, and help position Hologic’s gynecological surgical solutions within clinical guidelines and standard of care, ultimately contributing to the advancement of women’s health worldwide. What To Expect • A strategically important, highly visible role at the interface of science, clinical practice and business for a market-leading women’s health company, • Close collaboration with international KOLs, professional societies and leading centres in gynecological surgery, • Responsibility for driving and supporting evidence generation activities, including clinical studies, real-world data initiatives and health-economic projects, • Involvement in the development and delivery of impactful medical education programs, symposia and training for healthcare professionals, • A dynamic, international environment with frequent cross-functional interaction and the opportunity to influence global and regional strategy for the GSS portfolio, • Regular travel, approximately 40%, to attend scientific congresses, educational events, internal meetings and site visits across Europe and beyond What We Expect • Proven experience in Scientific or Medical Affairs within the medical device industry, ideally with a focus on surgical devices, • Experience in gynaecology or women’s health is highly desirable, • Demonstrated experience working across multiple countries or regions, with an understanding of how clinical practice, regulation and reimbursement differ between markets, • Ability to engage confidently and credibly with healthcare professionals, KOLs and payer-facing stakeholders on scientific, clinical and health-economic topics, • Strong analytical skills to interpret data and develop clear, balanced scientific narratives that support both clinical practice and Market Access needs, • A structured, organised approach to managing multiple projects and deadlines across markets, • Effective collaboration with colleagues from Medical Affairs, Clinical, Marketing, Regulatory, Commercial and Market Access teams Why Hologic? • You will contribute to a clear, meaningful purpose: improving women’s health through better gynaecological care and broader access to minimally invasive solutions, • You will work with innovative, procedure-focused technologies supported by a strong and growing clinical and health-economic evidence base, • You will join a company that places science, data, value demonstration and clinical partnership at the centre of its strategy, • You will be part of a collaborative culture that values initiative, openness and continuous learning Salary: UK £64,000-£95,000, Belgium €75,000-€125,000, Spain €54,000-€100,000, France €70,000-€120,000, Germany €83,000-€145,000, Italy €60,000-€120,000 gross per year. The final offer will depend on experience, skills, and alignment with internal pay structures. In addition, we offer a comprehensive benefits package including pension and insurances. Apply today! #LI-AB1 #LI-Remote

Join Hologic’s Diagnostics team as an Applications Specialist and become a trusted partner to laboratories across South East England. In this field‑based role, you’ll combine scientific expertise, technical troubleshooting, and customer engagement to help laboratories maximise the value of Hologic’s diagnostic solutions while delivering exceptional user experiences. What to Expect • Act as a key technical and applications expert for Hologic customers within your territory, supporting laboratories in the effective use of our diagnostic platforms., • Deliver engaging training for new and existing users, ensuring they feel confident operating and optimising Hologic systems., • Provide advanced applications troubleshooting and guidance to help customers resolve complex issues quickly and effectively., • Support the full customer journey—from pre‑site and site assessments to ongoing post‑installation support., • Build strong, long‑term relationships that drive customer satisfaction and retention., • Identify opportunities to grow existing accounts while gathering insights from competitive sites to support market expansion., • Represent Hologic at conferences, trade shows, and customer events, providing technical expertise and commercial support., • Work closely with cross‑functional teams including Sales, Field Service Engineering, Marketing, Technical Solutions, and Customer Service to deliver a seamless customer experience. What We Expect • A Bachelor’s degree in Life Sciences, Biomedical Sciences, or a related discipline., • Strong experience working within a diagnostic laboratory environment, with advanced applications knowledge in a relevant field., • Solid knowledge of diagnostic technologies and the ability to confidently support Hologic products and services., • Experience using tools such as Microsoft Office, with familiarity in systems like Salesforce CRM and Oracle ERP., • Up‑to‑date awareness of local accreditation standards and clinical training requirements related to medical devices., • Excellent communication and interpersonal skills, with the ability to explain complex scientific concepts clearly to diverse audiences., • Strong analytical and troubleshooting abilities, with a systematic approach to solving technical challenges., • Confidence delivering engaging training sessions to different user groups., • The ability to interpret scientific literature and communicate key insights effectively., • A full driving licence and the ability to travel extensively within the territory. We’re looking for someone who is customer‑focused, proactive, and collaborative—someone who can represent the voice of the customer internally while working independently in the field. You’ll thrive in a fast‑moving environment, bring thoughtful problem‑solving to complex situations, and continuously look for ways to improve the customer experience. If you enjoy combining scientific expertise with relationship‑building and want to make a meaningful impact in diagnostic healthcare, this role offers the opportunity to do exactly that. Salary: £45,000 - £55,000 + bonus- The final offer will depend on experience, skills, and alignment with internal pay structures. In addition, we offer a comprehensive benefits package including company car or car allowance, pension and insurances. Territory: South East UK Location: Ideally based in Epsom, Croydon, Watford, Harlow, or Kent Travel: Approximately 70–80% (around 4 days per week) #LI-HE1 #LI-Remote

Refrigeration Engineer £50K - £55K (DOE) Permanent Birmingham My client is on the lookout for an experienced Refrigeration Engineer to join their team where you will be working across East Midlands .You will be responsible for ensuring that refrigeration systems are Serviced & Maintained correctly which include heavy commercial and Industrial systems (CO2, Freon, and Chilled water applications – Ammonia experience advantageous, but not essential )You will be working closely with the Service admin team, Service Supervisors, and other senior service engineers to ensure that the refrigeration systems meet the required specifications and standard for our clients. You will need to make sure clients systems are running to their optimum condition to meet site operating requirements, always ensuring safe systems of work • .Qualifications & Experience – Refrigeration EngineerMinimum 5 years’ relevant experienc, • eRelevant qualifications: City & Guilds Refrigerant handling 2079, CO2 (Ammonia would be advantageous but not essential, • )Proven experience in large commercial, or industrial refrigeratio, • nPrevious experience in a senior rol, • eExcellent communication, leadership, and problem-solving skill, • sThorough understanding of electrical control, • sUp to date knowledge of COSHH regulation, • sUnderstanding of the principles of refrigeration and of the comprising component, • sServicing of systems utilising approved methods and practice, • sExcellent skills in diagnostics to identify & resolve system failure, • sAbility to work unsupervise, • dCSCS approve, • dWork within current Health and Safety guideline, • sFull driving licenc, • eOperation of Mobile Elevated Working Platfor, • m On Offer – Refrigeration Engineer£50K - £55K • (DOE)On call 1 week in 4 (Standby fee £225.00 per, • week)40 hour week – 8am to 4, • :30pm25 days + 8 bank hol, • idaysTravel time door to, • doorVan, fuel card,, • toolsCompany Pension – Employer 3% and Employ, • ee 5%Private Health (Following a successful probationary pe, • riod)Health Support Scheme (Following a successful probationary pe, • riod)Death in Service Benefit (Following a successful probationary pe riod)For more information on this role, please contact Kieren Provis on 01453 829776, or send a copy of your CV to kieren.provis@omegaresource. co.ukOmega Resource Group is an employment agency specialising in opportunities at all levels within the Engineering, Aerospace, Automotive, Electronics, Defence, Scientific, Oil & Gas, Construction and Manufacturing sec tors.For details of other opportunities available within your chosen field please visit our website www.omegaresource. co.uk

Mechanical Maintenance Technician Location: Birmingham Working Pattern: Days (Mon–Fri) Salary: Experience Dependent This is a hands-on Mechanical Maintenance Technician position within a highly regarded global engineering and manufacturing environment. You will play a key role in ensuring production equipment and facilities operate reliably and efficiently, supporting continuous improvement and minimising downtime. Working as part of a skilled maintenance team, you will be responsible for diagnosing faults, maintaining equipment, and contributing to projects that improve operational performance, safety, and energy efficiency. Responsibilities - Mechanical Maintenance Technician • Diagnose and repair mechanical faults across a range of production equipment (including bearings, conveyors, pneumatics, and associated systems), • Support electrical engineers with basic fault finding on sensors, motors, and control panels, • Carry out planned preventative maintenance (PPM) and reactive maintenance activities, • Maintain tools and equipment to ensure safe and effective operation, • Respond quickly to breakdowns and emergencies to minimise production disruption, • Manage and update technical documentation for machinery and production lines, • Support tooling activities, including tool setting and machine setup, • Work with workshop machinery such as lathes, milling machines, drills, and grinders, • Contribute to continuous improvement and maintenance reduction projects, • Use CMMS systems to record work, analyse trends, and improve equipment performance, • Propose and implement improvements to enhance reliability, efficiency, and safety across production processes Experience / Qualifications - Mechanical Maintenance Technician • Time-served apprentice or formally qualified in Mechanical Engineering, • Proven experience in a manufacturing or production maintenance environment, • Strong mechanical fault-finding and repair skills, • Basic to intermediate electrical knowledge (motors, sensors, panels), • Experience with tool setting and machine tool setup, • Familiarity with workshop machinery (lathes, milling, drilling, grinding), • Experience using CMMS systems for maintenance tracking and analysis, • Ability to read and interpret mechanical drawings, • Strong communication skills with the ability to work across departments, • Proactive approach to problem solving and continuous improvement Benefits - Mechanical Maintenance Technician • Competitive salary, • 25 days holiday + bank holidays, • Competitive pension scheme, • Life assurance, • Flexible benefits platform (including holiday buy/sell, health checks, dental, eye care, gym memberships, cycle to work, and retail discounts), • Employee Assistance Programme, • Internal mobility and career development opportunities, • Access to global projects and mentorship programmes, • Generous employee referral scheme, • Recognised as a Top UK Employer For more information on this role, please contact Andy Haddon on 01453 796617, or send a copy of your CV to andrew.haddon@omegaresource.co.uk For details of other opportunities available within your chosen field, please visit _ Omega is an employment agency specialising in opportunities at all levels within the Engineering, Manufacturing, Aerospace, Automotive, Electronics, Defence, Scientific, Energy & Renewables and Tech sectors. Ideal background / Previous roles may include: Mechanical Maintenance Engineer, Maintenance Technician, Mechanical Fitter, Multi-Skilled Maintenance Technician, Plant Maintenance Engineer, Shift Maintenance Engineer, Production Maintenance Technician, Engineering Technician.

ZEISS is technology and innovation. We develop, manufacture and sell highly innovative products and solutions for our customers in a variety of business fields – always testing the limits of what is feasible. ZEISS is an internationally leading technology enterprise operating in the optics and optoelectronics industries generating more than 11.8 billion euros in revenue with around 46,000 employees across 50 countries around the globe. Position Summary • Lead the global Quality function for Consumer Eyecare across the US, EU, China, and future markets, • Build, lead, and continuously improve a scalable global Quality organization covering QMS, Pharmacovigilance / Post-Market Surveillance, Supplier Quality, and Contract Manufacturing Quality, • Ensure ZEISS Consumer Eyecare products are developed, sourced, manufactured (including external/contract manufacturing), released, distributed, and monitored in line with applicable quality, safety, and regulatory requirements, • Act as the senior Quality partner to the business for launches, market expansion, supplier and contract manufacturing decisions, product changes, and quality risk management across Consumer Eyecare categories such as eye drops, eye vitamins, lid care, and other adjacent eye health products. Responsibilities • Define and lead the global Quality strategy, governance, and operating model for Consumer Eyecare, including external and contract manufacturing, • Build, implement, and maintain a fit-for-purpose global QMS across regions, product categories, and manufacturing models (internal and external), • Lead local Quality teams in the US, EU, and China, ensuring strong capability, clear accountability, and consistent execution, • Own global quality governance for complaints, deviations, non-conformances, investigations, CAPAs, change controls, recalls, and management review, • Oversee quality processes for Pharmacovigilance / vigilance / Post-Market Surveillance, including compliant reporting, escalation, trend monitoring, and inspection readiness, • Lead Supplier Quality and Contract Manufacturing Quality across CDMOs, contract manufacturers, packers, and critical suppliers, • Ensure compliance with applicable regulatory frameworks, including but not limited to: United States: U.S. Food and Drug Administration regulations (e.g., 21 CFR Part 820 (QSR), 21 CFR Part 11, OTC drug requirements, dietary supplement cGMPs); European Union: EU MDR (2017/745), IVDR (2017/746), EU GMP guidelines, ISO 13485, ISO 14971, and applicable directives for consumer health products; China: National Medical Products Administration (NMPA) requirements, China GMP, Medical Device Regulations, filing/registration requirements, and local vigilance reporting obligations, • Own supplier and contract manufacturer qualification, audits, onboarding, quality agreements, performance management, and risk-based oversight, • Ensure end-to-end quality oversight of externally manufactured products, including tech transfer, process validation, batch release governance, and ongoing performance monitoring, • Ensure readiness for internal audits, supplier audits, partner audits, and health authority inspections across all relevant markets, • Serve as the senior escalation point for critical quality issues, product quality events, serious complaints, field actions, and market actions, • Partner closely with Regulatory, Supply Chain, Procurement, Operations, R&D/Product Development, Medical/Safety, Commercial, Legal, and IT to embed quality into business processes and launch readiness, • Provide Quality leadership for new product launches, market entries, tech transfers, supplier and contract manufacturer changes, artwork or label changes, and lifecycle management, • Define and track global quality KPIs, dashboards, and management reporting, and drive continuous improvement across the function, • Support quality due diligence and risk assessment for new suppliers, contract manufacturers, partnerships, acquisitions, and future market expansions Required Knowledge & Experience Essential Criteria • Degree in Pharmacy, Chemistry, Life Sciences, Engineering, or another relevant scientific discipline; advanced degree is a plus, • Proven experience in relevant Quality experience in regulated healthcare categories, • Strong experience in Consumer Healthcare / Consumer Eyecare, ideally across categories such as OTC, medical devices, pharmaceuticals, food supplements, or adjacent eye health products, • Proven leadership experience in global or multi-region Quality roles, including line management of geographically dispersed teams, • Demonstrated experience building or upgrading Quality systems in a growing international business, • Deep expertise in QMS, audits, inspections, deviations, investigations, CAPAs, change control, management review, and continuous improvement, • Strong experience in Supplier Quality and Contract Manufacturing oversight, including CDMO governance, supplier qualification, audits, and quality agreements, • Solid experience with PV / vigilance / PMS / complaint handling and post-market quality processes, • Strong understanding of regulatory and compliance requirements across the US, EU, and China, including FDA, EU MDR/IVDR, ISO standards, and NMPA frameworksStrong understanding of quality and compliance requirements across the US, EU, and China, • Experience across multiple product categories with different regulatory requirements is highly desirable, • Strong business judgment and risk-management capability, with the ability to make pragmatic decisions in a fast-moving environment, • Excellent leadership, communication, and stakeholder management skills, with the ability to influence senior cross-functional leaders in a matrix organization, • Fluent in English; additional languages, especially Mandarin and/or German, are a plus, • Willingness to travel internationally, • Strong transformational leadership with ability to operate in a matrix organization, • Hands-on mindset combined with strategic thinking, • Ability to drive change, alignment, and performance in a complex global environment

About the Role Mission To ensure Safety is priority number one and that the UK sites maintain a safe work environment with zero injuries and that the business is sustainable, minimizing any negative impact on the surroundings and making sure to protect the environment. Duties and Responsibilities Together with respective site management team set goals, targets and activities, and drive follow up of the annual road map/action plans to improve HSE, aligned with EMEA strategy and plans and other mandatory documents. Responsibilities • Monitor laws and regulations linked to HSE in the business, plan and support the implementation of necessary measures to meet current and future legislation., • Ensure that local processes needed for the HSE Management System are established and maintained and train the organization in the Management System., • Systematically identify, assess and document environmental, health and safety, and fire safety risks and develop processes and action plans to mitigate the risks., • Develop and hands-on support the implementation of proactive safety tools and activities on site, such as hazard identification, near miss reporting, safety alert stand downs, toolbox talks, BBS etc., • Drive and hands-on support the organization to continuously improve HSE at UK sites., • Plan and ensure that internal and external audits and other obligatory HSE-related inspections and controls are performed according to the plan., • Identify and make sure necessary trainings for employees related to HSE, including mandatory refreshing/updating training., • Summarize and analyze historical HSE related data and KPIs in order to be able to prioritize the future., • Responsible for monthly data collection and reporting., • Attend group-wide HSE resource group(s). Qualifications • Bachelor’s Degree in Health, Safety, Environmental or scientific or related engineering field., • Languages: Excellent command of English. Required Skills • At least 5 years’ industry experience., • Practical working knowledge of HSE tools and techniques., • Several years of experience from working with Safety Culture change and development., • Several years of practical work experience and continuous improving waste-, water-, energy- and chemical management., • Specialist knowledge, awareness and understanding of different relevant UK laws and regulations and of most widely used international standards., • 3+ years’ experience in ISO14001, ISO45001 or similar accredited HSE management systems., • Auditor experiences., • Driver’s licence is a requirement due to the travel ratio associated with the role. Characteristics • Builds credibility by rolling up their sleeves and being visible regularly in operational areas, • Leads by example rather than managing from reports, • Is comfortable challenging poor practices and influencing change, • Teaches teams why environmental and health & safety matters, not just issues a procedure, • Is resilient and demonstrates integrity during times of pressure, conflict and non-conformance, • Demonstrates and upholds fairness, consistency and teamwork Additional Information • The position is 100% site-based at Cradley Heath, Birmingham site., • Candidates applying for this role must reside within a commutable distance of Cradley Heath, Birmingham site and be willing to be on-site daily. This role does not include working from home., • There is a regular travel requirement to visit locations based in Chester and in Waterlooville., • The role has zero direct reports., • QHSE Manager at Waterlooville refers to this position for functional guidance/strategy for HSE only., • Candidates must be able to explicitly demonstrate the documented right to work in the UK.

A World-Changing Company at Lifebit At Lifebit, we're driven by the mission to make complex data analysis simpler and more accessible. We empower key institutions worldwide to revolutionize their data utilization and technology integration. Lifebit is powering the world’s federated data platforms for population-scale health and life sciences. Our Federated AI Platform is trusted across national health systems, global pharma, and research biobanks to unlock sensitive biomedical and real-world data securely, compliantly, and at scale. As we scale through our Series B growth phase, we are expanding our product organization to meet the demands of a global market. Join us if you're inspired to tackle meaningful challenges and want to lead the next generation of health technology and cloud-based genomic solutions. The Role We are looking for a high-performing Product Manager to join our growing team and drive the evolution of our platform. In this role, you will be instrumental in bridging the gap between cutting-edge science and world-class software, ensuring our federated solutions solve the most pressing challenges for clinicians and researchers. Lifebit specializes in managing the world’s most sensitive genomics data. We need a PM who thrives in an Agile environment, possesses a deep technical intuition, and can translate high-level business goals into a concrete, impactful product roadmap. Your Role and Responsibilities • AI-Powered Platform Development: Lead the design and delivery of AI capabilities within a chat-based product interface, building agentic solutions that leverage tools, skills, agents, and diverse data sources to create a comprehensive agentic platform for users and researchers., • Data Architecture & Integration: Drive the strategy for data modeling, transformation, and standardization across the platform. Own the data ingestion pipeline and ensure seamless connectivity that makes data AI-ready and optimized for advanced analytics., • Agile Product Leadership: Drive the full product lifecycle within an Agile framework, leading cross-functional squads to deliver high-quality features in continuous cycles., • Strategic Roadmapping: Own and plan your product area’s roadmap, moving beyond feature lists to focus on outcome-based goals that align with Series B scaling targets., • User Analytics & Design: Lead the integration of advanced user analytics and partner with Design and User Research teams to create intuitive interfaces for complex scientific workflows., • Stakeholder & KPI Management: Measure, track, and report on product KPIs to internal and external stakeholders, providing data-driven rationale for product pivots and investments., • Infrastructure & Tools: Utilise Jira and Confluence as the "source of truth" for technical specifications, ensuring seamless communication across Engineering and Product teams., • Regulatory Compliance: Work closely with Legal and Clinical teams to ensure all product features comply with UK-specific data residency requirements, GDPR, and international health data standards (ISO/IG). What You Bring to the Table • Experience: 4+ years of experience in product management specifically within an Agile team., • AI Ownership: 2+ years of demonstrated work experience with agentic products., • Proven Track Record: Demonstrated experience owning and executing complex product roadmaps from inception to launch., • Technical Proficiency: Expert-level command of Jira and Confluence; ability to hold technical discussions with engineers regarding API architecture and data schemas., • Analytical Rigor: Strong experience with design-thinking principles and utilizing user analytics to drive iteration., • Growth Mindset: Experience working in a high-growth Series B startup environment, demonstrating the ability to build scalable processes while remaining adaptable. Preferred Qualifications • Biotech Acumen: Experience in genetics, medical sciences, or Bioinformatics is a significant plus, but a passion for the field is essential. What We Offer Lifebit is synonymous with a dynamic work culture that encourages both personal and professional growth. Our mission-driven organization is dedicated to making a significant impact in science and healthcare. We provide a comprehensive benefits package, including: • Compensation: £60,000 - £80,000 gross annually + performance-based bonus., • AI Upskilling: Use up to £10,000 and 10 dedicated days per year for qualified AI-related professional development (AI certification, LLM workshop, or AI bootcamp)., • Professional Development & Wellbeing: An annual personal development budget of £1,000 for conferences, training, certifications and personal wellbeing., • Remote-First Culture: Work from anywhere in the UK with a home-office stipend. In accordance with 2026 UK employment reforms, we provide Day One access to paternity and unpaid parental leave., • Flexible Working: Receive 25 days of annual leave plus bank holidays and flexible hours to maintain a healthy work-life balance., • Diverse Team: Join an international and diverse team passionate about transforming healthcare through data., • Deep Technology & Science: Get exposure to problems and applications in the cloud, data analysis, ML, life sciences, and big data fields. Join us at Lifebit for a career that promises to be your next significant venture, dedicated to advancing the scientific and healthcare fields. Don't miss the chance to be part of our mission! Life at Lifebit Lifebit is dedicated to fostering an environment where employees can flourish, valuing individual strengths, skills, and passions. We prioritize health and well-being, offering comprehensive benefits and support. Our fully remote model is built on trust and asynchronous communication, utilizing virtual workshops and occasional off-sites to maximize creativity and innovation. Lifebit is proud to be an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment. In compliance with the UK Employment Rights Act and Fair Work Agency guidelines, we ensure transparent pay structures and robust data privacy for all staff. Compliance & Eligibility All applicants must have the right to work in the UK. This role is subject to a standard Disclosure and Barring Service (DBS) check given the sensitive nature of the medical data platforms we manage. Join us in reshaping the future of data analysis and technology integration.

Science Technician required for college in Birmingham WeDoData has recently partnered with a well-established multi-academy trust in Birmingham that is looking to appoint a Science Technician ahead of the next academic year. This is a full-time, permanent opportunity to join one of the trust’s schools and become part of a supportive and ambitious Science Department. Our client is highly regarded for its hands-on learning approach, outstanding facilities and immersive teaching environments, strong partnerships with leading universities, and excellent student outcomes. To be considered, you must have a scientific background (education experience is not essential), be looking for a long-term opportunity within a growing organisation, demonstrate strong awareness of health and safety procedures, and be enthusiastic about supporting practical science education. In return, my client can offer: • Between £23,000 and £26,500 per annum, • Excellent career development opportunities, • The opportunity to be involved in the growth of the organisation, • Additional employee benefits package If you have the relevant experience and would be open to finding out more, please call Jean at WeDoData on 01173027500 or apply as soon as possible. If this role isn't quite right for you, please feel free to forward it to anyone you think might be a better fit. WeDoData (Bristol) Ltd is committed to safeguarding and promoting the welfare of children and young people and expects all staff, applicants, and clients to share this commitment. Any appointment will be made subject to strict vetting and screening checks and receipt of a satisfactory enhanced DBS check. In accordance with the DfE statutory guidance 'Keeping Children Safe in Education', this may also include an online search as part of our due diligence on shortlisted applicants.

Do you have a passion for clinical training and education? Do you have experience of enteral feeding or digestive therapies? If so, this role would definitely suit your skillset and ambition! My client is a reputable and well established organisation who prides themselves on advancing digestive health and introducing innovation into the medical devices market place. They are looking for someone to fulfil an immediate, 9 - 12 month fixed term contract The position is to cover the Southern regions of England. Responsibilities in this role include: • Performing product demonstrations to clinicians & patients, and gathering their feedback., • You will be tasked with facilitating training sessions with hospital sites, as well as providing patient support and assisting with product installation with patients Functions of the role include: • Schedule training sessions and attending multi-disciplinary team meetings as required, • Provide a responsive and caring customer service that focuses on clear communication, problem solving and empathy., • Involved in the on boarding of new hospitals & patients., • Develop and implement training materials for clinicians and nurses, • Regular travel within the South England region About you: • Experience within the medical devices market place and in-depth knowledge of the current landscape, • Experience with public speaking and providing education to a range of disciplines, • Familiar and comfortable with technology, • Confident socially, • Ability to work autonomously and be self-driven. In return, you will join an organisation that is expanding rapidly. They are very much changing patient lives and are keen to have someone join them on this journey of growth and development. There is a strong opportunity for growth and development within this role.

ZEISS is technology and innovation. We develop, manufacture and sell highly innovative products and solutions for our customers in a variety of business fields – always testing the limits of what is feasible. ZEISS is an internationally leading technology enterprise operating in the optics and optoelectronics industries generating more than 11.8 billion euros in revenue with around 46,000 employees across 50 countries around the globe. Founded in Germany in 1846, we are proud of our rich heritage. As a company wholly owned by a foundation, ZEISS is rooted in and committed to responsibility in all its activities. Therefore, 15% of revenue is currently invested in science and R&D. ZEISS is convinced that innovation and technology are the key to a sustainable future and solutions for global challenges. If you want to enable business success and make a difference with us, ZEISS is the right place for you! Head of Product Innovation is responsible for leading the definition, design, development, and execution of product initiatives across the OTC, medical devices, vitamins & food supplements and cosmetics, aligned with the business strategy. This includes establishing project scope, product performance targets, claims development and substantiation, and rigorous problem-solving approaches while leveraging deep technical expertise and working closely with CDMOs. This position requires product innovation leadership and strong technical expertise throughout project execution, integrating consumer insights and data driven decision making. This role will collaborate closely across the CDMOs and multifunctional teams (local and global regulatory, quality, marketing teams) – ensuring cohesive partnership and the successful translation of consumer and business needs into competitive project product solutions. The role of Head of Product Innovation will involve: Project Leadership & Execution • Working with CDMOs to deliver the project pipeline. For ZEISS exclusive formulations, lead and own end to end technical execution of product development projects, managing CDMOs to develop robust process development and ensure full delivery, • Define project pathways, ensure milestone delivery on time., • Independently drive technical problem solving and lead technical risk management., • In collaboration with marketing, develop a robust product and claims pipeline., • Develop and lead any studies required to substantiate the claims. This includes working closely with CROs if required, • Drive consumer centric product science visualisation in collaboration with global marketing, • Partner with cross functional teams – regulatory, quality, marketing, procurement, supply chain to align deliverables, resources and project priorities., • Closely manage existing products and product innovation relationship with CDMOs and ensure all development and validation work complies with internal and external standards (Quality, Medical, Regulatory) Product Innovation Expertise and Leadership • Provide deep expertise in formulation science, chemistry and process understanding, • Establish appropriate product specifications, testing and stability requirements based on product classifications and use., • Manage CDMOs in OTC, Medical Devices, VMS or cosmetic categories including providing the technical requirement to support RFQ process, • Conduct technical due diligence on established products and formulations, • Lead CDMOs, testing laboratories, research organisations (incl CROs) to support new product or new claims development., • Optimise ingredients / formulations to meet performance, claims, cost and supply requirements., • Identify opportunities to enhance processes, share knowledge and strengthen the project scientific capabilities. As the Head of Product Innovation you will have: • Bachelor’s / Master’s degree / PHD in Science or Pharmacy with extensive professional R&D experience, • Proven experience in a consumer product organisation with a strong focus on new product development and commercialisation within OTC, MD, Cosmetics or VMS categories, • Strong technical foundation and experience in formulated and engineering products with experience across dosage formats being beneficial, • Solid understanding of end-to-end product development including GLP and GMP/GCP, • Experience collaborating with manufacturing teams and /or CDMOs and proven evidence in delivering NPD, • Ability to work effectively in a matrixed organisation, building strong functional relationships across Marketing, Regulatory, Quality, Procurement and Project Management, • Ability to influence and align diverse stakeholders, • Agile, proactive and highly motivated, thriving in fast-moving environments, • Excellent verbal and written communication skills Desirable Criteria • Experience in start-up or incubation environments, with a track record of developing and scaling new products., • Familiarity with regulatory requirements in healthcare/OTC, medical devices., • Experience integrating consumer insights into product development. Apply now to take the next step in joining ZEISS, where you can push technological boundaries, shape markets and contribute to the advancement of society. Your ZEISS Recruiting Team: Kate Campbell _ Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, ideology, disability, age or sexual orientation and identity.

The Opportunity Trident are seeking to recruit a chartered building surveyor to join our established team in Birmingham. There is scope for fast career progression, to get involved in the direction of the business, and work with a wide range of clients on differing asset types. The successful candidate would get direct exposure to clients, so that they can understand our client’s aspirations and help us to achieve these. We work with various client types and their representatives when acquiring, improving and managing all types of commercial properties. The successful candidate would also get the opportunity to grow their network of local and National contacts as we work with a variety of property agents, managing agents, solicitors and other property professionals. The opportunity is for a chartered surveyor with good experience of both professional and project work, to include; acquisition and dilapidations surveys and negotiation, planned preventative maintenance, contract administration / project management and statutory compliance. Trident will offer a highly competitive salary package including a range of benefits: • iPhone & Laptop to support our agile & hybrid working policy, • Enhanced maternity / paternity and adoption leave policy (after a successful probationary period), • Competitive private pension scheme (5% employer & minimum 3% employee contribution), • Private Health Care (after 3 months), • Tax-free EOT bonus scheme – after 12 months continuous employment, • Membership to our life insurance scheme (x2 annual salary), • Upon passing probation the company will provide you with a £20.00 monthly allowance to spend on our benefits package provider, Zhoosh, to further enhance your benefits package:, • Top up your pension contributions, • Purchase critical illness cover, in steps of £25,000 up to £250,000 maximum cover, • Purchase life insurance, in steps of £25,000 up to £250,000 maximum cover, • Purchase a bike through our cycle scheme, • Lease an electric car, • Car allowance, • Company and team profit shares, • Career development investment, • Payment of professional fees and membership subscriptions, • Minimum 25 days holiday + bank holidays, • Opportunity to accrue an additional 4 long service days, • Opportunity to buy a maximum of two weeks’ additional annual leave each year, • Electric Car Scheme, • Cycle to Work Scheme, • Perkbox benefits platform, • Company annual staff team building day and regular local social events About Trident In June 2022 Trident proudly became an Employee Ownership Trust. Trident has recently been awarded “Investors in People” Gold accreditation, which demonstrates that our people are our most important asset. Trident’s culture embraces diversity, equality and inclusion (DEI) across our offices and our team enjoy a healthy work life balance that supports physical and mental wellbeing. Trident are B Corp certified and were featured in the Sunday Times, Best Places to Work 2025! We have also partnered up with PREACH Inclusion to implement our DEI Framework. We've meticulously measured our carbon footprint and set a science-based target through SBTi (Science Based Targets Initiative), ensuring our goals are grounded in scientific consensus. Our network of national regional and offices work as a collaborative team to provide the highest level of Building Surveying and Project Management to our enviable client list. Our agile working policy has operated since 2019 and it recognises that work is not just performed “9 to 5” in the office, allowing our staff the flexibility to vary working hours and to work remotely although we encourage staff to attend the office regularly to help promote our core values of team working and collaboration. To Apply Please apply via the LinkedIn job post.

About the role We are seeking a Domain Architect for the In Silico stream to assess the current research data, computational biology, bioinformatics and AI/ML environments. The role is hybrid, with expected visits to Oxford or London for onsite collaboration. Responsibilities • Design research data platforms and cloud analytics environments., • Define environments supporting model development, validation, deployment and reproducible research., • Define the target-state architecture for:, • human genetics;, • genome-wide association studies;, • rare-disease genetics;, • target prioritisation;, • translational science;, • computational biology;, • bioinformatics;, • multi-omics;, • multimodal evidence integration. What we expect: • Deep experience in pharmaceutical R&D digital transformation., • Practical experience in computational biology, bioinformatics and translational science., • Strong understanding of human genetics, GWAS, rare-disease genetics and target discovery., • Experience with multi-omics and multimodal evidence integration., • Experience designing research data platforms and data-intensive scientific workflows., • Experience designing cloud analytics and AI/ML platform architectures., • Understanding of the full machine-learning lifecycle, including development, validation, deployment, monitoring and reproducibility., • Experience with knowledge graphs, semantic technologies, retrieval-augmented generation or scientific copilots., • Experience integrating research, clinical, real-world evidence, literature and public data sources., • Knowledge of FAIR principles, data governance, privacy, security, responsible AI and model governance., • Experience working within enterprise architecture governance and Technical Design Authority processes. Nice to have: • Experience with Databricks, Genestack, Mystra, PlutoBio or comparable solutions.

Walker Cole International is searching for a Senior Clinical Quality Assurance Manager to join a rapidly expanding international Pharmaceutical business based in the UK. In this position, you will play a key leadership role within the global quality function, overseeing the delivery of UK and EU compliance services whilst supporting global quality initiatives across a diverse portfolio. This position offers an excellent opportunity for an experienced GCP Quality professional looking to progress into a senior leadership role with future progression pathways made transparent. The role can be based remotely with some travel across the UK and Europe, with occasional international travel. Your responsibilities will be to: • Lead and perform a range of GCP audit programmes covering clinical studies, service providers, quality systems, and operational processes., • Evaluate and strengthen quality systems through various assessments and improvements., • Contribute to the strategic direction of the global quality function, supporting the development of new initiatives., • Maintain and continuously improve internal quality processes to ensure operational excellence and regulatory compliance., • Provide technical leadership and guidance to colleagues, supporting capability development across the wider compliance team. The successful candidate will have: • An academic background in Life Sciences or a related scientific discipline, with postgraduate qualifications considered advantageous., • Demonstrable experience leading and executing GCP audits across clinical trial operations, vendors, CROs, suppliers, and quality systems., • Strong understanding of international GCP regulations and expectations within pharmaceutical, biotechnology, or clinical research environments., • Outstanding communication and relationship-building skills, with confidence interacting at all organisational levels., • Professional GCP training and certification, alongside a commitment to maintaining current regulatory knowledge. Quality Assurance | QA | Clinical Quality | GCP | Good Clinical Practice | GCP Auditor | Lead Auditor | Quality Consultant | CRO Oversight | Sponsor Oversight | Vendor Qualification | Vendor Management | Clinical Trials | Inspection Readiness | CAPA | SOP Authoring | Quality Management System | QMS | Risk Management | Regulatory Compliance | Clinical Research | Biotechnology | Pharmaceutical | Clinical Development | ICH GCP | Global Quality | Audit | Quality Systems ID - 108871

Director of Quality Assurance (OSD) Type: Permanent On-site: 4 days per week/ 1 day from home Industry: Pharmaceutical Manufacturing (Oral Solid Dose) Overview An established pharmaceutical manufacturer is seeking a Director of Quality Assurance to lead the QA function across a complex Oral Solid Dose (OSD) manufacturing operation. This is a strategic leadership position responsible for driving quality culture, regulatory compliance, inspection readiness, and continuous improvement while partnering with Manufacturing, Supply Chain, Technical Operations and senior site leadership. The successful candidate will provide direction to multiple QA teams, ensuring products are manufactured in accordance with GMP requirements and global regulatory expectations. Key Responsibilities • Provide strategic leadership for the site Quality Assurance function across OSD manufacturing operations., • Lead and develop multiple QA teams, fostering a strong quality culture and high-performance environment., • Ensure ongoing compliance with EU GMP, FDA and other applicable regulatory requirements., • Maintain inspection readiness and lead regulatory inspections from agencies including FDA, MHRA and EMA., • Oversee batch disposition processes and ensure robust quality decision-making., • Drive continuous improvement initiatives across Quality Systems and manufacturing processes., • Provide oversight of deviations, CAPAs, change controls, investigations and risk management activities., • Partner closely with Manufacturing, MS&T, Engineering, Validation, QC and Supply Chain to support operational excellence., • Review quality metrics and identify trends to proactively improve performance., • Ensure effective implementation and maintenance of the site's Quality Management System (QMS)., • Support new product introductions, technology transfers and commercial manufacturing activities., • Manage quality-related risks and ensure appropriate governance across the site., • Act as a key member of the site leadership team, influencing business strategy from a quality perspective. Requirements • Degree in Pharmacy, Chemistry, Pharmaceutical Sciences or another relevant scientific discipline., • Extensive Quality Assurance leadership experience within a GMP-regulated pharmaceutical manufacturing environment., • Significant experience supporting Oral Solid Dose (OSD) manufacturing., • Strong working knowledge of EU GMP, FDA regulations, ICH guidelines and global quality standards., • Demonstrated experience leading regulatory inspections and managing audit responses., • Proven ability to lead large multidisciplinary QA teams., • Experience working with complex manufacturing operations and cross-functional stakeholders., • Strong leadership, communication and stakeholder management skills., • Strategic mindset with the ability to balance quality, compliance and business objectives. Desirable • Experience within a multinational pharmaceutical manufacturing environment., • Exposure to new product introduction (NPI), technology transfer or site expansion programmes., • Knowledge of digital quality systems and continuous improvement methodologies (Lean/Six Sigma). What's on Offer • Senior leadership opportunity within a highly regulated pharmaceutical manufacturing site., • Strategic role with significant influence across site operations., • Opportunity to lead a well-established Quality organisation supporting complex OSD manufacturing., • Competitive salary and comprehensive benefits package.

Senior ML Engineer – Remote (UK) Most AI products are wrappers. We're building the real thing, an agent that takes on genuine tasks for everyday users: running errands, managing workflows, holding context across long and complex conversations. Reliable by design, not by luck. We're small, we move fast, and the ML layer is the product. We need someone to own it. The role You'll bridge research and production, taking ideas and turning them into systems that run at scale, stay reliable, and get better over time. Full-stack ML ownership: from raw data to deployed model. Day to day that looks like: • Building end-to-end pipelines across data, training, evaluation, and inference, • Adapting and fine-tuning models with modern techniques: LoRA, QLoRA, SFT, DPO, distillation, • Architecting inference systems that hold up under real latency and cost constraints, • Creating data pipelines that produce high-quality synthetic and real-world training data, • Running evaluation that goes beyond benchmarks: robustness, safety, bias, production behaviour, • Owning deployment: GPU optimisation, quantisation, memory efficiency, scaling, • Working directly with application engineers so ML integrates cleanly into backend, mobile, and desktop Your skills and experience • Deep understanding of deep learning and transformer architectures, • Proven experience training, fine-tuning, or shipping large-scale models in production, • Strong with at least one major ML framework (PyTorch, JAX) and quick to pick up others, • Familiar with distributed training and inference tooling: DeepSpeed, FSDP, Megatron, ZeRO, Ray, • Engineering discipline: code that's readable, robust, and maintainable, • Experience optimising for GPU constraints: quantisation, mixed precision, memory, • Comfortable taking ownership of ambiguous problems from zero to one, • Ships, iterates, learns from production Nice to have • LLM inference frameworks: vLLM, TensorRT-LLM, FasterTransformer, • RLHF: PPO, DPO, ORPO, • Open-source contributions to ML or systems libraries, • Scientific computing, compiler, or GPU kernel experience, • Multimodal or diffusion model background, • Large-scale data processing: Arrow, Spark, Ray Why join At a big company, ML work gets absorbed into a machine. Here, your systems are the product. You'll work closely with research and engineering leadership, have real influence over how the architecture evolves, and see the direct impact of your work on users. If you want to build ML infrastructure that actually matters, this is it.

About the role We are looking for a Domain Architect to design lab informatics and scientific data-management architectures across multiple systems, and to align them with scientific and business needs. What we expect • Deep experience in life-science, pharmaceutical or biotech laboratory digital transformation., • Practical experience with ELN, laboratory inventory, scientific registration and sample-management solutions., • Strong understanding of plate-based assays, imaging, omics and high-throughput laboratory workflows., • Experience with laboratory automation, robotics, instrument integration and scheduling or orchestration., • Experience designing lab informatics and scientific data-management architectures across multiple systems., • Strong knowledge of APIs, event-driven architecture, microservices, cloud-native patterns and domain-driven design., • Experience designing FAIR-aligned scientific data architectures., • Practical experience with metadata, data lineage, ownership, data catalogues and reusable research data products., • Experience leading or supporting technical product evaluations and proofs of concept., • Experience working within enterprise architecture governance and Technical Design Authority processes., • Ability to explain complex architecture options to scientific, business and technical stakeholders. Nice to have • Hands-on experience with platforms such as Dotmatics, Revvity Signals, Benchling, Mosaic, LabVantage, TetraScience or comparable solutions.

We are partnering with one of the world's leading healthcare communications organizations as they continue to expand their Regulatory Writing team. Due to ongoing growth, they are seeking experienced Senior Regulatory Medical Writers who are passionate about scientific excellence, client partnership, and delivering high-quality regulatory documentation across a diverse portfolio of pharmaceutical and biotechnology clients. This is an opportunity to join a highly respected organization that values strategic thinking, collaboration, and long-term career development. The team is looking for individuals who want to make a meaningful impact, build strong client relationships, and contribute to the continued growth and evolution of the regulatory writing function. The Opportunity: As a Senior Regulatory Medical Writer, you will be responsible for developing and reviewing a range of regulatory documents while serving as a trusted scientific partner to both clients and internal stakeholders. You will work closely with multidisciplinary teams to ensure the delivery of clear, accurate, and compliant regulatory communications that support global development and submission strategies. This role offers exposure to a broad range of therapeutic areas and the opportunity to work directly with leading pharmaceutical and biotechnology companies. Key Responsibilities • Author, edit, and review a variety of regulatory documents for global pharmaceutical and biotechnology clients., • Ensure all deliverables meet scientific, regulatory, and quality standards., • Partner closely with clients to understand project objectives and provide strategic writing support., • Collaborate with Regulatory Affairs, Clinical Development, Medical Affairs, Biostatistics, and project teams to deliver high-quality submissions., • Manage multiple projects simultaneously while maintaining timelines and quality expectations., • Contribute to client meetings and serve as a trusted scientific resource throughout project delivery., • Support the development of best practices and contribute to the continued growth of the regulatory writing team., • Stay informed of evolving regulatory guidance and industry developments. Qualifications • Advanced scientific degree preferred (PhD, PharmD, MD, MSc, or equivalent)., • Significant experience in regulatory medical writing within a pharmaceutical company, biotechnology organization, CRO, or healthcare communications agency., • Strong experience authoring and reviewing regulatory documents for global submissions., • Excellent scientific writing, communication, and stakeholder management skills., • Ability to build strong relationships with clients and collaborate effectively across multidisciplinary teams., • Strong project management and organizational skills with the ability to manage competing priorities., • Experience within a client-facing environment is highly desirable. Why Consider This Opportunity? • Join a globally recognized healthcare communications organization with a strong reputation in regulatory and scientific communications., • Work alongside industry-leading experts across a diverse portfolio of pharmaceutical and biotechnology clients., • Be part of a growing team where your contributions will help shape future processes, capabilities, and client partnerships., • Gain exposure to a wide range of therapeutic areas, products, and development programs., • Excellent opportunities for professional growth, development, and career progression. If you are an experienced regulatory writer looking to combine scientific excellence with strategic client engagement, we would welcome the opportunity to speak with you.

Who We Are Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40 manufacturing facilities and more than 40.000 employees around the globe, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market, and are rapidly ramping up their presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. Values At Sun Pharma our core values—Humility, Integrity, Passion, and Innovation—are part of our unique culture, known as Sunology. We are empowering our employees to create their “Own Sunshine”. We believe in being Better Everyday by investing on lifelong learning, Taking Charge by owning our impact, and Thriving Together in a workplace where collaboration is encouraged. We are committed to being an inclusive and equitable employer, valuing diverse perspectives and creating an environment where all individuals feel respected, heard, and inspired to bring their best selves to work. Overall Job Purpose The Medical Manager Ophthalmology (MM) is responsible for leading Medical Affairs activities in the UK for a branded Ophthalmology product in the post‑launch phase. In alignment with the Brand Strategy and medical Plan, the MM works closely with UK Key Opinion Leaders (KOLs) to drive scientific engagement and ensure high‑quality medical support. Key responsibilities include initiating and managing clinical research projects, organizing national advisory boards, and delivering scientific publications, congress posters, and presentations in collaboration with KOLs. As the medical expert for the product, the MM provides medical and scientific education to KOLs and field colleagues through presentations, training, and ongoing scientific support. The MM also develops medical content and provides strategic briefings for KOLs attending congresses. In addition, the MM partners closely with the Marketing Manager, offering medical insights and content to support marketing materials and projects, while ensuring strict adherence to pharmaceutical industry codes and compliance standards. Major tasks & responsibilities (70% field) Strategic plan development in close collaboration with Marketing and Head Medical Affairs Execution of the Medical Affairs launch strategy plan at country level. • Mapping and management of KOLs on the disease, • Develop links with and support national networks in the therapeutic area, • In collaboration with Market Access, ensure product Access and in local guidelines, • Organizing local Advisory Boards (content, objectives, speakers, attendees), • Local publications and congress posters within strategy of the product, • First medical HCP contact at Congresses and symposia,, • Content input, providing medical slide decks, briefing KOLs for congress and symposia presentations, within brand strategy, • Medical information on requests to HCPs and medical Presentations to HCPs within Brand strategy, • Handling Investigator-Initiated trials (IIT): Internal approval and contracting, • Approval of contracts for external (consultancy/speaker) activities with HCPs, • Develop medical training decks and give medical training for commercial colleagues in the field on disease and product, • Medical scientific and strategic input on Marketing projects and materials in collaboration with Marketing Manager, • Ensure all Medical and Marketing projects, materials and presentations are compliant to pharmaceutical codes. Education Qualifications • (Bio) medical (scientific) academic degree, • Training in the code of Pharmaceutical Compliance rules, • Presentation and training skills Work experience • Minimum of five years of Medical Affairs experience in the pharmaceutical industry, • Ophthalmology network and experience, • Strategic and operational experience in launch activities, • Experience in Marketing and or Commercial function in Pharmaceutical Industry Technical skills/job specific competencies • Mandatory - Fluent in English, • Setting up and run Medical projects, • Good developed influential skills use internally and internationally in the medical field, • Outgoing personality, likes to interact with people, being in the field, • Goal oriented and strategic thinking, • Good understanding of pharmaceutical industry codes, • Good collaboration with Marketing and Sales colleagues, • Good sense of the Brand strategy and follow up in all projects, • Good teaching and presentation skills, • Flexibility and patience, • Positive creative mindset to challenges Accountability • Takes responsibility and owns up to all activities and personal actions, • Executes with agility, without compromising on core values, • Follows through and implements agreed decisions within agreed timelines consistently, • Takes responsibility for personal and team actions, and learns from part mistakes, • Clearly defines accountability within the team and drives them to achieve high performance standards Collaboration • Builds strong internal networks and communicates across departments and functions to meet business objectives, • Proactively contributes to the success of other departments and shares credit., • Does not hesitate to seek help, • Focuses on overall business value to Sun over own department/function, • Is culturally sensitive and comfortable working in a global context Customer Centricity • Understands and responds to customer/ stakeholder needs, • Develops positive long-term relationships with customers/ stakeholders, • Displays an entrepreneurial mind-set and identifies opportunities and ways to stay ahead of competition

Develop your career in a role where you’ll take the lead in delivering high quality, patient focused diagnostic services. As a Specialist Biomedical Scientist with extensive experience in Blood Transfusion, you will lead a team of specialist biomedical scientists and support staff, applying advanced scientific knowledge, methods and technology to the investigation of blood samples. Your expertise will guide clinical diagnosis and the management of disease, while ensuring the safety of the island’s blood supply for the benefit of islanders’ health. Working in a collaborative and forward-thinking environment, you will lead a team performing a broad range of blood transfusion laboratory analyses on patients’ and donors’ samples. You will provide expert advice on appropriate techniques, contributing to clinical diagnoses, treatments and the evaluation of therapeutic interventions. Your leadership will help shape patient care and accelerate scientific progress. You will also manage the blood transfusion and donation processing and testing workload through effective teamwork, ensuring urgent clinical needs and agreed turnaround times are consistently met, aligned to good manufacturing and transfusion best practice. Our Biomedical Scientists cover a range of services in blood sciences including haematology, clinical chemistry, blood transfusion and the Jersey Blood Donor Service. We are investing in our people and are devoted to building on our excellent scientific centre to deliver outstanding pathology services to our island community. Jersey is a unique place to live and work, and being a Biomedical Scientist here is different. As a Crown Dependency, we are an Island nation with our own healthcare service. With our patients and health professionals at the centre of all we do, as a Biomedical Scientist you have more time to deliver your role, and we give more time to you for your development and wellbeing. And as with many aspects of island life, our healthcare system is familiar enough for comfort but offers variances that mean our Biomedical Scientists have a truly different experience. For an informal discussion please contact: pathologycareers@health.gov.je For a full job description: JD - _ For more information about Jersey and relocating to the island: _

Senior Spacecraft Software Engineer Glasgow, UK - Hybrid £85,000 - £100,000 Depending on experience & Qualifications We are proud to be supporting a world-leading space-to-cloud analytics company in their search for a Senior Spacecraft Software Engineer. Because this engagement is sensitive, we'll share the client's name with candidates at the shortlisting stage. The Opportunity Our client owns and operates one of the world's largest multi-purpose satellite constellations, delivering advanced maritime, aviation, and weather tracking globally. Their infrastructure spans a proprietary satellite constellation, a global ground station network, and 24/7 operations providing real-time coverage of every point on Earth. This role sits at the intersection of satellite payloads, scientific computing, and data delivery systems. You will be responsible for developing and maintaining both the flight and ground software that powers GNSS-based satellite missions, working across system layers from embedded software through to mission data pipelines. It is a high-impact, high-autonomy position where technical breadth and ownership are essential. Key Responsibilities Flight & Payload Software • Develop and maintain scientific and command & control software for GNSS-based satellite payloads, • Work across embedded system layers to ensure accurate and timely scientific data output, • Engage with payload developers and mission operators to evolve software in support of scientific objectives Ground Systems & Data Delivery • Build and operate ground-based automation systems for data extraction, transformation, and delivery, • Collaborate with flight operations to troubleshoot and ensure consistent, high-quality data delivery, • Participate in code reviews, testing, and documentation to maintain software reliability and traceability What We're Looking For Our client is seeking a Senior Spacecraft Software Engineer with deep technical foundations in embedded systems and GNSS signal processing. You'll take strong ownership of your work and be comfortable operating independently across hardware and software boundaries. Core Requirements • Proficient in Embedded C/C++ for hardware development in constrained environments, • Solid background in DSP techniques and theory, particularly in the context of RF or GNSS signal processing, • Hands-on experience with GNSS signal processing algorithms and/or scientific applications such as GNSS-RO, GNSS-R, or PNT Desirable • Python proficiency and ability to pick up new tools and languages as needed, • Experience with cloud-based systems (e.g. AWS), backend development, and scalable data storage, • Prior experience working on satellite payloads or in the aerospace domain, • Experience building telemetry and data visualisation tools, • Contributions to open-source scientific or aerospace-related software projects Why This Role Stands Out • Work on a real, operational satellite constellation delivering mission-critical scientific data globally, • High autonomy from day one, design, build, and own your work end-to-end, • Join a technically exceptional team operating at the cutting edge of space and clean technology infrastructure, • Generous benefits including education assistance, stock purchase programme, fitness reimbursement, family leave, and more, • An opportunity to contribute to work that genuinely improves life on Earth Apply via Cleantech Talent This role is being managed exclusively by Cleantech Talent on behalf of our client. If you have the background and ambition to take on this challenge, we would love to hear from you. Please apply directly through LinkedIn or reach out to the Cleantech Talent team with your CV and a brief note on your interest and relevant experience. All applications are handled in strict confidence.

Medical Science Liaison - UK - Remote (Travel across the UK is required 60-80%) with some visits to our UK offices About the Company Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally by revitalising niche, tried-and-trusted medicines. Our core behaviours are: • We act decisively, but we never compromise on quality, • We keep our promises and do as we say, • We value our heritage and foster an entrepreneurial spirit, • We reinvest in our future – in our products, our brands and our people, • We give back to our communities Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers worldwide. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees from 29 nationalities and operates from offices in the UK, Denmark, the Netherlands, Switzerland, Italy, Spain, Germany, the U.A.E., India, Australia and Singapore. We are an agile, committed, and innovative global speciality pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce. Pharmanovia’s therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology About the Role Reporting to the Medical Department, you will be a member of the MSL team, whose primary responsibility is to interact with influential stakeholders and healthcare providers nationally. You will collaborate with physicians and other medical experts to support trial management, RWE initiatives, interact with patient organisations, and ensure that healthcare professionals have the most up-to-date information about the medical and clinical benefits of Pharmanovia’s products Responsibilites • Setting up strategies to target the most relevant HCPs for Pharmanovia’s therapeutic efforts and coordinate and align key messages to position Pharmanovia as a credible partner and provider of effective treatments and medicines, • Identifying, developing, and maintaining professional relationships with national KOLs, establishing peer-to-peer collaborations with key medical experts in the therapeutic areas covered by Pharmanovia, • Supporting evidence generation initiatives, including potential investigator site identification, trial recruitment, registries, and presentation of final approved data, involving experts to generate scientific data, including investigator-initiated trials, • .Collaborating with physicians on medical affairs initiatives, including publication and communication plans, advisory boards, medical education opportunities, webinars, training, and speaker development, • Serving as a scientific peer-to-peer resource to external disease experts and internal stakeholders, • Supporting the medical community with up-to-date medical information, robust disease expertise, and product information, • Communicating clinical insights on new data to the company, • Coordinating the gathering of insights from HCPs to support business strategy, such as new product development and market access, • Fostering cross-functional collaboration with internal teams: KAMs, local marketing, market access, etc, • Generating national plans to provide needs-based, value-added support of the medical and scientific community in line with company goals, • Using systems to strategically map, identify, profile, and prioritise thought leaders in line with the medical plan and goals, • Being a credible scientific expert in the given therapeutic area and in the product(s) themselves, • Reporting and documentation of MSL’s daily activities Qualific • A scientific degree (e.g. PhD, PharmD or MD)., • Medically trained and/or clinical experience in Oncology, Gyn-oncology, Internal Medicine, or a related field., • Prior MSL experience of 3-6 years within Oncology Required Skills • Appropriate focus on performance and delivery, • Must excel at working independently and in cross-functional teams. Demonstrates excellent time management skills and can adapt to new circumstances and ideas., • Inclination to seek and analyse data from a variety of sources to support decisions and to align others with the organisation’s overall strategy., • Knowledge of compliance requirements and adherence to all relevant standards., • An entrepreneurial approach to developing new, innovative ideas that will stretch the organisation and push the boundaries within the industry, • Fluency in spoken and written business English is essential, • Travel required Pay range and compensation Package We offer a competitive salary plus a bonus and rewards package, including holidays, employee recognition awards, social events, a pension scheme, and hybrid Working Equal Opportunity Statement Pharmanovia is an equal-opportunity employer. Pharmanovia does not unlawfully discriminate against employees or applicants for employment based on an individual’s race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Pharmanovia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Territory will include multiple countries in the EU. Serving as a value-added resource and extension of the Company the Clinical Trial Liaison (CTL) will support the company's Ophthalmology pipeline. The CTL supports the execution of country medical plans related to clinical trial engagements. The CTL will work full time to educate, analyze, and resolve issues with clinical research sites and investigators. This role involves compliant collaboration with KOLs, investigators, research staff members, advocacy groups to build strong professional partnerships, provide credible scientific expertise, and serve as a field-based extension to support the company's clinical trial programs. Essential Duties And Responsibilities Site and Investigator Partnerships • Create investigator engagement plans to support site identification and selection, • Build and maintain partnerships with potential PIs for company clinical trials, • Conduct compliant scientific exchange to educate on company clinical trials, • Provide clinical trial liaison support to site investigators involved in sponsored studies including protocol support, screening barriers, and clinical trial recruitment and retention, • Collection of key medical insights from PIs to inform refinement of strategies, • Serve as a liaison to internal R&D functions to ensure the effective support of PIs, • Respond in a timely manner to unsolicited inquiries from external stakeholders and HCPs Building Company & Pipeline Advocacy • Through compliant scientific exchange, build and maintain professional relationships with external stakeholders to expand research, company advocacy, and educational partnerships, • Collect key strategic insights from top research KOLs and HCPs to support strategic initiatives, • Support execution of strategy through creation of national and regional congress plans for your assigned territories to attend and execute activities Qualifications • An advanced degree in life sciences (MD, PharmD or PhD or equivalent), • Has established scientific relationships and the ability to deliver effective presentations to HCPs, • Experience in clinical trial operations, design, site support and scientific engagement with clinical trial sites required., • General Ophthalmology or Anterior segment ophthalmology therapeutic area experience and/or Neurology, • At least 2 years of therapeutic, research or substantive patient care experience is required, • Frequent travel is required. Availability to travel up to 75% of time, • Availability to attend meetings on holidays and weekends, • Ability to travel internationally as needed with valid passport, • Clean and valid driver’s license

We are recruiting a PV QA Manager to join a leading Pharmaceutical company in the UK on a remote basis. This role is inside IR35 and is pivotal in ensuring excellence in Pharmacovigilance Quality Assurance (PVQA) activities. As the QA Manager, you will play a crucial role in supporting the PV system and the collection and reporting of safety information This is an initial 12 month contract and offers fully remote working. Please note you must have the full right to work in the UK. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QA Manager will be varied however the key duties and responsibilities are as follows: 1. As the QA Manager, you will execute regional, cross-regional, and global audit programs, including planning, conducting, and reporting audits, and liaising with customers on audit findings., 2. As the QA Manager, you will provide expert GPvP advice to key personnel, including coaching QA colleagues and interpreting health authorities' requirements for implementation., 3. As the QA Manager, you will support the development and maintenance of the Quality System by addressing non-conformances and managing quality issues related to critical non-conformities., 4. As the QA Manager, you will develop and manage interfaces with QA departments of service providers to ensure oversight and mitigate risks to the business. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the QA Manager, we are looking to identify the following on your profile and past history: 1. Relevant degree in a related field., 2. Proven industry experience in clinical/Pharmacovigilance QA or the pharmacovigilance function., 3. A working knowledge and practical experience with QA Standards, particularly Good Clinical and GPvP Practice Guidelines and Regulations. Key Words: QA Manager / Pharmacovigilance / PVQA / Quality Assurance / Clinical QA / GPvP / Audit Programs / Regulatory Compliance / Risk Management / Continuous Improvement / Clinical / Pharmaceutical / Biotechnology / Remote / PV / Veeva / eQMS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.

We are looking for an experienced LabWare LIMS Developer with a strong scientific background complemented by hands-on experience within regulated laboratory and medical device manufacturing environments. They will be responsible for the design, development, configuration, validation and ongoing enhancement of LabWare LIMS solutions, supporting laboratory operations through the implementation of efficient, compliant and user-focused systems. Playing a key role in driving the introduction and optimisation of functional LIMS platforms, improving data management, workflow automation, and operational efficiency . They will work closely with laboratory, quality, regulatory and technical stakeholders to gather requirements, develop system functionality and ensure solutions align with business and compliance needs. Demonstrating strong project management capabilities, leading initiatives from planning and development through to validation, deployment, and completio n. Key areas of expertise inclu • de:LabWare LIMS configuration, development, and implementat, • ionLaboratory workflow analysis and process optimisat, • ionComputer System Validation (CSV) and GxP complia, • nceDocumentation lifecycle management and regulatory requireme, • ntsProject planning, delivery, and stakeholder managem, • entMolecular biology and microbiology laboratory environme, • ntsMedical device manufacturing and quality syst, • emsUser training, knowledge transfer, and customer supp, • ortCross-functional collaboration and communicat ion The ideal candidate will be proactive and a self-motivated professional with a strong aptitude for learning new technologies, solving complex problems, and delivering high-quality solutions within regulated laboratory environme nts.

In this decade, the world will create Artificial General Intelligence. There will only be a small number of companies who will achieve this. Their ability to stack advantages and pull ahead will define the winners. These companies will move faster than anyone else. They will attract the world's most capable talent. They will be on the forefront of applied research, engineering, infrastructure and deployment at scale. They will continue to scale their training to larger & more capable models. They will be given the right to raise large amounts of capital along their journey to enable this. They will create powerful economic engines. They will obsess over the success of their users and customers. Poolside exists to be this company: to build a world where AI will be the engine behind economically valuable work and scientific progress. We believe the fastest way to reach AGI lies in accelerating software development itself, by reshaping the developer experience with agentic systems, coding assistants, and the frontier models that power them. We deploy these systems directly into the development environments of security-conscious enterprises. We were founded in the US and have our home there, but our team is distributed across Europe and North America. We get our fix of in-person collaboration (and croissants) in Paris each month for 3 days, always Monday-Wednesday, with an open invitation to stay the whole week. We also do longer off-sites once a year. Our team is a multidisciplinary blend of research, engineering, and business experts. What unites us is our deep care for what we build together. We’re in a race that requires hard work, intellectual curiosity, and obsession; to balance this intensity, we’ve assembled a team of low ego and kind-hearted individuals who have built the special culture Poolside has. By building collaboratively and with intention, we create a compounding effect that moves the entire company forward towards our mission: reaching AGI through intelligence systems built for software development. You'll be working alongside our pre-training data team, focused on one of the most foundational challenges in training frontier LLMs: acquiring the best possible pre-training data. The data we collect is upstream of everything. It directly shapes the capability of the models we train. As our first dedicated data acquisition engineer, you will spearhead and evolve systems that crawl the web at massive scale, rapidly ingest data from strategic partnerships, and build specialized tooling to maximize recall from high-value sources. You'll collaborate closely with pre-training data researchers and engineers to ensure that our sourcing of data maps to our training needs, to ensure we have the most capable pre-trained models. To deliver the highest-quality, diverse, and most comprehensive data corpus to fuel the pre-training of frontier models for software development. Design, build, and operate a large-scale web crawler responsible for acquiring all openly accessible data on the internet Develop specialized deep crawlers targeting high-value sources to improve recall and coverage In collaboration with data researchers, own a long-term road map for data acquisition Build observability, monitoring, and debugging tooling to ensure reliability and transparency across crawl infrastructure Collaborate with pre-training, post-training, and evaluations teams to align data acquisition priorities with model training needs Build high-throughput ingestion pipelines for rapidly onboarding partner data and evaluating it for quality Strong distributed systems background with proven experience building and operating large-scale infrastructure — data pipelines, web crawlers, or similar Proficiency in Python, and comfortable optimizing performance and debugging complex systems under production conditions Hands-on experience with web crawling or large-scale data extraction: understanding of HTTP protocols, distributed job queues, and data parsing at scale Familiarity with cloud platforms (AWS) and container orchestration (Kubernetes, Docker) for deploying and managing high-throughput workloads Awareness of the non-technical dimensions of internet-scale crawling: data privacy, robots.txt adherence, and responsible crawl practices Nice to have: Prior experience pre-training LLMs Experience in building trillion-scale SOTA pre-training datasets Experience translating research to production at scale Intro call with one of our Founding Engineers Technical Interview(s) with one of our Members of Engineering Team fit call with the People team Final interview with one of our Founding Engineers Fully remote work & flexible hours 37 days/year of vacation & holidays 16 weeks of flexible, full-pay parental leave Health insurance allowance for you & dependents Company-provided equipment Well-being, always-be-learning & home office allowances Frequent team get togethers Diverse & inclusive people-first culture

Precision AQ is growing! Our team is looking for a Senior Account Executive to join our Medical Education team based in the UK. Location: Remote, but with opportunity to go into Salisbury office. Team: One of our oncology teams initially, but with scope to work across other therapy areas. Job Summary and Scope: The Senior Account Executive (SAE) works as part of a function, supporting them in the day-to-day servicing of accounts. As part of the team, they are responsible for supporting the Account Manager (AM), Senior Account Manager (SAM) and/or Account Director (AD) with the efficient, profitable delivery of projects, creating status reports and financial updates and supporting with the internal scheduling of work. They will also take a lead on organising logistics for meetings and facilitating PromoMats (or other client review platform) uploads. Key responsibilities: Client • Complete weekly status reports (with oversight from the AM/SAM/AD) as required and ensure projects/campaigns are tracking to planned timelines., • Attend client calls when required and develop contact reports., • Support in the development and delivery of materials for specific projects and campaigns as outlined by the account lead and/or AM/SAM/AD., • Book in timely Click-Ups with Creative, Digital, Client Services and Editorial teams to ensure smooth workflow, and ensure POs are raised for external subcontractors and suppliers as required., • Organise logistics for internal team or client update meetings and support AM/SAM/AD with organisation of logistics for external meetings and events., • Ensure thorough knowledge of client review platforms for your accounts and facilitate this process (including briefing CST, ensuring content/editorials checks as needed, and conducting uploads if required), • Maintain the high-quality of all deliverables through appropriate accuracy and quality checks prior to final QC., • Support the account lead in following up on all projects to gain feedback. Financial • Understand how to maintain financial profitability of all projects you are working on by understanding the requirements of realistic budget estimates and how to review costs on an ongoing basis., • Gain complete familiarity with financial platforms and processes to enable you to understand servicing levels (budget vs. actual hours) and direct costs, in order to accurately brief internal team members on the hours allocated to tasks., • Proactively manage and track project costs to ensure these do not exceed the budget., • Review of supplier invoices and provision of project code / task line to finance department on request. Management • Comply with Makara Health policies and procedures and demonstrate a personal commitment to their adherence and implementation. Other responsibilities • Travel to client meetings may be required as part of this role., • Undertake any duties as may be required from time to time that can reasonably be regarded as within the remit of the post., • Aware of and conform to legal requirements in all activities, both internal and external. Implicit in this is that all managers and employees conform to the appropriate standards in terms of Data Protection, Health and Safety and Information Security requirements but also to the highest standards of business ethics. Requirements: • One year of relevant experience within medical communications agency, • Scientific degree preferred, but not mandatory, • Strong communication, management and multitasking skills #LI-Remote #LI-TB1 Any data provided as a part of this application will be stored in accordance with our For CA applicants, please also refer to our . Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at _. It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

The business take a brilliant approach to hiring, in that they will consider candidates whether it be recent scientific graduates requiring lots of training and development, through to experienced Field Sales individuals. The role will be focussing on Medical Sales, liaising with contacts within th

We’re looking for a Lead Product Manager to help us turn complex nutritional science into life-changing habits. You will be the engine behind our core mobile experience, ensuring our members understand their biology through a product that is as intuitive as it is scientifically rigorous. In your first 6 months, you will: Own the delivery and strategic health of a major system or small domain, impacting 1-2 squads. Lead complex projects spanning 2+ teams to launch high-impact mobile features. Proactively identify and drive a complex, cross-team project that moves a core business metric. You’ll join our Product Management team, reporting directly to the Chief Product Officer. You’ll sit alongside 4 other Product Managers across the UK and EU, leading a cross-functional squad of engineers and product designers. Depending on your project, you’ll partner with Science or Marketing teams to keep our evidence-based impact front and centre. The B2C Expert: You have a deep mastery of digital products, specifically high-growth mobile applications. You understand the nuances of consumer psychology and D2C habit loops. Scientific Mindset: You don't guess; you look for the data. You are obsessed with user research and running experiments to validate every step of the roadmap. Bias for Action: You thrive at "startup speed". You’d rather ship a "good" version today and iterate based on feedback than wait for a "perfect" version next month. ZOE Energy: You are passionate about health-tech and move with the autonomy of a pillar strategist. You are a multiplier who elevates the capability of everyone around you. Solve: Take ownership of complex, cross-functional problems that impact the long-term health and growth of our core business verticals. Build: Design and implement a roadmap based on continuous user interviews and research, ensuring we build what our members actually need. Scale: Lead projects spanning 2+ teams, moving our mobile metrics from current performance to industry-leading benchmarks. Collaborate: Act as a strategic partner to the SLT, translating executive vision into measurable organisational impact. We value your time as much as our own. We’ve designed a streamlined, 4-step process to get us from "Hello" to "Welcome to the team" as quickly as possible. Step 1: 👋 Intro chat with Talent Team A high-energy intro to see if our missions align. We’ll chat about your journey, what makes ZOE tick, and make sure the basics (role, impact, and expectations) are a match. Step 2: 🧠 Hiring Manager Interview A tactical conversation focused on your craft. We skip the generic scripts and dive straight into how you solve problems, your past wins, and the specific challenges this role is here to tackle. Step 3: 🔄 The Remote Loop This is where we get into the details. Depending on the role and level, this stage consists of 2 to 4 focused interviews designed to assess different areas (e.g., technical skills, cross-team collaboration, or strategic thinking). Step 4: 🎉 The Finish Line (Offer & Onboarding) If there’s a match, we don’t hang around. We’ll extend an offer, talk through equity and benefits, and get you ready for your ZOE onboarding journey. Let’s change the world’s health together. The experience, skills, and attributes we’ve outlined are what we believe will help someone truly thrive in this role. However, we understand that talent comes in many forms. If you are genuinely excited about ZOE's mission and this opportunity, please don't hesitate to apply—even if you don't meet every single requirement listed. We fundamentally value potential and commitment above all else. We are dedicated to fostering growth and providing opportunities for you to learn and develop alongside us.

Area Sales Manager - Medical Devices Southern Territory C.£40k basic + uncapped commission + Car allowance An award-winning medical device company, home to a strong portfolio of recognised brands. As a top supplier to the NHS with a global presence, this company are seeing significant growth. They have a fantastic culture, are supportive and offer great training and career development opportunities. Due to growth the business is now looking to add a dynamic and passionate Area Sales Manager to develop end build business across the South East region. Responsibilities will include: • Achieve sales targets and weekly and monthly KPIs, • Building long lasting relationships within hospital departments, • Support with training on your products, • Analyse the marketplace and competitor activities, • Develop an effective territory/account sales strategy, • Manage sales process from product introduction, presentation and trial to closing and contract negotiation, • Attends and presents at external customer meetings and internal meetings You will have: • At least 2 years selling experience, managing a territory, • Previously Medical Sales experience is desirable, along with an understanding of The NHS marketplace - however FMCG backgrounds will also be considered, • Degree educated or relevant experience, • Results Orientated, • Self-motivated, • Full driving licence On offer for this exciting new roles is: • C.£40,000 basic DOE, • uncapped commission, • Car allowance

A highly successful Medical Technology business with roots and presence throughout Europe are working with DB Charles Recruitment to hire a new Key Account Manager to cover new & existing clients in areas predominantly around the East Anglia (North London, Essex, Cambridge, Peterborough, Coventry, Nottingham, Leicester, Louth, Boston) etc. The business take a brilliant approach to hiring, in that they will consider candidates whether it be recent scientific graduates requiring lots of training and development, through to experienced Field Sales individuals. Personality and attitude are key to the hiring of this business. The role will be focussing on Medical Sales, liaising with contacts within the NHS, Private Hospitals (surgeons / nursing staff) through to procurement & finance professionals. The hired candidate will report directly into the UK Sales Director and key duties for the role will include: • Developing new clients and maintaining existing business, • Lead follow ups, • Product training, • CRM Management, • Pitches & presentations The client will consider candidates with the following skill sets: • A recent graduate with a strong Biological / Medical /Anatomy focussed degree through to candidates such as Senior Sales Representatives / Account Managers within the Medical Industry, • Contacts within the medical industry would be highly advantageous however not essential, • Must hold a full UK Driving License and have there own vehicle, • Must be based in the region they will be operating in, • Must be highly motivated and sales driven, • Strong ability to learn The role will be working Monday to Friday, 9:00am to 5:00pm and the client is seeking to pay a salary of £35,000 per annum rising to £38,000 after the probation period with additional benefits such as: • Car allowance, • Fuel mileage claim, • x25 days annual leave + bank holidays + Xmas shutdown period, • Uncapped quarterly commission schemes, • Laptop & mobile phone, • Plus many others Please get in touch with your application if interested in this position.

Marketing and Communications Manager (EU-based) Clinglobal is a global, science-driven Animal Health services group dedicated to advancing veterinary research, innovation, and the delivery of high-quality scientific solutions. We are expanding our Business Development team and seeking an experienced Marketing Manager who can operate independently and play a pivotal role in supporting our Business Development Director. This role is ideal for a marketing professional who thrives in a regulated, scientific environment and enjoys creating high-quality marketing materials rather than engaging in direct, field-based sales activity. Primary Job Purpose As our Marketing Manager, you will be responsible for developing and managing marketing content and digital platforms to support our commercial growth. Your work will help ensure that Clinglobal’s capabilities are communicated clearly, consistently, and compliantly across all channels. Key focus areas include: • Creating and maintaining brochures, presentations, capability sheets, and digital content., • Managing marketing assets across websites, social media channels, and internal platforms., • Supporting the Business Development Director with strategic marketing initiatives., • Preparing client-ready materials for proposals, conferences, and events., • Ensuring marketing communications meet scientific expectations and industry standards., • Translating scientific information into compelling, market-ready messaging. This role does not require travel-intensive sales activity; instead, it is content-driven, strategic, and operational. Qualification, Training and Experience Requirements • Bachelor’s degree in Marketing, Design, Communications, Business, Animal Health, or a related field., • Minimum of 5 years of professional experience in marketing or communications roles., • Experience working within a regulated environment, ideally within the Animal Health, Animal Nutrition, or Pharmaceutical frameworks., • Strong written and visual communication skills in English with the ability to translate technical concepts into accessible marketing content. Other European languages will be valuable., • Demonstrated experience managing digital platforms, website content, and social media channels., • Preferred / Advantageous:, • Experience in the Animal Health, CRO, pharmaceutical, or scientific services industry., • Understanding of regulatory constraints for marketing scientific or health-related services., • Familiarity with digital marketing tools. Other Requirements • Remote or hybrid, depending on the country., • Occasional international travel for internal meetings or events may be required. Why Join Clinglobal? At Clinglobal, you will be part of an innovative, scientifically driven organization that is shaping the future of Animal Health research. We offer: • A collaborative, international work environment, • Opportunities to support meaningful scientific and veterinary advancements, • Professional growth within a rapidly developing global group, • The ability to make a real impact on how our capabilities are communicated to the world Important Note to Applicants Please be aware that Internet Explorer is not compatible with BambooHire. The Company complies with local and international data protection and privacy legislation. This includes transparency in the processing of personal information processed about job applicants during the recruitment process. By applying for this position, applicants agree to the processing of their personal data in accordance with our recruitment procedure and Privacy Notice available from our website. As part of the hiring process, candidates need to willingly take part in personality and behaviour assessments to determine a good fit for the job role. These assessments assist with the evaluation of candidates in a fair and thorough manner. All information gathered is kept private and only used to assess suitability for the job role. The Company may perform criminal and/or other relevant checks (as is relevant to the position) on all applicants applying for this position. Ready to Apply? If you are a proactive marketing professional who enjoys working in a dynamic scientific environment, we would love to hear from you!

At Data Intellect it has never been just about data or technology, they are our tools. It’s about human intellect, collaboration and providing solutions for the most complex of challenges. We do this by living the [DI] code: We are Problem Solvers who are Humble, possess a Can-do Attitude with a focus on Togetherness. “We are not big on egos, but we’re not for the faint-hearted either” – Steve Turner, CEO We are hiring for developers for our growing Market Abuse Surveillance practice. What you’ll be doing: • Working with business users to define requirements for new application functionality, • Developing, testing, supporting and maintaining all code for client applications, • Assisting the Project Manager with all aspects of project delivery, • Working as part of a team to deliver projects on time and on budget, • Analysing data and creating reports for clients to present findings, • Mentorship and training of junior developers Experience and skills required: • Minimum 3+ years kdb+ development experience, • Knowledge and experience in KX Surveillance, or of technical solution development in a surveillance, context is highly advantageous, • Ability to learn new programming languages and financial concepts quickly - logical thinkers and problem solvers wanted, • Familiarity with Software Development Methodologies, • Good knowledge of the Systems Development Life Cycle, • Detail-orientated, results driven and in possession of a can-do attitude, • Capable of working both independently and within a team, • Excellent client facing skills, • Minimum 2:1 degree in Mathematics, Physics, Computer Science or any other scientific/engineering discipline Experience and skills desired*: *But don’t rule yourself out if you haven’t had the opportunity to develop these skills yet • Knowledge of Trade Surveillance technology and Market Abuse regulations in one or more jurisdictions, • Experience of other programming languages, e.g. Python, • KX Surveillance deployment and enhancement, • Experience with application of AI and Machine Learning, • Cloud development experience, • Experience of other data solutions, specifically Time Series Experience in an investment bank or large financial organisation, • People management experience, • Technical lead of project or sub-team What we offer: • Flexible working – we offer hybrid working so our people can achieve that elusive work/life balance., • Professional development – we offer extensive training, ranging from leadership to specific technical skills., • Progression opportunities - we run a biannual promotion process. Monthly 121s with your People Leader provides support to guide you and your career in the right direction., • International travel opportunities – we offer the opportunity to work internationally, with teams in Belfast, London, New York, Hong Kong & Singapore, • Healthcare cover – provider is dependent on region, UK is provided by Benenden Health, including 24/7 GP Service & Mental Health Helpline to give you peace of mind when it comes to your health, • Generous referral scheme – we love to see referrals and referring a friend means cash for you!, • Regular social events, prizes and giveaways – our talented social committee work hard all year round to provide exciting events across all regions to promote our value of togetherness A little background on DI Simply put – we turn big data problems into smart data solutions At our core, Data Intellect is a data and technology consultancy firm. Our key area of expertise is financial and capital markets technology solutions. However, the utility of these solutions allow us to apply fintech data expertise to other industries such as smart energy and healthcare. This proprietary offering is complemented by a wealth of experience in data engineering, electronic trading systems, data capture applications, regulatory and compliance systems and middle and back-office enterprise web solutions. Fair employment and equal opportunities Data Intellect is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Accommodations are available on request throughout the assessment and selection process. Welcome to Data Intellect. #ChallengeAccepted

At Bruker Biosensors we are committed to strengthening our customer relations team to promote our new innovative heliX® and SPR #64 ‘Triceratops’ biosensors and are seeking highly motivated individuals to join us as Technical Sales Managers. • people and science, • speaking with high-level scientists about their research activities to identify technical fits, • developing opportunities to implement our cutting-edge technology, • promoting a great technology with the capability to fight cancer and other diseases at the forefront of next-generation drug development, • advanced scientific instruments for high-end research challenges in academia and industry, • getting to know new people by attending conferences and trade shows, learning about their technical challenges, and engaging in scientific discussions, • explaining cutting edge technology in a comprehensible way by giving presentations and organizing seminars, • coordinating technology evaluation projects and managing the collaboration of scientists, • traveling and an international work environment, • being part of a dynamically growing team, • a friendly and outgoing personality with great team spirit and a natural sales talent, • excellent communication and presentation skills, plus a keenness to start conversation, • a background in biotechnology, biophysics, chemistry, molecular biology, pharmacology, or similar (BSc, MSc, or PhD degree), • the ability to manage several projects simultaneously and self-organized by using a structured, well-organized approach, • experience in one or some of the following areas is a plus: sales, biophysical methods for molecular interaction analysis (SPR or other), drug discovery, advanced laboratory equipment, • remote work position based within the assigned territory, • visit and stay connected with our office and application labs in Munich and Hamburg, Germany, • 50 % travel involves business trips to customers, collaboration partners and HQ in Munich, • a fun and dynamic work environment with a young, multicultural team, • scientific training in the biophysical analysis of molecular interactions, • training in the sales process of CapEx scientific equipment, • competitive compensation and the possibility for rapid career development alongside a growing team

This opportunity is only for candidates currently residing in the specified country. Your location may affect eligibility and rates. Please submit your resume in English and indicate your level of English proficiency. At _, innovation meets opportunity. We believe in using the power of collective intelligence to ethically shape the future of AI. What we do The Mindrift platform connects specialists with AI projects from major tech innovators. Our mission is to unlock the potential of Generative AI by tapping into real-world expertise from across the globe. About the Role GenAI models are improving very quickly, and one of our goals is to make them capable of addressing specialized questions and achieving complex reasoning skills. If you join the platform as a Machine Learning expert, you’ll have the opportunity to collaborate on these projects. Although every project is unique, you might typically: • Design original computational STEM problems that simulate real scientific workflows., • Create problems that require Python programming to solve., • Ensure problems are computationally intensive and cannot be solved manually within reasonable timeframes (days/weeks)., • Develop problems requiring non-trivial reasoning chains and creative problem-solving approaches., • Verify solutions using Python with standard libraries (numpy, pandas, scipy, sklearn)., • Document problem statements clearly and provide verified correct answers. Compensation On this project, contributors can earn up to $55 per hour equivalent, depending on their level and pace of contribution. Compensation varies across projects depending on scope, complexity, and required expertise. Please note that other projects on the platform may offer different earning levels based on their requirements. How to get started Simply apply to this post, qualify, and get the chance to contribute to projects aligned with your skills, on your own schedule. From creating training prompts to refining model responses, you’ll help shape the future of AI while ensuring technology benefits everyone. • You hold a Master’s or PhD Degree in Computer Science, Mathematics, Physics, Engineering, or a similar STEM field., • You have at least 5 years of Machine Learning experience with proven business impact., • Strong programming skills in Python (numpy, pandas, scipy, sklearn)., • Solid understanding of numerical methods and computational algorithms., • Research or industry experience involving computational problem-solving., • Your level of English is advanced (C1) or above., • You are ready to learn new methods, able to switch between tasks and topics quickly and sometimes work with challenging, complex guidelines., • Our freelance role is fully remote so, you just need a laptop, internet connection, time available and enthusiasm to take on a challenge. Why this freelance opportunity might be a great fit for you? • Take part in a part-time, remote, freelance project that fits around your primary professional or academic commitments., • Work on advanced AI projects and gain valuable experience that enhances your portfolio., • Influence how future AI models understand and communicate in your field of expertise.

TetraScience is the Scientific Data and AI company.We are catalyzing the Scientific AI revolution by designing and industrializing AI-native scientific data sets, which we bring to life in a growing suite of next gen lab data management solutions, scientific use cases, and AI-enabled outcomes.TetraS

Do you want to work on production AI systems used by global pharmaceutical companies? Have you built LLM or data platforms that needed to work reliably in real customer environments? Are you ready to operate at the intersection of AI Engineering, platform architecture, and enterprise delivery? A Series A biotech AI startup is hiring a Forward Deployed Engineer to help enterprise customers integrate cutting-edge AI and knowledge graph technology into production workflows. Their platform combines NLP, LLMs, retrieval systems, and biomedical knowledge graphs to uncover relationships between diseases, proteins, and drugs across millions of scientific documents. The business works with pharmaceutical and biotech organisations globally and is scaling customer onboarding significantly following strong commercial traction. You’ll join a highly technical, remote-first team focused on solving complex scientific and engineering problems with real-world healthcare impact. This role sits between AI Engineering, Solutions Engineering, and customer delivery. You’ll work directly with technical customer teams to scope, architect, and deploy production AI workflows while also contributing to the company’s core platform and reusable capabilities. Key Responsibilities • Lead customer AI/data integrations from discovery through deployment, • Design and implement RAG, retrieval, and agentic AI workflows, • Build integrations around APIs, orchestration systems, and data pipelines, • Support deployment of LLM-powered systems into production environments, • Contribute to reusable platform capabilities and internal tooling, • Work closely with enterprise stakeholders and customer engineering teams, • Help architect solutions involving knowledge graphs, vector search, and cloud infrastructure Key Details • Salary: £80k–£130k + equity/share options, • Working model: Fully remote (UK-based) with occasional travel, • Stack: Python, LLMs, RAG, Neo4j, vector databases, Spark, dbt, Airflow/Dagster/Prefect, cloud warehouses, • Sponsorship: Currently unavailable Interested? Please apply below.

We are looking for a new Clinical Support Specialist / Territory Sales Manager in Central Midlands and Wales. The Regional Clinical Support Specialist will play a central role in further growth of the market share in the UK, providing special attention to the north of the country, and assuming respo

To be considered for this opportunity you should have sales experience in channel sales and distributor management as well as expertise of Nitrogen/LCMS—Hydrogen/GC markets. Furthermore, you will analyse sales data and provide regular reports on channel performance as well as work closely with th

Due to growth, they are now looking to hire a European Territory Sales Manager to join their friendly team. Responsibilities will include managing current OEM clients in order to build relationships, upselling and cross selling in order to increase sales for the company. Furthermore, you will analys

Business Development Manager South East Dental / Medical Sales £55k DOE + Bonus + Car or Allowance A leading dental manufacturer is looking for a Business Development Manager to drive growth by identifying and converting new business opportunities across the South East. This role focuses on engaging with prospective clients, nurturing leads, and supporting the handover to the sales team for long-term account management. Key Responsibilities: • Identify, qualify, and convert new business opportunities via outbound calls, digital outreach, and social selling., • Build strong relationships with decision-makers, understand their needs, and offer tailored solutions., • Generate quotes and close sales where possible or set up qualified meetings for the field sales team., • Maintain accurate CRM records and ensure seamless handover of leads., • Support team development through coaching, onboarding, and mentoring., • Assist with temporary territory coverage as needed. What We’re Looking For: • Proven experience in business development or sales, ideally in the dental or healthcare sector., • Strong communication, relationship-building, and digital outreach skills., • Confident using CRM, quoting tools, and other digital platforms., • Self-motivated, organised, and results-driven., • Degree preferred; experience in supporting business growth for dental practices is a plus. This is a fantastic opportunity for someone passionate about sales who is looking to grow role within a dynamic and innovative industry.

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients in CVRM team. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Main Job Tasks and Responsibilities: The Senior Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Requirement: • Strong SAS programming experience within the pharmaceutical/CRO industry, • Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies, • Experience in generating and validating SDTM, ADaM, and TLFs, • Good understanding of CDISC standards and clinical trial processes, • Ability to work independently and manage multiple priorities in a fast-paced environment, • Experience supporting regulatory submissions is preferred, • Strong communication and stakeholder management skills Responsibilities: • Develop, validate, and maintain SAS programs for clinical study data analysis and reporting, • Create datasets, tables, listings, and figures according to study requirements, • Collaborate with Biostatistics, Data Management, and Clinical teams, • Ensure programming deliverables meet quality standards and project timelines, • Participate in study planning, review specifications, and support submission activities Education and Experience: • Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience., • Need to have Respiratory/Immunology TA experience., • Working knowledge of ICH and Good Clinical Practices, Clinical research, Clinical trial process, and related regulatory requirements and terminology. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful. Who will you be working for? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #LI-TT1 #LI-Remote #Senior #Contract

Join our team as a Territory Manager (South UK) Sentec is a Swiss-American medical device company specializing in respiratory care. Since its founding in 1999 the company utilizes a deep-tech approach that is founded on advanced science and avant-garde technologies for respiratory patients across care areas. The goal is to support enduring change in clinical practice that reduces challenges of respiratory patients, improves healthcare outcomes, and alleviates cost. Sentec applies latest scientific results and engineering technologies across the three core platforms transcutaneous monitoring, intrapulmonary percussive ventilation and electrical impedance tomography. The company researches, develops and manufactures all products exclusively in-house. Sentec earned Kununu’s Top Company award in 2025 and 2026. Key Responsibilities: • Achieve regional sales budget, • Build and expand a loyal reliable network of KOL's and reference centers, • Create early adopters (new technology), • Manage direct end user sales (targets, pricing, marketing plans), • Initiate and manage local product launches, • Perform high impact product launches, • Initiate and manage regional marketing and education programs, • A minimum of 5 years of sales experience with respiratory care products, patient monitoring or other neonatal care products / concepts is mandatory, • Clinical background in NICU, ICU or Respiratory desirable, • Proven track record within the targeted market segments selling capital equipment and related consumables / supplies, • Familiar with MS Office Suite, including MS Dynamics 365, • High energy level, can cope with 70-80% travel time, • Located in Greater London and Reading area, • Meaningful activity on products that enable a personalized therapy for patients, • Flat hierarchy, short decision-making processes, interdisciplinary collaboration, • Opportunity to contribute and develop your skills in an agile company Policy for unsolicited applications from recruiters and recruitment agencies We do not accept any unsolicited applications from recruiters or recruitment agencies without a prior written agreement between both parties. Therefore, we will not be liable for any commission, fee, or expense for candidates submitted spontaneously. Any application sent without a prior agreement will be considered a direct application and will not be subject to any commission rights.

Refrigeration Engineer £50K - £55K (DOE) Permanent Birmingham My client is on the lookout for an experienced Refrigeration Engineer to join their team where you will be working across East Midlands. You will be responsible for ensuring that refrigeration systems are Serviced & Maintained correctly which include heavy commercial and Industrial systems (CO2, Freon, and Chilled water applications - Ammonia experience advantageous, but not essential) You will be working closely with the Service admin team, Service Supervisors, and other senior service engineers to ensure that the refrigeration systems meet the required specifications and standard for our clients. You will need to make sure clients systems are running to their optimum condition to meet site operating requirements, always ensuring safe systems of work. Qualifications & Experience - Refrigeration Engineer Minimum 5 years' relevant experience Relevant qualifications: City & Guilds Refrigerant handling 2079, CO2 (Ammonia would be advantageous but not essential) Proven experience in large commercial, or industrial refrigeration Previous experience in a senior role Excellent communication, leadership, and problem-solving skills Thorough understanding of electrical controls Up to date knowledge of COSHH regulations Understanding of the principles of refrigeration and of the comprising components Servicing of systems utilising approved methods and practices Excellent skills in diagnostics to identify & resolve system failures Ability to work unsupervised CSCS approved Work within current Health and Safety guidelines Full driving licence Operation of Mobile Elevated Working Platform On Offer - Refrigeration Engineer £50K - £55K (DOE) On call 1 week in 4 (Standby fee £225.00 per week) 40 hour week - 8am to 4:30pm 25 days + 8 bank holidays Travel time door to door Van, fuel card, tools Company Pension - Employer 3% and Employee 5% Private Health (Following a successful probationary period) Health Support Scheme (Following a successful probationary period) Death in Service Benefit (Following a successful probationary period) For more information on this role, please contact Kieren Provis on 01453 829776, or send a copy of your CV to Omega Resource Group is an employment agency specialising in opportunities at all levels within the Engineering, Aerospace, Automotive, Electronics, Defence, Scientific, Oil & Gas, Construction and Manufacturing sectors. For details of other opportunities available within your chosen field please visit our website Omega is acting as an Employment Agency in relation to this vacancy. Omega does not charge candidates any recruitment or job-seeking fees at any stage of the hiring process. TPBN1_UKTJ

Our client is a leading chemical distributor of Resins and associated products to the Adhesives, Sealants, Coatings and Construction markets.This position is a full-time permanent role reporting to the Commercial Director.Joining a small, proactive and fast paced team.This position will be field / h

Scientific Instrumentation, Laboratory Technology, Laboratory Equipment, Analytical Instrumentation, Analytical Equipment, Technical Sales, Scientific Sales, Instrumentation Sales, Business Development, Account Management, Key Account Management, Strategic Accounts, Customer Relationship Management,

Talentmark are recruiting for an QA Administrator, to join a pharmaceutical company, based in Birmingham, on a permanent basis. The salary is around £27,000-£29,000 per annum. The Company: Our client are a Pharma manufacturing company who produce, import, and distribute bespoke medicines (Specials), and CBPMs (Cannabis-Based Products for Medicinal Use). Your main duties will be: Manage the lifecycle of all controlled documents within the paper-based QMS (SOPs, forms, master documents, batch records, policies and specifications). Provide administrative support for deviations, NCs, CAPAs, change controls, complaints and incident reports. Ensure document activities comply with EU GMP (as applicable to Specials), MHRA expectations, and internal quality procedures. Work closely with Production, QC and QA teams to ensure correct and timely use of controlled documents. Design and execute method validation/verification, method transfers and robustness studies as required. Your Background (Essential): Degree in scientific, pharmaceutical or quality-related discipline. Previous administration experience in an office or documentation-focused role. Strong command in Microsoft Excel. Your Background (Desireable): Familiarity with core GMP documentation. Experience in a GMP, pharmaceutical, specials or other regulated environment. Knowledge of Specials Manufacturing regulatory requirements and MHRA guidance. Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence. If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (Talentmark) and follow us to see our latest jobs and company news

Class 2 Driver We are looking for Class 2 Drivers on behalf of a specialist delivery company based in Birmingham The Business: The client deliver IT, Medical, Scientific, and large printing equipment throughout the UK, Ireland, and Europe. All deliveries involve positioning the goods where required, unpacking and removal of the outer packaging. Training is provided for this type of assignment. A successful candidate would expect to spend most of the time in UK, but trips to Ireland and Europe crop up from time to time. Nights out run at approximately one per week but can increase according to workflow. vehicles are well maintained and very high specification and have well-appointed high roof cabs. We have a settled and steadfast workforce with all staff having 10+ years’ service and many with much longer service up to 25+ years. Full uniform is provided and you will work in a friendly and relaxed environment. Class2 Driver - The Person: Hold a valid Class 2 Licence, CPC and Digicard, with at least 12 months experience for insurance Friendly and outgoing Capable of manual handling as needed Flexible to take on Nights out Happy to deliver and work in Ireland / Europe as and when needed Additional information: £16.00 Ph or £17.93 Ph with rolled up Holiday pay Weekends Time and a half / Double time Permanent contract after 12 weeks completed Job Type: Temp to perm Contract length: 12 weeks

Packaging & Compliance Technologist Permanent | Competitive Salary + Benefits We're recruiting on behalf of a leading food manufacturing business seeking a Packaging & Compliance Technologist to join their growing Technical team. This is an excellent opportunity for someone with experience in food compliance, regulatory affairs, or technical services to take ownership of packaging compliance across UK and European markets. Key Responsibilities • Ensure compliance with UK EPR and EU PPWR regulations., • Manage packaging compliance data and regulatory documentation., • Complete customer questionnaires and technical specifications., • Support artwork approval and pack copy development., • Create and maintain finished product specifications., • Gather and validate nutritional information. About You • Experience in Technical, Regulatory Affairs, or Compliance within food manufacturing., • Knowledge of packaging regulations and packaging materials., • Degree qualified in Food Science or a related scientific discipline., • Strong attention to detail and excellent organisational skills., • Able to manage multiple priorities and work to tight deadlines., • Confident communicator with a proactive approach. Why Apply? • Join a well-established and growing food business., • Work at the forefront of evolving UK and EU packaging legislation., • Broad role with exposure to compliance, artwork, and technical operations., • Excellent opportunity for career development. To find out more, apply today or contact us for a confidential discussion