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Experienced Pharmacovigilance Lead (Hybrid role) This is NOT an entry level role. At least 3-5 years PV experience in a CRO is required. 6 month initial Fixed Term Contract Immediate start preferred The Pharmacovigilance Lead provides operational and scientific leadership for assigned projects and/or functional PV activities, ensuring delivery of high‑quality, compliant PV services in accordance with the TMC PV QMS, contractual obligations, and regulatory expectations. THIS IS A HYBRID ROLE: we expect the successful candidate be able to come to the office in Hartley Wintney, Hampshire, at least twice a week. Role-specific tasks include; Case processing, reporting and team management • Responsible for day-to-day oversight of end-to-end case processing, including management of PV rota, functional guidance, and leadership of case processing team, • Management of case-processing flow, ensuring regulatory reporting compliance., • Oversight of case-processing KPIs and maintaining and reporting on internal metrics and KPIs, • Provide expertise, support and active participation in case processing and routine departmental PV activities (e.g. MedDRA coding, eTMF, reconciliations), • Support PV Manager in preparation and maintenance of key client documentation (e.g. SMPs and PSMFS), • Ensure PV deliverables are executed, and delivered in compliance with the TMC PV QMS, SOPs, and applicable regulations., • Ensure inspection readiness for assigned projects, including support for audits and regulatory inspections., • Review and approve PV documents (inc. Project-specific and departmental controlled documents), reports, and outputs in line with delegated authority., • Support PV managers as point of contact for assigned clients or internal stakeholders., • Support PV governance activities, including oversight meetings, metrics review, and performance reporting. Other key information: Education and experience • Advanced life sciences degree (or equivalent experience)., • Significant experience in pharmacovigilance within a CRO and/or MAH environment., • Proven leadership and decision‑making capability., • Strong regulatory and scientific judgement., • Excellent stakeholder and client management skills., • Ability to balance operational delivery with quality and compliance oversight.

Formulation Chemist Rate: £18.34 per hour Location: Bracknell Contract Length: 24 months We are looking for a Formulation Chemist for one of our top client to join their Formulation Technology Group. This position would be suitable for new graduates or scientists with fewer than 5 years of experience. Your role will include researching novel formulation technologies, understanding how growers apply their products, and developing new chemical crop protection products, using automation where appropriate. More specifically, this involves applying a fundamental understanding of chemistry and a scientific approach to design, prepare, and characterize novel formulations in the lab and at grower‑relevant scale, as well as testing their performance through representative experiments. You’ll be planning and conducting experimental work programmes, so a love of practical work, good organisation skills, scientific curiosity, and an ability to solve technical problems are all critical for the role. We are also looking for someone who can integrate well into the lab community and take responsibility for specific equipment and lab spaces. As our client is a global company, you will work within multidisciplinary project teams, so high attention to detail and strong communication skills will be key to your success as you work with scientists from other functions to record, report, present, and discuss your data. The work will be at the forefront of Crop Protection research, so we are looking for scientists with a passion to learn and stay up to date with technological advancements. Skills • Experience of working independently and safely in a chemical lab environment, • Scientific curiosity and a passion for continuous learning, • Good organisational and project management skills, • A dynamic and enthusiastic attitude to problem solving, • Excellent communication, teamwork, and networking skills This is a great opportunity for an individual with passion for practical work who is early in their career or taking their first steps into industry, with the chance to work and learn alongside highly qualified and experienced employees. We embrace and encourage diversity—this drives our innovation and enables us to outperform the market. If this role excites you and you believe you have what we need, then we’d love to hear from you! Education • Degree in Chemistry, Biochemistry or a related scientific subject, • We will also consider applications from candidates with equivalent work experience

QC Analytical Manager – Diagnostics | £50,000 – £65,000 | Berkshire We're seeking an experienced and driven QC Analytical Manager to lead quality control and analytical operations in a fast-growing diagnostic manufacturing environment. If you have a strong background in ELISA-based testing, team leadership, and compliance within diagnostics or biopharma, this could be the ideal next step in your career. About the Role This leadership role sits at the heart of the QC and production function, overseeing a team of scientists and technicians responsible for testing, releasing, and continuously improving ELISA diagnostic kits. You’ll provide technical direction, manage resources, drive compliance, and ensure that products meet rigorous quality standards across the entire lifecycle – from raw materials to finished goods. You’ll collaborate closely with R&D, QA, and Manufacturing teams to ensure process efficiency and product excellence, while also fostering a high-performing, quality-focused culture across your department. Key Responsibilities • Lead, mentor, and develop QC and Analytical teams, • Oversee testing of raw materials, antigens, conjugates, and final ELISA kits, • Ensure analytical data review, trending, and compliance with SOPs and regulatory standards, • Drive method validation, transfer, and troubleshooting, • Manage equipment calibration and qualification, • Lead investigations, audits, and CAPA implementation, • Develop and monitor KPIs, using data to improve performance, • Identify and implement process improvements (Lean, Six Sigma), • Support regulatory readiness and continuous improvement initiatives What We’re Looking For • Degree in Biochemistry, Immunology, Biomedical Science, or related discipline (BSc or higher), • 5–10 years’ experience in QC, manufacturing science, or diagnostics, • Experience/knowledge in ELISA/immunoassay lab environments - strongly desired, • Strong expertise in method validation, data integrity, and documentation compliance, • Skilled in statistical analysis tools (e.g. SoftMax Pro, Minitab, JMP), • Experience supporting regulatory submissions and audit readiness, • Lean Six Sigma certification or equivalent process improvement experience, • Excellent problem-solving, communication, and team development skills Salary, Benefits & Location • Salary: £50,000 – £65,000 (depending on experience), • Location: Berkshire Apply Today If you’re ready to lead from the front and make a measurable impact in diagnostic product quality, we’d love to hear from you. Apply now to bring your scientific leadership into a business that values innovation, quality, and people.

Research Scientist (Biokinetics & Fungal Genetics) Location: Jealott’s Hill, UK Contract length: 2 years Salary: £17.74 Department: Bioscience – Crop Protection About the Role An exciting opportunity has arisen for a Research Scientist to join the Bioscience function within Crop Protection, supporting disease control research at a leading international research centre based at Jealott’s Hill. This role will be split equally between Fungicide Biokinetics and Fungal Genetics, supporting projects that aim to deliver new insights into fungicide behaviour and fungal pathogen biology. The work combines applied biokinetics studies with advanced molecular and microbiological techniques. Role Purpose The successful candidate will work closely with Science Leaders and multidisciplinary project teams to deliver high‑quality experimental data within agreed timelines. The role requires strong technical capability in microbiology and molecular biology, alongside excellent organisational, communication and teamwork skills. All work must be carried out in compliance with strict Health, Safety and Environment (HSE) standards. Key Responsibilities • Design and conduct in vivo biokinetics studies in fungi and plants to assess fungicide bioavailability, • Perform fungal genetics experiments, including mutagenesis, transformation, CRISPR‑based genome editing and sensitivity assays in fungal and oomycete pathogens, • Carry out molecular biology workflows including cloning, PCR, DNA/RNA extraction, plasmid preparation, Oxford Nanopore sequencing and genome analysis, • Interpret and analyse experimental data, producing detailed reports and presentations for project teams, • Maintain fungal cultures, ensuring high‑quality, contamination‑free operations, • Review and improve existing protocols to enhance capacity, efficiency and reproducibility, • Transfer knowledge and build new capabilities to strengthen disease control research toolkits, • Implement HSE actions to ensure all laboratory operations meet defined safety standards Essential Requirements • BSc or MSc (preferred) in Biological Sciences, Microbiology, Plant Science or a related discipline, • 1–2 years’ laboratory‑based experience in an academic or industrial setting, • Competence in microbiology and molecular biology techniques (e.g. cloning, PCR, DNA/RNA extraction, aseptic techniques), • Fundamental understanding of genetic transformation principles, • Strong scientific writing and verbal communication skills (fluent in English), • Excellent organisational skills with the ability to follow science plans and deliver results to deadlines, • Team‑oriented mindset with the ability to work collaboratively across disciplines and manage multiple priorities Desirable Experience • Experience culturing microorganisms and fungal pathogens (e.g. Zymoseptoria, Fusarium, Phytophthora, Aspergillus), • Hands‑on experience with fungal transformation and CRISPR‑based genome editing, • Understanding of ADME studies for active ingredients, • Experience with LC‑MS analysis for small molecule detection, • Handling large datasets, including data storage, analysis, reporting and visualisation, • Experience running automated laboratory workflows

Research Scientist (Biokinetics / Bioperformance) Location: Jealott’s Hill, UK Contract length: 2 years Pay rate: £17.74 per hour Department: Bioscience – Crop Protection R&D About the Organisation Our client is a global, R&D‑driven agricultural science organisation focused on improving food security worldwide. Through world‑class science and innovative crop solutions, their teams work internationally to transform how crops are grown and protected. About the Role An exciting opportunity has arisen for a Research Scientist to join the Bioperformance group within the Bioscience function at an international research centre based at Jealott’s Hill. The Bioperformance group conducts research into the ADME (Absorption, Distribution, Metabolism and Elimination) behaviour of active ingredients in both target and non‑target species. This work supports the understanding of product performance, selectivity, resistance, and translation from laboratory studies to field application. The successful candidate will support a variety of product development and market support projects, generating high‑quality scientific data using laboratory, glasshouse and analytical techniques. Key Responsibilities • Provide scientific and technical support to assess the bioavailability of novel agrochemicals, • Independently design, plan, execute and analyse experiments involving whole plants (in vivo) and plant parts (ex vivo), • Generate, interpret and present scientific data through detailed reports and presentations, • Deliver agreed scientific priorities in line with project timelines, • Ensure all work complies with Health, Safety and Environment (HSE) standards, • Review and improve existing protocols to enhance capability and efficiency, • Share knowledge and contribute to the development of new scientific capabilities Essential Requirements • BSc or MSc (preferred) in Plant Biology, Biochemistry, Chemistry, Soil Science or a related biological science, • Minimum of 2 years’ relevant laboratory‑based experience in an academic or industrial setting, • Strong scientific writing and verbal communication skills (fluent in English), • Good organisational and time‑management skills, • Ability to work effectively within multidisciplinary teams Desirable Experience • Professional experience in Pharmacology, Agronomy, Crop Protection, Biochemistry or Analytical Chemistry, • Experience with ADME studies of active ingredients, • LC‑MS analysis of small molecules, • Handling and analysing large datasets, including data visualisation, • Experience working with soil, seeds or plant physiology, • Understanding of plant responses to biotic and abiotic stress

Job Title: Laboratory Technician Location: Bracknell Contract Length: 12 months Schedule: 20 hours per week Overview We are seeking a motivated and detail-oriented Laboratory Technician to support day-to-day laboratory operations. This role is ideal for someone with strong organisational skills and an eagerness to learn. The successful candidate will contribute to maintaining a safe, efficient, and high‑quality laboratory environment, with opportunities to grow into more advanced scientific and analytical tasks. Key Responsibilities Health, Safety & Environment (HSE) • Support routine HSE tasks and ensure compliance with regulatory and internal safety standards., • Perform general housekeeping to ensure laboratory organisation and cleanliness., • Support laboratory instrument management, including routine checks and basic maintenance. For high-performing candidates, responsibilities may expand to include: • Conducting routine laboratory analyses., • Operating state-of-the-art analytical equipment. Skills & Competencies • Strong ability to work collaboratively within a diverse team., • Effective written and verbal communication skills., • Quick learner with the ability to apply new skills promptly., • Excellent timekeeping and organisational abilities., • Good attention to detail is essential., • Inventory management experience is desirable., • Experience working with radio chemicals—particularly carbon‑14—is beneficial but not essential. Education Requirements • Minimum A-levels, with Chemistry or Biology at grade C or above.

Job Type: Full-TimeSalary: Additional Benefits Senior Radioactive Waste Specialist Location: RG7 4PR , located between Reading and Basingstoke, with free onsite parking. Package: £47,800 to £75,000 (depending on your suitability, qualifications, and level of experience). Working pattern: AWE operates a 9-day working fortnight. We will consider flexible working requests so that your work may fit in with your lifestyle. Just let us know your preferred working pattern on your application. Ready to play your part? At AWE, it's not just a job, it's far more than that. Our shared purpose is to help keep the nation safe. Could this role be the opportunity for you to play your part? As a Senior Radioactive Waste Specialist at AWE, you will provide expert leadership and technical guidance for the management of radioactive waste across the organisation. You will define the standards, functional requirements, and strategic direction for radioactive waste, ensuring consistent interpretation of legislation and policy while maintaining essential environmental permitting responsibilities. As a first‑level leader, you will support and motivate your team of Waste Officers, championing a culture of inclusion, continuous improvement, and high standards in safety, security, and environmental performance. You will be responsible for ensuring waste generators and waste routes remain compliant with regulatory and company requirements, managing authorisations, and overseeing inspection and auditing programmes. The role includes developing and maintaining competent Waste Officer capability, driving sustainable waste management improvements, and providing authoritative technical advice to internal stakeholders. You will also act as a key interface with regulators such as the ONR and EA, ensuring effective communication, operational learning, and robust governance across all waste‑related activities Who are we looking for? We do need you to have the following: * A degree in an engineering or scientific discipline enhanced by experience or post-graduate qualification; or equivalent combination of relevant qualifications and/or experience. * Significant experience working in a responsible role within radioactive waste management or waste regulatory field. Whilst not to be considered a tick list, we'd like you to have experience in some of the following: * Detailed knowledge of UK and European radioactive waste legislation, standards and guidelines and those systems that exist to enable industry to comply. * Knowledge of the Environmental Management System and the requirements of ISO 14001. * Knowledge of health and safety requirements appropriate to the job * Excellent stakeholder engagement skills and experience of dealing with different levels of stakeholder * Experience of Line Management and Matrix Management of Staff. You'll need to have the ability to work calmly and constructively in a priority changing environment and be able to manage your own workload. You will also have initiative, enthusiasm, a flexible approach, and ability to work to tight deadlines. Work hard, be rewarded: We ask a lot and set the bar high because our work truly matters. In return we offer balance, with award winning benefits including: * 9-day working fortnight - meaning you get every other Friday off work, in addition to 270 hours of annual leave. * Market leading contributory pension scheme (we will pay between 9% and 13% of your pensionable pay depending on your contributions). * Family friendly policies: Maternity Leave - 39 Weeks Full Pay and Paternity Leave - 4 Weeks Full Pay. * Opportunities for Professional Career Development including funding for annual membership of a relevant professional body. * Employee Assistance Programme and Occupational Health Services. * Life Assurance (4 x annual salary). * Discounts - access to savings on a wide range of everyday spending. * Special Leave Policy including paid time off for volunteering, public service (including reserve forces) and caring. The 'Working at AWE' page on our website is where you can find full details in the 'AWE Benefits Guide'. Hybrid working is available for this role on an informal, non-contractual basis. Typically, 3 or 4 days onsite per week. #LI-ZB1

You’ll work closely with experienced team members to develop your skills in: * Conducting inspections and audits * Reviewing Standard Operating Procedures (SOPs) * Investigating deviations and supporting CAPA management * Delivering quality training and guidance to scientific staff

Salary: £27,000 - £29,000 Benefits: Competitive Annual Leave Entitlement Matched pension contributions with length of service Family feel company Flexible working hours Training and progression opportunities Annual performance and salary review Competitive annual leave entitlement Generous Company contribution toward gym membership Matched pension contributions with length of service Cycle to Work Scheme We are looking to recruit a detail-oriented and proactive Technical Labelling Coordinator who will be responsible for managing and overseeing labelling projects of Instructions for Use (IFUs) and related product labelling. This position will be joining our thriving UK medical device manufacturing company to work within our Technical Department. This role plays an important part in supporting regulatory compliance and ensuring our Instructions for Use (IFUs) and product labelling are accurate, compliant and meet applicable regulatory requirements, industry standards and internal specifications. As a Technical Labelling Coordinator, you will be responsible for coordinating reviews with key stakeholders, managing document changes and approvals, and ensuring labelling content is accurate, compliant, and that all claims in the Instructions for Use (IFUs) are fully supported by appropriate data and evidence. The successful candidate will bring an understanding of regulatory or technical documentation, along with the ability to coordinate document reviews involving multiple stakeholders. This role requires strong organisational skills, excellent attention to detail and the ability to maintain comprehensive records of changes and decisions throughout the Instructions for Use (IFUs) lifecycle. Essential Experience/Qualifications Qualification or degree ina scientific discipline(Chemistry, Biology, Physics, Materials or a related subject) or relevant documentation experience. Strong organisational skills and the ability to work effectively with cross-functional teams. Able to manage documentation workflows and maintain detailed records of changes and decisions. Able to function effectively in a highly regulated environment with a strong focus on compliance. Experience working within a regulated quality management systemor familiarity with controlled documentation processes. Desirable Experience/Qualifications Experience in reviewing and evaluating technical and regulatory documentationfor accuracy, compliance, and completeness. Experience working within a medical device, pharmaceutical, or regulated manufacturing environment. Knowledge and understanding of regulatory requirements related to labelling and Instructions for Use (IFUs) (e.g., FDA regulations, EU MDR/IVDR, ISO 15223, ISO 20417). Key Skills Methodical, organised and structured approach to work. Able to gather, evaluate, critically interpret and communicate information. Excellent verbal and written communication skills. Able to build and maintain strong working relationships. Able to work well under pressure and meet deadlines. Strong multitasking and prioritisation skills. Able to work both independently and collaboratively within a team. Able to work effectively across multiple interrelated departments. Self-motivated with a can-do attitude and an enthusiastic approach to work. IT literate, with proficiency in Microsoft Office. Excellent attention to detail. Hours of Work 40 hours per week Equal Opportunities We are committed to creating a diverse and inclusive workplace for all. We are an Equal Opportunities Employer and welcome applications from all individuals, regardless of age; disability; gender; gender reassignment; marital or civil partnership status; pregnancy and maternity; race; religion or belief; sexual orientation, or any other characteristic protected by law. We believe that diversity enriches our workplace and enhances our ability to deliver exceptional results. We assess all applications based on skills, qualifications, and experience, ensuring a fair and equitable recruitment process. * REF- 227 506 TPBN1_UKTJ

ROLE OVERVIEW: Our client is seeking a Tender & Bid Team Leader to join a leading medical equipment company based in the Berkshire area. As the Tender & Bid Team Leader, you will play a pivotal role in managing the full tender and bid process across all business units, ensuring high-quality submissions that support the delivery of profitable sales and outcomes-based solutions for customers and patients. KEY DUTIES AND RESPONSIBILITIES: Your duties as the Tender & Bid Team Leader will be varied however the key duties and responsibilities are as follows: 1. Lead, support, and develop a team of Tender & Bid Specialists and Administrators, fostering a culture of excellence and continuous improvement., 2. Oversee end-to-end tender and bid processes and Standard Operating Procedures, ensuring legal and procedural compliance., 3. Champion ESG, Sustainability, and Social Value within the tender process, aligning submissions with evolving market and regulatory expectations., 4. Monitor performance metrics and generate regular reporting to support strategic decisions. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the Tender & Bid Team Leader, we are looking to identify the following on your profile and past history: 1. Relevant degree in a business, science, or economics-related discipline., 2. Proven industry experience in tender and bid or related commercial roles., 3. A working knowledge and practical experience with MS Office applications; SharePoint and Power BI is a plus. Key Words: Tender / Bid Team Leader / Medical Equipment / Sales Support / Tender Process / Bid Management / Healthcare Procurement / NHS Procurement / Leadership / Sales Marketing 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.

The Transactional Finance Analyst is responsible for delivering high-quality end-to-end transactional finance support across Accounts Receivable (main activity), Billing (main activity) Accounts Payable (cover). Transactional Finance Analyst Responsibilities. Ability to identify process inefficienci

A leading provider of analytical services is seeking a Transactional Finance Analyst to join their growing team in Bracknell, UK.This remote role requires delivering high-quality transactional finance support, focusing on Accounts Receivable and Accounts Payable in a fast-paced environment.Candidate

Key words: Quality management, Auditor, Quality Assurance, QA, Compliance, GLP, GCP, GMP, GxP, CAPA, MHRA, FDA, South East, Berkshire, Reading, Wokingham, Slough, London VRS9150AW. As a QA Officer, you’ll be responsible for auditing data and reports across a variety of scientific studies and proje

A quality assurance provider in Wokingham seeks a QA Officer to ensure compliance in scientific data audits and reports. A full benefits package with pension, private healthcare, and life insurance is also included, providing a supportive entry into the field of quality assurance.

A leading scientific group in Bracknell is offering a Summer Internship Opportunity as an Operational Excellence Intern.

Zest Scientific is partnering with a rapidly expanding, award-winning digital healthcare provider delivering specialist weight management services across the UK and Europe.

Our client is a leading 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 Managing Director.Joining a small, proactive and fast paced team.This position will be field / home based a

We are working with a global leader in the food and pharmaceutical sector, a trusted brand dedicated to maintaining the highest standards of product integrity and consumer safety.Operating from their on-site laboratory facility in Lancashire, they are looking for aQC Manager.This role is a key leade

Sales Specialist – Scientific Instrumentation Territory: South West England Salary: to ~£45,000 plus car/allowance and bonus Portfolio: Lab and in-process Instrumentation Are you a scientifically qualified sales professional looking to work with cutting-edge laboratory technology and

Our client is a fast-growing chemical distributor that recognises delivering value begins with its people.By placing employee development at the core of its strategy, the organisation empowers its teams to grow, innovate, and excel in their roles.Alongside this, a strong focus on employee wellbeing

Our client is a leading 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 Managing Director.Joining a small, proactive and fast paced team.This position will be field / home based a

Our client is a fast-growing chemical distributor that recognises delivering value begins with its people.By placing employee development at the core of its strategy, the organisation empowers its teams to grow, innovate, and excel in their roles.Alongside this, a strong focus on employee wellbeing

A Home Based Technical Sales Engineerwith strong customer facing skills and proven experience of working within a Sales / Inside Sales /Applications role within a Scientific products, Life Science or related electronics environment will join an established High-Tech Company.

Senior Technical Service ManagerPermanent opportunityStockport/MacclesfieldWe are working with an established coatings business within the Speciality Coatings sector.Following internal change and continued growth within NPD and compliance functions, they are seeking a Senior Technical Service Manage

As part of continued growth, they are seeking a Scientific Of.

Senior Director of Toxicology and PathologyEdinburghPermanent opportunityWe are working with a multinational company in the recruitment for aSenior Director of Toxicology and Pathology.This is a high-impact leadership role which will work on improving global health and bringing life-changing medicin

Zest Scientific is partnering with a rapidly expanding, award-winning digital healthcare provider delivering specialist weight management services across the UK and Europe.

Senior Systematic Literature Reviewer / Evidence Synthesis Consultant.An exciting opportunity to join a steadily growing Global HEOR & Access consultancy with one of the best staff turnover rates in the entire healthcare consulting space, offering full remote flexibility, a non-corporate culture, fl

Medical Affairs Scientific Partner - Oncology Diagnostics. Medical Affairs Scientific Partner. Build and maintain strong scientific relationships with KOLs in pathology, oncology diagnostics, and laboratory medicine.

As Scientific Director, you’ll take a strategic leadership role, ensuring excellence across scientific content, client engagement, and team performance. Are you a seasoned scientific leader ready to make a real impact on global healthcare communications? I’m partnering with a well-established, i

As Head of Scientific Research, you will provide strategic, scientific and operational leadership of the firms research function. You will drive innovation, secure research funding, oversee multi-disciplinary research programmes and bring alignment and integration between commercial objectives and s

Network Scientific Recruitment, part of Network Scientific Ltd. Network Scientific is an award-winning science recruitment agency specialising in the provision of temporary, permanent and contract recruitment services to the scientific and related technical industries. Are you a graduate of a scient

Network Scientific is a multi‑award‑winning scientific agency with bold growth plans and a reputation for doing things differently. Recruitment Consultant – Scientific Recruitment. For more than a decade, we’ve partnered with pioneering organisations across the scientific, healthcare, and te

Represent the company at scientific conferences and events. Scientific degree (preferably in chemistry or biology). Sell scientific software solutions into the drug discovery space.

Network Scientific Recruitment, part of Network Scientific Ltd. Network Scientific is an award-winning science recruitment agency specialising in the provision of temporary, permanent and contract recruitment services to the scientific and related technical industries. Relevant Scientific degree (or

EPM Scientific have partnered exclusively with a true market leader in the.