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Warehouse Operative Location: Slough Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: Join Lonza AG as a Warehouse Operative and be a part of our outstanding team in the United Kingdom! Our ambitious and world-class Manufacturing division is growing, and we need dedicated individuals to help us continue our success story. This role is critical in ensuring our operations run efficiently and our customers receive flawless service. Shift Patterns: Monday to Friday 8am - 4.30pm Saturday & Sunday 6am to 2pm (1 in 3 Weekends) Shift Premium and Callout Premium in addition to your base salary! Key responsibilities: * Perform raw material management activities, including receipt, inspection, labelling, put away, storage, picking, checking, delivery, returns, and cycle counting. * Manage bulk and sample material activities, from receipt and checking to packing and shipping, following (Good manufacturing Practice (GMP) and customer specifications. * Ensure all areas are stocked with necessary consumables, engineering items, gases, and equipment. * Conduct usability, expiry, and labelling checks for materials delivered to production areas. * Maintain accurate stock levels and records, ensuring all documentation is up to date. * Monitor cold rooms, freezers, and warehouse temperatures to ensure accurate storage conditions. * Adhere to GMP standards and safety precautions, completing all required training and keeping records compliant. * Perform housekeeping activities, promptly reporting issues and ensuring audit readiness. * Support Lean practices and engage in continuous improvement activities. * Be responsible for on-call warehouse duties as required. Key requirements: * Proven experience in large warehouse or a manufacturing environment is essential for this role. * Working within a regulated environment is highly desirable. * Outstanding attention to detail and accuracy in record-keeping. * Ability to operate forklift and other manual handling equipment is desirable but not essential. * Reliable, with good time-keeping and a proactive approach to tasks. * Dedication to maintaining high standards and continuous improvement. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: Are you a strategic thinker with a passion for sourcing high-quality materials at the best value? As part of our ongoing expansion, we are growing the onsite procurement team to meet increasing project demands. You will take a proactive role in managing the performance of raw material suppliers to ensure the successful execution of the Material Requirement Plan (MRP). This includes maintaining accurate Procurement Master Data in SAP, enabling reliable MRP calculations and efficient purchase order creation. You will also support the category manager and strategic buyers in implementing supply strategies and work closely with Accounts Payable to resolve any invoice queries. We’re seeking candidates with direct procurement experience and a proven track record of managing client escalations, both internal and external. Responsibilities * Manage and resolve all vendor delivery escalation issues promptly and effectively. * Monitor and evaluate supplier performance, providing regular feedback to Strategic Buyers and Category Managers. * Support the implementation of supplier changes and other procurement initiatives led by Central Category Managers and Site Strategic Buyers. * Collaborate with the broader Procurement team to ensure all relevant material and vendor master data, as well as outline agreements, are accurately maintained and up to date in SAP. * Conduct price negotiations with vendors to secure favorable terms. * Address and resolve delivery and shipping-related issues and inquiries. * Oversee vendor performance, driving continuous improvements in on-time delivery, quality compliance, and adherence to contractual obligations. * Manage and resolve vendor returns efficiently. * Resolve all invoice-related queries in collaboration with relevant departments. Key Requirements * Proven track record of managing escalations with vendors effectively. * Experience managing multiple vendors, product lines, and escalation processes. * Demonstrated capability and proactive approach to managing an annual procurement spend exceeding £10 million. * Solid experience in direct procurement. * Experience within the pharmaceutical industry is highly desirable. * Strong customer service orientation with the ability to manage multiple priorities concurrently. * Experience in supplier management and conducting low-value negotiations. * Proficiency in SAP ERP (or equivalent systems) within a purchasing or procurement environment is highly advantageous. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: As an Associate Principal Scientist at Lonza AG, you will lead scientific breakthroughs and drive innovative research to enhance lives through outstanding investigations. Situated in Slough, UK, you will play a vital role in our Protein and Peptide Analytics (PPA) R&D team, applying your expertise in protein interaction measurements to advance our projects. Your responsibilities include independent and team-based research, guaranteeing precise analytical project delivery and supporting our top-tier scientific direction. Your work will not only advance our technical capabilities but also encourage and mentor junior scientists within the team. Your expertise in quantifying antigen interactions for biopharmaceutical using diverse analytical methods is crucial! Key responsibilities: * Plan and complete scientific activities including study development, method creation, laboratory tasks, scientific evaluation, mentoring of junior scientists, project oversight, and technology exploration. * Evaluate and develop innovative protein interaction workflows to support biologics process development and drive innovation. * Perform a range of analyses using SPR, ELISA, and related methods for the characterisation of proteins and their relevant post-translational modifications (PTMs) and critical quality attributes (CQAs). * Analyse and interpret complex data, presenting findings to internal collaborators to inform project decisions. * Take charge of scientific leadership within the team, facilitating collaboration across the Bio R&D department to align alliances and impact. * Act as a Protein Interaction Subject Matter Expert (SME) in multiple collaborative projects, guiding analytical discussions, translating data into project context, and supporting decision-making processes. Key requirements: * Degree or equivalent experience in Life Sciences or a related field, with a preferred focus on Biochemistry, Biomanufacturing, or Biotechnology. * Extensive practical experience in an analytical laboratory with a focus on protein analysis. * In-depth knowledge and practical expertise in SPR/ELISA for protein characterisation, including related hardware and software. * Attitude towards innovation in the biologics field, with a keen interest in research and excellent scientific writing abilities. * Robust foundation in proven analytical methods within the industry, with knowledge of innovative technologies and their applications in biotherapeutic characterisation. * Strong communication and interpersonal skills, able to influence collaborators in a scientific capacity and accomplish technical projects within a matrix organisation. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Title: Laboratory Systems Specialist Location: Slough Visa and Relocation support is offered with this role. Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: The role of a Laboratory Systems Specialist is to lead the development and implementation of robust Lab/digital infrastructure within our R&D laboratories for the UK and US locations. This is pivotal in enabling efficient, automated data exchange between laboratory instruments and enterprise informatics systems such as Electronic Lab notebooks (ELN)s, Laboratory Information Management Systems (LIMS) and other relevant data setups. The ideal candidate would have experience in implementing robust digital infrastructures within lab environment automation. You will be pivotal in connecting scientific users, automation scientist, and IT teams together . Be willing to travel within the UK and Europe, accounting for approximately 10% of working time! Key responsibilities: * Design, implement, and maintain secure, scalable IT/OT interfaces between lab instruments (e.g., bioreactors, plate readers, liquid handlers) and informatics systems (ELN, LIMS, SDMS, etc.) * Collaborate with IT, Data science and scientific teams in R&D to identify integration needs and define architecture for real-time or scheduled automated data transfer. * Develop or configure middleware, APIs, and custom connectors—either in-house or in collaboration with external vendors—to enable automated data capture, contextualization, and storage. * Manage instrument network connectivity (e.g., OPC-UA, MQTT, REST APIs, TCP/IP) and data pipelines from edge devices to cloud/on-premise environments. * Support system validation efforts (e.g., CSV, 21 CFR Part 11 compliance) in partnership with QA and IT Compliance teams, while also providing technical troubleshooting and support for instrument connectivity and data integration issues. * Contribute to long-term digital strategy for lab automation, analytics, and operational efficiency. Support scale-up and tech transfer of automated workflows to operational areas or QC environments outside of R&D when needed. * Participate in required Lonza training programs. Key requirements: * Bachelor’s or Master’s degree in Computer Science, Engineering, Scientific or a related field. * Experience in a similar IT/OT integration or lab informatics/digitalisation role within biotech, pharma, or CDMO environment. * Proven hands-on experience integrating lab instruments with ELNs, LIMS, Scientific Data Management System (SDMS), or other data systems. * Proficiency with data integration technologies and protocols: OPC UA, MQTT, REST/SOAP APIs, SQL, Python, etc. * Familiarity with lab automation platforms (e.g., Tecan, Hamilton, Agilent, Beckman, Sartorius) and related data workflows. * A good understanding of GxP, 21 CFR Part 11, data integrity principles, and validated environments is a plus. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Warehouse Operative - 12 month FTC Available Location: Slough Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: Join Lonza AG as a Warehouse Operative and be a part of our outstanding team in the United Kingdom! Our ambitious and world-class Manufacturing division is growing, and we need dedicated individuals to help us continue our success story. This role is critical in ensuring our operations run efficiently and our customers receive flawless service. Shift Patterns: Monday to Friday 8am - 4.30pm Saturday & Sunday 6am to 2pm (1 in 3 Weekends) Shift Premium and Callout Premium in addition to your base salary! Key responsibilities: * Perform raw material management activities, including receipt, inspection, labelling, put away, storage, picking, checking, delivery, returns, and cycle counting. * Manage bulk and sample material activities, from receipt and checking to packing and shipping, following (Good manufacturing Practice (GMP) and customer specifications. * Ensure all areas are stocked with necessary consumables, engineering items, gases, and equipment. * Conduct usability, expiry, and labelling checks for materials delivered to production areas. * Maintain accurate stock levels and records, ensuring all documentation is up to date. * Monitor cold rooms, freezers, and warehouse temperatures to ensure accurate storage conditions. * Adhere to GMP standards and safety precautions, completing all required training and keeping records compliant. * Perform housekeeping activities, promptly reporting issues and ensuring audit readiness. * Support Lean practices and engage in continuous improvement activities. * Be responsible for on-call warehouse duties as required. Key requirements: * Proven experience in large warehouse or a manufacturing environment is essential for this role. * Working within a regulated environment is highly desirable. * Outstanding attention to detail and accuracy in record-keeping. * Ability to operate forklift and other manual handling equipment is desirable but not essential. * Reliable, with good time-keeping and a proactive approach to tasks. * Dedication to maintaining high standards and continuous improvement. Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role: At Lonza, the Laboratory technician is responsible for working as part of a team in providing support services to laboratory-based activities. You will be responsible for ensuring that all equipment is calibrated and ready to be use, consumables and buffers are always stocked and the laboratory are at GMP standard at all times. Candidates for this role must previously have worked/studied in a Laboratory environment, with strong knowledge of calibrating/using laboratory equipment! Responsibilities * Completion of routine (daily and weekly) equipment calibration checks * Responsible for generating analytical buffers for laboratory methods and processes for large quantities * Laboratory consumables stock management - checking and unpacking laboratory stock and replenishment of stocks at stores/ point of use * Ordering consumables from internal stores using the Warehouse Management System (WMS) and external orders using Sharepoint * Glassware and plastic ware cleaning, maintaining high levels of cleanliness and tidiness in the washroom environment * Processing of laboratory deliveries, receipt, storage and notifications * Cleaning and preparation of water baths according to Good Manufacturing Practice (GMP) procedures * Recording of all data and results in specified forms (electronic and paper) with accuracy and responsibility and keeping accurate records with GMP and Data Integrity principles in mind What we’re looking for: * A degree or relevant experience within a scientific background is highly desirable * Proven experience in a laboratory setting, ideally within a support or technician role * Strong knowledge of laboratory equipment and calibrating equipment * Familiarity with health, safety, and quality standards in a laboratory environment * Attention to detail and the ability to maintain high standards of cleanliness and operational efficiency * Excellent communication skills and ability to work collaboratively as part of a team Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Job Title: QA Customer Support Location: Slough, UK - 3 days onsite in a week Duration: 1 year Contract Job Description: • Significant experience (5-10 yrs) working within a GMP-regulated pharmaceutical – ideally biologics or biopharmaceutical – environments and/or relevant QA experience Level* Advanced - 5-10 years, • Education/Degree Required - Field of Study Science related discipline, • Leads the timely establishment of customer Quality Agreements (QAA) between Client and Customer, • Acts as primary Point of Contact for Quality Agreements for the functional teams, • Represents Client with regard to manufacturing and analytical testing in negotiations, • Quality Agreements for both the Client internal network and the face to the customer, • Provides the consistency between Client internal processes/standards and commitments in QAAs, • Setting up an efficient system to track the completion status of QAAs and monitor the requirements for periodic review, initiate periodic review where required · Executes establishment and maintenance of the QAA process within Client, • Participates in global QAA SOP revision working group, • Improves currently existing tracking tools and established way of working, • Creates new solutions in the field of QAA-related document life cycle, • Provides training about the QAA structure and content to the functional teams within Client

The Senior Project Planner will oversee and manage project schedules, ensuring timely delivery within the life science industry.Based in Slough, this role requires attention to detail and expertise in planning complex projects.This opportunity is with a large organisation in the life science sector.

Job Title: Life Science Customer Operations Agent. This role offers the opportunity to work in a dynamic environment where accuracy, communication, and customer care are key to success.

Job Title: QAA Writer– Global Biopharmaceutical Contract: 12 months Location: Slough (onsite) Salary: £31.52 PAYE, £41.10 Umbrella per hour (Inside IR35) Hours: 37.5 hours per week QA responsible for establishment, review and update of customer Quality Agreements (QAA) between the client and the Customer. Job Responsibilities: • Leads the timely establishment of customer Quality Agreements (QAA) between the client in Slough and the Customer., • Acts as primary Point of Contact for Quality Agreements for the functional teams in Slough., • Represents the client with regard to manufacturing and analytical testing in negotiations of Quality Agreements for both the internal network and the face to the customer., • Provides the consistency between internal processes/standards and commitments in QAAs., • Setting up an efficient system to track the completion status of QAAs and monitor the requirements for periodic review, initiate periodic review where required., • Executes establishment and maintenance of the QAA process within the company., • Participates in global QAA SOP revision working group., • Improves currently existing tracking tools and established way of working., • Creates new solutions in the field of QAA-related document life cycle., • Provides training about the QAA structure and content to the functional teams. Essential Requirements: • BSc in Science or QA discipline., • Significant experience (5-10 yrs) working within a GMP-regulated pharmaceutical – ideally biologics or biopharmaceutical – environments and/or relevant QA experience., • Excellent communication skills (verbal and written), • Excellent risk based decision-making and problem solving skills., • Accurate data entry skills. Attention to detail., • Ability to meet strict deadlines., • Ability to work in team and solo capacity.

Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful medicines that drives healthcare innovation! Hobson Prior is seeking a Drug Product Development Specialist to join a dynamic team within Pharmaceutical Development Sciences. This role focuses on injectable drug product manufacturing processes, supporting clinical and regulatory activities. You will collaborate with internal teams and external partners to ensure the successful development and production of sterile drug products. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: • Develop and refine manufacturing processes for injectable drug products from early studies to regulatory approval., • Select and define manufacturing parameters for clinical production., • Collaborate with internal teams and external manufacturers to meet project goals., • Conduct lab studies, analyse data, and document findings (e.g., filter selection, fill volume assessments, compatibility tests)., • Analyse manufacturing data to improve process understanding and performance., • Perform risk assessments for manufacturing processes., • Design processes for sterile injectable products in various forms (e.g., liquid, lyophilized powder, pre-filled syringes)., • Support clinical trial preparation and ensure timely production of stability and clinical batches., • Assist in process validation and ensure compliance with quality standards and regulations., • Contribute to regulatory submissions and respond to authority queries., • Investigate and resolve quality-related issues, such as deviations or complaints., • Facilitate knowledge transfer from late-phase development to commercial production., • Help improve departmental processes and ways of working. Key Skills and Requirements: • Experience in developing or manufacturing liquid drug products in the pharmaceutical industry., • Familiarity with biopharmaceuticals is a plus., • Knowledge of aseptic manufacturing processes, including vial, cartridge, and pre-filled syringe filling, is advantageous., • Understanding of sterile drug product development, including components, process transfer, scale-up, and optimization, is beneficial. For more information, please contact Jessica Taylor. If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - .

An established, full-service agency is looking for a Senior Medical Writer to join their brilliant team in Berkshire. With broad expertise across medical education, brand comms and multichannel marketing, this dynamic, independent agency enjoys strong client relationships and has several exciting new projects in the works. As SMW, you’ll be responsible for translating clinical data into informative and engaging content for an interesting mix of deliverables and therapy areas including Rare Disease, Neuroscience and Oncology. You’ll provide scientific expertise on accounts, liaise with client services teams, and ensure work is completed on brief and to the highest standards. This mid-size agency has a sociable and collaborative culture; you’ll be joining an ambitious team who are passionate about working on meaningful campaigns that make a difference in healthcare. You’ll enjoy opportunities to further your skills and plenty of support to help you progress. Requirements • Experience to SMW level within a healthcare communications agency setting, and knowledge across a broad range of medcomms activities., • Life science degree, ideally combined with a higher qualification (MSc, PhD), • Superb working knowledge of the pharmaceutical industry., • Strong organisation and time management skills.

A leading Pharmaceutical company in the Berkshire area, is seeking a dedicated QA Specialist. As the QA Specialist, you will play a crucial role in ensuring the timely establishment and maintenance of customer Quality Agreements (QAA) between our client and its customers. This role offers a balanced work arrangement with 3 days onsite and 2 days from home, providing flexibility and is an initial 12 month contract. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QA Specialist will be varied however the key duties and responsibilities are as follows: 1. As the QA Specialist, you will act as the primary point of contact for Quality Agreements, representing the company in negotiations and ensuring consistency between internal processes and commitments in QAAs., 2. As the QA Specialist, you will set up and manage an efficient system to track the completion status of QAAs, monitor requirements for periodic review, and initiate reviews as needed., 3. As the QA Specialist, you will participate in global QAA SOP revision working groups, improve existing tracking tools, and create new solutions for QAA-related document life cycles., 4. As the QA Specialist, you will provide training on the QAA structure and content to functional teams within the company. ROLE REQUIREMENTS: To be successful in your application to this exciting role as the QA Specialist we are looking to identify the following on your profile and past history: 1. Relevant degree in a science-related discipline., 2. Extensive industry experience within a GMP-regulated pharmaceutical environment, ideally in biologics or biopharmaceuticals, and/or relevant QA experience., 3. A working knowledge and practical experience with risk-based decision-making, problem-solving, and accurate data entry skills. Key Words: Quality Agreements Specialist / QA Specialist / Quality Assurance Specialist / QAA / pharmaceutical industry / GMP-regulated / biologics / biopharmaceuticals / risk-based decision-making / data entry / customer relations / SOP revision / document life cycle 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.

Project Architect (Life Science), slough.

Principal Investigator (PI) – Clinical Research Site Network - Multiple Locations.This is a chance to be part of an innovative organisation transforming trial delivery with modern infrastructure, operational excellence, and a collaborative investigator community.As a PI, you will oversee clinical

Global Life Science Jobs by 2x. Other TAs include Neuroscience, Ophthalmology, Cell/Gene therapies, Respiratory, Cardiovascular, Infectious disease, Nephrology, Endocrinology & Gastroenterology.

Support the implementation and continuous improvement of quality and regulatory compliance processes, including design control, product development lifecycle, and change management.

Advanced degree in pharmacy or life-science.

Ensure clinical project audit and inspection readiness through the study lifecycle.

Discovers and follows up on sales leads; conducts sales calls and visits within a region, industry, or product category; completes orders and sets up internal sales logistics; addresses customer complaints; keeps an eye on rival activity and shifting customer wants; and creates sales targets, budget

University/college degree in life sciences or a relevant allied health field. Global Life Science Jobs by 2x.

Lead design and execution of display campaigns.Optimize display systems and screening workflows.Support development of antibody assessment tools.Collaborate with internal teams to advance pipeline projects.Mentor junior team members and support lab infrastructure.Coordinate with external partners on

Global Life Science Jobs by 2x. Other therapeutic areas include Neuroscience, Ophthalmology, Cell/Gene therapies, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology, and Gastroenterology.

For this role you will be a highly motivated and enthusiastic individual with successful Life Science/laboratory sales experience. Alternatively you could be a graduate (ideally Biomedical Science, Biology or Sports Science etc.

Direct message the job poster from Apsida Life Science. Referrals increase your chances of interviewing at Apsida Life Science by 2x.

University/college degree in life sciences or a relevant allied health field.

As a Senior Program Manager you will support the delivery of medium to large, complex, cross-functional projects and programs in the life science sector. Detailed knowledge of laboratory projects across all lifecycle stages is highly advantageous. Project Management, Science, and Strategy/Planning.

Please feel free to email your CV at cv@life-science. Demonstrated ability to oversee the autonomous completion of several projects or programs using comprehensive data management research life cycles.

Identify and engage potential customers in the life sciences sector such as research institutions, universities, and biotechnology firms. A Bachelor’s degree in Cell Biology, Biology, Life Sciences, or a related field. A strong understanding of life science applications and laboratory workflows, w

Focus on science and patient care while we handle operations and compliance.

Set across three floors with generous ensuite bedrooms, dedicated staff teams and secure landscaped gardens, the home offers a safe, supportive and welcoming environment designed for comfort, dignity and quality of life.

A healthy, nutritious diet is vital to ensuring our residents' wellbeing and helping them enjoy daily life with us, which is why the role of Kitchen Assistant is so important.

As a Bank Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and companionship and sharing great moments and memories too.It's a chance to bring your dedi

As a Bank Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and companionship and sharing great moments and memories too.It's a chance to bring your dedi

A £500 Golden Hello is just one of the ways we'll reward you when you join Barchester in this role.As a Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support

PLEASE NOTE THAT WE ARE UNABLE TO PROVIDE SPONSORSHIP OR THE 20 HOURS WORKING FOR THIS ROLE**.As a Care Assistant at a Barchester care home, you'll help residents enjoy each day by making sure they get the quality care and support they deserve.You'll assist with daily living, providing support and c

Graduate SEN Teaching Assistant - Hounslow, West London.Contract: Permanent, Full-Time.Salary: £26,000 - £28,000 per annum.Start your career in education with a meaningful and rewarding role.Are you a recent graduate in Psychology, Education, or a related field with a genuine interest in supportin

We are looking for a highly motivated.Lettings Support Centre based in Wirral, Birkenhead, CH41 5BX.The main purpose of your role is to provide a.You will also co-ordinate and prepare renewal of tenancies and liaise with contractors to ensure repair/maintenance works are carrier out in time and to a

You will be responsible for delivering specialist support to patients in community-based or residential settings, helping them maintain independence and improving their quality of life.

Support with education, activities, and life skills.

Manage ML lifecycle with tools such as.

Youll have oversight for the full lifecycle of each project, management of risk and compliance, budget control and stakeholder relationships. That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leav

Youll have oversight for the full lifecycle of each project, management of risk and compliance, budget control and stakeholder relationships. That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leav

That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leave options to support your life priorities, such as parental pay and leave and volunteering days, as well as benefits to support your physical

That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leave options to support your life priorities, such as parental pay and leave and volunteering days, as well as benefits to support your physical

Youll have oversight for the full lifecycle of each project, management of risk and compliance, budget control and stakeholder relationships. That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leav

Support Worker – Accessibility Support (Hybrid, Northampton).Northampton (Hybrid – 1 days per week in office).Location: Northampton (Hybrid – 1 day on-site, 4 days from home, Tuesdays on-site).We are looking for a reliable and detail-oriented Support Worker to provide workplace assistance to a

Youll have oversight for the full lifecycle of each project, management of risk and compliance, budget control and stakeholder relationships. That’s why at the Royal Household we offer a generous benefits package designed to support your wellbeing and life priorities. We also offer a range of leav