146 jobs found

Location: Swindon FTC - 18 month contract. Catalent are currently recruiting for a QC apprentice to join the Swindon site. The Apprentice QC Analyst will learn and assist in many aspects of the QC Chemistry role and then put these learnings into practice within the laboratories. The Apprentice will perform analysis for analytical samples in accordance with defined analytical methods and Standard Operating Procedures and within timelines as agreed with line management. Catalent seeks people with the desire to make a difference in the health of patients and consumers globally. Your talents, ideas and passion are essential to your success and our mission: to deliver more products, better treatments, reliably supplied. This is the opportunity you've been looking for to learn, develop, and be part of a growing business. The Role: Complete any college-based courses and be prepared to undertake any future training, internally or externally, as required by Catalent. Responsibilities To comply with all Catalent EH&S requirements. To ensure that all tasks are conducted in accordance with defined risk assessments and that tasks are carried out with regards to the safety of others. To understand the cGMP requirements as related to the role, to follow the training provided and ensure that all activities are performed according to the appropriate procedures. To participate in laboratory housekeeping and maintenance duties. To prepare laboratory chemicals and reagents as required for analysis and documenting/labelling them according to laboratory procedures. Gain a proficient understanding for the use of some of the simpler items of analytical equipment used within the laboratory, including analytical balances, pH meters, dissolution baths, disintegration bath. Help to troubleshoot these instruments when they do not work as expected. Provide timely feedback to more senior staff and to the laboratory analysts. Qualifications Basic knowledge of the main site Quality Systems for example LIMS and QUMAS. A minimum of 3 GCSEs (or equivalent) including English and Math's at grade C/5 or above. Good analytical thinking, dynamic, pro active approach to the workload. Have a positive attitude, taking personal accountability for your work. To demonstrate ability for attention to detail. Catalent offers rewarding opportunities to further your career. Legal Statements Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. Proud member of the Disability Confident employer scheme.

At the Ellison Institute of Technology (EIT), we're on a mission to translate scientific discovery into real world impact. We bring together visionary scientists, technologists, engineers, researchers, educators and innovators to tackle humanity's greatest challenges in four transformative areas: Health, Medical Science & Generative Biology Food Security & Sustainable Agriculture Climate Change & Managing CO Artificial Intelligence & Robotics This is ambitious work - work that demands curiosity, courage, and a relentless drive to make a difference. At EIT, you'll join a community built on excellence, innovation, tenacity, trust, and collaboration, where bold ideas become real-world breakthroughs. Together, we push boundaries, embrace complexity, and create solutions to scale ideas from lab to society. Explore more at . Welcome to the Pathogen Project Within this ecosystem, the Pathogen Mission exemplifies EIT's commitment to transformative science. It aims to revolutionise the diagnosis and treatment of infectious diseases by leveraging whole genome sequencing (WGS)-based metagenomic and pathogen specific analytical tools. This remit includes the development of a decentralised, sample to answer sequencing diagnostic platform for infectious diseases, enabling rapid and accurate analysis of patient samples without prior assumptions. Supported by Oracle Inc.'s cloud computing scale and security infrastructure, the Pathogen Mission is progressing towards certified diagnostic products for deployment in laboratories, hospitals, and public health organisations worldwide. Your Role We are seeking a Scientist or Senior Scientist with a strong interest in method development to join our growing Applications team, focused on advancing sequencing based diagnostics. In this role, you will contribute to the design and optimisation of novel targeted and semi targeted approaches for the rapid sequencing of clinically relevant pathogens. This laboratory based position encompasses end to end experimental workflows, including sample preparation, target enrichment and amplification, library preparation, and sequencing. You will support the development of strategies for comprehensive, high sensitivity sequencing across a large number of targets, using approaches such as targeted amplification, hybridisation, and related techniques. The role encourages creative problem solving, with opportunities to propose, explore, and evaluate new ideas. You will work collaboratively within a multidisciplinary team of microbiologists, molecular biologists, engineers, and data scientists to develop assays for integration into an automated, device based platform. Drawing on your experience, you will help define experimental strategies, design and execute studies, and contribute to advancing the application of sequencing technologies in pathogen detection and related areas. Key Responsibilities Design, develop, and optimise end to end sequencing assays (targeted and semi targeted) Execute experiments, analyse and interpret data, and contribute ideas for improvement Troubleshoot complex technical challenges across a range of sample types Maintain clear documentation to support reproducibility of experimental work Collaborate closely with colleagues across disciplines to progress shared goals Contribute to scientific discussions and decision making as projects evolve Essential Knowledge, Skills, and Experience PhD in molecular biology, microbiology, genomics, biochemistry or a related field Experience using molecular biology techniques (e.g. PCR, RT PCR, nucleic acid extraction, library preparation) Experience developing and optimising PCRs and/or related experimental workflows Ability to troubleshoot experimental challenges and adapt methods as needed Experience with DNA/RNA sequencing data Strong experimental design and data interpretation skills Good organisation, record keeping and communication skills Desirable We recognise that strong candidates may not meet every criterion below. Experience in any of the following would be beneficial: Multiplex PCR assay development, particularly for sequencing applications Enrichment or capture methods for pathogens or pathogen derived nucleic acids Work with bacteria, fungi, viruses, or other pathogens Handling clinical samples RNA based workflows (e.g. transcriptomics, viral genomics) Background in virology Exposure to metagenomics workflows Biochemistry knowledge relevant to assay development (e.g. enzyme optimisation, reaction conditions, assay development) Key Attributes Scientific and Technical Enjoys exploring new ideas and approaches to experimental challenges Curious and motivated to solve complex problems Able to balance scientific rigour with speed and pragmatism Working Style and Collaboration Takes ownership of work while valuing collaboration and shared success Proactive and supportive team member, with a willingness to contribute beyond immediate responsibilities Comfortable working in a dynamic research environment, with support from colleagues Our Benefits Salary: Competitive + travel allowance + bonus Enhanced holiday pay Pension Life Assurance Income Protection Private Medical Insurance Hospital Cash Plan Therapy Services Perk Box Electric Car Scheme Working Together - What It Involves You must have the right to work permanently in the UK with a willingness to travel as necessary. In certain cases, we can consider sponsorship, and this will be assessed on a case by case basis. For this role we would expect someone to be fully on site in Oxford You will live in, or within easy commuting distance of, Oxford (or be willing to relocate).

Senior Scientist, Analytical Development (Chemistry) (Bedford, MA) We are looking to recruit a hands on highly talented Senior Scientist to manage the Analytical Development (AD) Chemistry team, providing onsite support and development for chemistry assays. This onsite Bedford, MA based role is an exciting opportunity to join an experienced organization whose mission is to enable our clients to deliver life changing therapies to patients. Responsibilities Lead and manage the Analytical Development Chemistry team responsible for installation of new equipment, assay development and the daily operation of HPLC, LC/MS, CE SDS, SEC and AUC development operations. Work in close collaboration with the AD Chemistry team to support client projects serving as the analytical methods expert to client teams. Lead and support the transfer, qualification, and validation of GMP analytical methods including but not limited to LC/MS, HPLC, Capillary Electrophoresis, (CE SDS), and AUC assays. Ensure AD Chemistry team members write protocols and generate reports related to QC method transfer, qualification, and validation activities. Provide training and supervision to junior scientists on assay development, instrumentation, and data interpretation. Support and monitor ongoing analytical method performance (e.g., system suitability trending, costing for new client projects) to drive continued improvement and optimization of client's analytical methods. Assist with data trending of assay controls and reference standards, as needed. Lead and support analytical method troubleshooting, as needed. Partner with internal and cross functional departments (e.g., QC and QA) to ensure on time delivery of client projects. Qualifications MS/PhD in Chemistry or related area. Over 10 years of related experience with LC/MS, HPLC, CE SDS and AUC. Proven people manager with the ability to shape teams. Strong expertise in analytical HPLC and LC/MS method development and basic troubleshooting. Independently motivated, detail oriented, and strong problem solving ability. Hands on experience in method development, qualification, validation and/or transfer. Knowledge of quality principles and GMP, ICH and GLP regulations. Experience creating/revising/reviewing operational SOPs, technical documents, protocols, and reports. Ability to work effectively in a fast paced environment. Excellent communication, technical, organizational, and interpersonal skills are essential. Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view.

A leading life sciences company is seeking a highly talented Senior Scientist to manage their Analytical Development Chemistry team. This role will involve leading assay development, ensuring timely delivery of client projects, and providing training to junior scientists. Candidates must possess a MS/PhD in Chemistry, over 10 years of experience with various analytical methods, and strong team leadership skills. This is an exciting opportunity to contribute to life-changing therapies in a dynamic environment.

Summary: The Laboratory Quality Analyst for Nijhuis Saur Industries in Stoke is responsible for ensuring the laboratory and Riventa business unit operate to the highest quality standards by managing accreditation compliance, internal and external audits, QA/QC processes, instrument calibration, data analysis, and documentation control. The role provides technical guidance to staff, supports method development, oversees customer satisfaction and performance metrics, leads accreditation audit representation, and manages non conformance investigations. It also involves collaborating with management and customers, producing performance reports, supporting routine and specialised testing, and maintaining ISO 9001 and ISO 17025 quality systems for both laboratory and manufactured parts environments. Duties and Responsibilities: Ensure compliance with laboratory accreditation, regulatory standards and provide guidance to staff to ensure that quality policies, processes and procedures are established, current and adhered to by all laboratory staff. Oversee laboratory internal audit processes, external proficiency testing programs, document control systems, competency assessment, training, and other quality processes. Support the development of instrument techniques, ensuring adequate calibrations and QC are in place. Monitor customer satisfaction and performance metrics of the laboratory. Liaise with management throughout the business as well as customers when reporting on quality and statistical data. Oversee the Riventa business unit quality system including manufactured parts QA/QC process, calibration of temperature probes to approved methods, warranty, repair and returns process for Riventa parts. Maintain a quality management system for Riventa. Work to the global NSI ISO 9001 accredited quality management system. Work to the NSI WTL ISO 17025 accredited quality management system. Manage, document and audit the Riventa incoming and assembled products/parts testing and acceptance QA/QC process at the Stoke facility, in collaboration with the Riventa team. Manage, document and audit the Riventa temperature and pressure probe calibration process to relevant standards. Conduct lab testing to high standards through busy periods or during periods of absence of Laboratory Analyst or Develop Analysts. Audit the analytical performance of the analysts, content of laboratory methodology and documentation to ensure compliance with the quality system. Represent the laboratory during annual accreditation audits. Oversee the laboratories non conformance log to ensure its appropriate use and investigations are completed in full, with appropriate actions. Analyse data, identify trends, monitor prevention and correction of quality deviations, and develop reports for management utilising regulatory knowledge, technical knowledge and laboratory experience. To provide quality support to the laboratory for routine testing when required as well as providing quality support to the Technical Development Scientist and the wider technical team with specialised testing and the growth of these methods. Report periodically to management, customers on the quality performance of the laboratory. Presenting data to stakeholders on laboratory performance statistics. Support the creation and reviewing of validation reports for new and current tests. Perform Uncertainty of Measurement calculations when required. This is not a fully comprehensive list of responsibilities, and other duties will be expected to be completed within the limits of the position. Required Skills/Qualifications (Essential): Knowledge and experience of quality management systems such as ISO 9001 and ISO 17025 and quality improvement tools and techniques Knowledge and experience of UKAS accreditation and audits is advantageous. Experienced in the auditing of quality systems and laboratory testing procedures. Experience working with a QC process for manufactured parts. Working knowledge of accreditation standards, practices, and guidelines sufficient to advise and guide the laboratory manager and laboratory team as they implement new methodology and maintain accreditation. Working knowledge of computer and analytical software programs sufficient for the evaluation of electronic data, data interpretation, and report development (A good understanding of the Microsoft Office Suite would be advantageous). Experience working with LIMS. Excellent organisational skills allowing the coordination of multi faceted QA activities. Experience in performing data analysis such as uncertainty of measurement. Working experience of overseeing the development of new analytical techniques. Good awareness of all HSE aspects in a laboratory environment (i.e., COSHH, RA). Required Skills/Qualifications (Desirable): Degree/HND in Biochemistry/Chemistry or related science (Highly Desirable) Consideration will be given to applicants with Certifications in Quality (Highly Desirable) Consideration will be given to those candidates with 2 years' experience in a similar position (Highly desirable) Knowledge and/or previous experience of GC FID, Ion chromatography, FT IR, wet chemistry, spectrophotometry experience of water, wastewater, cooling water and boiler water in the Oil & Gas, Petrochemical, food & beverage industries (Highly desirable). Working for us means: The salary is between £33,000 & £38,000 per year, depending on your professional experience. Hours of Work - 40 hours per week, Monday to Friday Holidays - 25 days + 8 statutory days (pro-rata) Probationary Period - 6 months. Pension - Can join immediately or auto enrolled after 3 months - Employee 5% and Employer 5% via salary sacrifice. Eligible to join Private Healthcare after successfully completing probation. Enrolled in Group Income Protection and Death in Service (4 x basic salary) upon commencement of employment. Notice - 1 Week during probation, increasing to 1 months thereafter. Nijhuis Saur Industries UK & Ireland are committed to maintaining Environmental & Social Impact goals: To reach Net Zero emissions across our value chain by 2040. To continuously meet high standards of social and environmental performance, transparency, accountability, maintaining B Corp Certification. To be a socially responsible company creating a positive impact to all stakeholders including workers, communities, customers, and our planet. Nijhuis Saur Industries UK & Ireland are an equal opportunity employer; we are committed to providing equal opportunities in all aspects of employment in line with the Equality Act 2010.