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You will be responsible for maintaining high standards of food safety and quality by implementing suitable controls and Good Manufacturing Practice (GMP) during maintenance activities. Manage site assets using the CMMS system, ensuring effective planning of maintenance activi.

Perform and record manufacturing operations within the cleanrooms / chemistry labs. BSc degree or equivalent qualification or relevant industry experience in chemistry (or closely related discipline). Knowledge of practical organic chemistry.

Joining a globally recognized team provides a unique opportunity for professional growth in cell and gene therapy manufacturing. Ideal candidates will have a BSc in Life Sciences and experience in GMP environments, including mammalian cell culture.

Candidates should possess a BSc in Chemistry or a related field and have strong attention to detail, teamwork, and communication skills.

A leading biotechnology firm is seeking a QC Analyst for a 12-month contract in Bristol. Candidates should possess a degree in Chemistry or a related field and ideally have 1-3 years of QC experience.

Xmoor Pharma is seeking a Senior GMP Production Scientist to supervise GMP production teams in Bristol. The role involves managing clinical grade ATMP products, ensuring compliance with production standards, and developing SOPs.

Key tasks include processing materials, QC sampling, and ensuring compliance with shipping regulations.

A leading biotechnology firm based in Bristol seeks a dedicated individual for a lab-based manufacturing role focused on ancillary materials for stem cell research.The successful candidate will engage in high-quality production processes, ensuring adherence to safety and quality standards.A solid BS

Candidates should hold a degree in Chemistry or a related field with 1-3 years of QC experience.

A leading biotechnology company in Bristol is seeking an Operations Associate to join their distribution team.

A biotechnology company in Bristol is seeking a Senior GMP Production Scientist to lead GMP manufacturing operations for ATMP clinical products.This role involves supervising production teams, ensuring compliance with regulatory standards, and developing production methods.Candidates should have sub

The Senior GMP Production Scientist will be responsible for routine operations in eXmoor’s GMP production suites & take the lead role for establishing GMP Production for a varied range of ATMP clinical products in the eXmoor GMP facility. The Senior GMP Production Scientists will take responsibili

The types of projects you may be asked to work on will include, but is not limited to, GMP Implementation projects; De-risking activity including projects relating to insurance transactions; individual technical or high priority projects; Pensions Dashboard Data Projects; data work; CETV Top Up Exer

A leading pharmaceutical company in Bristol is seeking a Reliability Engineer to enhance reliability and improve maintenance processes. The ideal candidate will monitor equipment performance, ensure compliance with GMP standards, and provide technical guidance to the engineering team.

A leading biotechnology firm is seeking an Analytical Development Research Associate for their GMP Analytical Development Team in Bristol. The role involves method development, validation activities, and analytical testing to support product development.

Location: Bristol, BS20 Job Role: Mixing Operative Hours: Monday to Friday 6.00am - 2.00pm and 2.00pm - 10.00pm on rotations Role Type: Temporary to permanent Hourly rate: £15.97 per hour gap Personnel Bristol is operating as an employment business and is hiring 2 Mixing Operatives to work in a food production environment. The role involves weighing and mixing ingredient batches, operating mixing equipment, completing quality checks, and maintaining high food safety and hygiene standards. The job role: Weigh, measure, and prepare raw ingredients according to recipes and production plans Operate mixing and blending equipment safely and efficiently Follow batch sheets and standard operating procedures to ensure product consistency Carry out quality checks during mixing to meet food safety and quality standards Record production data accurately, including ingredient usage and batch details Maintain high standards of hygiene, housekeeping, and GMP Clean mixing equipment and work areas between batches Adhere to all health & safety and food safety regulations Support production targets by working effectively as part of a team The Candidate: Punctual and good time management Manufacturing experience beneficial Attention to details Driving licence essential Ability to communicate well If you are interested, please get in touch on (phone number removed) or click Apply now

Location: London, Watford or Bristol Office Canada Life UK looks after the retirement, investment and protection needs of individuals, families and companies. We help to build better futures for our customers, our intermediaries and our employees by operating as a modern, agile and welcoming organisation. Part of our parent company Great-West Lifeco, Canada Life UK has operated in the United Kingdom since 1903. We have hundreds of respected and supported employees committed to doing the right thing for our customers and colleagues. Canada Life UK is transforming to create a more customer-focused business by providing our customers with expertise on financial and tax planning, offering home finance and annuities propositions, and providing collective fund solutions to third party customers. Job Summary: • Develop and deliver technical support: Responsibility for providing timely and accurate product/tax technical information and support to internal teams and change projects. • Provide specialist training: Delivery of technical training to internal stakeholders including design and preparation of key materials, presentations, etc. • Support management of technical documentation: Responsibility for maintaining key documents/forms including Policy Provisions, Scheme Rules, Application Forms, etc; and provide technical input to marketing collateral, campaign management, and online content. • Represent Canada Life in Industry/Technical discussions and events: Represent Canada Life at industry technical forums (e.g. Origo, Criterion, Equity Release Council, etc) and supporting development and creation of internal responses to proposed changes to UK Government policy and FS regulation impacting Retirement product lines. What will you be doing: 1. Technical support for internal teams: • Act as product/tax technical lead for retirement queries to support decision-making on industry standards, product terms & conditions, product technical rules/guidelines, product technical documentation, product reviews, transaction guidelines, complex cases, GMP equalization queries, complaint handling, and tax treatment on the company, its customers, and other beneficiaries covering death claims, pensions in divorce, trusts, monies in, and monies out. • Lead review, interpretation, impact analysis, and delivery of guidance in respect of changes to technical standards and/or legislation impacting retirement product lines, including HMRC Pension Newsletters, HMRC Tax Manual, and Equity Release Council Product Standards. • Act as principal intermediary with HMRC to interpret requirements/ensure compliance with correct reporting and filing for retirement product lines (including Pensions Increase Orders/GMP Increase Orders, HMRC Event Reporting for accounting for tax, HMRC Band Reporting). • Act as key point of contact with relevant tax authorities for tax treatment/queries in respect of income/benefit payments made to non-UK tax jurisdictions including Isle of Man, Jersey, and Guernsey 2. Technical support to change projects: • Act as product/tax technical lead on change projects impacting retirement product lines, including product developments/changes, annual changes to escalation rates, annual changes to tax year-end processes and documentation. • Support creation/validation of technical product requirements to deliver successful change and UAT to ensure requirements translated correctly. • Proactively develop and maintain productive relationships with key stakeholders to support identification and implementation of changes required to ensure technical compliance 3. Design and delivery of training to internal teams: • Delivery of technical training to internal stakeholders including design and preparation of key materials, presentations, etc. • Training on impact of new legislation, new technical standards, and new products/product changes/process changes. 4. Technical documentation: • Act as technical lead in management, review and approval in Aprimo of key documents/forms including Policy Provisions, Scheme Rules, Application Forms, etc. • Provide technical input/guidance to support creation and maintenance of marketing collateral, campaign management, and online content. 5. Support public policy team: • Collaborate with Public Policy team to support development and creation of internal responses to proposed changes to UK Government policy and FS regulation impacting Retirement product lines What Experience do you require for the position: • Excellent communication skills • Self-motivated, engaging, good with people, with a keen eye for detail • Demonstrate the ability to communicate complex technical information in a simple and understandable way • Ability to understand, highlight and clearly articulate the opportunities arising from complex technical and legislative changes. • Ability to disseminate information from industry groups, UK Government, UK Regulators, UK and non-UK tax authorities, and to identify emerging opportunities • Act as a specialist to encourage open and constructive relationship and help others develop skills to be effective • Demonstrate the ability to coach • Ability to write clear technical accurate reports/articles • Able to demonstrate in-depth understanding of the Retirement product lines and provide training in support of these, and the surrounding legislative and tax framework Qualifications • Preferably suitable qualifications in pensions, tax or estate planning - such as PFS diploma, G60/AF3 pensions specialist qualification, or equivalent Benefits of working at Canada Life We believe in recognising and rewarding our people, so we offer a competitive salary and benefits package that's regularly reviewed. As a Canada Life UK colleague, you'll receive a competitive salary and comprehensive reward package including a generous pension and bonus scheme, along with, income protection, private medical insurance and life assurance. We have a fantastic number of other benefits and support services as well as regular personal and professional development. How we work at Canada Life Our culture is unique and incredibly important to us. We care about doing the right thing for our people, customers and community and helping others to build better futures. Our blueprint behaviours shape and influence how we work, and are central to the relationships we have with others. Every day we are encouraged to be more curious, own the outcome, face into things together and find a way forward. We want colleagues to have rewarding careers with us so we invest in the development of our people, technology and workplaces. That's why we offer a range of training, flexible working and opportunities to grow and develop. Diversity and inclusion Building an inclusive workplace with a diverse workforce where everyone can feel they belong and achieve their potential regardless of gender, ethnicity or any other characteristic is a key commitment for us. We are proud of the progress we're making in DEI, and we continue for it to be a significant focus. "At Canada Life we believe in the power of great people from different backgrounds, experiences and perspectives coming together to build better futures. Emerging talent is crucial to our growth and creating an environment that continues to inspire us all." Nick Harding, Chief People Officer, Canada Life UK We appreciate that everyone has different work and life responsibilities. We're happy to discuss flexible working arrangements, including part time, for any of our roles should this be a requirement for you. TPBN1_UKTJ

Our client is a global manufacturer of specialist scientific instrumentation, helping laboratories around the world enable advancements in many areas such as pharmaceutical, food, environmental and healthcare. To ensure the efficiency of their operations, they are currently looking for an enthusiastic and motivated Field Service engineer to join their team in the South of England. As a Field Service Engineer, your key responsibilities will include: • Servicing, installing and repairing Scientific instrumentation onsite, specialising in the company’s Inorganic product range (ICP, FT-IR, UV/Vis, GC & AA instrumentation), • Covering a local territory across the M4 corridor with travel further afield in the South of England, • Diagnosing faults on complex scientific equipment ensuring prompt, flexible and customer focused support, • Managing equipment parts and spare parts To be considered for this role, you will have: • HND in engineering or equivalent qualification, • Previous experience servicing complex scientific instrumentation (Chromatography, Mass Spectrometry, Automation) from a range of instrument vendors, • Knowledge of GMP, • Full driving license and willingness to travel up to 80% of your time, • Excellent communication skills and ability to work well in a team Applications are also invited from candidates from a lab background looking to transition into an instrument focussed role! Full training will be provided to assist you with the transition! For your work you will be rewarded with an excellent remuneration and benefits package (including bonus and company car!) Keywords: Inorganics, ICP, ICP-OES, ICP-MS, FT-IR, UV/Vis, AA, Atomic Absorbance, GC-MS, Waters, Agilent, Sciex, TFS, Shimadzu, service engineer, FSE, instrument technician, repair, maintenance, M4, London, Reading, Oxford, Swindon, Bristol, VRS9160PC Please note that by submitting your application to VRS Ltd your details will be registered with us so that we can contact you about suitable job opportunities now and in future. You may unsubscribe at any time by emailing us directly via our website

Location: Bristol, BS20 Job Role: Packing Operative Hours: Monday to Friday 6.00am - 2.00pm and 2.00pm - 10.00pm on rotations Role Type: Temporary to permanent Hourly rate: £15.97per hour gap personnel Bristol are operating as an employment business and is hiring 2x Packaging Operatives to work in a food production environment, supporting the packing and preparation of ingredient products. The role involves operating packing equipment, completing quality checks, and maintaining food safety and hygiene standards. The job role: Operate and monitor packaging machinery to ensure efficient and accurate packing of ingredients Pack, label, and palletise products in line with production schedules and specifications Carry out visual and weight quality checks to ensure products meet Kerry quality standards Follow food safety, hygiene, and GMP procedures at all times Maintain a clean, safe, and organised work area Report equipment faults, product issues, or safety concerns to supervisors Adhere to health & safety policies and company procedures Support team members to meet daily production targets The Candidate: Punctual and good time management Manufacturing experience beneficial Attention to details Driving licence essential Ability to communicate well If you are interested, please get in touch on (phone number removed) or click Apply now

CBRE Global Workplace Solutions (GWS) is a leading global provider of integrated facilities and corporate real estate services. We operate across complex, multi-site portfolios and are committed to delivering safe, compliant, and high‑performing workplaces for our clients. We are recruiting a Finance Lead to provide high‑quality client reporting and commercial financial support across a large, complex contract environment. This is a highly visible role, partnering closely with operational teams, Account Leadership, and Client Finance to ensure robust governance, effective cost control, and strong financial performance This role is ideal for a commercially minded finance professional who enjoys working close to the operation, adding value through insight, analysis, and strong stakeholder relationships. Key Responsibilities Client & Commercial Finance Build strong, trusted relationships with client operational and finance teams Take ownership of client financial reporting, providing clear, value‑adding commentary and insight Support annual budgets and quarterly forecasts, working collaboratively with the client and operations Ensure compliance with the commercial model (GMP), driving governance and financial discipline Identify savings and efficiency opportunities, supporting delivery of financial targets Coordinate monthly accruals and deliver accurate results to tight deadlines across multi‑site and multi‑country portfolios CBRE Financial Management Provide hands‑on financial support to the account, working closely with the Finance Contract Manager and Account Manager Manage and report monthly actuals, supporting GMP reconciliation and cost control Deliver ad‑hoc financial analysis and support business improvement projects Ensure finance policies and procedures are followed, escalating risks where required Contribute to CBRE annual budgets and quarterly forecasting cycles Quality & Stakeholder Engagement Support consistent contract delivery across regions, sharing best practice and financial innovation Influence decision‑making through clear insight and confident communication Act as a positive culture carrier, aligned to CBRE values and customer expectations What We're Looking For Educated to A‑Level or Degree level (or equivalent) Part‑qualified or newly qualified accountant (ACA / ACCA / CIMA) - desirable Strong commercial finance experience in a fast‑paced, deadline‑driven environment Excellent Excel skills (including lookups, pivots and financial modelling); confident with Word, PowerPoint and Outlook Experience working with complex contracts, GMP models, or multi‑currency environments - desirable Confident communicator, able to engage and influence senior stakeholders and clients Highly organised, detail‑focused, and comfortable managing competing priorities under pressure Willingness to travel as required by the role

A European manufacturer of hygienic components based in West Yorkshire is seeking a Quality Technician to ensure product quality and compliance with internal standards.The role involves conducting inspections, managing quality concerns, and supporting continuous improvements.Candidates should have p

Successful candidates will have a relevant engineering qualification and experience in GMP environments.

An established industry player is seeking a Quality Assurance Officer to join their dynamic team in Oxfordshire.This pivotal role involves ensuring the highest standards of quality and regulatory compliance in the biotechnology sector.You will manage batch reviews, oversee audits, and maintain Quali

You will provide invaluable technical expertise and support to our UK Retirement market, particularly in the critical areas of GMP rectification and equalisation, while also engaging in a variety of actuarial project work across different pension-related initiatives. Lead in team meetings to discuss

A leading UK consultancy is seeking a Senior Project Analyst to join their GMP Data Solutions team.

Responsibilities include performing inspections of raw materials, maintaining documentation to GMP standards, and ensuring material status for release. A leading biopharmaceutical company in Greater London seeks a Quality Control Specialist to manage incoming materials and support GMP-compliant acti

A leading NHS trust in London is seeking an enthusiastic Band 5 Radiopharmacy Technician to join their Radiopharmacy team.Candidates should have attention to detail, effective communication skills, and the ability to work under pressure.Experience in aseptic manufacturing and working with radioactiv

Deep GMP experience not essential (you will be trained) but previous experience in GMP calculations at some level is. A fantastic role offering the opportunity to carve a career within the GMP space now and lots of opportunity thereafter!. Technical GMP Actuary or Specialist (Pensions).

Candidates should possess a strong understanding of GMP and HACCP, with excellent communication skills.

A pharmaceutical company in Greater London is seeking a Process Technician to support production operations within a GMP-regulated environment. Candidates should have experience in GMP or manufacturing environments, and strong attention to detail is essential.

This senior technical position focuses on the delivery and cost control of capital projects in compliance with cGMP and EHS standards. The successful candidate will lead cross-functional teams, manage project proposals, and ensure adherence to GMP regulations.

Responsibilities include ensuring GMP compliance, training junior staff, and maintaining high standards of production.

A healthcare agency is seeking an experienced Pharmacist with NHS Hospital experience to join their team in Greater London.The ideal candidate will be GPhC registered, compliant with regulations, and able to work flexible hours, both part-time and full-time.In return, the agency offers excellent pay

This role involves managing validation compliance activities and ensuring all processes meet GMP and corporate standards.

A global consulting firm seeks an Actuarial Consultant to drive GMP equalisation and engage in actuarial projects.

A leading medical technology company in Cirencester is seeking a Senior Validation Engineer to maintain the validated state of critical medical device manufacturing processes.The role involves leading validation projects, supervising a team, and ensuring compliance with regulatory standards.Candidat

The ideal candidate will have over 7 years of experience in the Biotech or pharmaceutical sectors, particularly in cGMP environments.

A leading recruitment firm in Greater London is seeking a detail-oriented QC Materials Technician to ensure compliance and quality standards in a GMP-regulated environment. The ideal candidate should have at least 1 year of experience in a GxP or GMP setting, possess strong communication skills, and

Ideal candidates will have strong knowledge of GMP, HACCP, and tracing in manufacturing environments.

The GMP Production Manager will be responsible for establishing the GMP production team and taking a lead role in the operation of the GMP production suites. The GMP Production Manager will lead and develop the GMP production team and will be responsible for leading the day-to-day management, operat

The role involves operating filling and packing equipment in a GMP environment, ensuring compliance with quality standards.

A global ecommerce group is hiring a Machine Operative for their production team in Blackpool, England.In this role, you will ensure safety and quality standards while operating and maintaining high-speed production equipment.Ideal candidates possess strong communication skills, attention to detail,

Greencore Group plc is seeking a Night Shift Quality Auditor for its Spalding site in the United Kingdom.The successful candidate will ensure compliance with quality management systems and food safety standards while supporting continuous improvement initiatives.Key responsibilities include conducti

Ipsen Group in Dublin is looking for a talented Plant Engineer to contribute to the production of Active Pharmaceutical Ingredients (APIs).The ideal candidate will have 5 years' experience in maintenance engineering within the pharmaceutical industry, focusing on HVAC, lyophilization, and process ab

Required: degree in engineering or a related field, extensive GMP experience, and significant leadership experience.

Experienced throughout the GMP tech stack. Integrating new capabilities for prototyping of tech solutions for both Assembly and GMP Clients. Be an evangelist to help our clients be at the top of their game by helping with their technical solutions of the GMP & GCP tools.

You will manage projects from concept to completion, ensuring compliance with GMP standards while optimizing plant infrastructure.

Candidates must have a degree in a relevant scientific discipline and prior experience in highly regulated environments such as cGMP or ISO.