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Role Summary We are looking for a skilled and driven Formulation Development Scientist to join our UK manufacturing site. This role acts as the critical technical bridge between our India-based R&D center and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing. Key Responsibilities • Lead and support pilot batch manufacturing, scale-up batches, and troubleshooting of commercial batch failures at the UK site., • Serve as the primary technical liaison between the India R&D team and the UK TT department, ensuring effective knowledge transfer and alignment on formulation strategies., • Execute and oversee technology transfer activities for oral liquid and suspension products, ensuring compliance with regulatory requirements and internal quality standards., • Develop and optimize homogenisation processes for large-volume liquid products, ensuring product uniformity, stability, and consistency at scale., • Prepare and review technical documents including batch manufacturing records, technology transfer reports, process descriptions, and deviation investigations., • Identify root causes of manufacturing issues and implement robust corrective and preventive actions (CAPAs)., • Collaborate cross-functionally with QA, QC, Regulatory Affairs, and Manufacturing teams to support product lifecycle activities., • Contribute to process validation, equipment qualification, and process analytical technology (PAT) initiatives as applicable., • Stay current with regulatory guidelines (ICH, MHRA, EMA) relevant to liquid dosage form development and manufacturing. Qualifications & Experience Education • M.Pharm / M.Sc. in Pharmaceutics, Pharmaceutical Sciences, or a closely related discipline., • 6-12 years of hands-on experience in pharmaceutical formulation development, with a focus on oral liquids and suspensions., • Demonstrated experience in scale-up and technology transfer of liquid dosage forms., • Practical experience with homogenisation equipment (high-shear mixers, rotor-stator homogenisers) at pilot and commercial scale., • Strong understanding of formulation principles for oral liquids and suspensions (rheology, particle size, physicochemical stability)., • Familiarity with ICH Q8/Q9/Q10 guidelines and QbD principles., • Experience with GMP manufacturing environments and documentation practices., • Strong communication skills — able to operate effectively across geographies and functions., • Analytical and structured problem-solving mindset., • Self-driven with the ability to manage multiple priorities independently., • Collaborative team player with a proactive approach. What We Offer • A technically stimulating role at the interface of R&D and commercial manufacturing., • Opportunity to work across international sites with a high-calibre scientific team., • Competitive salary and benefits package in line with UK industry standards.

As a Maintenance Engineer, you will be working within a regulated GMP manufacturing environment, ensuring all machinery and site services are maintained to a high standard. Engineering qualification (NVQ Level 3 or equivalent).

A leading healthcare staffing organization in Watford seeks a Pharmacy Technician.

The role involves assisting in Phase I studies, managing drug assembly, and ensuring compliance with GMP and GCP regulations.

A leading biopharmaceutical company is seeking a Microbiology Analyst 1 in Elstree to support microbiological quality functions and ensure high standards of testing and data integrity.

A leading recruitment firm is seeking a Maintenance Engineer for a position in Bushey. In this role, you will work within a regulated GMP manufacturing environment, performing both reactive and planned maintenance on machinery and site utilities. Ideal candidates will have a strong electrical or mec

A healthcare provider in Watford is seeking an Advanced Pharmacist for its Technical/Cancer Services Department. Ideal candidates should hold an MPharm degree and possess significant experience in hospital pharmacy, particularly with cancer therapies.

Graduate Electrical Design Engineer Location: Hertfordshire, UK Salary: Competitive + Benefits + Structured Training The Company A specialist technical engineering consultancy based in Hertfordshire, delivering complex building services solutions across highly regulated and mission-critical environments. The business is recognised for its expertise in pharmaceutical and data centre projects, working with global clients to deliver high-performance, compliant, and resilient electrical infrastructure across the full project lifecycle — from concept design through to commissioning. Due to continued project wins and growth, they are now looking to appoint a Graduate Electrical Design Engineer to join their expanding design team. Role Overview As a Graduate Electrical Design Engineer, you will support the design and delivery of electrical building services systems across technically challenging projects. You’ll gain exposure to mission-critical environments where reliability, compliance, and performance are paramount. You’ll work closely with senior engineers and multidisciplinary teams, receiving structured mentoring and hands-on project involvement from day one. Key Responsibilities Assist in the design of electrical building services systems including: Power distribution Lighting design UPS & standby power systems Earthing & lightning protection Containment & cable routing Produce electrical calculations and design documentation Support the development of schematics, layouts, and technical drawings Use design software such as AutoCAD, Revit, and Amtech/Dialux (training provided if needed) Attend design meetings and collaborate with mechanical and project teams Assist with site surveys and inspections Ensure designs meet industry standards and client specifications Support commissioning and handover phases where required Project Exposure You will gain experience working on: Pharmaceutical manufacturing facilities Cleanrooms & laboratory environments Mission-critical data centres High-spec technical engineering installations Regulated and GMP-compliant facilities Candidate Requirements Degree qualified in: Electrical Engineering, or Building Services Engineering (Electrical bias) Strong academic background Understanding of electrical design fundamentals Desirable (Not Essential) Placement year or internship experience Familiarity with AutoCAD or Revit Knowledge of data centre or pharma environments Understanding of UK building regulations and standards

Reporting to the QC Supervisor the QC Analyst will be Responsible for Ensuring High-Quality Analytical Testing and Compliance within the QC Laboratory The QC Analyst will be Responsible for Managing Laboratory Activities, Overseeing Analytical Work, Supporting Junior Staff, and Ensuring Adherence to cGMP and Company Procedures ROLE Duties Broadly Include * Laboratory Management and Coordination * Analytical Testing * Compliance & Documentation * Quality Systems & Continuous Improvement * Systems & Cross-Functional Support REQUIRED Qualifications and Experience Requirements Include * Relevant Degree in Chemistry or Related Scientific Discipline * Previous Experience in a Pharmaceutical Laboratory Environment * Practical Experience with HPLC Analysis and Troubleshooting * Understanding of GMP and Pharmacopeial Requirements * Working According to Standard Operating Procedures * Detail-Oriented and Highly Organised * Professional and Approachable * Proficient in Microsoft Office eg Word and Excel * Proactive and Solution-Focused * Strong Written and Effective Communication Skills

Quality Assurance Officer – Pharmaceuticals (GDP) Overview Our client is looking for a proactive and detail-focused Quality Assurance Officer to support a busy pharmaceutical quality function. This role will play a key part in maintaining GDP compliance, supporting the Quality Management System (QMS), and ensuring regulatory standards are consistently met. You will work closely with the QA Manager / Responsible Person (RP) and will have the opportunity to deputise when required. Key Responsibilities Quality Management System (QMS) Support the ongoing maintenance and improvement of the QMS Manage QA logs including deviations, CAPAs, change controls, complaints, recalls, and SOP tracking Assist with implementation and maintenance of electronic QMS systems Ensure all quality documentation is correctly issued, controlled, and archived Compliance & Regulatory Ensure compliance with GDP and relevant regulatory requirements (MHRA, EU guidelines) Support supplier and customer qualification activities Assist in ensuring all licensed activities (procurement, storage, distribution, export) remain compliant Deviations, CAPAs & Investigations Log, investigate, and track deviations, CAPAs, complaints, and temperature excursions Support root cause analysis and risk assessments Ensure timely completion of corrective and preventative actions Documentation & SOPs Draft, review, and update Standard Operating Procedures (SOPs) Maintain accurate and up-to-date quality documentation, including training records and validation files Audits & Inspections Support internal audits, self-inspections, and external audits Assist with supplier/vendor audits and compliance checks Review returned goods, damaged stock, and support recall processes Training & Reporting Support GDP training activities and maintain training records Attend quality review meetings and provide documentation support Assist in preparing quality metrics and reports Additional Responsibilities Support change control processes and risk assessments (ICH Q9) Liaise with manufacturers and external stakeholders on quality matters Ensure compliance with Health & Safety and internal procedures Support wider QA activities as required Experience & Qualifications Degree in Life Sciences (or equivalent, RQF Level 6 or above) Previous experience or understanding of GDP/GMP within pharmaceuticals Familiarity with MHRA, EU GDP guidelines, and quality systems Strong organisational and documentation skills Comfortable using Microsoft Office (Excel, Word, Outlook) Key Skills High attention to detail Strong written and verbal communication Ability to manage multiple priorities Problem-solving mindset Team-oriented with a proactive approach

We are looking for a skilled and driven Formulation Development Scientist to join our UK manufacturing site. This role acts as the critical technical bridge between our India-based R&D centre and the UK Technology Transfer (TT) department, supporting the seamless transition of liquid products from development through to commercial manufacturing. Key Responsibilities • Lead and support pilot batch manufacturing, scale-up batches, and troubleshooting of commercial batch failures at the UK site., • Serve as the primary technical liaison between the India R&D team and the UK TT department, ensuring effective knowledge transfer and alignment on formulation strategies., • Execute and oversee technology transfer activities for oral liquid and suspension products, ensuring compliance with regulatory requirements and internal quality standards., • Develop and optimize homogenisation processes for large-volume liquid products, ensuring product uniformity, stability, and consistency at scale., • Prepare and review technical documents including batch manufacturing records, technology transfer reports, process descriptions, and deviation investigations., • Identify root causes of manufacturing issues and implement robust corrective and preventive actions (CAPAs)., • Collaborate cross-functionally with QA, QC, Regulatory Affairs, and Manufacturing teams to support product lifecycle activities., • Contribute to process validation, equipment qualification, and process analytical technology (PAT) initiatives as applicable., • Stay current with regulatory guidelines (ICH, MHRA, EMA) relevant to liquid dosage form development and manufacturing. Qualifications & Experience Education • M.Pharm / M.Sc. in Pharmaceutics, Pharmaceutical Sciences, or a closely related discipline., • Ph.D. is an advantage but not mandatory. Experience • 6-12 years of hands-on experience in pharmaceutical formulation development, with a focus on oral liquids and suspensions., • Demonstrated experience in scale-up and technology transfer of liquid dosage forms., • Practical experience with homogenisation equipment (high-shear mixers, rotor-stator homogenisers) at pilot and commercial scale., • Prior exposure to a cross-site or cross-functional TT role is highly desirable. Technical Skills • Strong understanding of formulation principles for oral liquids and suspensions (rheology, particle size, physicochemical stability)., • Familiarity with ICH Q8/Q9/Q10 guidelines and QbD principles., • Experience with GMP manufacturing environments and documentation practices., • Working knowledge of relevant regulatory frameworks (MHRA, EMA, ANDA/CTD as applicable). Soft Skills • Strong communication skills — able to operate effectively across geographies and functions., • Analytical and structured problem-solving mindset., • Self-driven with the ability to manage multiple priorities independently., • Collaborative team player with a proactive approach

STEM recruitment solutions have a superb opportunity for a Maintenance Technician to work with their highly respected client in the Elstree area. The position would suit an engineer/technician who has a manufacturing background and experience of working to GMP regulations. You will work across the facility, performing a combination of reactive and proactive maintenance on both the manufacturing equipment and the facility itself. There will also be a variety of other duties such as calibrations, support with production set up, document completion and continuing improvement initiatives The role operates on a early/back shift rotation covering Monday to Friday and would suit someone from a food, pharmaceutical or medical device background. STEM Recruitment Solutions Ltd operates as both a Recruitment Agency and a Recruitment Business. We endeavour to reply to all applications when possible however on occasions this may not be possible due to volumes of responses. STEM Recruitment is a Scientific, Engineering and Manufacturing Recruitment business supplying talented staff to permanent and temporary opportunities

Multi Skilled Engineer - Hertfordshire Salary: £53,000 Shifts: 4 on 4 off days Commutable from; Harlow, Bishop's Stortford, Chelmsford, Cambridge, Stevenage, Hertford, Ware, Cheshunt, Enfield, Watford, St Albans, Luton, Hitchin, Braintree, Colchester Are you an electrically biased engineer or a multi skilled engineer looking for your next big move in manufacturing? We are partnering with a market leading FMCG company, working in a highly skilled, specialised engineering team. Key responsibilities: • Deliver planned preventative maintenance and respond efficiently to breakdowns in a timely manner to maximise equipment uptime * Carry out electrical and mechanical fault finding on a variety of equipment * Use system to record maintenance activity and planned maintenance and track KPI's * Work effectively with external contractors and production teams to ensure smooth running of the factory * Ensure full compliance with food safety, environmental and health and safety standards * Maintain a daily engineering report log * Ensure work orders are completed effectively and on time * Adhere to technical procedures and GMP Key skills & experience: • Time served or relevant level 3 engineering qualifications * 17th or 18th Edition electrical certification * Previous maintenance or engineering experience within the FMCG industry * Good communication and problem-solving skills * High attention to detail and health and safety standards * Flexibility to cover shifts if required. * Ability to work under pressure and meet tight deadlines * Experience in low and high care environments If this sounds like the right opportunity for you, please contact Alexa or Oli on (phone number removed). As you know over here at Zest we like to do things properly and always want to keep you, the candidate in the loop. Applying to this 'one of a kind' role you give Zest permission to hold your information. If you want to know more about how Zest look after your personal information please visit our privacy policy on the website (url removed)

Reporting to the Quality Systems Manager, the QA Officer will be responsible for Ensuring the Quality Management System is Robust, Compliant, and Aligned with Regulatory Requirements The QA Officer will Support Quality Oversight, Across Manufacturing, Documentation, Supplier Management, Risk Assessment, and Regulatory Submissions to Maintain the Highest Standards of Product Quality and Regulatory Compliance ROLE Duties Broadly Include * Quality Management System * Documentation and Controlled Documents * Regulatory and Compliance * Quality Operations * Supplier and Vendor Quality * KPIs and Reporting REQUIRED Qualifications and Experience Requirements Include * Bachelor’s Degree in Pharmaceutical Sciences, Chemistry, Life Sciences, Quality Management, or Closely Related Field * Strong Knowledge of cGMP, GDP, ISO Standards, and MHRA/FDA Regulatory Requirements * Experience in a Pharmaceutical, Medical Device, or Regulated GMP Environment * Hands-On Experience with QMS Operations eg Change Control, Deviations, CAPA’s, Document Management * Experience Preparing for Internal/External Regulatory Audits. * Experience with Batch Documentation, (BPR/Bar Review) and Manufacturing Quality Oversight * Experience with ERP Systems eg Sage * Excellent Attention to Detail and Accuracy * Strong Organisational and Time Management Capabilities * Strong Written and Effective Communication Skills * Ability to Work Cross Functionally with Multiple Departments * Analytical Approach with Strong Problem Solving Skills * Ability to Manage Multiple Tasks and Work to Strict Deadlines

You will oversee maintenance activities, manage technical documentation, and ensure compliance with GMP regulations. The ideal candidate has experience in GMP environments and relevant engineering education.

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

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

You’ll be part of our GMP Data Solutions team, the specialists behind the delivery and implementation of GMP equalisation and rectification projects. Senior Project Analyst - GMP Data Solutions.

A global biopharmaceutical organization is seeking an experienced Commissioning Engineer for a 12-month contract in Surrey.The role involves leading commissioning activities for Heat Pumps and HVAC systems, ensuring adherence to project schedules while collaborating with various teams.Ideal candidat

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

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

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

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

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

A leading pharmaceutical company in the United Kingdom is seeking a highly motivated Manufacturing Technician.This role entails operating and maintaining manufacturing equipment, ensuring adherence to safety and quality standards, and supporting production efficiency.Candidates should have a High Sc

This role supports training compliance and competency activities in a fast-paced GMP manufacturing environment.

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.

Elix Sourcing Solutions is looking for a Production Supervisor in Prudhoe to lead a team of approximately 20 staff in a fast-paced manufacturing setting.This hands-off supervisory role emphasizes productivity, quality, and safety improvements with great progression opportunities.Suitable candidates

GMP Recruitment Agency Limited are proud to be partnered with a well-established ad vastly successful Estate Agency based in the Forest of Dean.

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

Ideal candidates will have qualifications in pharmaceutical sciences, significant GMP experience, and a dedication to patient-focused service.

A leading pharmaceutical company based in Derby is seeking a Project Manager to oversee multiple projects in pharmaceutical storage and distribution.The successful candidate will ensure compliance with GxP standards and drive continuous improvement through LEAN principles.Essential qualifications in

The role requires extensive experience in pharmaceutical equipment maintenance, fault finding, and adherence to GMP standards.

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

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,

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).

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

Ideal candidates will have experience in aseptic services and quality assurance, a keen eye for detail, and understand GMP.

A leading pharmaceutical manufacturer in the UK seeks a Multi Skilled Engineer.This permanent position involves supporting the maintenance team with breakdowns and scheduled activities.Ideal candidates will have a minimum City & Guilds qualification with significant maintenance engineering experienc

This key leadership role requires proven expertise in GMP-regulated environments, focusing on production output, team management, and compliance.

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

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.

This senior leadership position involves overseeing all engineering and technical operations within a GMP-regulated manufacturing facility.

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

The role requires adherence to GMP standards and involves managing service contractors and vendor relationships.

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

A leading biotechnology firm in the UK seeks a QC Analytical Scientist to oversee testing of gene therapy products, adhering to EU and FDA GMP requirements. Ideal candidates will have a degree in Human Health or Sciences and prior experience in a GMP environment.

Key responsibilities include preparing, compounding, and dispensing aseptic products under GMP standards.