Senior QC Analyst

Added 05/06/2025

Role: Senior Quality Control AnalystLocation: CardiffSalary: £30,000 - £40,000 This is an exciting opportunity for a Quality Control Analyst to join an experienced team on the South Coast of Wales. The role: Senior QC Analyst As an Analyst you will:Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis. The successful QC Analyst will have: A relevant science degree or equivalent qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or...

GC Analyst

Added 09/05/2025

GC-MS Analyst - Fragrance IndustryLocation: LancashireSector: Fragrance / Analytical ChemistryJob Type: Full-time, PermanentAn exciting opportunity has arisen for a GC-MS Analyst to join a global manufacturer specialising in high-quality fragrance compounds, perfumes, and aroma ingredients used across various industries.Due to continued growth, we're looking to expand the analytical department with a motivated individual who will support the preparation, analysis, and formulation of fragrance compositions. Please note, this is primarily a desk-based, computer-focused role.Key Responsibilities:Prepare samples for GC-MS (Gas Chromatography-Mass Spectrometry) analysisAnalyse fragrance samples to identify and quantify component materialsInterpret essential oil data to determine specific oils presentCreate and develop fragrance...

GC Analyst

Added 09/05/2025

GC-MS Analyst - Fragrance IndustryLocation: LancashireSector: Fragrance / Analytical ChemistryJob Type: Full-time, PermanentAn exciting opportunity has arisen for a GC-MS Analyst to join a global manufacturer specialising in high-quality fragrance compounds, perfumes, and aroma ingredients used across various industries.Due to continued growth, we're looking to expand the analytical department with a motivated individual who will support the preparation, analysis, and formulation of fragrance compositions. Please note, this is primarily a desk-based, computer-focused role.Key Responsibilities:Prepare samples for GC-MS (Gas Chromatography-Mass Spectrometry) analysisAnalyse fragrance samples to identify and quantify component materialsInterpret essential oil data to determine specific oils presentCreate and develop fragrance...

GC Analyst

Added 08/05/2025

GC-MS Analyst - Fragrance IndustryLocation: LancashireSector: Fragrance / Analytical ChemistryJob Type: Full-time, PermanentAn exciting opportunity has arisen for a GC-MS Analyst to join a global manufacturer specialising in high-quality fragrance compounds, perfumes, and aroma ingredients used across various industries.Due to continued growth, we're looking to expand the analytical department with a motivated individual who will support the preparation, analysis, and formulation of fragrance compositions. Please note, this is primarily a desk-based, computer-focused role.Key Responsibilities:Prepare samples for GC-MS (Gas Chromatography-Mass Spectrometry) analysisAnalyse fragrance samples to identify and quantify component materialsInterpret essential oil data to determine specific oils presentCreate and develop fragrance...

Senior QC Analyst

Added 02/05/2025

Role: Senior QC AnalystSalary: Circa £35,000 (Negotiable)Monday - FridayLocation: Chester areaThe role: Carry out Analytical testing using a range of techniques such as UV, HPLC and GCCoaching/Mentoring junior members of the teamSupport management with timetabling analytical dutiesReporting any issues into Management The candidate: Degree in scientific disciplineUnderstanding and previous experience of working in a GMP EnvironmentExperienced in analytical techniques such as HPLC, GC, EVThe ability to lead a team If you would like to apply for this position or require further information, please email a copy of your CV to Jack Challinor on

Stability Analyst

Added 30/04/2025

Role: Stability AnalystLocation: DerbyshireSalary: £27,000 - £32,000Monday - Friday 8:30am - 4pmThe role: Focused on HPLC Analysis for stability studies and validation of analytical methods. We're looking for degree qualified candidates that are experienced in the following:HPLC AnalysisStability studiesMethod developmentICH ValidationExperience in GMP environmentStrong Analytical SkillsResponsibilities Conducting stability studies on raw materialsAnalysing stability dataEnsure compliance with relevant regulatory guidelinesSupport process validation activitiesPreparing stability protocolsMaintaining stability chambersIf you want to apply or require further information please contact Jack Challinor at

Senior QC Analyst

Added 17/04/2025

Role: Senior QC AnalystSalary: Circa £35,000 (Negotiable)Monday - FridayLocation: Chester areaThe role: Carry out Analytical testing using a range of techniques such as UV, HPLC and GCCoaching/Mentoring junior members of the teamSupport management with timetabling analytical dutiesReporting any issues into Management The candidate: Degree in scientific disciplineUnderstanding and previous experience of working in a GMP EnvironmentExperienced in analytical techniques such as HPLC, GC, EVThe ability to lead a team If you would like to apply for this position or require further information, please email a copy of your CV to Jack Challinor on

QC Analyst

Added 13/03/2025

Role: QC Analyst Location: HullFull timeSalary: Around £30,000 - £32,000A fantastic opportunity has arisen for Senior QC Analysts to join a sterile manufacturing facility in Hull. The role: QC Analyst As an Analyst you will:Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis. The successful QC Analyst will have: A relevant science degree or equivalent qualificationUnderstanding of current GMP, Health and Safety and COSHH regulationsExperience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able...

QC Analyst

Added 04/03/2025

Role: QC Analyst Location: Preston Full timeSalary: Up to £28,000 A fantastic opportunity has arisen for a QC Analysts to join a sterile manufacturing facility in North Wales. We offer a fantastic package plus benefits such as:7 % matched pensionDiscounts on common retail outlets through our rewards platformGenerous holidaysSalary sacrifice schemeSubsidised canteenFree parking The role: QC Analyst As an Analyst you will:Design and carry out HPLC/UPLC/UV/GC analytical method validation and/or verificationSupport the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis. The successful QC Analyst will have: A relevant science degree...

QA Officer - Pharmaceuticals

Added 13/06/2025

QA Officer - Pharmaceutical Manufacturing - HULLJoin a Growing Pharmaceutical Company with a Passion for Quality and Innovation!We are partnering with an ambitious and rapidly expanding pharmaceutical manufacturing company based in Hull to recruit a QA Officer. This is an exciting opportunity to be part of a company making significant investments in their facilities, people, and future.As a QA Officer, you'll play a vital role in ensuring that quality standards are upheld across all stages of manufacturing and supply. Whether you're an experienced QA Associate looking to take the next step, or already operating as a QA Officer, this role...

Qualified Person - Pharmaceuticals

Added 11/06/2025

Qualified Person (QP) - Sterile ManufacturingAre you a Qualified Person with experience in sterile pharmaceutical manufacturing? Looking to make an impact in a forward-thinking company where quality and patient safety come first?Smart4 Sciences are working with a pharmaceutical manufacturer in Essex specialising in the production of sterile and non-sterile products. As part of their continued expansion, they're seeking an experienced and proactive Qualified Person to join their quality team.The Role:As a QP, you'll be responsible for ensuring that products released to market meet the highest standards of GMP compliance and patient safety. Working in a modern GMP facility, you will:Act...

QA Officer - Pharmaceuticals

Added 13/05/2025

Smart4Sciences are currently working with a Pharmaceutical Company in the North West to recruit a QA Officer to join a small team responsible for all aspects GMP compliance within their Sterile manufacturing facility on a 12 month fixed term contract.This QA Officer position is a brilliant opportunity for candidates with prior GMP experience to further their career within QA with a company who can provide strong progression opportunities or for people with a background in GMP laboratories who are keen to transition to QA.Key ResponsibilitiesRespond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments,...

QA Officer - Pharmaceuticals

Added 12/05/2025

Smart4 Sciences are currently working with a Pharmaceutical Company in North Wales to recruit a QA Officer to join a small team responsible for all aspects of GDP and GMP compliance.This QA Officer position is a brilliant opportunity for candidates with 1+ years GDP/GMP experience to further their career within QA with a company who can provide strong progression opportunitiesKey ResponsibilitiesRespond to and action quality enquiries and quality management activities including deviations, change controls, risk assessments, complaints etc.Support internal and external GDP/GMP auditsAuthor, review and archive quality documentation including SOPs, PQRs, supplier agreementsEnsure GMP/GDP compliance at all timesKey RequirementsPrior GDP/GMP...

Qualified Person - Pharmaceuticals

Added 02/05/2025

Smart4Sciences are currently working with a Pharmaceutical Company in the north of England to recruit a Qualified Person responsible for sign off and release of finished Pharmaceutical productsAs a QP you will be responsible for reviewing and evaluating batch records and performing batch certification and release of solid-dose products in accordance with GMP and the Human Medicines Regulations. Key ResponsibilitiesPerforming QP batch certification of licensed medicines (per applicable regulations) and providing QP support as required for Quality issues.To act as 'Qualified Person' in approving Finished Product for release onto the marketplace.Verify and ensure that the products are manufactured, packed and...

Formulation/Development Lead - Pharmaceuticals

Added 02/05/2025

Formulation/Development Lead - Pharmaceuticals - North London Smart4Sciences are currently recruiting for a Formulation/Development Lead who will be responsible for working with one of North London's leading CDMOs of pharmaceutical products and lead all NPI and Tech Transfer activity.This Formulation/Development Lead position is a brand new role that has been created due to increased business and is a brilliant opportunity for a Scientist with a strong background in Formulation/Process Development to take a leading role in future projects within the companyKey responsibilitiesLead all Formulation/Development activities, working with clients and customers from the outset to interpret requirements and ensure projects are...