Senior QC Analyst

Added 09/07/2025

Senior QC Analyst I am currently recruiting for a Senior QC Analyst for a Sterile Manufacturing organisation based in North Wales, this is an exciting opportunity for an established leader within QC to progress their career. Key responsibilities for the Senior QC Analyst Perform routine analytical testing via HPLC, GC, UV, FTIR, in compliance with cGMP regulations.Review analytical data and laboratory documentation.Provide technical guidance and support to junior analysts.Work with the Section Leader and QA team to Investigate OOS and OOT results, deviations, and support CAPAs. Requirements for the Senior QC Analyst Bachelor's degree in Chemistry or related subject.2-3 years...

Analyst - Method Validation

Added 17/06/2025

Contract Analyst - Method Validation - Bristol - 4-6 Month Contract *** Urgent Vacancy to support method validation for a new generic tablet formulation ****Do you have experience in method validation for HPLC methods for products registered under MHRA/GMP ?Are you skilled in report writing & protocol generation for HPLC & dissolution testing methods ?Are you immediately available for a new contract ?Please apply now or contact Simon Fowler at NGAGE Smart4Sciences on 01925239725 or to process your application

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

Regulatory Affairs Specialist - Pharmaceuticals

Added 11/07/2025

Pharmaceutical Regulatory Affairs Specialist | £40k - £45k | Hertfordshire | PermanentAre you a Regulatory Affairs professional with a sharp eye for compliance and a passion for guiding pharmaceutical products through every stage of their lifecycle?Smart4 Sciences are working with a pharmaceutical manufacturing company that's looking for an experienced Regulatory Affairs Specialist to join their team. This is an exciting opportunity to play a vital role in ensuring the company's products meet UK and EU regulatory standards from early development through post-marketing.Whether you're preparing submissions or staying ahead of evolving MHRA/EMA guidelines, this is a key position with real influence...

Cost Engineer- Pharmaceuticals

Added 10/07/2025

Cost Engineer- Pharmaceuticals I am currently working with a leading pharmaceutical manufacturer who are looking for a Cost Engineer to join the team on a 12-month FTC. This is a good opportunity for a contract Cost Engineer to develop their skillset within pharmaceuticals and work with one of the leading pharmaceutical organisations in the world. Key responsibilities for the Cost Engineer- Pharmaceuticals Monitor budgets and forecasts, perform cost-benefit analysis, for up to 200 different Projects worth up to £2Million.Registration of new Projects using the internal Capital Approval Scheme.Implementation onto SAP for various projects, providing work structures.Manage Project budgets within SAP...

Regulatory Affairs Manager - Pharmaceuticals

Added 10/07/2025

Join a pharmaceutical leader dedicated to improving access to essential medicines and make your mark in regulatory excellence. We are seeking a proactive and experienced Regulatory Affairs Manager to lead their Regulatory Affairs team and ensure full compliance with EU and GDP regulations. If you are a collaborative leader with a strong background in pharmaceutical distribution and regulatory affairs, this could be your next career-defining move.Key ResponsibilitiesLead, motivate, and supervise the regulatory approval team.Act as the main point of contact for team members and facilitate effective collaboration.Maintain and oversee accurate quality records, CAPAs, deviations, and SOPs.Coordinate with manufacturers and oversee...

QC Section Leader- Pharmaceuticals

Added 03/07/2025

QC Section Leader- Pharmaceuticals I am currently recruiting for a QC Section Leader for a Sterile Manufacturing organisation based in North Wales, this is an exciting opportunity for an established leader within QC to progress their career. Key responsibilities for the QC Section Leader- Pharmaceuticals Lead and Supervise the QC Team ensuring deadlines are met within cGMP standards.Review any CAPAs, Change Controls and Deviations prior to QA approval.Write, review and develop internal SOPs for the most efficient process.Support method development, method validation and any equipment qualification.Lead batch release within the QC department. Requirements for the QC Section Leader- Pharmaceuticals Bachelor's...

Regulatory Affairs Officer - Pharmaceuticals

Added 25/06/2025

Regulatory Affairs Officer - Pharmaceuticals & Medical Devices - HullAre you a Regulatory Affairs professional with a keen eye for compliance and a passion for bringing life-changing products to market? Smart4 Sciences partnering with a well-established pharmaceutical company who are looking to add a Regulatory Affairs Officer to their growing team.About the Role:As the Regulatory Affairs Officer, you'll play a critical part in ensuring regulatory compliance across UK, EU, and international markets. From product registration to post-market vigilance, you'll support the full lifecycle of innovative pharmaceutical and medical device products.Key Responsibilities:Compile and submit regulatory dossiers (new registrations, variations, renewals, CTAs).Maintain...

QA Manager - Pharmaceuticals

Added 19/06/2025

QA Manager - Pharmaceutical ManufacturingNorthamptonshire | Competitive Salary + Benefits | Permanent, Full-TimeAre you an experienced QA professional ready to take the next step in your career? Smart4 Sciences are working with a leading pharmaceutical manufacturing company in Northamptonshire that's on the lookout for a skilled QA Manager to join their growing team.This is a fantastic opportunity to take ownership of the Quality Assurance function on a busy GMP site, support a collaborative and quality-driven culture, and help shape the future of pharmaceutical manufacturing.The Role:As QA Manager, you'll lead a small but experienced QA team and take responsibility for the...