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

Validation Engineer

Added 06/06/2025

Validation Engineer - Pharmaceuticals - Hull Salary negotiable Are you looking for your next step in Pharmaceutical Validation ?This company is experiencing an exciting period of growth, known for internal progression & variation, this is great place to progress your skills & expertise in Validation Engineering.As the Validation Engineer, you will benefit from working on various projects including exposure to the full validation life from Design Qualification through to operational handover & inclusive of CSV. Desirable Experience & QualificationsBroad validation experience in GMP Experience in cGMP Annex 11, 21 CFR Part 11, GAMP 5. Able to write URS and VMP...

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 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...

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...