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 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...

Validation Officer- Pharmacueticals

Added 28/04/2025

Smart4 Sciences are currently working with a GMP regulated Pharmaceutical Manufacturer to recruit a Validation Officer to their site in HertfordshireAs a Validation Officer you be part of a small team responsible for maintaining the site Validation Master Plan and will be required to lead, author and perform IQ, OQ, PQ protocols including Process, Cleaning, Equipment and Computer Systems; completing all associated documentation in accordance with ICH guidelines and GMP standards.Key ResponsibilitiesLead, author and execute IQ, OQ, PQ protocols on specific projects including Process Validation, Cleaning Validation, Computer System Validation and Facilities ValidationManage all validation documentation including commissioning test scripts,...

Quality Assurance Officer

Added 17/03/2025

Role: Quality Assurance Officer Location: WirralSalary: £35,000 (negotiable) An exciting opportunity has become available for a QA Specialist to join a growing pharmaceutical company that specialise in pharmaceutical manufacturing. The position will be based on the Wirral. This would be a great opportunity for an experienced quality professional with one or two years of experience to join a growing team to accelerate progression within their career Job Description, Quality Assurance Officer Conduct regular audits and inspectionsAssist in training staff on quality standards and best practicesError Recording, execution of CAPAs and QMS complianceOversee the quality of all manufactured products and ensure...

QA Officer

Added 11/03/2025

Role: QA OfficerLocation: WidnesSalary: £30,000 - £32,000 Due to expansion we are looking to build our team! We're expanding our team and need to recruit a QA Officer for our team based in Widnes. The role: Reviewing Batch records and creating the associated checklists to support batch certificationArchiving GMP critical documents in line with company policyEnsuring current versions of controlled documents are available to site personnelAssist in AuditsProactively identifying risks within the QMS and supporting the development of action plans to address and drive continuous improvementTo foster collaborative working with sister departments across the globeTo perform out of specification /...

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...

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...

QA Manager, RP, RPi - Pharmaceuticals

Added 17/06/2025

QA Manager / RP / RPi - Pharmaceuticals - Greater London AreaAre you an experienced Quality Assurance professional with RP and RPi eligibility, looking for your next challenge in a dynamic and expanding pharmaceutical company?Our client, a rapidly growing and innovative pharmaceutical business based just outside London, is seeking a QA Manager who is also eligible to act as the Responsible Person (RP) and Responsible Person for Import (RPi) under GDP regulations. This is a hybrid role with excellent development prospects and the chance to make a significant impact in a highly collaborative team environment.Key Responsibilities:Oversee and continuously improve the...

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...

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...

Quality Director - Pharmaceuticals

Added 02/05/2025

Smart4Sciences - Quality Director - PharmaceuticalsSmart4Sciences are currently working with a Pharmaceutical company in Bedfordshire to recruit an experienced Quality Director to lead and the develop an experienced Quality team and ensure all products are manufactured inline with GMP and MHRA Regulations.As the Quality Director you will be part of the SLT; essential in driving the business forward, developing current processes and delivering continuous improvement throughout the Quality function.Key ResponsibilitiesVerify and ensure that all processes and procedures to include effective data management systems, policies, processes and programmes to provide assurances of ongoing statutory, regulatory and MA compliance.As a key member...

Head of Quality - Pharmaceuticals

Added 28/04/2025

Smart4Sciences - Head of Quality - PharmaceuticalsSmart4Sciences are currently working with a Pharmaceutical Manufacturing company in Hertfordshire to recruit an experienced Head of Quality to lead and the develop an experienced Quality team and ensure all products are manufactured inline with GMP and MHRA Regulations.As the Head of Quality you will be part of the SLT; essential in driving the business forward, developing current processes and delivering continuous improvement throughout the Quality function.Key ResponsibilitiesVerify and ensure that all processes and procedures to include effective data management systems, policies, processes and programmes to provide assurances of ongoing statutory, regulatory and MA...

Qualified Person - Pharmaceuticals

Added 28/03/2025

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...