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...

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...

QA Manager and Responsible Person (RP)

Added 10/07/2025

Join a leading logistics partner to the healthcare and pharmaceutical industry, as a Quality Manager & Responsible Person (RP). This is a crucial leadership role, responsible for site-level Quality operations, ensuring full compliance with GDP, MHRA, ISO, and internal quality systems. Key ResponsibilitiesLead and manage the on-site Quality department, overseeing personnel, operations, and performance.Act as the named Responsible Person for MHRA licences, ensuring adherence to GDP (2013/C 343/01).Ensure robust implementation of the Quality Management System including deviations, CAPAs, change control, and self-inspections.Maintain compliance with GxP, ISO 9001, ISO 13485, and regulatory standards.Conduct internal and external training on key QA topics...

Regulatory Affairs Manager

Added 26/06/2025

Regulatory Affairs Manager I am working with a pharmaceutical/ Medical Device manufacturing site based in Deeside specialising in challenge meals, this is a good opportunity for a experienced Regulatory Affairs Manager to develop their career with an expanding company. Key responsibilities for the Regulatory Affairs Manager Develop and implement regulatory strategies for FDA and MHRA submissions.Lead the preparation, submission, and lifecycle management of regulatory dossiers.Work closely with the director with FDA and MHRA, coordinating meetings, and inspection readiness.Monitor changes in global regulatory landscapes and assess impact on ongoing and future projects.Provide regulatory guidance during product development, labelling, and promotional review...

Construction Project Manager- French Speaking

Added 19/06/2025

Construction Project Manager- French Speaking I am currently recruiting for a Construction Project Manager on a contract basis based in Northern France for a new build of a pharmaceutical plant. As a Construction Project Manager, you'll be responsible for the end-to-end delivery of the project coordinating teams, managing budgets and timelines, and liaising with clients, contractors, and subcontractors. Key responsibilities for the Construction Project Manager- French Speaking Plan and execute, construction projects in line with deadlines and budgets.Oversee and manage the lifecycle of the project from pre-construction and construction..Lead on-site, off-site, contractors and suppliers to work within SLAs and ensure...

Utilities Manager

Added 02/05/2025

Role: Utilities ManagerSalary: £50,000 - £55,000Location: Liverpool Due to the expansion of the business an exciting role has become available for a Utilities Manager. We are a giant within the Chemical Process industry and are looking for an experienced manager to ensure we stay at the forefront of the market. The role: Ensure that the utilities are produced and distributed in a manner that meets Safety, Quality, Cost, Environmental and Service Requirements.Ensure access to equipment in order that maintenance activities and programs are carried out in a proactive manner to improve Safety, Reliability, Quality and Efficiency.Oversee all aspects of the...

QA Manager, RP, RPi

Added 02/05/2025

Smart4 Sciences - QA Manager/RP/RPi - London - hybrid positionSmart4 Sciences are currently partnered with a Global Biopharmaceutical company looking to recruit a QA Manager/RP/RPi to join their team on a hybrid basis at their UK Head Office in London.As a QA Manager/RP/RPi you will responsible for the upkeep of the QDA wholesale licence for the company, working closely with CMOs across the EU on supplier quality incidents and releasing finished product in line with RP/RPi requirements.Key Requirements.RPi certification with experience operating on and managing a WDA LicenceA strong background in all aspects of GMP/GDP Quality Assurance within the Pharmaceutical/Biopharmaceutical...

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...

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 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...