Project Manager - Pharmaceutical (Contract, Outside IR35)

Added 01/05/2026

Engineering Project Manager (Pharmaceutical)(6 Month Contract, Outside IR35)We're working with a well-established and growing healthcare organisation to recruit a Project Manager to support the delivery of a complex engineering and facility expansion project.The RoleAs Engineering Project Manager, you'll play a key role in delivering installation, commissioning, and validation activities for an expansion of a pharmaceutical facility. Working closely with cross-functional teams, you'll help ensure projects are delivered safely, on time, and to the highest standards.You'll be involved throughout the full project life-cycle, from planning and installation through to validation, training, and handover.Key ResponsibilitiesSupport the delivery of engineering and facility-based projects...

CQV Engineer (Contract, Outside IR35 + Shifts)

Added 01/05/2026

CQV Engineer (Contract, Outside IR35 + Shifts)Smart4 Sciences Craigavon, Northern Ireland, United Kingdom (On-site)CQV Engineer - API Manufacturing (Contract, Shifts) Northern IrelandAbout the ProjectExpansion of API manufacturing capability, including a suite of chemical reactors controlled by Emerson DeltaV DCSFinancialHighly competitive package + shift allowance (percentage uplift) - financially lucrative opportunityThe role is determined as outside IR35This is a fantastic opportunity to join a cutting-edge expansion project with excellent earning potential through shift-based upliftsResponsibilitiesCommissioning phase for a new API plantWorking with mechanical/process equipment (reactors, skids, valves, interlocks)Managing and interfacing with vendor packagesSupporting DCS/PLC integration (Emerson DeltaV preferred)Vender package review (Mechanical equipment,...

CQV Engineer (Contract, Outside IR35 + Shifts)

Added 01/05/2026

CQV Engineer (Contract, Outside IR35 + Shifts)Smart4 Sciences Craigavon, Northern Ireland, United Kingdom (On-site)CQV Engineer - API Manufacturing (Contract, Shifts) Northern IrelandAbout the ProjectExpansion of API manufacturing capability, including a suite of chemical reactors controlled by Emerson DeltaV DCSFinancialHighly competitive package + shift allowance (percentage uplift) - financially lucrative opportunityThe role is determined as outside IR35This is a fantastic opportunity to join a cutting-edge expansion project with excellent earning potential through shift-based upliftsResponsibilitiesCommissioning phase for a new API plantWorking with mechanical/process equipment (reactors, skids, valves, interlocks)Managing and interfacing with vendor packagesSupporting DCS/PLC integration (Emerson DeltaV preferred)Vender package review (Mechanical equipment,...

Document Manager, Pharmaceuticals (Contract, Outside IR35)

Added 01/05/2026

Document Manager - CAPEX Projects (Pharmaceutical Industry) Contract, Outside IR35We are seeking an experienced and detail-oriented Document Manager to support CAPEX (Capital Expenditure) projects within a dynamic pharmaceutical environment. This role is critical in ensuring the effective control, organization, and compliance of project documentation across all phases of delivery.Key Responsibilities:Establish and maintain document control systems for CAPEX projects, ensuring accuracy, version control, and accessibility.Manage the lifecycle of engineering, construction, and validation documents in line with regulatory and company standards.Coordinate with project managers, engineers, contractors, and quality teams to ensure timely submission, review, and approval of documents.Ensure compliance with industry regulations...

Automation Engineer - Pharmaceutical

Added 11/05/2026

Automation & CSV Engineer (Permanent) - West YorkshirePharmaceutical Manufacturing | High-Tech GMP Environment | Career Growth OpportunityAn exciting opportunity is available for an Automation & Computer System Validation (CSV) Engineer to join a highly regulated manufacturing environment within the pharmaceutical/life sciences sector.This role is ideal for an engineer who enjoys working at the intersection of automation, validation, digital systems, and manufacturing operations. You'll play a key role in supporting critical production systems, driving continuous improvement initiatives, and ensuring compliance across computerized and automated processes.Key ResponsibilitiesSupport and maintain automation and control systems across manufacturing operationsTroubleshoot equipment and process-related automation issuesParticipate in...

Project Engineer - Pharmaceutical Manufacturing

Added 01/05/2026

Project Engineer - Pharmaceutical Manufacturing I am currently recruiting for an experienced Project Engineer for a highly regulated pharmaceutical manufacturing organisation; the role is for the develop of their manufacturing facility, clean room experience will be an advantage. Key Responsibilities for the Project Engineer Manage end-to-end delivery of engineering projects such as, equipment installation, upgrades, facility improvements.Support validation activities IQ/OQ/PQ)and documentation for these.Troubleshoot new equipment, communicate with Vendors and Suppliers for this.Coordinate internal teams and external contractors, ensuring the timeline is being met and within budget.Identify and implement process and equipment improvements.Support Qualification of new facilities such as Clean Rooms....

Senior Project Engineer - Pharmaceutical

Added 26/03/2026

Senior Project EngineerSmart4Sciences West Yorkshire, England, United Kingdom (On-site)Senior Project Engineer - Pharmaceutical Utilities & Facilities (Permanent)Location: West Yorkshire Salary: £50-£60kThe RoleWe're looking for a Senior Project Engineer with a Chemical or Mechanical Engineering degree to lead CAPEX improvement projects in utilities and facilities within the pharmaceutical sector.If you've successfully delivered projects in HVAC, Boiler, and Water systems and thrive in a regulated, GMP environment, you'll play a pivotal role in upgrading and optimising critical plant infrastructure.Key ResponsibilitiesLead and manage CAPEX projects across HVAC, Boiler, and Water processes from concept to completion.Define project scope, technical specifications, budgets, and schedules.Collaborate with...

Contract CSV Engineer

Added 13/04/2026

Contract CSV Engineer - 12 Months Outside IR35 - Ireland (GBP)Join one of the best DeltaV Project teams in the UK & IrelandBenefit from excellent rates and outside IR35 Cross boarder tax affiliates to manage your compliance aspects for Southern Irish contractorsScenic location with plenty of options for temporary accommodation & relocation to the local area. Flights from Leeds, Glasgow, Liverpool & Manchester (20 minutes from the local airport) Significant Capital Investment in expansion of API manufacturing.Calling versatile CSV Contractors who have experience of Computer Systems Validation & Commissioning of DeltaV Distribution and Batch Control Systems. Some very good people...

Contract CQV Engineer

Added 13/04/2026

Contract CQV Engineer - 12 Months Outside IR35 - Ireland (GBP)Scenic location with plenty of options for temporary accommodation & relocation to the local area. Flights from Leeds, Glasgow, Liverpool & Manchester (20 minutes from the local airport) Significant Capital Investment in expansion of API manufacturing.Calling versatile CQV Contractors who have experience of commissioning & validating equipment commonly used on a chemical API site (Active Pharmaceutical Ingredients) such as glass lined reactors, centrifuges and pressure filters. Some very good people on this Project which could last up to 3 years.Please contact Simon Fowler Lead GMP Contract Specialist at NGAGE Smart4Sciences

Pharmaceutical Analyst

Added 16/04/2026

Are you a detail-driven scientist with a passion for analytical testing and pharmaceutical development? Smart4 Sciences are working with an established and innovative pharmaceutical services provider to recruit a Pharmaceutical Development Analyst into their Pharmaceutical Development team. The RoleThis is an exciting opportunity to carry out high-quality analytical testing for complex pharmaceutical products in a GMP-regulated environment. You'll be an integral part of a specialist team working on product development projects with a focus on respiratory and inhalation drug products. Key Responsibilities:Perform experimental testing of pharmaceutical products using validated analytical methods.Prepare and handle solutions, mobile phases, and reagents in line...

QA Officer (6m Contract)

Added 03/03/2026

Quality Assurance Officer (6‑Month Contract) - Pharmaceuticals - BedfordSmart4 Sciences is working with a respected pharmaceutical supplier to recruit a Quality Assurance Officer. This full‑time 6-month contract role sits within a close‑knit QA team and offers hands‑on involvement in GMP compliance, quality systems, and key operational processes.This position is ideal for candidates with GMP experience in pharmaceuticals who are keen to strengthen their QA expertise and gain exposure across a broad range of compliance activities. Role Overview As a Quality Assurance Officer, you will play a central role in maintaining GMP standards and supporting the company's Quality Management System. You...

Quality Manager

Added 11/06/2026

Quality Manager - Cwmbran (Near Newport, South Wales) A leading CRO is looking for a Quality Manager to join its Cwmbran team, taking ownership of day‑to‑day Quality Assurance operations and ensuring both GMP and non‑GMP activities meet the highest standards of compliance, integrity, and client commitment.In this pivotal role, you'll provide hands‑on QA leadership across the full spectrum of quality system activities - from laboratory oversight and supplier audits to inspection readiness and documentation review. You'll be expected to apply pragmatic, risk‑based judgement suited to a dynamic contract laboratory environment where regulated and non‑regulated activities coexist.As a senior quality practitioner...

Quality Officer - Audit & Self Inspection

Added 20/05/2026

Quality Audit Officer - BedfordAre you a detail‑driven quality professional with a passion for compliance and client engagement? One of our leading pharmaceutical partners is seeking a Quality Audit Officer to join the Bedford team, where you'll play a pivotal role in hosting client audits and driving the self‑inspection programme across the business. This client‑facing role places you at the forefront of audit activities, ensuring compliance with ISO 9001, ISO 13485, and GDP regulations while building strong relationships with client quality teams.Working alongside the Quality Integration Manager, you'll arrange and host audits, draft and submit audit responses, and act as...

Quality Assurance Manager - FMCG Manufacturing

Added 11/05/2026

Quality Assurance Manager - FMCG Manufacturing 📍 WorcestershireAn established and growing manufacturing business is seeking an experienced Quality Assurance Manager to lead site quality and compliance activities within a fast-paced production environment.This is a highly visible role with responsibility for maintaining and improving quality systems, audit readiness, product compliance, and operational standards across the site.The RoleKey responsibilities will include:Managing and developing the site Quality Management SystemLeading HACCP reviews and site risk assessmentsCoordinating internal audits and supporting external audits/customer visitsDriving GMP, hygiene, and continuous improvement standardsManaging investigations, non-conformances, CAPAs, and root cause analysisOverseeing SOP control and quality documentation processesSupporting supplier and...

Head of Quality - Pharmaceuticals

Added 10/03/2026

Smart4 Sciences - specialists in pharmaceutical recruitment - are currently partnering with an established pharmaceutical organisation to recruit a Head of Quality to join their Site Leadership Team.This is a senior leadership role with full responsibility for the QA and QC functions, driving the site's quality strategy and ensuring compliance across manufacturing, licensing and parallel import operations.You will play a key role in maintaining an inspection-ready environment, leading regulatory audits and acting as the primary contact for the Medicines and Healthcare products Regulatory Agency.Lead and develop the site Quality Management SystemOversee QA & QC teams and departmental performanceHost regulatory and...