420 jobs for “Pharmaceutical Quality Assessor”
Carries out planned preventative maintenance, fault finding and repairs on manufacturing, packaging and utility equipment in a sterile pharmaceutical plant, responding to breakdowns to minimise downtime. Works within a shift-based cross-functional team, using SAP CMMS and GMP documentation, and supports root cause investigations, CAPAs and continuous improvement.
SAP · CMMS
IQVIA
Supervises a team of laboratory staff in a central laboratory services environment, setting day-to-day operational activities and ensuring effective delivery. Oversees hiring, training, performance management, safety compliance, CAPA and quality incident resolution, and reviews laboratory metrics to drive process improvement. Requires immunology-based clinical laboratory or clinical trials experience and proficiency with LIMS.
LIMS
Eurofins
Acts as the key analytical point of contact for clients, leading the transfer of commercial analytical methods across multiple laboratory sites and ensuring their robustness, performance and compliance for drug substances. Coordinates analytical activities, supports change programmes and market access projects, and leads a small team of scientists while working with Quality, Regulatory and Manufacturing. Based at a pharmaceutical client facility in Macclesfield.
Taylorollinson
Combines technical applications support with outbound sales for a Life Sciences SME supplying cell biology and recombinant protein products. You'll troubleshoot customer issues, recommend products, follow up leads and quotations, and proactively develop new business by phone and email, working in a small team.
Thermo Fisher Scientific
Performs chemical, physical and microbiological testing of raw materials, in-process, finished and stability samples in a GMP pharmaceutical QC lab. Uses wet chemistry techniques, auto titrators, Karl Fischer, FTIR and UV-Vis, plus LIMS, with instrument calibration, COSHH risk assessments and 6S housekeeping duties.
LIMS · Microsoft Office · Auto Titrators +4
IQVIA
Conducts site qualification, initiation, monitoring and close-out visits for clinical trials, ensuring GCP compliance, patient safety and data integrity. Builds relationships with investigators, resolves data queries, mentors junior staff and travels up to 40-60% within the region. Embedded in a sponsor-dedicated functional service partnership model.
Investigator Site Files · Trial Master Files
Mackie Myers
Lead client-facing formulation development programmes for biologic drug products, combining hands-on lab science with project ownership and people management. Design and oversee complex experimental studies, manage client interactions and technical reports, and mentor scientists within a growing team while driving innovation and technical excellence.
Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and Key Risk Indicators, translating complex risk signals into actionable insights for Clinical Trial Teams. Works in a global matrix with clinical, data and risk-surveillance teams, driving continuous improvement through analytics and technology.
Artificial Intelligence
Lead and develop a team of Central Monitors while shaping risk-based monitoring strategies across a global clinical development portfolio. Oversee trial-data surveillance, signal detection and insight generation, translating complex risk signals into actionable insights and designing study-specific Key Risk Indicators and Quality Tolerance Limits.
Artificial Intelligence
Leads authoring, review and lifecycle management of clinical and performance evaluation documentation for a global diagnostics organisation, including protocols, study reports, investigator brochures and regulatory submissions. Works cross-functionally with regulatory, quality, R&D and medical affairs teams, conducting literature reviews and synthesising complex clinical data under IVDR and GCP.
AI-enabled tools
Leads the Operational Excellence function at a major influenza vaccine manufacturing site, deploying Lean, Six Sigma and the CSL Operating System to translate strategy into operational priorities and financial benefits. Owns the site management system, structured problem solving and continuous improvement, coaching senior leaders and leading the OE team. Reports to the Manufacturing Site Lead and sits on the Site Leadership Team.
CSL Operating System
Supports the Value Stream Operations Manager in running a sterile manufacturing value stream, coordinating daily and weekly performance across Operations, Engineering, Quality, Supply Chain and MSAT. Drives safety, quality, delivery and cost objectives, leads continuous improvement using Lean and Six Sigma, and deputises for the Operations Manager when required.
GSK Production System
Eurofins
Develops, optimises and validates trace analysis methods using LC-MS and Orbitrap technologies to detect and quantify trace-level small molecules in raw materials, intermediates and drug substances. Provides technical expertise on mutagenic impurities and nitrosamines at parts-per-billion levels, performing complex analytical investigations and authoring method development reports and validation protocols. Based at a client pharmaceutical facility, collaborating with multidisciplinary internal and external teams.
LC-MS · Orbitrap · GC-MS +6
Moderna · 1001–5000 people · Late stage
Hands-on individual contributor role operating production equipment for mRNA vaccine manufacturing at the Harwell site, following cGMP, SOPs and safety requirements. Involves troubleshooting equipment and digital issues, basic maintenance, documentation with Quality Assurance, and RCA/CAPA investigations, with exposure to continuous improvement and Generative AI tools.
Generative AI
Orchard Therapeutics
Leads global pharmacovigilance operations, overseeing case intake, ICSR processing and regulatory reporting across clinical and post-marketing portfolios. Acts as business administrator for the Veeva Safety database and primary interface with PV vendors, while driving SOPs, inspection readiness and safety data exchange agreements.
Veeva Safety
