346 jobs for “Product Field Sales Specialist - Laborat”
Diagnose, repair and maintain electro-mechanical, fluidic and electronic diagnostic systems across the South and South West England region, covering installations, preventative and corrective maintenance. Deliver on-site and office-based customer training and support new product launches while working with the Regional Technical Manager and wider Technical Services team.
Roche Diagnostics
GSK · 10000+ people · Public
Support a secondary manufacturing site's production area with technical services including new product introduction, troubleshooting, and technical projects. Design and validate manufacturing processes, drive improvements using lean and Six Sigma, and lead FMEAs, risk assessments and change controls under cGMP and EHS standards.
Leads CMC's scientific data, application and agentic AI product portfolio, setting integrated strategy and roadmap across forward-deployed engineering, product management and AI product strategy. Accountable for delivery quality, GxP compliance, governance, budget and headcount, and for representing the capability to R&D, Global Supply Chain, Quality and enterprise leadership.
Isomorphic Labs · 201–500 people · Series A
Build and evolve a large-scale ML infrastructure platform that supports training and deploying novel models across vast compute and data pools. Work cross-functionally with research, engineering and product teams, exploring agent deployment and distributed, performance-critical workloads. Hybrid role in London requiring three office days a week.
Kubernetes · Google Cloud Platform · GCP +1
Isomorphic Labs · 201–500 people · Series A
Research engineers translate frontier research concepts into practical implementations, building and optimising state-of-the-art AI models such as Transformers, GNNs and diffusion models, plus the codebases, data pipelines and infrastructure for training and evaluation. The role sits in an interdisciplinary team of drug discovery experts and ML specialists, with a strong emphasis on experimentation, benchmarking and taking models from conception to production.
JAX · PyTorch · XLA +6
Nuclera
Formulate, dispense and quality-control reagents for a protein discovery platform, operating lab equipment such as pipettes, centrifuges and UPLC systems. The role covers batch documentation, inventory management via ERP and troubleshooting production deviations, working closely with R&D, QA and Supply Chain in a fast-paced lab environment.
UPLC · ERP
LGC
Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.
Microsoft Word · Microsoft Excel
Autolus · 101–500 people · Series C
Serves as the primary point of contact for Advanced Therapy Treatment Centres across South UK, driving appropriate utilisation of CAR T therapies and coordinating site qualification, setup and patient treatment logistics. Works cross-functionally with Marketing, Medical Affairs and Market Access, and is 80% field based with UK travel.
Ipsen
Field-based medical affairs role acting as a scientific partner to healthcare professionals and thought leaders across the East Midlands, Yorkshire and East of England. Involves non-promotional scientific exchange, medical education, advisory boards, and supporting investigator-sponsored and real-world evidence studies within a neuroscience portfolio, working closely with UK, Ireland and global teams.
ABPI Code
AstraZeneca · 10000+ people · Public
Owns International regulatory strategy for complex cell therapy programs, embedding regional requirements into evidence generation, submissions and labeling. Leads BLA/MAA planning, Health Authority engagements and labeling negotiations, integrating clinical, CMC, safety and commercial input. Also leads a matrix regulatory team, coaching colleagues and shaping policy and process improvements.
BLA · MAA · IND +2
Autolus · 101–500 people · Series C
Field-based commercial role owning relationships with Advanced Therapy Treatment Centres across the South UK, acting as the primary point of contact for CAR T therapy accounts. Responsibilities span site onboarding and qualification, coordinating patient treatment logistics and chain of identity, compliance audits, and strategic account planning with Marketing, Medical Affairs and Market Access. Requires deep haematology/oncology and cell therapy expertise, with around 80% travel.
IQVIA
Monitors Phase I-IV clinical trials across UK sites, conducting evaluation, initiation, interim and close-out visits in line with GCP and sponsor requirements. Works closely with the Clinical Trial Manager and Lead CRA, handling source verification, eCRF/EDC data review, query resolution and site training. Requires oncology monitoring experience and involves travel plus mentoring of less experienced CRAs.
EDC · eCRF
EMBL-EBI
Develops the user-facing Europe PMC service, building fast, accessible interfaces for searching and navigating a corpus of over 47 million biomedical publications. Works with UX, product, back-end and data science colleagues to create reusable components, integrate REST APIs and JSON data, and improve performance, accessibility and maintainability within an Agile team.
React · Vue · Git +2
Thermo Fisher Scientific
Monitors investigator sites using a risk-based approach, conducting remote and on-site visits to assess protocol and regulatory compliance, performing SDR, SDV and CRF review, and documenting findings in reports. Acts as a site processes specialist ensuring trials follow ICH-GCP, applicable regulations and SOPs, while developing collaborative relationships with investigational sites and supporting audit readiness.
CTMS · Microsoft Office
Bristol Myers Squibb
Leads clinical strategy and execution for one or more GI oncology indications of a given asset, owning the Target Product Profile and disease area strategy. Manages a team of physicians and scientists designing, running, analysing and interpreting all clinical studies, and acts as internal and external clinical authority for regulatory interactions and business development. Requires deep therapeutic expertise and 8+ years of drug development experience, with international and domestic travel.
