362 jobs for “Product Support Application Specialist”
Senior operational lead for GSK's Global Supply Chain Digital & Technology function, acting as trusted advisor to the SVP. Owns strategic planning, portfolio governance, PMO orchestration, business operations, workforce planning, change leadership and communications, using AI and automation to drive simplification across a complex global matrix.
AI · Automation
GSK · 10000+ people · Public
Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then hand proven solutions to a Solutions Engineer for scale-up. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP, and AI coding assistants are the default mode of building, turning manual lab and process workflows into agentic automation.
Claude Code · GitHub Copilot · Databricks AI Assistant +3
Acts as case management subject matter expert for assigned clinical trials, overseeing safety reporting plans, vendor performance and ICSR compliance. Leads pharmacovigilance processes, supports GxP inspections and audits, and provides study-specific training to vendors and internal teams. Requires deep PV and regulatory knowledge in a multinational pharmaceutical setting.
Drug Safety Database
AstraZeneca · 10000+ people · Public
Leads three mandates for an infectious disease portfolio: defining end-to-end publication strategy from target selection to clinical development, securing grants and partnerships with NGOs and philanthropic funders, and horizon-scanning emerging biotechnology. Partners with discovery, clinical, data and external academic stakeholders, coaching teams and influencing senior decision-makers.
Genomics
Owns the transition from discovery to delivery on Mystra, a scientific data platform, breaking strategic initiatives into well-scoped epics and features. Works with scientific SMEs, data services, engineering and design to ensure requirements are scientifically valid and technically sound, running kick-offs and bi-weekly check-ins. Requires fluency with genomic data such as GWAS papers, p-values and effect sizes.
Mystra
Genomics
Staff-level product engineer leading a petabyte-scale analytical data platform built on multi-tenant ClickHouse, spanning database internals through to data-serving systems. Work includes sharding and replication strategy, materialised views, self-healing pipeline automation, and Data-as-a-Service productisation, plus shaping data foundations for an agentic AI layer. The role combines hands-on engineering with line management of a small team and setting platform-wide technical direction.
ClickHouse · Mystra · MystraAI
Danaher
Provides advanced third-level technical support for Digital Pathology products including the Aperio GT Platform, CytoVision and CytoInsight, resolving complex escalations and communicating guidance to field teams. Owns service readiness for change requests and new product development, partnering with R&D, Quality and Product Management to turn findings into documented defects and service improvements.
Aperio GT Platform · Aperio FL · CytoVision +7
Vertex Pharmaceuticals
Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.
LIMS
Moderna · 1001–5000 people · Late stage
Performs routine environmental monitoring and critical utility sampling, plus water testing for TOC, conductivity, bioburden and endotoxin in a GMP manufacturing facility. Executes QC microbiology methods including sterility, bioburden and endotoxin testing, supports method transfers and qualifications, and authors quality records such as deviations and CAPAs. Site-based role working closely with AS&T groups and contract labs on mRNA products.
Vitek · Isolator Technology · LIMS
Thermo Fisher Scientific
Lead a medical information operations team, overseeing the development and dissemination of accurate medical and drug information while ensuring regulatory compliance. Responsibilities include supervising staff, quality review of medical/clinical work, client reporting, training, and acting as liaison between clients and program staff. Requires proficiency in English and French.
Helical
Provide scientific leadership across model evaluation and applied use cases, ensuring foundation models stay grounded in drug development and translational research challenges. Act as a senior individual contributor and key scientific partner, mentoring junior colleagues and working with Product and Business Development to turn biology and ML into customer-facing deliverables as the team scales.
Orchard Therapeutics
Safety expert serving as global PV lead for gene therapy products across investigational and marketed phases, owning benefit-risk strategy, aggregate reports (PSURs, DSURs) and risk management plans. Also acts as medical monitor, providing clinical oversight, real-time AE/SAE review and signal detection in close collaboration with cross-functional teams and health authorities.
Veeva
Platform Recruitment
Develops FPGA and embedded firmware for high-performance data acquisition and signal processing systems used in biomedical research products. Writes VHDL for FPGA design and C for low-level hardware control, integrating with interfaces such as SPI, I2C, UART, USB and Ethernet. Works alongside hardware and software engineers across the full product lifecycle, with real project ownership and a progression route to senior roles.
AMD/Xilinx Vivado · Intel Quartus · USB +1
SoCode
Job Title: Senior QA Validation EngineerLocation - Cambridge: On Site (some flex on occasionSalary - £80k - £100k (depending on experience) + up to 10% bonus (company performance dependent) + equityOverviewWe are seeking an experienced Senior QA Validation Engineer to…
Moderna · 1001–5000 people · Late stage
Hands-on automation engineering role supporting drug product packaging and drug substance manufacturing at a new mRNA facility. Involves commissioning and optimising Emerson DeltaV and Allen-Bradley/Rockwell PLC systems, automated labelling and secondary packaging equipment, plus GxP validation, root cause analysis and lifecycle documentation. Works independently as a technical specialist across manufacturing, engineering, quality and digital teams.
Emerson DeltaV · Allen-Bradley · Rockwell Automation +7
