362 jobs for “Product Support Application Specialist”
Ipsen
Leads Cell Line Development and Upstream Process Development strategies for biologic products, from candidate selection through commercial manufacturing. Acts as subject matter expert within cross-functional CMC teams, managing CDMO partnerships, supporting regulatory submissions and technology transfer, and mentoring junior scientists.
CHO
Ipsen
Leads Ipsen's global Biologics Process Development organisation, owning CMC drug substance strategy for toxins, monoclonal antibodies, ADCs and enzymes from candidate selection through launch and lifecycle. Manages process and analytical development teams, acts as CMC sponsor, and directs CDMO partnerships, tech transfer and regulatory submissions. Also serves as PharmDev/R&D site lead in Wrexham on the cross-divisional Site Leadership Team.
CDMOs
Pfizer · 10000+ people · Public
Leads the strategy, design and lifecycle management of digital clinical supply chain systems for Global Clinical Supply, working with product managers and business SMEs on a 3-5 year roadmap. Drives process and technology integration, system modernisation and retirement, and enterprise-level portfolio prioritisation while reporting progress to senior management. Hybrid role with up to 15% travel.
Pfizer · 10000+ people · Public
Lead the digital transformation of Pfizer's clinical supply chain systems, overseeing the full lifecycle from concept to decommissioning. Define multi-year product strategies, drive process and technology integration, and guide cross-functional teams to ensure regulatory compliance and efficient delivery of investigational products worldwide.
Sits within GSK's Chemical Manufacturing & Control function, shaping how AI transforms manufacturing sites worldwide. Runs day-to-day tech transfer engagement with sites and CMOs, sizes AI opportunities, defines target process, data and agent architecture, and drives agentification and recipe building for new products alongside forward deployed engineering pods.
MES · LIMS · ERP +6
Sits within GSK's Chemical Manufacturing & Control function, running day-to-day tech transfer engagement with manufacturing sites and CMOs while redesigning processes in detail. Shapes NPI launch strategy covering site impact assessment, capacity management, digital twins, scenario planning and virtual line commissioning, and defines the target process, data and agent architecture. Owns the tech transfer package and drives agentification and MES-ready recipe building alongside forward deployed engineering pods.
MES · LIMS · ERP +6
Lead the development and maintenance of global labelling documents for neuroscience medicines, translating clinical and safety data into compliant product information. Facilitate cross-functional discussions, support Health Authority responses, and ensure timely implementation of labelling changes across global and major markets.
CSL · 10001+ people · Public
Leads a cross-functional Clinical Development Team as the lead scientific expert, owning the clinical strategy, plan and medical monitoring for immunoglobulin programs. Accountable for clinical content of regulatory submissions and study documents, and serves as medical monitor across trials in a matrixed environment.
CSL · 10001+ people · Public
Leads the cross-functional Clinical Development Team as lead scientific expert, owning the Clinical Development Plan and integrating internal and external contributions into program strategy. Serves as medical monitor, authors key regulatory and study documents, and presents to safety and review committees.
Vertex Pharmaceuticals
Leads the development and execution of international regulatory strategy across European and Rest of World markets, from first-in-human through post-marketing. Represents Global Regulatory Affairs on core development teams, manages project plans and resources, and advises senior management. Also a people manager within the International GRA leadership team, driving process improvement and regulatory policy engagement.
EMA
Plans and executes medical and scientific engagement activities such as advisory boards, congress symposia, external expert engagements and medical education programmes across oncology, cardiovascular, renal, neuroscience and immunology. Works within the International Medical Affairs Center of Excellence, translating engagement strategy into operational plans, managing vendors, logistics and budgets, and reinforcing compliant, audit-ready ways of working.
CRM Software
Danaher
Field-based role servicing, repairing, installing and testing microscopy and imaging systems at customer sites across South UK, with occasional EMEA support and up to 70% travel. Involves diagnosing failures, escalating complex technical or quality issues, and building customer relationships while driving continuous improvement within a remote North EMEA service team.
Microsoft Office · Word · Excel +1
Johnson & Johnson Innovative Medicine
A 12-month student placement in the clinical research department, supporting international trials of medical technology products. Duties include administering and coordinating the logistical aspects of clinical studies, tracking essential documents, and collecting and recording study data, with meetings alongside cross-functional partners.
Microsoft Excel · Microsoft Word · Microsoft PowerPoint
Fortrea
Owns product strategy, roadmap and innovation for clinical pharmacology clinics and bioanalytical labs, spanning early-phase platforms like ClinSpark, LIMS/LIS, ELN, instrument connectivity and lab automation. Builds business cases and secures funding, governs a regulated portfolio, and leads multidisciplinary product teams and vendors across distributed sites.
ClinSpark · LIMS · LIS +7
IQVIA
Provides strategic medical and scientific subject matter expertise in hematology-oncology, advising internal stakeholders on protocol design, clinical development plans and proposals, and supporting client bid-defense meetings. Acts as an internal and external consultant across the research and development lifecycle, coaching project teams and collaborating with business development and operations. Greater independence is expected over time under the therapeutic area head.
