Jobs at Orion Pharma

Leads development and implementation of innovative in vitro toxicology screening methods, laboratory automation, and human-relevant safety assessment approaches. Provides scientific leadership in assay development, data interpretation, experimental planning, and strategic decision-making for drug discovery programs. Coaches scientists and research associates, collaborates with internal and external stakeholders, and drives continuous improvement of toxicology workflows, technologies, and practices.

Leads production operations development projects across Fermion’s Oulu and Hanko pharmaceutical manufacturing sites. Responsibilities include harmonizing equipment-cleaning processes, coordinating controlled-substance handling, improving cross-functional collaboration, implementing 5S practices, developing documentation, and driving initiatives from concept through implementation in a GMP-regulated environment.

Lead development and improvement of eClinical systems and processes supporting clinical trials. Manage Medidata configurations, access, data outputs, reporting, coding dictionaries, validation, and regulatory compliance. Program in SAS, R, and Python; create Spotfire visualizations; apply CDISC standards; and provide technical guidance and training. Collaborate with clinical, statistical, quality, and vendor teams to improve automation, data quality, and AI-enabled solutions across the clinical development lifecycle.

Supports pharmaceutical API manufacturing investment projects and technical changes at Fermion’s Oulu site. Responsibilities include preparing engineering documentation, feasibility studies, designs, calculations, qualification materials, and P&ID updates; coordinating equipment procurement, installation, commissioning, suppliers, and contractors; and supporting project execution, shutdowns, and handover to production while meeting GMP requirements.

Lead an independent oncology research project identifying target-effector protein pairs for induced proximity medicines. Integrate clinical omics, functional genomics, and protein interaction data; design and analyze studies; develop validation strategies using functional genomics and chemical biology; interpret findings; collaborate with Orion scientists and academic partners; prepare publications, reports, and presentations; and comply with quality, safety, data integrity, and intellectual property requirements.

Maintains veterinary medicine marketing authorizations, prepares variation submissions, writes quality dossier sections, responds to regulatory authorities, monitors change requests, and verifies French-market artwork and promotional materials. The role collaborates with Regulatory Affairs, Quality Assurance, R&D, Manufacturing, and other international teams to ensure regulatory compliance and product quality. CMC dossier-writing experience, English and French fluency, a relevant scientific degree, and a valid French work permit are required.

Develop and maintain production-critical MES, recipe management, reporting, automation, and OT systems across pharmaceutical manufacturing sites. Responsibilities include system functionality, compliance, cybersecurity, virtualization, documentation, supplier coordination, digitalization projects, system validation, and ensuring reliable long-term performance in a GMP-compliant environment.

Field sales of a pharmaceutical product to urologists and oncologists; provide expert consultation to office-based and hospital physicians; build networks; perform target-group analyses and territory management; plan and run professional events; manage budgets, reporting, customer data, and administrative tasks to meet sales targets.

Own and develop OT and IT solution architecture for Animal Health, support OT environment as technical expert, design and deliver IT solutions, manage vendor and lifecycle activities, align stakeholders, and enable digitalization for real-time decision-making across manufacturing sites.

Manage and coordinate high-quality product information (CCDS, SmPCs, PLs, labelling). Write and control PI documents, perform quality checks, manage document change control, and guide global PI processes in collaboration with Regulatory Affairs, Pharmacovigilance, Medical Affairs and Commercial Operations.

As a Pharmaceutical Sales Representative, you will sell pharma products, manage customer accounts, achieve targets, and organize events, focusing on Pulmonology, Neurology, and Gynecology.

Field sales representative responsible for building relationships with medical specialists, providing compliant medico-scientific information, mapping and developing territory, managing stakeholders, reporting activities in company systems, maintaining promotional materials, and monitoring market and competitors to support product growth.

Pharmaceutical field sales role focused on pulmonology (and neurology). Responsible for selling to specialists, GPs and pharmacies, acquiring and managing customers, achieving targets, planning events, administrative tasks, maintaining CRM data, budget and territory management with reporting.

Lead the Biove site finance function, overseeing accounting, reporting, tax, treasury, and compliance. Manage month-end closes, statutory reporting and audits, cash and working capital. Support costing, budgeting, forecasting, and financial planning. Lead a small finance team, drive process improvements, harmonization, automation and stakeholder collaboration.