Jobs at Orion Corporation

Leads the development and implementation of innovative in vitro toxicology methods, cell-based assays, laboratory automation, and safety assessment workflows for pharmaceutical discovery and development. The role interprets complex biological data, supports project decisions, drives scientific innovation, coordinates in vitro and in silico assessments, and coaches scientists. It is a permanent, full-time, on-site position in Turku, Finland, requiring collaboration across multidisciplinary teams and external partners.

Leads development, administration, validation, and improvement of GxP-regulated clinical data systems and eClinical processes. Manages Medidata configurations, permissions, coding dictionaries, reporting, data outputs, and Spotfire visualizations. Provides expertise in CDISC standards, clinical trial data management, automation, AI-enabled tools, compliance, user training, and cross-functional collaboration across clinical development teams and vendors.

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

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 validation studies using functional genomics and chemical biology; collaborate with Orion scientists and academic partners; communicate findings through reports, publications, presentations, and project updates while meeting quality, safety, data integrity, and intellectual property requirements.

Supports pharmaceutical manufacturing investment projects and technical changes at Fermion’s Oulu site. Responsibilities include preparing engineering calculations, feasibility studies, technical documentation, qualification materials, and P&ID updates; coordinating equipment procurement, suppliers, contractors, installation, commissioning, and handover; supporting project activities and maintenance shutdowns; and improving manufacturing facilities and engineering practices in compliance with GMP requirements.

Maintains veterinary medicine marketing authorizations, prepares variation submissions for manufacturing transfers, writes quality dossier sections, responds to regulatory authorities, ensures product information compliance, monitors change requests, and verifies French-market artwork and promotional materials. The role collaborates with Regulatory Affairs, Quality Assurance, R&D, and Manufacturing teams across international markets.

Develop and maintain production-critical MES, recipe management, reporting, automation, and OT systems across Fermion’s pharmaceutical manufacturing sites. Responsibilities include system harmonization, cybersecurity and virtualization initiatives, supplier coordination, system validation, GMP compliance, documentation, and ensuring system reliability and availability.

Field sales role promoting a pharmaceutical product to urologists and oncologists. Responsibilities include territory and budget management, customer network development, target analyses, event planning, reporting, and achieving quantitative and qualitative sales goals.

Manage and coordinate regulatory product information (PI) documents including CCDS, SmPCs, PLs and labelling. Write and quality-control PI content, manage document change control, provide global coordination and guidance on PI processes, and ensure compliance with internal guidelines and SOPs while collaborating with Regulatory Affairs, Pharmacovigilance, Medical Affairs and commercial teams.

Lead the Biove site finance function including accounting, reporting, tax, treasury, and compliance. Manage month/quarter/year closings, statutory reporting and audits, cash and working capital. Partner with Controlling, HR and local management on costing, budgeting, forecasting and financial planning. Lead a two-person finance team, strengthen controls, drive process harmonization, automation and digitalization across the Animal Health finance organization.

Design, maintain and govern OT and IT solution architecture for Animal Health. Provide technical OT expertise, support implementation projects, manage vendor lifecycle, enable digitalization and real-time data-driven decisions, and align solutions with business stakeholders.

Field sales role focused on pulmonology (plus neurology and gynecology). Sell pharmaceutical products to specialists, GPs, and pharmacies; acquire and manage customers; meet quantitative and qualitative targets; plan events; handle administrative tasks, database maintenance, budget and territory management with reporting.

Field pharmaceutical sales representative for CNS and Womens Health in Milan. Build and maintain relationships with medical specialists and opinion leaders, map and develop territory, manage stakeholders, deliver medico-scientific information in compliance with regulations and company procedures, ensure pharmacovigilance and proper handling of promotional materials, monitor market and competition, and report activities using company systems.

Field-based pharmaceutical sales role covering a defined German territory selling to specialists, GPs and pharmacies. Tasks include customer acquisition and account management, meeting quantitative and qualitative targets, event planning, administrative duties, database upkeep, budget and territory reporting. Requires certified pharmareferent or natural science degree and recent pulmonary field experience; neurology is an additional focus.