Jobs at Orion Pharma

Manage supplier relationships and operational purchasing to ensure timely availability of finished pharmaceutical products. Handle forecasting, purchase orders, delivery follow-up, invoicing, logistics coordination, and SAP product data maintenance. Serve as primary contact for suppliers and internal stakeholders, support supplier/category development, and participate in cross-functional operational meetings.

Plans and coordinates pharmaceutical stability studies, validation, and analytical method transfers with CROs and internal quality control teams. Reviews protocols, reports, analytical methods, deviations, change controls, stability data, and regulatory documents. Prepares CTD documents, Product Quality Reviews, and related technical documentation while coordinating data collection, vendor follow-up, and in-licensing support for Orion’s Indian pharmaceutical operations.

Design, develop, and maintain Semarchy xDM master data solutions across product and business partner domains. Build data models, workflows, match/merge rules, validations, integrations, and governance processes. Support data quality monitoring, stewardship, lineage, and issue resolution while expanding into reference, finance, and asset master data. Collaborate with business and technical stakeholders, provide technical guidance, and contribute to continuous improvement of the organization’s global MDM landscape.

Manage and support Veeva CRM across multiple countries by administering configurations, troubleshooting issues, maintaining data integrity, creating reports, and supporting integrations. Train users, drive CRM adoption, implement business rules, monitor metrics, and improve customer engagement processes. Collaborate with sales, marketing, medical, and global CRM teams to translate business requirements into technical solutions and support platform rollouts.

Prepares and reviews pharmaceutical and quality registration dossiers, variations, amendments, annual reports, renewals, and responses to regulatory deficiencies under EU requirements. The role classifies regulatory changes, maintains regulatory records and internal systems, collaborates with stakeholders, and supports regulatory capability development. Candidates need 5–8 years of international pharmaceutical regulatory affairs experience, EU and ICH knowledge, and a Pharmacy or Chemistry degree.