Jobs at Orion Corporation

Manage supplier relationships and operational purchasing to ensure timely availability of finished pharmaceutical products. Own purchase orders, forecasts, delivery follow-up, invoicing, stock adequacy, and SAP product data updates. Act as primary operational contact internally and with suppliers, support supplier/category management, and coordinate logistics and EU re-analysis.

Plans and coordinates pharmaceutical stability studies, method validation, and method transfers with CROs and quality-control laboratories. Prepares and reviews CTD technical documents, analytical methods, validation reports, change controls, deviations, stability data, and Product Quality Reviews. Supports regulatory responses, vendor coordination, externally supplied product reviews, drug-product property evaluations, local in-licensing, and Indian pharmaceutical team activities.

Develop and maintain Semarchy xDM master data solutions, including data models, workflows, match/merge rules, quality validations, integrations, and governance processes. Focus initially on product and business partner data, expanding to reference, finance, and asset domains. Collaborate with business and technical stakeholders, support stewardship and issue resolution, and provide technical guidance while ensuring data quality, lineage, and compliance.

Administer and improve Veeva CRM across multiple countries, supporting sales and marketing users, configuring systems, troubleshooting integrations, and maintaining data integrity. Develop reports, training materials, business rules, and adoption initiatives while supporting segmentation, targeting, customer engagement, and commercial performance tracking. Collaborate with global CRM, sales, marketing, and medical teams to translate business requirements into technical solutions and streamline operations.

Prepare, review, and maintain pharmaceutical and quality regulatory dossiers, variations, amendments, annual reports, renewals, and responses to regulatory deficiencies under EU requirements. Classify regulatory changes, maintain records and internal systems, collaborate with departments and partners, meet deadlines, and support regulatory capability development. The role requires international pharmaceutical regulatory affairs experience, EU and ICH knowledge, strong English communication, and a pharmacy or chemistry degree.