Acting as a pharmaceutical expert in product industrialization projects and/or product lifecycle management activities including deviation management and CAPA processes.
Planning, implementation, and documentation of product changes. Organizing and monitoring trial and process validation batches in production.
Identification and implementation of process improvements in working processes and production processes in close collaboration with other experts and stakeholder organizations.
Working closely with production, quality assurance, quality control, engineering, production planning and CPD & LCM experts. Collaborating with Orion’s subsidiaries and partners and participating in inspections conducted by regulatory authorities and partners.

A relevant higher university degree (e.g., M.Sc. in Pharmacy or M.Sc. in Engineering).
Willingness to work in a production environment and, when needed, in a non-GMP manufacturing laboratory.
Experience in a GMP or other regulated environment is an advantage.
Understanding of authority requirements related to marketing authorizations and product lifecycle management, especially regarding product change management, is an advantage.
Experience/knowledge of gel and ointment manufacturing processes is of advantage.
A solution-oriented and proactive working style.
Ability to adapt to changing situations and tasks, and to face challenging situations with a positive attitude.
Strong interpersonal and collaboration skills.
Fluent communicator in Finnish and English both written and verbal.

Development Manager

Key skills