October 11, 2024

Orion Corporation

Espoo

QA Manager

Description of position
As the QA Manager, GVP (Good Pharmacovigilance Practices) you are responsible for quality assurance in pharmacovigilance. Your duties include planning, conducting and monitoring internal and external audits and you actively participate in regulatory authority inspections and partner audits. You are involved in approving pharmacovigilance SOPs, deviations, CAPAs and change management. You monitor international regulatory authority guidances, and provide support, advice and training in GVP.
The location of this permanent role is in Espoo.
Description of unit
R&D QA is part of Quality Management organisation and is responsible for quality assurance in R&D and pharmacovigilance. Main tasks of R&D QA include assuring that processes comply with Gx P requirements and are continuously developed, internal and external auditing of Gx P activities and monitoring regulatory authority guidance.
We offer
We offer you an exciting and challenging position which is versatile and include both teamwork and independency. You work actively in an international environment with highly professional colleagues. Please visit our website to find further information about our values and Orion as an employer https://www.orion.fi/en/careers/orion-as-an-employer/.
Requirements
To be successful in this role, you will need:

University degree in e.g. pharmacy or life sciences
Experience in pharmaceutical or medical device industry
Experience in pharmacovigilance and/or quality assurance and auditing
Good co-operation skills, but also capability to work independently
Readiness to take responsibility and willingness to develop processes further
Strong interpersonal skills and the ability to positively influence and guide others
Excellent problem solving, risk analysis and negotiation skills
Ability to manage multiple activities and timelines, and see both the big picture and pay attention to the details
Fluency in written and spoken English
Fluency in IT skills and e.g. experience from document management and quality management systems used in pharmaceutical industry
Readiness to travel abroad occationally

Additional Information
If you are interested in this opportunity, please submit your cover letter and CV at the latest 30th October 2024.
For more information on the position, please contact Sari Launonen, Director, QA R&D, tel. +358 50 966 7178 (best available during the following times: 15th October between 14-15, 23rd October between 9-10 and 29th October between 14-15)
#LI-ORION
Orion Corporation operates in more than 30 countries, where we Orionees, 3600 in total, work in all kinds of positions. Among us there are Research Scientists, Laboratory Technicians, Engineers and IT Specialists as well as people working in Production, just to mention some examples. We offer diverse and responsible jobs to our personnel in a truly multi-disciplinary work environment. We encourage people to develop their competences and offer opportunities to affect the job description and creating their own career path at Orion. We are searching for top talents who are ready to share our passion for the work that we do.