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Salary
≈ $33k – $92k per year (Estimated)
Location
Hybrid (Turku, Finland)

Confirmed on the employer's own hiring board on Oct 7, 2026. First seen by Alion on Oct 5, 2026. Orion Corporation scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Founded in 1917, Orion Corporation is a prominent Nordic pharmaceutical enterprise headquartered in Espoo, Finland. The company develops, manufactures, and markets human and veterinary prescription drugs, over-the-counter products, and active pharmaceutical ingredients. Leveraging robust in-house research and manufacturing facilities, it provides innovative therapies across key therapeutic fields such as oncology, neurology, and respiratory care to global markets.

Your role

In this role, you will be responsible for the validation of equipment and computerised systems across our manufacturing operations.

You will also contribute to technical projects as a validation expert, working closely with project teams and other stakeholders.

This is a permanent, full-time position based primarily in Turku, with the possibility for hybrid working. The role involves some travel, mainly between our manufacturing sites. Travel frequency and the duration of business trips will vary depending on the project and its phase.

Responsibilities

Your key responsibilities include:

  • Defining validation and testing strategies for assigned projects
  • Planning, performing, and leading qualification and validation activities for GxP-critical equipment and computerised systems
  • Ensuring validation documentation complies with applicable regulatory requirements and internal procedures
  • Maintaining the validated state of GxP-critical equipment and computerised systems through change control, periodic reviews, and revalidation
  • Providing qualification and validation expertise during audits and inspections

What you can expect from us

We offer a versatile and challenging role with excellent opportunities for professional development. As part of the Validation and Calibration group, you will work in a collaborative and supportive team with strong professional expertise.

In this role, you will collaborate closely with a wide range of stakeholders, including QA, Automation, Own Manufacturing, and external suppliers.

At Orion, your work creates true impact and well-being for our customers, patients and society at large. Our culture of friendliness, respect, mutual appreciation and diversity creates a safe working environment where you can strive for excellence. We offer a wealth of career paths and development opportunities that support the development of innovative solutions and improving the quality of life.

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/

What are we looking for?

  • A relevant degree in engineering, technology, life sciences or a related field, along with relevant work experience
  • Good understanding of GxP requirements
  • Strong documentation skills and attention to detail
  • Good problem-solving and communication skills
  • Fluency in both Finnish and English

Previous experience in qualification and validation, as well as with computerised systems in a regulated environment, is considered an advantage.

You are solution-oriented and work in a systematic and conscientious manner. You are comfortable taking responsibility, working independently, and managing multiple tasks and projects. At the same time, you enjoy collaborating with different stakeholders and are motivated to continuously develop your expertise in qualification and validation.

How to apply

If you are interested in this opportunity, please submit your application by Sunday 18 October 2026. We typically review applications already during the application period and may start video-interviewing candidates before the application deadline. Therefore, we invite you to send your application as soon as possible.

For further information about the position, please contact Maija Halonen, Head of Validation & Calibration, at +358 50 966 5461 on Friday 9 October between 9.00 and 10.00 or on Thursday 15 October between 12.00 and 13.00.

Approved medical examination which also includes drug testing is required prior to the employment. We will also carry out a security clearance prior to the employment for the selected person.

Your new team

Orion's Global Operations covers the entire pharmaceutical manufacturing process, from sourcing of raw materials to the manufacture of products, packaging and delivery to customers. We are also responsible for the industrialisation of new products and product lifecycle management.

In Global Operations we have approximately 1,600 professionals working in Production, our external supplier network (Externally Sourced Operations) and Fermion Oy (API manufacturing and marketing). In addition, the organisation includes Supply Chain & Procurement, Technical Operations, Facility Management, EHS (Environment, Health and Safety), CPD&LCM (Commercial Product Development & Product lifecycle management) and Operations Development.

The Technical Operations unit is responsible for Orion's supply chain production technology and its maintenance. The main task of the unit is to ensure that the production equipment, facilities and systems meet the quality, safety and capacity requirements set for them. In the Validation and Calibration department, our team of around 25 experts is responsible for the validation and calibration of systems, equipment and facilities.

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