QC Technical Operations Specialist — GMP & Equipment

Orion Corporation; Espoo; On-site; EUR 47,000 - 65,000; Full time

Job summary

Orion Pharma in Espoo, Finland, seeks a Technical Associate for QC Technical Operations to maintain laboratory equipment and IT systems, perform validation testing, commissioning, troubleshooting, and system administration in a GMP environment.

You will work with laboratories, QA, equipment suppliers, and external service providers to ensure safe, efficient, and timely operations, with opportunities for development in a multidisciplinary team.

Qualifications

• Bachelor's degree in chemistry, analytical chemistry, or a related field.
• Experience in laboratory work and chemical analytical instrumentation techniques (e.g., HPLC, GC, spectrophotometers).
• Good technical skills and ability to learn new systems.
• Proactive, solution-oriented, innovative with positive attitude toward challenging tasks; works independently and in a team with good networking and communication skills.
• Able to prioritize and manage multiple assignments simultaneously.
• Fluency in Finnish and English (written and spoken).
• GMP experience is an advantage.

Responsibilities

• Coordinate laboratory equipment and facility-related activities with laboratories and stakeholders.
• Prepare and maintain GMP documentation (SOPs, deviation reports).
• Support laboratory equipment maintenance and related operational activities.
• Acquire, qualify and validate new laboratory instrumentation per GMP and regulatory requirements.
• Participate in laboratory and departmental development projects.
• Collaborate with internal stakeholders, equipment suppliers, and external service providers.

Skills

Laboratory experience

Analytical instrumentation

Teamwork

Fluent English

Finnish language

Education

Bachelor's degree in chemistry or related field

Tools

HPLC

GC

Spectrophotometers

Job description

Orion Pharma in Espoo, Finland, seeks a Technical Associate for QC Technical Operations to maintain laboratory equipment and IT systems, perform validation testing, commissioning, troubleshooting, and system administration in a GMP environment.

You will work with laboratories, QA, equipment suppliers, and external service providers to ensure safe, efficient, and timely operations, with opportunities for development in a multidisciplinary team.