Technical Associate

About this role

Responsibilities

• As our Technical Associate, Quality Control (QC) Technical Operations, you will be responsible for various tasks in the QC Technical Operations Unit, such as maintenance of laboratory equipment and IT systems. Your duties will also include validation testing, commissioning, troubleshooting, and system administration of laboratory equipment and facilities. You will work closely with laboratories, quality assurance (QA), equipment suppliers, and external service providers to help ensure that laboratory operations run safely, efficiently, and in a timely manner.
• The position is permanent and based in Espoo.
• Your key responsibilities include:
• Coordinating laboratory equipment and facility-related activities in collaboration with laboratories and other stakeholder groups
• Preparing and maintaining GMP documentation, such as SOPs and deviation reports
• Supporting laboratory equipment maintenance and related operational activities
• Acquiring, qualifying and validating new laboratory instrumentation in accordance with GMP and regulatory requirements
• Participating in laboratory and departmental development projects
• Collaborating with internal stakeholders, equipment suppliers, and external service providers
• What you can expect from us
• We offer a diverse and varied role in a successful company, along with opportunities for professional development. You will work in a team of experts in a multidisciplinary environment with various stakeholders. You will be supported by a skilled and friendly team with good team spirit and helpful colleagues. You will receive a comprehensive induction for the role.
• At Orion Pharma, 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 th