Software Validation Engineer- LabView

Software Validation Engineer - LabVIEW Medical Devices / Diagnostics Location: Copenhagen, Denmark - On-site Contract: 12 months (potential to extend) Start: ASAP Hours: Full-time Role Overview We are looking for an experienced Software Validation Engineer to join a leading organisation within the medical device and diagnostics industry. This role will focus heavily on LabVIEW and software validation, so we are looking for someone with hands-on LabVIEW experience combined with a strong background in validating software within a regulated environment. You will support a range of software validation activities, working closely with engineering and quality teams to ensure systems meet relevant quality and regulatory requirements. Key Responsibilities

• Perform software validation activities within a medically regulated environment
• Work hands-on with LabVIEW, including programming, troubleshooting and/or modification of LabVIEW applications
• Develop, execute and maintain software validation protocols and documentation
• Ensure software and associated systems meet defined requirements and quality standards
• Support the investigation and resolution of issues identified during validation activities
• Work closely with engineering, software, quality and validation teams
• Support change control and revalidation activities where required
• Contribute to process validation activities where applicable
• Support the preparation and execution of validation protocols such as IQ, OQ and PQ, where relevant to the project
• Maintain clear and compliant validation documentation within the quality system

Essential Experience

• Hands-on LabVIEW experience
• Software validation experience
• Strong understanding of validation methodologies and documentation
• Experience working within a regulated engineering environment, ideally medical devices, diagnostics, pharmaceutical or life sciences
• Ability to work cross-functionally with engineering, software and quality stakeholders

Highly Desirable

• Process validation experience
• Experience with IQ/OQ/PQ
• Wider equipment, test system or manufacturing validation experience
• Previous experience within medical devices or diagnostics
• Experience supporting software-controlled equipment or test systems