Software Validation Engineer- LabView
Copenhagen
Contract
Research and Development
CR/613881_1791553362
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
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