Validation Engineer Role
We are seeking a highly driven and skilled Validation Engineer to join our team on a 12-month contractual basis. This role focuses on the validation of test systems and manufacturing processes to meet stringent industry standards and internal quality protocols.
Key Responsibilities:
* Design and Execution of Validations
Plan, design, and execute validations of test methodologies used in production and quality assurance, ensuring alignment with regulatory frameworks and company procedures.
* Process Validation Leadership
Lead process validation efforts for medical device manufacturing operations, driving compliance and quality.
* Installation and Verification
Determine the necessary criteria and documentation for installing new testing fixtures and production tools. Perform verification testing to confirm process consistency and reliability.
* Data Analysis and Reporting
Conduct thorough analysis of processes, defining key performance parameters and acceptable output criteria. Compile comprehensive validation protocols and reports that adhere to industry and organizational requirements.
Candidate Profile:
To be successful in this role, you should possess:
* A degree in Engineering or a related scientific/technical field (preferred).
* At least five years of hands-on experience in validation within a regulated industry, ideally medical devices.
* Strong project management skills and ability to meet deadlines in a high-pressure environment.
* Excellent communication and collaboration skills, with the capacity to engage effectively across teams and management levels.
* Strong organizational capabilities and attention to detail.
* Proven aptitude for troubleshooting and process improvement.
* An enthusiastic team player with a proactive mindset and a passion for delivering quality results.
* A commitment to personal development and maintaining all required job-related certifications or training.