Validation Engineer Role Summary
The Validation Engineer will manage and develop validations within the Quality Management System to ensure products and processes meet specifications and acceptance criteria.
This includes planning, execution, and closure of process validations and/or trial activities in a high-volume medical device environment.
The ideal candidate will have relevant academic qualifications, previous work experience in GMP compliant manufacturing, excellent communication skills, and data analysis abilities.
Key Responsibilities:
* Planning and execution of process validations and trial activities
* Closure of validation activities to ensure compliance with regulations
* Collaboration with cross-functional teams to achieve business objectives
* Analysis and interpretation of data to inform decision-making
Requirements:
* Relevant academic qualifications in a related field
* Previous work experience in GMP compliant manufacturing
* Excellent communication and interpersonal skills
* Data analysis and interpretation abilities
This role requires a strong understanding of quality management systems, process validation, and regulatory requirements. If you are a motivated and detail-oriented individual with a passion for quality and excellence, we encourage you to apply.