Job Overview
* We are seeking a highly skilled Engineering Validation Specialist to join our team.
About the Role
The successful candidate will be responsible for ensuring that all equipment and processes meet the required standards of quality and compliance. This will involve designing, authoring, reviewing and approving qualification and validation documentation, as well as executing cycle development studies in line with standard approval processes.
The ideal candidate will have relevant technical qualifications in applied pharmaceutical or biological sciences, and at least 3-4 years of experience in a comparable role. They should also have excellent communication and interpersonal skills, as well as proficiency in Microsoft Office and job-related computer applications.
Key Responsibilities
* Design, author, review and approve qualification and validation documentation
* Execute cycle development studies in line with standard approval processes
* Collaborate with cross-functional teams to ensure effective execution of projects
* Analyse and interpret complex data to identify areas for improvement
* Develop and implement continuous improvement initiatives using Lean Six Sigma methodologies
Requirements
* Relevant technical qualifications in applied pharmaceutical or biological sciences
* At least 3-4 years of experience in a comparable role
* Excellent communication and interpersonal skills
* Proficiency in Microsoft Office and job-related computer applications
Benefits
* Opportunity to work on high-profile projects
* Professional growth and development opportunities
* A dynamic and collaborative work environment