Job Details
Role Overview
We are currently looking for a Validation Engineer to join a leading pharmaceutical company based in Oxford on a 7 month contract. As the Validation Engineer you will work as part of a larger validation team to ensure the biotech facility equipment, utilities, instrumentation and computerized systems are qualified and maintained in a validated state in accordance with appropriate regulatoryKey Duties and Responsibilities
Your duties as the Validation Engineer will be as follows:1. Establish, revise, and maintain validation plans and procedures for qualification of equipment required for cGMP compliance
2. Be responsible for writing and executing qualification protocols and report generation, including acceptance criteria generation
3. Perform equipment requalification to ensure utilities and equipment remain compliant with required procedures and regulations
Role Requirements
To be successful in your application to this exciting opportunity as a Validation Engineer we are looking to identify the following on your profile and past history:1. A minimum of five years professional experience in validation, engineering, or operations
2. Experience with GMP utilities and equipment is preferred
3. Excellent communication and interpersonal skills are required. Attention to detail, flexibility and technical writing skills are important for this position
