Job Description
We are seeking an experienced Validation Engineer for the role of Pharmaceutical Technology Specialist.
About the Role
The successful candidate will be part of the Validation Department, responsible for qualifying and validating all CGMP equipment, systems, and processes.
Key Responsibilities
* Oversee and coordinate site validation master plans under prospective, concurrent, and retrospective validation studies in a timely manner.
* Ensure all validation requirements are met for new processes, equipment, or changes to existing processes or equipment.
* Actively work on validation projects, completing associated project documentation in line with current corporate and regulatory expectations.
* Facilitate PQR review process and laboratory equipment review process as per the current rota.
* Keep up-to-date with current and changing regulatory guidance for relevant areas of validation.
Requirements
* Rélevant 3rd Level Qualification is essential.
* Experience in Pharmaceuticals Manufacturing/Production is essential.
* Demonstrate exceptional project management skills, proficient in Microsoft Office suite of programs, and experience with Validations processes.
* Excellent communication, organization, time-management, and teamwork skills.