Validation Opportunities
We are seeking a highly skilled Validation Engineer to lead the development of our site's EMPQ strategy and implement environmental monitoring protocols.
Key Responsibilities:
* Drive the development of site EMPQ strategy and implement/maintain EM protocols for graded pharmaceutical areas, ensuring compliance with regulatory guidelines.
The ideal candidate will have experience in cleaning validation, temperature mapping activities, qualification of parts washers and/or autoclaves, drug substance/drug product process performance qualification and validation.
A Bachelor's degree in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry or related field is required. Strong technical writing and oral communication skills are also necessary.
You will be working closely with production and quality control teams to establish environmental procedures. Experience in global regulatory submissions, internal audits external inspections as needed would be an advantage. Possess minimal work direction needed but high levels initiative to facilitate problem solving risk assessment projects meetings making problems visible striving continuous improvement leading supporting organizational initiatives e.g safety financial forecasting etc.
This role requires a commitment to quality safety compliance focus customer satisfaction]