Are you interested in working at the intersection of pharmaceutical manufacturing, process validation, and sterile production? We are looking for a Validation Analyst to support a large-scale validation project within Animal Health. In this role, you will contribute to ensuring compliance, product quality, and reliable sterile manufacturing processes within a highly regulated GMP environment.
Job Description
My client is a global leader in the pharmaceutical industry, where quality, compliance, and continuous improvement are at the heart of operations. This newly created project-based role focuses on the validation and optimization of sterilization and filtration processes within a sterile manufacturing environment.
In this position, you will investigate and evaluate filtration processes to ensure they meet sterilization and regulatory requirements. You will develop, execute, and document validation activities, including protocols, reports, and technical assessments in accordance with GMP standards.
This role offers the opportunity to make a direct impact on critical manufacturing processes within an international and highly regulated pharmaceutical environment.
Responsibilities
Profile
Employment Conditions
Use our AI to tailor your resume for this Validation Engineer Pharma position at Oxford Global Resources.