Associate Director – Validation
Listed on 2026-10-11
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Quality Engineering -
Engineering
Regulatory Compliance Specialist, Pharma Engineer, Quality Engineering
Associate Director of Validation within Facilities and Engineering, overseeing site-wide validation programs supporting GMP compliance in a pharmaceutical setting.
Responsibilitiesestablishing validation strategies aligned with cGMP, leading validation projects for facilities, equipment, and processes, and ensuring documentation and system compliance; managing validation lifecycle activities from commissioning to qualification and validation audits.
RequirementsBachelor's in Engineering or related field; 10-12 years in validation management, engineering, or capital projects in regulated industries, with extensive GMP, FDA knowledge, and experience leading complex validation programs; strong project management, analytical, and communication skills.
High-Valuepharmaceutical manufacturing, facility and equipment validation, cGMP compliance, validation lifecycle management, capital projects, and regulatory audits.
Work setupinvolves office and on-site environments with occasional travel to various sites and possible after-hours work.
Consider building your career as a Associate Director – Validation at AstraZeneca.
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