Job Description
Job Description
The Validation Manager leads the end-to-end planning, coordination, and execution of a portfolio of site projects focused on process and product validation, product and technology transfer, and validation and qualification workstreams. This role partners closely with cross-functional stakeholders to ensure all projects are delivered on time, within scope, and within budget, while maintaining robust GMP documentation and a constant state of inspection readiness. The Validation Manager provides strategic oversight, technical guidance, and leadership to ensure that validation activities support compliant, efficient, and reliable pharmaceutical manufacturing operations.
Responsibilities
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- Location Cherry Hill, New Jersey
- Job Type Full-time
- Category Operations Specialties Managers
- Posted Date July 08, 2026
- Application Deadline August 17, 2026