Global Validation Program Lead

Integrated Resources Inc.; Baltimore (MD); On-site; USD 110,000 - 150,000; Full time

Job summary

A leading pharmaceutical company is seeking a Validation Manager to oversee the Baltimore Site Validation Program. The role involves managing compliance, preparing validation documents, and training staff to ensure global regulatory adherence. Candidates should have extensive experience in validation protocols and management within the pharmaceutical industry to contribute effectively to maintaining product supply and compliance.

Qualifications

• 8-12 years of related experience within pharmaceutical industry.
• Minimum of 8 years of validation experience including writing and executing protocols.
• Minimum of 5 years of validation management experience.

Responsibilities

• Responsible for oversight of the Baltimore Site Validation Program.
• Prepares and executes validation master plans and protocols.
• Trains and directs staff in validation protocol execution.

Skills

Project Management

Communication

Troubleshooting

Education

B.S. degree in engineering, biology, pharmaceutics, or related science discipline

Tools

Kaye data logger equipment

Job description

A leading pharmaceutical company is seeking a Validation Manager to oversee the Baltimore Site Validation Program. The role involves managing compliance, preparing validation documents, and training staff to ensure global regulatory adherence. Candidates should have extensive experience in validation protocols and management within the pharmaceutical industry to contribute effectively to maintaining product supply and compliance.