Minimum of +8 years working in a GMP environment. Must have experience creating or managing QA Batch Record documentation for a pharmaceutical manufacturing environment.
• Demonstrated ability in leading cross-functional teams
• Extensive knowledge and experience with Master Batch Record systems / processes
• Exceptional oral and written communication skills with proficiency in MS Office (specifically Word and Visio)
• Detail oriented and organized with the ability to problem solve and create efficient, effective workflows
Headquartered in Chicago metropolitan area, Protocol Link is a leading project management and strategy consulting firm providing comprehensive regulatory affairs, cGMP compliance, quality assurance, and validation services to the FDA-regulated companies worldwide. Protocol Link’s mission is to provide customer-focused services with ethical conduct, mutual trust, and personnel empowerment while striving to offer the best of both quality and efficiency. It's how we've been doing business since 1996. The right way.