Coordinator, Clinical Supply Operations

📋 Description

• Generate batch records for clinical packaging activities performed in Lake County
• Coordinate with relevant partners to gather and confirm information needed to prepare accurate
• Check records for completeness, consistency, and alignment with approved source information
• Route records for review and approval, track status, and follow up on outstanding actions
• Incorporate approved changes and maintain clear version control
• Resolve record questions and discrepancies with subject-matter experts

🎯 Requirements

• Associates Degree or High School Diploma with equivalent experience
• 2 years of closely related cGMP manufacturing and supervision experience
• Demonstrated knowledge of cGMP requirements
• Goal-oriented, able to lead within a team environment, self-motivated
• Extensive experience with generating/completing cGMP documentation
• Strong organizational skills and ability to make quick decisions

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k)
• Short-term incentive programs