Quality Assurance - Associate Director/Director

Wilmington PharmaTech (WPT) is looking for a Quality Assurance Specialist with GMP experience in the API / pharmaceutical industry for our brand new API pilot plant. The role includes leading and overseeing Document Review & Batch Release, QA Product Management, Customer Complaints, CAPAs, Document Change Control, Management Review/KPI & Compliance Initiatives in an FDA regulated environment. Ideal candidates should have: A strong understanding of Good Manufacturing Practices and API / pharmaceutical manufacturing Experience in new product development projects Project management experience Demonstrated proficiency in acting as a customer-facing quality representative Proven managerial experience with demonstrated success in communicating, leading, and motivating others to succeed Experience building teams and developing succession plans is highly desirable Must be a strategic driver of change with excellent writing skills.

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