Quality Assurance - Associate Director/Director

Quality Assurance - Associate Director/Director

Key Responsibilities/Qualifications:

Wilmington PharmaTech (WPT) is looking for 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, 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, and must be a strategic, driver of change with excellent writing skills.

A degree in chemistry degree with a minimum of 3 years of experience is desired within either the API or pharmaceutical manufacturing environment is preferred; food or medical device industry experience may be considered. Strong cGMP knowledge & strong problem solving ability req'd.