$200K - $250K*
The incumbent in this position has primary responsibility of overseeing all aseptic and non-aseptic pharmaceutical manufacturing production while ensuring cGMP and DEA regulatory compliance.
Responsible for the support of site and company-wide objectives through the reporting of department Key Performance Indicators (KPI). Responsible for meeting site level quality, safety, delivery and productivity objectives. Ensures people and processes comply with current Good Manufacturing Practices and company procedures. Establishes and maintains cooperative cross-functional relationships with peers in Quality and Facilities Engineering to meet plant objectives.
In partnership with site leaders, sponsors a quality and compliance focused site culture which embraces RFT (right first time) and Continuous Improvement expectations.
Responsibilities may include:
Valid through: 2020-4-9