Sr. Director II, Site Quality Head
Greater Ft. Lauderdale Florida area
A large global leader in pharma is looking for a proven change agent to join their rapidly expanding team! This company has an established presence in generics, specialty, OTC and API, building on more than a century-old legacy, with a fully integrated R&D function, strong operational base and global infrastructure and scale. This particular site is a very large and complex and you would be responsible for over seeing Quality for R&D, manufacturing, and packing. If you are looking to reshape the quality culture of a well-established pharmaceutical leader than please don't hesitate to apply.
The Executive Director, Site Quality Head will have the following responsibilities:
Implementing, developing and monitoring the Quality policies, programs and procedures to ensure compliance with ISO standards, GxP standards, FDA, corporate policies and other regulatory body guidelines and regulations
Implementing continuous improvement initiatives to ensure maximum productivity and drive Quality programs
Ensure that systems meet the needs of all external and internal constituencies with an emphasis on quality, process, budget control, productivity, and profitability
Create active development and training plans for Quality staff
The Head of Quality will have the minimum requirements:
10+ Years of GMP experience
7+ Years in Quality Management - Associate Director, Director or Head positions in the past
OSD (Fluid Bed Processing) experience
Ability to handle large groups
Compensation:
Competitive base salary + Bonus + LTI + Full Medical Benefits + Relocation for the right candidate
