【COMPANY OVERVIEW】
A Global Pharmaceutical company and the fourth largest specialty generic pharmaceutical company in the world
【JOB RESPONSIBILITIES】
Support Quality activities at Contract Manufacturing Organizations (CMO) and API suppliers. Providing Quality oversight.
Accomplishes quality objectives by planning and evaluating project activities. Support may
include operations and validation.
Manage Operational Quality systems
QMS compliance
【People Management】
This position will manage 7 people
【REQUIREMENTS】
Minimum of 15 years of experience in Pharmaceuticals
or Medical Devices.
15+ years of related experience in a cGMP environment
Interaction with the global company in English.
Team player, task oriented, manage multiple complex priorities and keen on working in a cross‐cultural working
environment.
Certified Quality Auditor (e.g. ASQ) certification preferred.
English language fluency, both written and verbal, with the ability to communicate at all levels within the
organization; any other language fluency a plus