Position requires progressive, postBachelors experience 5 years with Masters OR 7 years with Bachelors, including the followingbr 3 years managing a quality assurance group in a GMP pharmaceuticalbiologics cell therapy contract manufacturing setting.br At least some experience in each of the following skills Managing the quality release and distribution of bulk drug substances and finished products to support Phase I and Phase II clinical trials; Adhering to a maintenance budget; Implementing and management of an electronic Quality Management System Trackwise, Documentum, QPulse; Providing guidancebr and leadership for site wide quality systems deviation, CAPA, change control, inspection; and Recruiting, developing and retaining a quality management team.br br Completion of a background investigation required.
Categories: eb3
0 Comments