Specialist Qa34

Descripción del Empleo:
Biotechnology industry experience •Detailed technical understanding of bio-processing unit operations
•Skilled in performance of GMP production operations
•Regulatory knowledge and interactions
•Participate and help lead cross-functional teams
•Ability to communicate and collaborate with technical and management staff within manufacturing, process development, and quality
•Organizational, technical writing and presentation skills
•Project management skills
•Knowledge of control charting
•Availability to support non-standard shift
•Experience in Root Cause Analysis (Fishbone, 5 Why’s, Kepner Tregoe)

ISHIHARA TEST is required
Requisitos:
•Master’s degree in Sciences/Engineering and 3 years of directly related experience or
•Bachelor’s degree in Sciences/Engineering and 5 years of Manufacturing experience in a GMP regulated industry