Job Description: Onsite!
Knowledge of process engineering and science generally attained through studies resulting in a B.S., in engineering, a related discipline, or its equivalent.
A minimum of 2 years relevant experience in biopharmaceutical industry or its equivalent.
Knowledge of SOPs, cGMPs and the knowhow to work and manage within a regulatory environment.
Understanding of process and equipment validation principles
Knowledge of biopharmaceutical facility design and manufacturing operations. Experience with biopharmaceutical regulatory submissions and interaction with regulatory agency inspectors is desirable.
Knowledge of project management principles including proficient use of project management tools and software such as MS Project and other collaborative systems.
Excellent verbal & written communications skills. Interpersonal / facilitation skills necessary to interface with and influence all levels of the organization.
Job Responsibilities-
Additional Job Requirements
None
Any Graduate