Independent scientist who demonstrates innovative technical knowledge and significantly contributes to the overall operations of the Virus Production group. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Contributes to the achievement of the company and departmental goals and objectives. Supports management of laboratory schedule with operations team. Performs and directs assays according to and in compliance with Good Laboratory Practice (GLP), current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Acts as Study Director as required.
Position Specific Responsibilities:
Equal Opportunity Employer Minorities/Women/Veterans/Disabled