Quality Manager

Description: Job: Senior Manager R&D Deviation and CAPA Management R&D Quality and Medical Governance Onsite - T/W/Th Location - Parsippany, NJ (preferred) or Foster City, CA Primary Responsibilities Lead and facilitate Quality Event Investigations and subsequent CAPA development in accordance with defined timelines and in collaboration with appropriate subject matter experts Build, deploy and reinforce learning tools and materials to support quality event management capability development Oversee the standard and timeliness of deviation and CAPA completion Work with the business process owners to identify issues and improvement requirements and lead those improvement initiatives In support of the quality management system module leads maintain records of issues, enhancement requests and support the implementation of system changes Administer notification to management and escalation process Participate in risk assessments and act as risk facilitator Candidate Requirements GxP experience is preferred 10+ years experience in Biopharma experience 6+ years managing investigations (deviations, CAPA, etc) Experience writing investigations Experience managing RCA Job Type: Contract Pay: $70.00 - $75.00 per hour Expected hours: 40 per week Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Vision insurance Schedule: 8 hour shift Monday to Friday Application Question(s): Do you have experience with Quality Event Investigations and subsequent CAPA development? If yes, Mention Client Name? Are you comfortable with Rate $75/hr on W2? Are you comfortable with onsite in Foster City CA? Experience: CAPA: 8 years (Required) R&D Deviation: 6 years (Required) Work Location: On the road