
Associate Director, Viral Vector Downstream Manufacturing
- Oceanside, CA
- Permanent
- Full-time
- Lead Kite Vector Downstream Manufacturing team that is responsible for safe, quality and efficient buffer prep, cell purification, and fill & finish/packaging of vector substance production
- Provide strategic and technical leadership, as well as training, coaching, staff development, and annual performance reviews
- Direct the activities of Downstream Manufacturing operations groups including Production and cGmP Cleaning as strong manufacturing partners
- Define, plan, and implement activities/projects related to campaign or production readiness, new product introduction (NPI), and product changeover operations to ensure production schedules are met
- Identify and implement process improvement opportunities and/or corrective actions to increase yield, maximize capacity, improve operational efficiency, reduce costs, and ensure safety while maintaining regulatory compliance
- Determine metrics for success and evaluate performance against metrics
- Partner with Vector Process Development, Quality, Validation, Engineering, Maintenance, BSO, MSAT, and Supply Chain (Warehouse/Materials Management/Planning) to ensure timelines, deliverables, and business operations are aligned and met
- Oversight of completion and closure of all deviations, CAPA's, incidents, and change managements within the Manufacturing department
- Lead or represent the department as a member of a cross-functional project team providing guidance, insight and recommendations relative to the goals and objectives of the Manufacturing operations’ function
- Identifies risks and creates working plans to prevent issues
- Leads supervisors to ensure safety and compliance are adhered to by team and drives culture of operational excellence
- Supports various governmental agencies/regulators and external and internal audits or inspections
- A Ph.D. and 2+ years of experience in manufacturing in the pharmaceutical industry OR
- A MS/MA and 8+ years of experience in manufacturing in the pharmaceutical industry OR
- A BS/BA and 10+ years of experience in manufacturing in the pharmaceutical industry OR
- A High School Diploma and 14+ years of experience in manufacturing in the pharmaceutical industry
- 10 years bio manufacturing management experience in a Current Good Manufacturing Practices (cGMP) bioprocess environment
- Experience in cell banking and cell purification and fill/finish/packaging (bio-manufacturing)
- Demonstrated influencer cross-functionally with senior leaders
- Strong knowledge of quality systems, validation principles, regulatory guidelines, and multi-product controls
- Experience with Single-Use Technology scale manufacturing equipment and distributed control systems (DCS) such as DeltaV and automated process equipment
- Experience with Clinical (Phase II/III) and Commercial production
- Experience with Electronic Batch Records in manufacturing
- Background in disposable technology and multi-product facility desired
- Consistent positive attitude and demonstrated ability to learn new skills
- Strict adherence to established safety and compliance practices and standards
- Ability to think critically, with demonstrated troubleshooting and problem-solving skills as applicable to manufacturing process, documentation, and equipment
- Self-motivated and willing to accept temporary responsibilities outside of initial job description
- Comfortable in a fast-paced environment with minimal direction and able to adjust workload based upon changing priorities
- Ablity to work off hours as well as weekends as needed
- Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.