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Sr Manager, Manufacturing - Viral Vector Downstream
Sr Manager, Manufacturing - Viral Vector DownstreamGilead Sciences • Oceanside, CA, US
Sr Manager, Manufacturing - Viral Vector Downstream

Sr Manager, Manufacturing - Viral Vector Downstream

Gilead Sciences • Oceanside, CA, US
2 days ago
Job type
  • Full-time
Job description

Kite Vector Downstream Manufacturing Team Leader

We're here for one reason and one reason only to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

Responsibilities include :

  • Leading 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
  • Providing strategic and technical leadership, as well as training, coaching, staff development, and annual performance reviews
  • Directing the activities of Downstream Manufacturing operations groups including Production and cGmP Cleaning as strong manufacturing partners
  • Defining, planning, and implementing activities / projects related to campaign or production readiness, new product introduction (NPI), and product changeover operations to ensure production schedules are met
  • Identifying and implementing process improvement opportunities and / or corrective actions to increase yield, maximize capacity, improve operational efficiency, reduce costs, and ensure safety while maintaining regulatory compliance
  • Determining metrics for success and evaluating performance against metrics
  • Partnering 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
  • Leading or representing 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
  • Identifying risks and creating working plans to prevent issues
  • Leading supervisors to ensure safety and compliance are adhered to by team and drives culture of operational excellence
  • Supporting various governmental agencies / regulators and external and internal audits or inspections

Basic Requirements :

  • A Ph.D. and 0+ years of experience in manufacturing in the pharmaceutical industry OR
  • A MS / MA and 6+ years of experience in manufacturing in the pharmaceutical industry OR
  • A BS / BA and 8+ years of experience in manufacturing in the pharmaceutical industry OR
  • A High School Diploma and 12+ years of experience in manufacturing in the pharmaceutical industry
  • Preferred Requirements :

  • 8 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
  • Ability to work off hours as well as weekends as needed
  • The salary range for this position is : $143,225.00 - $185,350.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans.

    Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.

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    Manager Manufacturing • Oceanside, CA, US

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