Job Description

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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 fulfill their aspirations. Join Kite and help create more tomorrows.

Job Description

We are seeking a highly effective Supervisor, Manufacturing to be responsible for supervising a team of cell therapy manufacturing specialists in our state-of-the-art commercial biotechnology facility in Frederick, MD.

In this role, the Supervisor will supervise the on-the-floor operations of our commercial cell therapy manufacturing facility in a cGMP environment including developing a team, and providing the necessary training and ongoing coaching, performance management and recognition of direct staff, including performing annual performance reviews.

• This position is for Front-end Swing shift (Sunday to Wednesday, from 3:00PM to 01:30 AM)
  Responsibilities (include but are not limited to):
  
• Supervise the on-the-floor operations of our commercial cell therapy manufacturing facility in a cGMP environment
  
• Build a team, provide necessary training and ongoing coaching, discipline and recognition of direct staff, including performing annual performance reviews
  
• Generate SOPs, MPRs, and SPRs for equipment and procedures used in routine biologics manufacture
  
• production and resource schedule against operational plan
  
• Ensure performance of all process steps specific to the phase or stage of operation
  
• Process monitoring, including manipulation of databases, documents and/or spreadsheets to support business reporting requirements
  
• Review of completed manufacturing documentation per compliance standards and established timelines
  
• Investigate and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior management
  
• Interact with outside vendors and senior management
  
• Participate in multi-functional project teams, as necessary
  
• Take corrective action to bring about required changes using change control procedures
  
• Other duties as assigned