Supervisor, Manufacturing

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.

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. **Shift – Sun- Wed, 1500-0130** 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 Execute 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   Basic Qualifications: Master’s and 3+ years of relevant experience OR Bachelor’s and 5+ years of relevant experience   Preferred Qualifications: Able to build and lead a team as well as train entry-level personnel Knowledgeable of the current Code of the Federal Regulations (CFR's) and Current Good Manufacturing Practices (cGMP's) Sufficient understanding of process, systems and equipment to troubleshoot problems and provide solutions to senior management Sufficient knowledge of electronic quality systems Must be able to work on off shift hours as well as part of the on-call rotation as needed is required; weekend shift likely Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment High energy level and a positive outlook coupled with the requisite “can do” attitude and a willingness to do what it takes to achieve personal and organizational goals and overcome obstacles Willingness to think outside of the box and adapt best practices to our small, but growing environment Ability to adapt in a constantly evolving environment Self-motivated with a strong sense of ownership in areas of responsibility Previous cell culture experience preferred/highly desired People Leader Accountabilities •Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and