Supervisor, Manufacturing (Back End Day Shift)

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. As a people leader, 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.

Requirements

• Provide oversight and/or supervision for the on-the-floor operations of cell therapy manufacturing in a cGMP environment.
• Build a team, provide leadership, guidance, and necessary training to staff in alignment with cGMP requirements.
• Clear communication with outgoing and incoming shift supervisors to disseminate all relevant information.
• Support the review and approval of procedural changes within controlled documentation.
• Participate in multi-functional project teams, as necessary.
• Responsible for oversight of on-the-floor execution of protocol driven production activities within manufacturing (APVs, PPQs, Engineering Runs, etc.)
• Execute production and resource schedule against operational plan
• Ensure performance of all process steps are in compliance with applicable SOPs, policies, and governing documents.
• 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 leadership.
• Take corrective action to bring about required changes using change control procedures.
• Support cross-functional meetings to ensure manufacturing representation as needed.

Benefits

• Paid time off
• Company-sponsored medical, dental, vision, and life insurance plans
• Discretionary annual bonus
• Discretionary stock-based long-term incentives