This role exists to support the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Supervisor will be responsible for managing a team, shall be an SME on assigned Manufacturing Unit Operations, scheduling of daily operations, training, maintaining compliance as it relates to Manufacturing Operations and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. The Supervisor will perform review/approval of documents such as deviations & validations. Work will be split between Grade B and Grade C aseptic manufacturing environment and the office area, but may also include support of process development runs in the Manufacturing Science and Technology laboratory.
DUTIES AND RESPONSIBILITIES:
The following reflects management's definition of essential functions for this job but does not restrict the tasks that may be assigned. Management may assign or reassign duties and responsibilities to this job at any time due to reasonable accommodation or other reasons.
Manages Partial to Full Shift Manufacturing Staff -includes performance reviews, team meetings, one on one meetings, development planning, coaching/mentoring, Manage PTO requests/Time Off, On-the-Floor Supervision, and training.
SME (Subject Matter Expert) Trainer on Manufacturing Unit Operations and Equipment. First line of response for troubleshooting and cross-functional problem solving. Escalates to Line Manager as necessary.
Performs cell manufacturing related activities while wearing clean room attire in an aseptic cGMP manner. Responsible for documenting all data in a compliant manner in MBR/eBRs and associated logbooks.
Responsible for authoring, editing, reviewing and/or approving manufacturing documents. These documents include but are not limited to:
Training records
Copies of patient batch records and the Certificates of Analysis of the Drug Product
SOPs and Batch Record versions
Equipment and other logbooks
Validation documentation
MEMOs, CAPAs/ Deviations
Executed logbooks and Batch Records
Involved in Quality Output- May include but not limited to: Engagement in Compliance Forums (e.g. Aseptic Behaviors, GDP)
Works with the Quality team to author and review out of specification (OOS) reports, deviation investigations and corrective and preventative actions.
Daily scheduling of Manufacturing Operations including use of electronic systems (e.g. LIMS, SedApta, PAS-X, etc)
QUALIFICATIONS:
COMPETENCIES: