Supervisor, All QC (Night Shift-6:00 p.m. to 6:00 a.m.)

Position Overview The Supervisor, All QC, 223 shift is responsible for providing day‑to‑day supervision, audit readiness, and planning activities for the laboratory. The supervisor will lead an All QC Team that performs routine testing for Urgent/STAT testing of manufacturing batch samples, clean utility, and environmental monitoring. This role is part of a 24x7 team supporting testing/sampling across all QC laboratories required for urgent testing/Manufacturing support. The role will learn and perform testing/sampling across multiple labs in QC. What You'll Do Provides supervision and scheduling of the 223 shifts in the All‑QC laboratory team. Applies expertise in laboratory methodology and compendial requirements for QC testing spanning all QC labs (e.g., Bioburden, Endotoxin, HPLC, UV280, TOC, etc.) per department SOPs and test methods for samples associated with manufactured batches. Acts as primary point of contact for the team and first‑line escalation point in areas of responsibility. Leads the team to meet project deliverables. Sets up and maintains operations of a QC testing laboratory. Assists senior management with resource planning and budget‑related tasks. Ensures efficient team scheduling and management of sample collection and testing to meet deliverables on time. Collects recommendations for enhancements and gaps in responsibilities, prioritizes and implements solutions with leadership. Maintains relationships with site‑based customers and global colleagues, providing updates to leadership as requested. Ensures allocation and planning of adequate resources for laboratory testing activities, QA support activities, and provides technical guidance to the team. Leads cross‑functional teams to achieve operational readiness objectives and new product introduction goals using a risk‑based, right‑size approach. Leads or guides laboratory staff in investigating lab deviations, excursions, and implementation of CAPAs as needed. Serves as Subject Matter Expert in audits and inspections for the laboratory, preparing and guiding the team to ensure audit readiness. Establishes and maintains internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements. Provides training, coaching, and mentorship to the team and peers as applicable. Works with the team to identify areas for improvement, reduce blind spots, and provide opportunities for increasing responsibility aligned with career objectives. Other duties, as assigned. Minimum Requirements Bachelors in Life Sciences (Biology or Microbiology) with 4+ years of relevant experience OR Masters in Life Sciences (Biology or Microbiology) with 2+ years of relevant experience 2+ years of team management experience Preferred Requirements Experience with management of complex projects Experience with leading startup activities and program‑forming initiatives, e.g. creation of systems or business processes that support Quality objectives Physical and Work Environment Requirements May work in mechanical/production spaces that may require hearing protection and enrollment in a hearing conservation program. Will work in an environment operating a motor vehicle or powered industrial truck. Ability to discern audible cues. Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color. EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (View email address on click.appcast.io). #J-18808-Ljbffr