Supervisor, Visual Inspection

Fujifilm

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profile Job Location:

Holly Springs, MS - USA

profile Monthly Salary: Not Disclosed
Posted on: 16 hours ago
Vacancies: 1 Vacancy

Department:

Manufacturing

Job Summary

Position Overview

The Supervisor Visual Inspection supports start-up and operational activities. This role leads a shift team supporting a 24/7 operating facility. The Supervisor Visual Inspection oversees daily manual and automated Visual inspection operations for Drug Product in a Good Manufacturing Practices (GMP) regulated environment. This role ensures inspection activities meet regulatory quality safety and production requirements while leading and developing inspection personnel. This role is integral in defect detection compliance continuous improvement and inspection readiness.

Company Overview

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs North Carolina. By end of 2025 well open North Americas largest end-to-end CDMO biopharmaceutical manufacturing facility offering drug substance production fill-finish and packaging under one roof.

Were looking for passionate mission-driven people to help us realize this exciting vision and deliver the next vaccine cure or therapy. We offer a dynamic work environment and were proud to cultivate a culture that will fuel your purpose energy and drivewhat we call Genki. Ready to shape the future of medicine Lets transform healthcare together!


Holly Springs North Carolina combines small-town warmth with proximity to Raleighs thriving tech scene making it the perfect blend of community and opportunity.


Fujifilm is globally headquartered in Tokyo with over 70000 employees across four key business segments of healthcare electronics business innovation and imaging. We are guided and united by our Group Purpose of giving our world more smiles. Visit: Description

What Youll Do

Provides on the floor leadership for a shift team of Manufacturing Associates
Oversees and coordinates the execution of the manufacturing schedule through daily shift assignments and huddles
Serves as the point of contact for escalations and provides guidance to resolve issues
Fosters an inclusive People-First Culture with regular communication conducting one-on-ones on a defined cadence with direct reports
Coaches and guides direct reports to cultivate professional development
Addresses employee questions and concerns performance gaps and partners with HR as needed for resolution
Maintains a safe and current good manufacturing practice (cGMP) compliant environment by ensuring direct reports have correct and up-to date training
Supports manufacturing investigations and continuous improvement projects
Coordinates with other functional areas for additional activities requiring access to the manufacturing space and equipment such as but not
Limited to maintenance calibration activities and the use of manufacturing equipment
Enforces company policies that directly impact employees (e.g. time reporting time off approvals shift work and inclement weather)
Completes required administrative tasks (e.g. timecard approvals time off approvals expense reports etc.)
Participates in the recruitment process and retention strategies to attract and retain talent as needed
Performs other duties as assigned

Basic Requirements

High School diploma/GED with 8 years of related experience in large pharma/biotech operations or projects; OR
Associates degree with 6 years of related experience in large pharma/biotech operations or projects; OR
Bachelors degree with 4 years of related experience in large pharma/biotech operations or projects
Previous experience leading supervising or managing others

Preferred Requirements

Bachelors degree in Life Science Engineering or related field with 4 years of related experience in large pharma/biotech operations or projects
Experience working in a facility start-up environment
Experience with electronic batch records root cause analysis technical writing and initiation of investigations

Lean Six Sigma or similar certification

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

To all agencies: Please no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email the internet or in any form and/or method will be deemed the sole property of FUJIFILM unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired no fee or payment of any kind will be paid.

EEO Information

ADA Information


Required Experience:

Manager

Position OverviewThe Supervisor Visual Inspection supports start-up and operational activities. This role leads a shift team supporting a 24/7 operating facility. The Supervisor Visual Inspection oversees daily manual and automated Visual inspection operations for Drug Product in a Good Manufacturin...
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