Manager, CQV

Fujifilm

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profile Job Location:

Holly Springs, MS - USA

profile Monthly Salary: Not Disclosed
Posted on: 3 days ago
Vacancies: 1 Vacancy

Job Summary

Position Overview

The Manager of CQV enables efficient tech transfer and new product introductions at the Holly Springs facility. This role is crucial for Upstream and Downstream process equipment (thaw to bulk fill) as it enables the right first time and on-time commercial production. This role provides technical expertise to the immediate team and other stakeholders as needed. Additionally this role leads a team of Engineers and provides coaching and direction.

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

Leads the Upstream and Downstream drug substance manufacturing validation engineering team including activities from thaw through bulk fill
Provides support and direction on commissioning and qualification by utilizing technical expertise
Oversees and manages a team of experienced engineers supporting operations technology transfers and projects on time and within budget
Drives project goals and deliverables to ensure the successful completion of the project phase through commercial manufacturing
Fosters and sustains a people first culture where the team feels valued respected and supported through servant leadership
Creates and implements the strategy for process equipment validation lifecycle such as Validation Master Plan (VMP) in close collaboration with the technical subject matter expert (SME) network and Large-Scale Business Unit counterparts
Manages departmental budget systems processes and team schedules
Provides leadership and direction to the site team to define the commissioning and qualification requirements for execution of clients processes
Partners with Client Process Engineering Process Sciences Quality Manufacturing and Global Engineering on large-scale platform development technology innovation scale-up and manufacturability as part of technology transfers as needed
Ensures that facilities laboratory equipment utility systems and process equipment are maintained in a qualified and validated state
Verifies and enforces that reports are written accurately and timely
Establishes systems and procedures to enable period review requalification analysis and reporting
Delivers effective engaging and informative presentations as needed
Presents site validation programs to regulatory and other agencies as necessary
Provides team support for critical manufacturing investigations and technical oversight of deviations change controls and corrective and preventive action (CAPA) regarding equipment qualification from Installation and Operational Performance Qualification
Enforces and ensures team adheres to company policies
Coaches and mentors direct reports to foster professional development and growth
Participates in the recruitment process and retention strategies to attract and retain talent
Addresses performance gaps employee concerns and partners with HR as needed for resolution
Other duties as assigned

Minimum Requirements:

Bachelors degree in an Engineering discipline with 12 years of experience in a related engineering (e.g. validation) or another
similar role
2 years of previous experience managing a team
Experience working in a cGMP manufacturing facility

Preferred Requirements:

Masters degree in an Engineering discipline with 8 years of experience in a related engineering (e.g. validation) or another
similar role
Prior experience working at a Greenfield site
Large Capex experience
Prior experience collaborating with global teams

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

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Required Experience:

Manager

Position OverviewThe Manager of CQV enables efficient tech transfer and new product introductions at the Holly Springs facility. This role is crucial for Upstream and Downstream process equipment (thaw to bulk fill) as it enables the right first time and on-time commercial production. This role prov...
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Key Skills

  • Restaurant Experience
  • Customer Service
  • Employee Evaluation
  • Management Experience
  • Math
  • Employment & Labor Law
  • Sanitation
  • Leadership Experience
  • P&L Management
  • Mentoring
  • Supervising Experience
  • Restaurant Management