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Position Overview

**_Summary_** **:** The Manufacturing Readiness Coordinator II assists the Manufacturing team to ensure right-first-time execution on the GMP manufacturing floor and on time starts by coordinating and delivering readiness milestones.

Company Overview

The work we do at FUJIFILM Diosynth Biotechnologies Texas has never been more important—and we are looking for passionate, mission-driven people like you who want to make a real difference in people’s lives.

From developing the next vaccine to advancing cell and gene therapies, we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.

If you’re ready to help transform the future of medicine, join FUJIFILM Diosynth Biotechnologies. We offer a flexible work environment and we’re proud to cultivate a culture that will fuel your passion, energy, and drive—what we call Genki.

Our state-of-the-art biomanufacturing facility is located in in College Station, Texas, which combines a small-town feel with vibrant culture, top-notch schools, and close proximity to big city life. Nestled between major hubs, it’s a dynamic location that blends convenience with innovation.

Fujifilm is globally headquartered in Tokyo with over 70,000 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: https://www.fujifilm.com/us/en/about/region/careers

Job Description

_Essential Functions:_

Responsible for participating in the following activities within the Manufacturing Support Services function:

Materials/Consumables

+ Draft and finalize process consumables list for new client programs

+ Work with Supply Chain, Process Development, Manufacturing Operations, Quality Control, and Quality Assurance to identify materials and consumables appropriate for GMP manufacture.

+ Familiar with preparing material specifications to enable purchasing and release of materials/consumables for use in GMP manufacture.

+ Coordinate purchase order creation for client owned/client delivered materials

+ Deliver inputs and outputs necessary for SAP recipe creation

+ Works with Manufacturing and Supply Chain to follow-up on material ordering and receipt status for GMP manufacturing.

+ Generate PO for consumables as applicable

Documents

+ Create standard work for manufacturing readiness, execution, and disposition activities for new customer programs

+ Author batch records

+ Generate SOP's and applicable forms for new equipment and route them in document control system

+ Generate WR for changes / service as needed.

+ Generate, route and close Change Controls for equipment as required

+ Familiar with drafting Batch Production Records from Process Specs, update per client review and route for approval

+ Review Unicorn Methods and DeltaV recipes with Process Engineer

+ Review product sample plans

+ Generate Intermediate and Final product labels and client approval forms as necessary

+ Review Process Specification

+ Create tier 2 placards for each new client program.

+ Review campaign summary report

+ Support Failure Modes and Effects Analysis (FMEA) risk assessments.

+ Support Potential Problem Analysis (PPA) events

Equipment and Readiness Coordination

+ Coordinate room/equipment changeover

+ Ensure all equipment is in the room prior cleaning and room release.

+ Coordinate room release

+ Coordinate with facilities any service or Preventive Maintenance/Corrective Maintenance that needs to be performed to the room or system/equipment in the room.

+ Identify availability and schedule equipment usage as necessary.

+ Review Unicorn methods

+ Assist Process Engineers with room layouts

+ Induct new/updated equipment into Blue Mountain asset management system

+ Ensure equipment location data is current in Blue Mountain

+ Generate work requests for changes/service as required

+ Assist Manufacturing Techs to identify / request / retrieve needs prior to process e.g. Post-use sanitization buffers, AKTA calibration buffers and materials, etc.

+ Provide PIP support

+ Originates and tracks manufacturing work orders as necessary.

+ Performs all other duties as assigned.

Continuous Learning and Improvement

+ Participates in team projects relating to Operational Excellence such as Problem Analysis and Prevention

_Required Skills & Abilities:_

+ Good oral and written communication skills, interpersonal and organizational skills.

+ Practical understanding of equipment used in bioprocessing (downstream and/or upstream)

+ Proficient with Microsoft Office applications.

+ Good self-discipline and attention to detail.

+ Must have flexible work hours – must be willing to work outside of normally-scheduled hours as necessary; including opportunities for alternative shift-hours and weekends as required.

+ Experience working in clean room environments.

+ Must have good planning skills and must be willing to interface with and support team members in many different roles and functions throughout the manufacturing facilities.

_Working Conditions & Physical Requirements:_

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:

+ Experience prolonged standing, some bending, stooping, pushing, pulling, reaching above shoulders and stretching.

+ Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment.

+ Lift up to 25 pounds frequently and up to 50 pounds, on occasion.

+ Attendance is mandatory.

_Qualifications:_

+ Master's Degree and two (2) years of experience, preferably in biopharmaceutical manufacturing (GLP or GMP) or supply chain operations; OR

+ Bachelor’s Degree and four (4) years of experience, preferably in biopharmaceutical manufacturing (GLP or GMP) or supply chain operations; OR

+ Associate degree and six (6) years of experience, preferably in biopharmaceutical manufacturing (GLP or GMP) or supply chain operations; OR

+ High School Diploma or GED and eight (8) years’ experience in biopharmaceutical manufacturing (GLP or GMP) or supply chain operations

+ All above requirements must include at least two (2) years’ of GLP or GMP experience

_Preferred Qualifications:_

+ Experience with both Upstream and Downstream cell culture processes

+ Experience with material control and testing requirements

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 ([email protected] or (979) 431-3500).

**Job Locations** _US-TX-College Station_

**Posted Date** _2 months ago_ _(3/20/2025 4:07 PM)_

**_Requisition ID_** _2025-33912_

**_Category_** _Manufacturing_

**_Company (Portal Searching)_** _FUJIFILM Diosynth Biotechnologies_