CQV Engineer 2 - FUJIFILM
Holly Springs, NC
About the Job
Overview
Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO
The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.
Join us
We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America.
The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.
External US
About the Role:
The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to include but not limited to equipment set up, building dashboards, and reading and reviewing documents. This role ensures equipment and systems comply with regulatory requirements and quality standards.
Major Accountabilities:
+ Configures, tests, and validates electronic systems to ensure the systems are properly qualified and validated per standards and regulatory requirements (e.g., Food & Drug Administration (FDA))
+ Reads piping & instrumentation diagrams (P&IDs) to walkthrough systems in the field
+ Drafts and implements validation protocols
+ Coordinates the execution of validation activities (e.g., equipment set up, material readiness, and work orders)
+ Creates work orders, generates calibration reports, maintenance plans, and other items in the computerized maintenance management system (CMMS)
+ Executes validation protocols for manufacturing equipment, lab and admin, process support equipment, etc.
+ Develops dashboards in Tableau to visualize and analyze CQV data to track progress and trends
+ Identifies potential risks and escalates to senior engineers or management for resolution
+ Creates, implements, and maintains equipment and system qualifications and validation protocols
+ Prepares and presents report packages for implementation into standard operating procedure (SOPs)
+ Prepares validation master plans for facilities, equipment, and systems
+ Other duties, as assigned
Basic Requirements:
+ Bachelor’s degree in Engineering with 2 years of experience in validation activities in facilities, commissioning, and systems qualifications
Preferred Requirements:
+ Master’s degree in Engineering with no prior experience
+ Prior experience with Good Manufacturing Practices (cGMP) or working in another highly regulated industry
+ Prior experience with mammalian cell culture process
Working Conditions & Physical Requirements
May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program.
Will work in 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.
Ability to ascend or descend ladders, scaffolding, ramps, etc.
Ability to stand for prolonged periods of time up to 240 minutes
Ability to sit for prolonged periods of time up to 240 minutes
Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers.
Ability to operate machinery and/or power tools.
Ability to conduct work that includes moving objects up to 50 pounds.
Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions.
Will work in warm/cold environments up to 100F Range (mechanical spaces)
Will work in outdoor elements such as precipitation and wind.
Will work in small and/or enclosed spaces.
Will work in heights greater than 4 feet.
_FDBN is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender identify or any other protected class. If an accommodation to the application process is needed, please email_ FDBN_PNC@fujifilm.com _._
_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 place. 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._
Job Locations _US-NC-Holly Springs_
Posted Date _1 month ago_ _(8/24/2024 9:54 PM)_
_Requisition ID_ _2024-27343_
_Category_ _Validation_
_Company (Portal Searching)_ _FUJIFILM Diosynth Biotechnologies_
Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO
The work we do at FDB has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy and drive - what we call Genki.
Join us
We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America.
The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States.
External US
About the Role:
The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to include but not limited to equipment set up, building dashboards, and reading and reviewing documents. This role ensures equipment and systems comply with regulatory requirements and quality standards.
Major Accountabilities:
+ Configures, tests, and validates electronic systems to ensure the systems are properly qualified and validated per standards and regulatory requirements (e.g., Food & Drug Administration (FDA))
+ Reads piping & instrumentation diagrams (P&IDs) to walkthrough systems in the field
+ Drafts and implements validation protocols
+ Coordinates the execution of validation activities (e.g., equipment set up, material readiness, and work orders)
+ Creates work orders, generates calibration reports, maintenance plans, and other items in the computerized maintenance management system (CMMS)
+ Executes validation protocols for manufacturing equipment, lab and admin, process support equipment, etc.
+ Develops dashboards in Tableau to visualize and analyze CQV data to track progress and trends
+ Identifies potential risks and escalates to senior engineers or management for resolution
+ Creates, implements, and maintains equipment and system qualifications and validation protocols
+ Prepares and presents report packages for implementation into standard operating procedure (SOPs)
+ Prepares validation master plans for facilities, equipment, and systems
+ Other duties, as assigned
Basic Requirements:
+ Bachelor’s degree in Engineering with 2 years of experience in validation activities in facilities, commissioning, and systems qualifications
Preferred Requirements:
+ Master’s degree in Engineering with no prior experience
+ Prior experience with Good Manufacturing Practices (cGMP) or working in another highly regulated industry
+ Prior experience with mammalian cell culture process
Working Conditions & Physical Requirements
May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program.
Will work in 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.
Ability to ascend or descend ladders, scaffolding, ramps, etc.
Ability to stand for prolonged periods of time up to 240 minutes
Ability to sit for prolonged periods of time up to 240 minutes
Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers.
Ability to operate machinery and/or power tools.
Ability to conduct work that includes moving objects up to 50 pounds.
Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions.
Will work in warm/cold environments up to 100F Range (mechanical spaces)
Will work in outdoor elements such as precipitation and wind.
Will work in small and/or enclosed spaces.
Will work in heights greater than 4 feet.
_FDBN is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender identify or any other protected class. If an accommodation to the application process is needed, please email_ FDBN_PNC@fujifilm.com _._
_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 place. 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._
Job Locations _US-NC-Holly Springs_
Posted Date _1 month ago_ _(8/24/2024 9:54 PM)_
_Requisition ID_ _2024-27343_
_Category_ _Validation_
_Company (Portal Searching)_ _FUJIFILM Diosynth Biotechnologies_
Source : FUJIFILM