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Engineer / Scientist 2/3, Downstream - MSAT

FUJIFILM Biotechnologies

FUJIFILM Biotechnologies

Holly Springs, NC, USA
Posted on Aug 18, 2025

Engineer / Scientist 2/3, Downstream - MSAT

Job Locations US-NC-Holly Springs
Posted Date 19 hours ago(9/12/2025 3:36 PM)
Requisition ID
2025-35180
Category
Engineering
Company (Portal Searching)
FUJIFILM Biotechnologies

Position Overview

The Engineer / Scientist 2/3, Downstream MSAT will provide tech transfer support and technical oversight for large scale purification activities for Monoclonal antibody production.

Job Description

What You’ll Do

  • Conducts lab and pilot plant experiments
  • Generates and coordinates execution sampling protocols
  • Serves as subject matter expert (SME) to lead and conduct troubleshooting, process impact assessments, and executes root cause analysis (RCA) and corrective and preventive action (CAPA) in response to deviations
  • Executes and analyzes lab and pilot plant work aimed at solving complex manufacturing problems
  • Leads and supports technology transfer (TT) across multiple unit operation
  • Coordinates, plans, and executes manufacturing process validation runs
  • Supports design and leads generation of sampling plans for process validation reports (PVRs) and investigations
  • Writes and reviews master batch records (MBRs) and standard operating procedures (SOPs), as needed
  • Generates and executes process training and consults on topics related to manufacturing and process
  • Leads technical risk assessments for new manufacturing processes
  • Contributes to the management of manufacturing data (i.e., databasing) and the statistical analysis aimed at both process monitoring and continued process verification
  • Writes documentation for internal and external use, such as manufacturing campaigns summary reports, process performance qualification (PPQ) protocol and reports, impact assessments etc.
  • Leads training of manufacturing staff and process sciences group on new processes, procedures, and use of equipment in the lab
  • Interprets and utilizes new knowledge to promptly drive data-based decisions
  • Collaborates with the manufacturing department to support commercial and clinical manufacturing campaigns, including on-floor support
  • Leads continuous improvement projects within unit operations, in partnership with manufacturing when applicable, to improve manufacturability, reliability, yield and cost
  • Supports supplier technical evaluations, risk assessments, and raw material evaluation and qualification
  • Other duties, as assigned

Knowledge and Skills

  • Proficient knowledge in Design of Experience (DOE)
  • Proficient knowledge in Statistical Process Control
  • Effective communication, both written and oral
  • Ability to effective present information to others
  • Proficient project management skills
  • Advanced problem-solving skills
  • Ability to provide feedback to others, including leaders
  • Ability to develop effective working relationships internally and externally
  • Ability to adapt communication style to differing audiences and advise others on difficult matters

Basic Requirements

• Associate degree in Engineering, Life Science or Chemical Engineering with 4 years of related work experience (e.g., manufacturing); or

• Bachelor’s degree in Engineering, Life Science or Chemical Engineering with 2 years of related work experience (e.g., manufacturing); or
• Master’s degree with no prior experience
• Experience using quality systems (e.g., deviation management, change control, CAPA, document management system)

Preferred Requirements

  • Associate degree in Engineering, Life Science or Chemical Engineering with 8 years related work experience (e.g., manufacturing); or
  • Bachelor’s degree in in Engineering, Life Science or Chemical Engineering with 6 years of related work experience (e.g., manufacturing)
  • Master’s degree with 3 years of related work experience; or
  • PhD with no prior experience
  • Large scale manufacturing support experience with chromatography for several types of chromatographic mediums operations, viral
    filtration, ultrafiltration, and bulk filling, troubleshooting, and deviation support
  • Experience using quality systems (e.g., deviation management system, change control, CAPA, document management system)
  • Experience using risk management and RCA tools

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

Will work in environment which may necessitate respiratory protection X No Yes
May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. X No Yes
Will work in environment operating a motor vehicle or Powered Industrial Truck. X No Yes
Ability to discern audible cues. No X Yes
Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color. X No Yes

Ability to ascend or descend ladders, scaffolding, ramps, etc. X No Yes
Ability to stand for prolonged periods of time. X No Yes
Ability to sit for prolonged periods of time. X No Yes
Ability to conduct activities using repetitive motions that include writs, hands and/or fingers. X No Yes
Ability to operate machinery and/or power tools. X No Yes
Ability to conduct work that includes moving objects up to X pounds. X No Yes If yes, 10 lbs. 33 lbs.
Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions. X No Yes

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