Manufacturing Specialist 1, Drug Product
Location : US-NC-Holly Springs
Requisition ID : 2025-35831
Position Overview
The Manufacturing Specialist 1, DP performs manufacturing support activities to ensure compliant and reliable production. This role may require flexibility with working hours and shift rotation to support a 24 / 7 manufacturing facility.
Job Description
What You'll Do
- During the project phase, support operational readiness initiatives as well as site commissioning and qualification efforts
- Supports troubleshooting including acting as a process subject matter expert (SME) for their process respective area(s)
- Coordinates Batch Planning including process template creation and import and management of Preventative Maintenance (PMs)
- Owns, performs, or drives documentation major documentation updates (i.e. Initiates new documents for new processes)
- Coordinates non-batch activities (e.g., Changeover, PMs, Aseptic Process Simulation [APS])
- Supports the MSAT group with tech transfer within manufacturing
- Ensures compliance and safety procedures are followed in manufacturing environment
- Create and updates Electronic Batch Records (EBRs) and Paper Batch Records
- Manages, performs, initiates, or supports change management records, investigations, Corrective and Preventive Actions (CAPAs) and Continuous Improvement (CI) activities
- Manages projects, leads execution, and participates in projects within Drug Product Finished Goods
- Assists and supports inspections and audits, providing support to ensure compliance within the manufacturing environment
- Assists Manager with projects and training, as needed
- Other duties, as needed
Basic Requirements
High School Diploma or Equivalent with 12 years of applicable industry experienceBachelor's degree with 8 years of applicable industry experienceMaster's degree with 6 years of applicable industry experiencePhD with 4 years of applicable industry experienceEquivalent Military ExperiencePreferred Requirements
High degree of understanding of operations sequence and cadence of activities in a manufacturing environmentBio Works or BTEC Capstone cGMP coursework preferredWorking Conditions & Physical Requirements
Will work in environment which may necessitate respiratory protectionMay work in Mechanical / Production spaces that may require hearing protection and enrollment in a hearing conservation programWill work in environment operating a motor vehicle or Powered Industrial TruckAbility to discern audible cuesAbility to inspect or perform a task with 20 / 20 corrected vision, visual acuity, including distinguishing colorAbility to ascend or descend ladders, scaffolding, ramps, etc.Ability to stand for prolonged periods of timeAbility to sit for prolonged periods of timeAbility to conduct activities using repetitive motions that include wrists, hands and / or fingersAbility to operate machinery and / or power toolsAbility to conduct work that includes moving objects up to 33 poundsAbility to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motionsWill work in warm / cold environmentsTo 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.
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