Process Engineer 1 (Upstream Engineering) Position Available In Wake, North Carolina

Tallo's Job Summary: The Process Engineer 1 at Diosynth Biotechnologies in Holly Springs, NC, supports capital projects, tech transfer, and manufacturing ops to ensure compliance with safety, regulatory, and engineering standards. This entry-level role requires a Bachelor's in Chemical Engineering or related field with 0-1 years of experience, preferably in a cGMP environment or with mammalian cell culture processes.

Company:
Fujifilm
Salary:
JobFull-timeOnsite

Job Description

Process Engineer 1 (Upstream Engineering)
Job Locations
US-NC-Holly Springs
Posted Date
6 days ago
(5/5/2025 6:44 PM)
Requisition

ID 2025-34484

Category Engineering Company (Portal Searching) Diosynth Biotechnologies
Position The Process Engineer 1 will provide engineering guidance to support capital projects, technology transfer, and manufacturing operations. This will ensurepliance with all safety, regulatory, and engineering requirements. This role will ad to product and customer requirements, and work towards optimizing plant efficiency and profitability. Company Follow Your Genki to North America’s largest, state-of-the-art Life Science Manufacturing Facility & CDMO The work we do at Diosynth Biotechnologies 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 Diosynth Biotechnologies and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharmapanies 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. Job Description What You’ll Do

  • Supports on time delivery and ensures quality from Fujifilm and Engineering, Procurement, Construction Management (EPCM) provider
  • Supports piping and instrumentation diagram (P&IDs) and other process design document review
  • Provides input to detailed design activities in partnership with EPCM provider
  • Writes User Requirement Specifications (URSs)
  • Supports Factory Acceptance Testing (FAT), Commissioning Qualification, and Validation (CQV), and start-up activities with supervision
  • Serves as on-call support for process equipment
  • Reviews, redlines, and approves P&IDs and other technical documents with supervision
  • Contributes to system impact assessments and quality risk assessments for process equipment
  • Supports technology transfer (TT) activities related to process equipment
  • Supports execution of Good Manufacturing Practices (GMP) runs
  • Provides technical support for root cause analysis (RCA) and process deviation investigations
  • Assists with deviations, change controls, corrective and preventive action (CAPA) closures
  • Supports technical risk assessments for new manufacturing equipment
  • Provides on-floor manufacturing support for equipment issues
  • Cross-trains on unit operations to assist team with meeting deliverables
  • Collaborates with other departments, such as Quality, Manufacturing, Maintenance, Validation, and Safety.
  • Other duties, as assigned Minimum Requirements
  • Bachelor’s degree in Chemical Engineering, Biotechnology Engineering, or another related field
  • 0-1 years of engineering or other relevant technical work experience Preferred Requirements
  • Experience working in a cGMP environment or other highly regulated industry
  • Prior experience with mammalian cell culture processes Working & Physical Conditions Will work in environment which may necessitate respiratory protection May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program.

Ability to discern audible cues. Ability to ascend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time up to 120 minutes. Ability to sit for prolonged periods of time up to 240 minutes. Ability to conduct activities using repetitive motions that include wrists, hands or fingers. Ability to operate machinery and/or power tools. Ability to conduct work that includes moving objects up to 33 pounds. Ability to bend, push or pull, reach to retrieve materials from 18″ to 60″ in height, and using twisting motions. Will work in warm/cold environments (60-90 range). Will work in small and/or enclosed spaces. Will work in heights greater than 4 feet.

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