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Bio Process Technician

Job in Wilson, Wilson County, North Carolina, 27893, USA
Listing for: EyeBio
Full Time position
Listed on 2026-01-17
Job specializations:
  • Manufacturing / Production
    Manufacturing Engineer, Operations Engineer
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below
Position: Bio Process Technician-10

Job Description

The Bio Process Technician is responsible for providing shop floor operations and environmental monitoring support to the aseptic manufacturing areas at the Wilson, NC site. Duties include formulation, CIP/SIP, packaging, inspection, aseptic primary filling, and routine room & equipment disinfection. The role also manages gowning, disinfectants, and materials movement, ensuring EHS and GMP compliance within the facility. This individual‑contributor will be part of the Operations team within the integrated process team (IPT).

This position is for 3rd Shift Wilson Rota POD IPT. Current hours are M – F 2pm to 10:30pm and will transition to M – F 10pm to 6:30am in May 2026.

Primary Responsibilities
  • Execute manufacturing operations, environmental monitoring, and facility disinfection in the pod vaccine manufacturing facility.
  • Set up and operate vaccines formulation, CIP/SIP, aseptic primary filling, packaging, inspection, and additional support equipment within qualified parameters.
  • Identify potential equipment problems and partner with other Vaccines Maintenance Technicians to ensure appropriate resolution.
  • Demonstrate ability to troubleshoot process, electronic systems, and equipment for routine and basic problems.
  • Perform other duties as requested by the Operations coach.
Compliance
  • Perform work safely, following identified safety procedures (hazardous work permitting, LOTO, HECPs) and using applicable PPE.
  • Operate in accordance with current Good Manufacturing Practices (cGMPs) and SOPs.
  • Complete documentation in batch records, electronic logs, or other systems per site procedure.
  • Maintain good housekeeping and 5S in assigned work area.
  • Adhere to the highest level of data integrity while performing duties.
  • Identify potential quality or safety issues, escalating per IPT management processes and assisting in investigation, root‑cause determination, and CAPA implementation.
Cost
  • Ensure startup activities for area of assignment are executed such that project deliverables and timelines are met.
  • Closely monitor team / process performance and improve reliability through problem solving and continuous improvement.
  • Set up and operate equipment in alignment with established training and procedures to ensure reliable operation with minimal delays or discards.
  • Identify and help implement continuous improvement and productivity enhancements within the IPT.
Team
  • Partner with Technicians and cross‑functional support groups for assigned area to maintain an inclusive and positive work environment.
  • Demonstrate a high degree of maturity and personal integrity. Strictly adhere to all site policies on personal conduct and attendance.
  • Train, develop, and mentor other team members to share experience and best practices.
  • Pursue knowledge and skills in assigned area from an operations perspective and share that information readily with team.
  • Maintain a culture of continuous improvement / MPS focused on standard work, making problems visible, minimizing waste, reducing process variability, and problem solving.
  • Routinely demonstrates leadership and conflict‑resolution ability. Demonstrates a willingness to provide and receive constructive feedback in 360° performance review.
Education Minimum Requirement
  • High School diploma or equivalent with previous experience operating, maintaining, troubleshooting, or repairing industrial equipment is preferred. Associates degree in Business, Science, or Technology‑based field and/or biopharma certificates such as Bioworks are preferred.
Required Experience and Skills
  • Three or more years in a GMP manufacturing facility (Aseptic/Cleanroom/Sterile Fill GMP preferred).
  • Ability to work independently as a team member.
  • Interpersonal skills with ability to influence and support others through a culture of inclusion, feedback, and empowerment.
  • Leadership ability, peer training experience, and/or productivity improvement activities strongly preferred.
  • Ability to gown and work in an aseptic environment.
  • Ability to work with computerized and automated systems.
  • Willingness to work irregular hours to support multi‑shift operation as needed.
Preferred Experience and Skills
  • Aseptic filling, visual inspection systems,…
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