Job Description

Position Description:

The Bio-Process Technician will be a member of the Maintenance & Operations team within the Vaccines integrated process team for a start-up vaccine manufacturing facility in Wilson, NC. This position is accountable for providing shop floor operations and environmental monitoring support to aseptic manufacturing within the vaccine manufacturing facility. Tasks will include formulation, aseptic primary filling, inspection, packaging, and CIP/SIP. This position will also perform various roles to include executing routine room and equipment disinfection as well as managing the movement of gowning, disinfectants, and materials. In addition to supporting operations activities, the role will be accountable for ensuring that EHS and GMP compliance is maintained within their area of assignment. This position will be an individual contributor and member of the Operations team.

Delivery

Execute manufacturing operations, environmental monitoring, and facility disinfection
Set up and operate vaccines formulation, aseptic primary filling, inspection, packaging, CIP/SIP, and additional equipment within qualified parameters
Identify potential equipment problems and partner with 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

Accountable for performing work in a safe manner, following identified safety procedures (hazardous work permitting, LOTO, HECPs), and using applicable safety equipment / personnel protective equipment (PPE)
Execute operations functions in accordance with current Good Manufacturing Practices (cGMPs) and standard operating procedures (SOPs)
Complete documentation in batch records, electronic logs, or other systems in accordance with 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. Escalate as per IPT management processes and assist in the investigation, root cause determination, and CAPA implementation.

Cost

Ensure that 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 groups for assigned area.
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.

Work Schedule:

8-hours, 2nd shift

Position Qualifications:

Minimum Education Requirement:

High School diploma or equivalent minimum.

Required Experience and Skills:

Three or more years of experience in a GMP manufacturing facility (aseptic GMP environment strongly preferred).
Demonstrated ability to work independently and as team member.
Demonstrated interpersonal skills with ability to influence and assist others through a culture of inclusion, feedback, and empowerment.
Demonstrated leadership ability, peer training experience, and/or productivity improvement activities strongly preferred.
Ability to gown and work in an aseptic environment.
Demonstrated ability to work with computerized and automated systems.
Willing to work irregular hours to support multi-shift operation on an as needed basis

Preferred Education, Experience and Skills:

Associate's degree in business, Science, or Technology-based field and/or bio-pharma focused certificates such as Bio-works preferred.
Experience with aseptic filling, visual inspection systems, CIP/SIP systems, packaging equipment and similar aseptic formulation and filling operations
Experience operating, maintaining, troubleshooting, and/or repairing industrial equipment
Experience working in a regulated environment (FDA, etc.) and basic knowledge of cGMPs as they apply to the vaccine/pharmaceutical industry
Experience in Continuous Improvement, Lean Manufacturing, Problem Solving, and/or Right First-Time methodologies
SAP / MES / electronic logbook basic knowledge from a production execution perspective
Demonstrated leadership ability, peer training experience, and/or productivity improvement activities.
Demonstrated ability and drive to work autonomously and help organize priorities and work with other team members.
Outstanding communication skills both within direct team and across multiple shifts to ensure success of overall team.
Ability to support technical writing of documents such as standard operating procedures (SOPs)

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WilsonTech

Our Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create a reliable global manufacturing network that’s devoted to delivering a high quality, reliable supply to customers and patients on time, every time.

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Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

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Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

3rd - Night

Valid Driving License:

No

Hazardous Material(s):

n/a

Required Skills:

Biopharmaceuticals, Biopharmaceutics, Continual Improvement Process, Data Integrity, Environmental Monitoring, Global Manufacturing, GMP Compliance, Lean Manufacturing, Machine Troubleshooting, Maintenance Processes, Manufacturing, Packaging Operations, Productivity Improvements, Standard Operating Procedure (SOP), Technical Writing, Troubleshooting

Preferred Skills:

Job Posting End Date:

07/18/2025

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.