• The BioProcess Technician is responsible for providing shop floor operations and environmental monitoring support to the aseptic manufacturing areas of the manufacturing facility at the Wilson, NC Site
• Responsibilities will include direct operational support for manufacturing activities including formulation, CIP/SIP, packaging, inspection and aseptic primary filling

This position will also be responsible for performing various supporting roles within the facility such as executing routine room and equipment disinfection and managing the movement of gowning, disinfectants, and materials to support the manufacturing areas

• In addition to supporting operations activities, the role will be responsible 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 within the integrated process team (IPT)
• Current hours for this position are M - F 2pm to 10:30pm and will transition to 3rd shift hours in May 2026
• Execute manufacturing operations, environmental monitoring, and facility disinfection within 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
• Responsible 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
• 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
• 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

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

• Required Experience and Skills
• Ability to work independently as Team member
• Interpersonal skills with ability to influence and support others through a culture of inclusion, feedback, and empowerment
• Ability to gown and work in an aseptic environment
• Ability to work with computerized and automated systems
• Willing to work irregular hours to support multi-shift operation on an as needed basis

No Travel Required

Accountability, Accountability, Analytical Problem Solving, Biological Manufacturing, Biopharmaceuticals, Biopharmaceutics, Cleanroom Gowning, Computer Literacy, Data Integrity, Environmental Monitoring, Environmental Monitoring Systems, Environment Management, Global Manufacturing, GMP Compliance, GMP Operations, Good Manufacturing Practices (GMP), Laboratory Processes, Lean Manufacturing, Machinery Operation, Manufacturing, Manufacturing Quality Control, Packaging Operations, Pharmaceutical Manufacturing, Production Scheduling, Productivity Improvements {+ 5 more}

$51,500 - $81,100 An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs

• The successful candidate will be eligible for annual bonus and long-term incentive, if applicable
• We offer a comprehensive package of benefits
• Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days

No relocation