Associate Technician, Operations

Merck

Wilson (NC)

On-site

USD 55,000 - 75,000

Full time

6 hours ago
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Job summary

Merck in Wilson, NC seeks a Bio Process Operations Associate Technician (2nd shift) to support aseptic filling, inspection, and packaging in a start-up vaccine facility. You will ensure cGMP compliance, execute disinfection and equipment setup, and collaborate with maintenance and operations teams.

The role requires attention to data integrity, adherence to safety procedures, and flexibility for multi-shift coverage.

Qualifications

  • One or more years of experience in a GMP manufacturing facility (aseptic GMP environment strongly preferred).
  • Ability to work independently and as part of a team.
  • Demonstrated ability to influence and assist others through inclusion and empowerment.
  • Ability to gown and work in an aseptic environment.
  • Experience with computerized and automated systems.
  • Willing to work irregular hours to support multi-shift operation.
  • Must be willing and able to wear a respirator as required.

Responsibilities

  • Execute manufacturing operations and facility disinfection.
  • Set up and perform aseptic vaccine manufacturing including primary filling, inspection, packaging, CIP/SIP.
  • Identify potential equipment problems and partner with Vaccines Maintenance Technicians for resolution.
  • Perform other duties as requested by the Operations coach.
  • Ensure cGMP compliance and SOP adherence; complete documentation in electronic records.
  • Maintain 5S and data integrity; escalate quality or safety issues as needed.
  • Support startup activities to meet deliverables and timelines.
  • Collaborate with Technicians and cross-functional teams; mentor others.

Education

High School diploma or equivalent
Associate's degree or biotech certificate (preferred)

Tools

SAP
MES
Electronic logbook

Job description

Bio Process Operations Associate Technician (2nd shift)

The Bio Process Operations 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 person is accountable for providing shop floor operations support to aseptic manufacturing within the vaccine manufacturing facility. Tasks will include 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 and facility disinfection

  • Set up and perform aseptic vaccine manufacturing to include 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 electronic batch records, electronic logs, and 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 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.


Reporting Relationships


  • Solid line report to: Manager, Maintenance & Operations

  • Dotted line report to: N/A

  • Position(s) reporting to this position: N/A (individual contributor)


Work Schedule

2nd shift 1400 to 2230


Minimum Education Requirement

High School diploma or equivalent


Required Experience And Skills


  • One 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

  • 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

  • Must be willing and able to wear a respirator for short periods of time, as required, and comply with all respiratory protection program requirements.


Preferred Education, Experience And Skills


  • Associate's degree in business, Science, or Technology-based field and/or bio-pharma focused certificates, such as Bioworks, 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)


Required Skills


  • Aseptic Handling

  • Biopharmaceuticals

  • Chemical Plant Operations

  • Computer Literacy

  • Continuous Improvement Techniques

  • Data Integrity

  • Environmental Controls

  • Good Manufacturing Practices (GMP)

  • Industrial Equipments

  • Industrial Maintenance

  • Interpersonal Communication

  • Manufacturing Operations

  • Operations Support

  • Pharmaceutical Production

  • Pharmaceutical Quality Assurance

  • Production Scheduling

  • Productivity Improvements

  • Safety

  • Health, Environment and Quality (SHEQ)

  • Safety Procedures

  • Shift Work

  • Technology Qualification


Preferred Skills

-- No specific skills listed --


US And Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.


Requisition ID: R425412


Job Posting End Date: 11/18/2026

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