Technician, Operations

Bio Process Operations Technician Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. The BioProcess Operations Technician is responsible for providing shop floor operations and environmental monitoring support to the aseptic manufacturing areas of the facility at the Wilson, NC site. This position includes direct operational support for manufacturing activities such as CIP / SIP, aseptic primary filling, inspection, packaging, and other operations activities as needed. It also involves executing routine room and equipment disinfection and managing the movement of gowning, disinfectants, and materials to support manufacturing areas. Additionally, the role ensures EHS and GMP compliance is maintained within their area of assignment. This position is an individual contributor and member of the Operations team within the integrated process team (IPT) for the 2nd Shift Wilson Rota POD IPT. Hours are Monday – Friday 2 pm to 10:30 pm. Primary Responsibilities Delivery 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 Compliance Work safely following identified safety procedures (hazardous work permitting, LOTO, HECPs) and using applicable safety equipment / PPE Execute operations functions in accordance with cGMPs and 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, and assist in investigations, root cause determination, and CAPA implementation Cost Ensure startup activities for area of assignment are executed to meet project deliverables and timelines 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 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 adhering 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 the team Maintain a culture of continuous improvement / MPS focused on standard work, making problems visible, minimizing waste, reducing process variability, and problem solving Routinely demonstrate leadership and conflict‑resolution ability; provide and receive constructive feedback in 360° performance reviews Education Minimum Requirement High School diploma or equivalent and previous experience operating, maintaining, troubleshooting, and/or repairing industrial equipment is preferred. Associates degree in Business, Science, or Technology‑based field and/or bio‑pharma focused certificates such as Bioworks preferred. Required Experience And Skills Three or more years in a GMP manufacturing facility (aseptic GMP environment strongly 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. Willing to work irregular hours to support multi‑shift operation on an as‑needed basis. Preferred Experience And Skills Aseptic filling, visual inspection systems, CIP/SIP systems, packaging equipment and similar aseptic formulation and filling operations. Working in a regulated environment (FDA, etc.) and basic knowledge of cGMPs as they apply to the vaccine/pharmaceutical industry. Continuous Improvement, Lean Manufacturing, Problem Solving, and/or Right First‑Time methodologies. SAP/MES/electronic log book basic knowledge from a production execution perspective. 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). Salary Range $57,900 – $91,200 (based on education, experience, skills, geographic location, and business needs). Benefits A comprehensive package of benefits including medical, dental, vision, healthcare, retirement benefits (401(k)), paid holidays, vacation, compassionate and sick days; and eligibility for annual bonus and long‑term incentive where applicable. Shift 2nd – Evening (Monday‑Friday 2 pm to 10:30 pm). EEO Statement We are an Equal Employment Opportunity Employer and provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. We comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit the EEOC websites. Validity The job posting is effective until 11:59 PM on the day before the listed posting end date (07/29/2026). #J-18808-Ljbffr Merck