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Added 5 mins ago
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Merck Sharp & Dohme LLC

Associate Technician, Operations

NC, United States

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Job details

Apply by: Nov 18, 2026
Posting language: English
Posted: Nov 3, 2026

Original job description

Job Description

Associate Tech, Operations

Job Description In Primary Posting Language (Include Requirements For Education, Experience And Skills)

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)
Job Description In Secondary Posting Language(s) (Include Requirements For Education, Experience And Skills)
Job Families for Job Profiles

#MSJR VETJOBS

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:

Current Employees apply HERE

Current Contingent Workers apply HERE

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. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we 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. As a federal contractor, 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:

EEOC Know Your Rights EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Not Applicable

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

11/18/2026*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.

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More about this job

Skills

Inspection
Packaging
SIP
Good manufacturing practices
Regulatory compliance
Troubleshoot
Electronics
Lockout/tagout
Documentation
Housekeeping
Problem solving
Process improvement
MPS
Leadership
Conflict resolution
Work independently
Troubleshooting
Pharmaceutical industry
Lean manufacturing
SAP
MES
Communication skills
Technical writing
Computer skills
Quality assurance
Schedule production

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