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Production Coordinator

Thermo Fisher Scientific

Thermo Fisher Scientific

Administration, Product
Greenville, NC, USA
Posted on Sep 16, 2025

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Summary:

Coordinates production activities and serves as liaison between cross-functional support groups and operations on production schedule. Ensures maximum efficiency of the production lines. Responsible for the effective execution the production schedule as well as rapidly and thoughtfully respond to unplanned events in production

Essential Functions:

Collaborates with supply chain scheduler to prioritize operations to ensure maximum performance. Coordinates production workflow for multiple products. Works collaboratively with functional leadership to understand impacts of the plan and opportunities to improve vision and value Participates in Supply & Demand meetings as part of the Supply Chain planning cycle Maintains detailed knowledge of production needs, requirements, problems, build and schedule. Awareness of production status in each area. Partners with Project Management, Schedulers, Maintenance, and other functional areas to accomplish project and group targets. Assist in resolving labor, equipment and raw materials needed to cover production demand. Aids and shares in accountability in production line readiness including setup and planning. Services as SME to address production issues when they arise striving for minimum disruption. Owns and reports overall production performance. Drives efficiency by applying data driven operational analytics. Able to optimally connect with all types of staff, including technical, professional, and upper management.

Job Scope:

Receives assignments in the form of objectives and determines how to meet schedules and goals.

Education / Experieince:

Bachelors Degree and 1+ years of prior proven experience OR High School Diploma and 5+ years of GMP experience. 3+ years of experience working in a supply chain or operations role.

Additional Experience Requirement:

Prior experience in manufacturing – parenteral filling and packaging operations. Knowledge of business processes supporting manufacturing operations. Robust understanding of quality and cGMP principles. Understanding the roles of cross-functional groups in a manufacturing setting. Fundamental knowledge of change control. Proficient skills in Microsoft Office and computer-based quality systems. Excellent oral and written communication skills

Equivalency:

Equivalent combinations of education, training, and relevant work experience may be considered.

Competencies:

Good understanding of Good Manufacturing Practices guidelines, Standard Operating Procedures and safety standards. Ability to work cross-functionally with other departments. Proficiency in operating autonomously and in a team setting with minimal direction. Digital literacy to include the Microsoft suite with particular strength in Excel. Excellent written and oral communication skills. Connects and collaborates with others to fulfill project and team targets.

Physical Requirements:

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; arm, hand and finger dexterity, including ability to type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, and read materials for prolonged periods of time.