Thermo Fisher

Supervisor, Automated Visual Inspection (12-hour days)

Greenville, North Carolina, USA Full time

Work Schedule

12 hr shift/days

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Fluctuating Temps hot/cold, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

s an Automated Visual Inspection Supervisor at Thermo Fisher Scientific, you'll play a key role in ensuring our pharmaceutical products meet quality standards. This position allows you to bring your skills to bear in a dynamic environment, supporting a hAealthier, cleaner, and safer world. This position works 12 hour days, 6a - 6p, on a 2-2-3 rotation.

Key responsibilities

  • Supervise, train, coach, and evaluate the performance of the visual inspection team, including trainers and qualified inspectors.

  • Oversee the daily operations of automated visual inspection systems, ensuring they are robust, efficient, and align with all relevant standards.

  • Ensure all processes and documentation are up-to-date and ready for regulatory inspections (e.g., FDA, EMA).

  • Act as a subject matter expert (SME) for visual inspection during audits and investigations.

  • Implement and manage corrective and preventive actions (CAPAs).

  • Develop, maintain, and revise training materials and programs.

  • Oversee the qualifications and re-qualifications of all inspectors.

  • Analyze quality and manufacturing data to identify trends and areas for improvement.

  • Lead or assist in projects to optimize inspection accuracy and reduce variability.

  • Work closely with production, engineering, quality, and other teams to support product flow and solve complex problems. 

Required Skills and Qualifications:

  • Bachelor's degree in Operations, Engineering, Business Management or related science preferred.

  • 3-5 years of experience in a manufacturing environment, preferably with a quality-driven background in pharmaceuticals or another GMP setting.

  • 2-3 years of experience in a leadership role.

  • Strong understanding of automated visual inspection systems and related technologies.

  • Working knowledge of USPs

  • Excellent communication, leadership, and interpersonal skills.

  • Knowledge of quality systems, regulatory compliance (e.g., cGMP), and audit preparation.

  • Ability to work independently and handle flexible schedules, including overtime. 

  • Strong computer skills and proficiency in Microsoft Office.

  • Statistical background helpful


We offer a competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team!