Quality Specialist III

Thermo Fisher Scientific•Greenville, NC

1d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. In this role, you will drive quality execution across sterile operations, including manufacturing, filling, packaging, and inspection. You will support both commercial and product development services while ensuring compliance with cGMP standards. This position also plays a key role in implementing process improvements and fostering a culture of continuous quality enhancement.

Requirements

Bachelor’s degree required (scientific field preferred)
Minimum of 5 years of experience in QA, QC, or Manufacturing
Pharmaceutical industry experience preferred (aseptic/sterile strongly preferred)
Experience in regulated environments (e.g., ISO) acceptable
Strong understanding of cGMP
Troubleshooting and problem-solving ability
Strong documentation and review skills
Ability to lead and support teams
Strong communication and collaboration
Ownership and accountability
Quality-focused mindset
Continuous improvement
Effective communication
Team collaboration
Ability to stand, walk, stoop, kneel, and crouch for extended periods
Lift and move 10–35 pounds
Manual dexterity and visual acuity
Ability to sit, reach, talk, and hear for extended periods
Use of PPE including safety glasses, lab coat, gloves, and respirator as needed

Responsibilities

Perform daily quality assessments of facilities, personnel, and documentation in classified and non-classified areas
Interact with employees to troubleshoot issues and reinforce aseptic techniques
Champion a strong quality culture
Review and approve procedures, training documents, and forms
Conduct quality batch record reviews
Participate in continuous improvement initiatives
Support client interactions and regulatory inspections
Develop and maintain SOPs and training materials
Partner with operations to improve documentation accuracy