Apply current Good Manufacturing Practices (cGMP) across all tasks. Perform specifications approvals, Incoming Inspections, and distribution shipment reviews. Conduct material and process inspections, including sampling activities. Review and approve Packaging Electronic Production Orders. Support root cause investigations and continuous improvement initiatives. Author, revise, and follow SOPs and Work Instructions; ensure accurate documentation. Escalate potential quality or compliance issues to leadership. Ensure timely issue resolution and implementation of corrective actions. Maintain a safe, compliant, and efficient working environment. Perform additional duties assigned to support business needs. Qualifications. Education:High School Diploma OR GED Required. Experience:3 years of relevant experience. Minimum 1 year of experience in a pharmaceutical or other regulated industry preferred. Familiarity with key Quality Systems (Change Control, Deviations, Complaints, Documentation Management). Ability to read, understand, and follow SOPs and Work Instructions in a GMP setting. Strong attention to detail and ability to work both independently and on cross-functional teams. Willingness to work various shifts, including overtime, as business needs require. Work Environment & Physical Requirements. Extensive standing and walking on the packaging floor. Ability to lift up to 25 lbs occasionally and 10 lbs regularly. Work in refrigerated (2–8°C) and freezer (-20°C) environments with provided PPE. Exposure to atmospheric conditions requiring specialized protective equipment. Must meet visual acuity and color-vision standards for inspection of products, components, and labels. Why Thermo Fisher Scientific? Meaningful work that directly impacts global health and safety. Industry-leading career development and training opportunities. Inclusive, diverse, and mission-driven culture. Competitive benefits and growth pathways. Apply Today. Be part of a team that’s making a difference. Apply now: