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Thermo Fisher Scientific

Lead QC Technician 2nd shift at Thermo Fisher Scientific

Thermo Fisher Scientific Allentown, GA

Job Description

Work ScheduleSecond Shift (Afternoons)Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety StandardsJob DescriptionQuality Inspector cGMP OperationsLocation:US -Allentown PACompany:Thermo Fisher ScientificAt Thermo Fisher Scientific youll join a team of 100000 professionals united by a missionto enable our customers to make the world healthier cleaner and safer. Those who are passionate about quality excel in regulated environments and seek to make a meaningful impact through their work are encouraged to apply.Position SummaryThe Quality Inspector supports cGMP manufacturing operations by performing material inspections documentation reviews and activities dedicated to meeting regulatory standards. This role ensures that materials components and processes meet quality and regulatory requirements while supporting continuous improvement across operations.Key ResponsibilitiesApply 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 as assigned to support business needs.QualificationsAssociate degreeorHigh School Diploma with 2 years of relevant experience.Minimum 1 year of experience in a pharmaceutical or other regulated industry.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 RequirementsExtensive standing and walking on the packaging floor.Ability to lift up to 25 lbs occasionally and 10 lbs regularly.Work in refrigerated (28C) and freezer (-20C) 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 ScientificMeaningful 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 TodayBe part of a team thats making a difference.Apply now:Thermo Fisher Scientific is an EEO/Affirmative Action Employer. We do not discriminate based on race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.Required Experience:IC Key Skills Laboratory Experience,Aseptic Technique,ELISA,FDA Regulations,PCR,High-Performance Liquid Chromatography,Microbiology,Quality Control,GLP,cGMP,Laboratory Information Management Systems,QA/QC Employment Type : Full-Time Experience: years Vacancy: 1

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