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. Location/Division Specific Information: Clinical Labeling Services, part of the Clinical Trials Division, located in Bohemia, New York provides leading clinical label design, production and management services for the pharmaceutical and biotechnology industry. Our advanced inspection software, full in-house print capabilities, and proprietary translation and regulatory approval system are designed to reduce overall clinical trial label cycle times. How Will You Make an Impact: The In Process Inspector role has a significant impact in ensuring the quality and integrity of the production process. Their responsibilities include monitoring and inspecting the various stages of manufacturing to identify any discrepancies while using automatic equipment or visually inspecting labels. Their vigilance and attention to detail play a crucial role in preventing defects, ensuring product safety, and maintaining overall process efficiency. A Day in the Life: Conducting inspections using automatic inspection equipment : Operates and monitors automatic inspection equipment to assess the quality and integrity of pharmaceutical labels during the manufacturing process including setting up the equipment, conducting routine checks, and interpreting the results to identify any defects or change requests from specifications. Ensures that labels meet the required standards for accuracy, legibility, and adherence to regulatory requirements Performing QC inspections : Conducts Quality Control (QC) inspections at various stages of the manufacturing process including visually examining labels, verifying label content, conducting accurate counts, checking for proper alignment, and assessing print quality. Uses appropriate tools and techniques, to ensure that labels meet the necessary quality standards and complies with regulatory guidelines. Documenting and reporting findings: Records all inspection results and documents any non-conformities or deviations identified during the inspections including generating detailed reports, maintaining inspection records, and communicating findings to area supervisor or manager. Effective documentation and reporting facilitate traceability, support corrective actions, and contribute to the overall quality assurance process. Physical Requirements / Work Environment Fast-paced environment which relies on teamwork to ensure jobs are completed within established timelines. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.