Quality Specialist II

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description 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. Discover Impactful Work Join our Clinical Trials Division (CTD) Quality team in Rockville, Maryland, and help ensure the quality and compliance of services supporting clinical trial products for a diverse portfolio of pharmaceutical and biotechnology clients. The Rockville site is not a manufacturing facility . The operation supports clinical trial product storage and repository activities, including temperature-controlled storage, shipping and receiving, with additional pharmacy and laboratory functions on site. As a Quality Specialist II , you will play a highly visible, client-facing role within the Quality organization. A significant part of your work will involve preparing for, hosting, and following through on external client audits. With client audits occurring regularly, this role is well suited to someone who can confidently represent Quality, communicate with different audiences, navigate detailed questions, and keep multiple activities moving in a fast-paced environment. When you are not supporting audits, you will perform day-to-day Quality activities including batch record review, validation protocol review, shipment label review, and quality system documentation. A Day in the Life Prepare for and host external client audits, serving as a primary Quality representative throughout the audit. Partner with site operations and coordinate with subject matter experts across functions to address client questions and retrieve supporting information during audits. Manage post-audit observations and findings through the quality system, including opening and maintaining records in TrackWise and coordinating responses through closure. Drive timely follow-up with cross-functional partners responsible for audit observations or findings, reviewing responses for completeness, accuracy, and appropriate client-facing language. Maintain clear communication with clients and internal stakeholders throughout audit preparation, execution, and follow-up. Review master batch records and post-execution documentation in accordance with applicable procedures. Review protocols associated with qualification and validation of temperature-controlled storage equipment, including freezers. Review labels associated with clinical trial product shipments entering and leaving the repository. Support Quality oversight activities within repository and storage areas, including periodic data-integrity and surveillance activities. Apply established procedures and quality requirements while helping internal partners understand and appropriately execute their responsibilities. Balance scheduled audit responsibilities with routine Quality work while maintaining accuracy, organization, and responsiveness. Keys to Success This role requires someone who is comfortable being highly visible with clients and taking ownership when priorities are moving quickly. You will be successful if you can remain composed during detailed or challenging client interactions, communicate clearly, and confidently guide an audit while knowing when to engage the appropriate subject matter expert. You should also be comfortable driving work across functions. Audit findings may involve departments outside Quality, so success requires persistence, sound judgment, strong follow-through, and the ability to keep stakeholders accountable to deadlines