(Fixed Term) Manufacturing Associate I

The Role: Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients. Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK. This long term investment will create skilled jobs and strengthen collaboration with academic, NHS, and government partners. We welcome experts ready to help expand access to life saving vaccines. Reporting to the Associate Director, Quality Control, this role sits at the heart of QC laboratory operations, enabling high-quality analytical and microbiological testing through robust lab support. You will ensure seamless execution of daily laboratory activities while upholding the highest standards of GxP compliance, data integrity, and operational excellence. This is an opportunity to work in a cutting-edge environment, with exposure to digital tools and emerging technologies, including opportunities to engage with AI-enabled systems that enhance laboratory workflows and data management. Here’s What You’ll Do: Perform solution preparation and reagent tracking to support QC laboratory activities Assist with and execute ordering of laboratory consumables and supplies, including management and stocking of QC lab inventory Execute simple laboratory testing such as pH and conductivity measurements as required Perform general laboratory support activities including reagent preparation, waste management, equipment maintenance, and housekeeping Assist with the receipt, processing, distribution, and shipment of samples to external laboratories Perform accurate data entry in accordance with Good Documentation Practices Establish and maintain a safe laboratory working environment aligned with internal and regulatory standards Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements Execute tasks precisely as defined in internal guiding documents, including standard operating procedures (SOPs) and work instructions Adhere to Data Integrity requirements, ensuring all data, documentation, and records are complete, accurate, and audit-ready Complete all training within the assigned learning plan according to defined timelines and requalification requirements The key Moderna Mindsets you’ll need to succeed in the role: We obsess over learning. We don’t have to be the smartest we have to learn the fastest. We digitize everywhere possible using the power of code to maximize our impact on patients. Here’s What You’ll Need (Basic Qualifications) Education: A-level in chemistry / biology or equivalent Previous work within a laboratory environment Flexibility and willingness to learn new techniques and adopt new practices when needed Proven ability to follow detailed SOPs and maintain accurate records Ability to work independently and as part of a team including strong communication skills Good working knowledge of Microsoft applications. Ability to collaborate effectively in a dynamic, cross-functional matrix environment. Ability to efficiently prioritise and complete multiple projects and tasks in a fast-paced environment. This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre-employment check. Pay & Benefits At Moderna, we believe that when you feel your best, you can do your best work.  That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. Best-in-class healthcare, plus voluntary benefit programs to support your unique needs A holisti ... (truncated, view full listing at source)