(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 is central to enabling the day-to-day success of QC laboratory operations. You will provide critical laboratory support while contributing to analytical and microbiological testing activities in a highly regulated GxP environment. This is a hands-on, individual contributor role with opportunities to engage with digital laboratory systems and emerging data-driven and AI-enabled tools that enhance quality and efficiency. Here’s What You’ll Do: Perform solution preparation and manage reagent tracking to ensure accurate inventory and availability Assist with and execute ordering of laboratory consumables and supplies, including management and stocking of QC lab materials 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 receipt, processing, distribution, and shipment of samples to external laboratories Perform data entry in alignment with Good Documentation Practices (GDP) Establish and maintain a safe laboratory working environment in accordance with internal 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 Follow Good Documentation Practices and Data Integrity requirements to ensure all data, documentation, and records are complete, accurate, and audit-ready Complete all required training within assigned learning plans according to defined timelines and requalification cadence The key Moderna Mindsets you’ll need to succeed in the role: We digitize everywhere possible using the power of code to maximize our impact on patients. We behave like owners. The solutions we’re building go beyond any job description. 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 holistic approach to well-being with access to fitness, mindfulness, and mental health su ... (truncated, view full listing at source)