Fixed Term Manufacturing Associate II

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. As a digitally savvy Operator within our mRNA vaccines production unit, you will play a central role in executing high-impact manufacturing activities in a cutting-edge, technology-driven environment. This position blends scientific thinking, operational execution, and digital fluency to ensure the production of safe, effective vaccines at scale. You will thrive in a fast-paced setting, contributing to continuous improvement while adopting innovative tools, including emerging generative AI capabilities, to enhance operational excellence. Here’s What You’ll Do: Practice safe work habits and strictly adhere to Moderna’s safety procedures and guidelines Follow gowning procedures and maintain housekeeping standards within assigned areas to ensure compliant and safe operations Execute manufacturing operations in accordance with current Good Manufacturing Practices (cGMP), standard operating procedures, and manufacturing documentation Partner closely with Quality Assurance (QA) to ensure timely documentation review and batch disposition for commercial production Participate in incident and deviation investigations, including root cause analysis (RCA), and contribute to CAPA implementation Apply performance management tools and collaborate with team members to achieve operational KPIs Troubleshoot routine equipment, process, and digital system issues with speed and precision Proactively identify and escalate compliance or health and safety concerns to Team Leads or Supervisors Maintain accurate and up-to-date training records and associated documentation Perform routine basic maintenance activities on equipment, including lubrication, mechanical checks, and filter changes using hand tools Contribute to continuous improvement initiatives and participate in multiple cross-functional projects in a dynamic environment Collaborate effectively within a matrixed, cross-functional team environment Demonstrate flexibility to work off-hours and overtime as required to meet production demands aligned with corporate and commercial objectives Operate with strong digital proficiency, contributing to innovation and process enhancements in a highly technological manufacturing setting 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 obsess over learning. We don’t have to be the smartest we have to learn the fastest. Here’s What You’ll Need (Basic Qualifications) 3 years of experience in a GMP manufacturing environment This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work. Here’s What You’ll Bring to the Table (Preferred Qualifications) A university degree with a specialization in Pharmaceutical production technology or equivalent Experience with filtration and chromatography, and cold chain management a plus Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines Ability to collaborate fluidly with peers, leadership and cross-functional support groups required Excellent written, oral communication, and organizational skills required. Ability to maintain attention to detail while executing multiple tasks with minimal supervision Demonstrated commitment to Moderna's values of Bold, Collaborative, Curious, and Relentless, embodying these value ... (truncated, view full listing at source)