(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. In this role, you will operate at the heart of Moderna’s mRNA vaccine production, combining hands-on manufacturing expertise with digital fluency in a highly advanced, technology-driven environment. You will play a critical role in ensuring the safe, compliant, and efficient production of vaccines while continuously advancing operational excellence. This is an opportunity to work with cutting-edge mRNA technologies and digital systems, contributing directly to innovation, continuous improvement, and patient impact. 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 to ensure a compliant and safe working environment Execute manufacturing operations in accordance with current Good Manufacturing Practices (cGMP), standard operating procedures, and manufacturing documentation Operate production equipment with a high level of technical skill and precision Troubleshoot routine equipment, process, and digital system issues with speed and accuracy Perform routine basic maintenance activities including lubrication, mechanical checks, and filter changes using hand tools Collaborate closely with Quality Assurance (QA) to ensure timely closure of documentation for commercial batch disposition Participate in deviation investigations, including root cause analysis (RCA), and contribute to CAPA activities Actively contribute to incident investigations and continuous improvement initiatives Apply performance management tools and work collaboratively to meet operational KPIs Proactively identify and escalate compliance, quality, and health & safety issues to Team Leads or Supervisors Maintain accurate and up-to-date training records and documentation Participate in multiple cross-functional projects within a fast-paced, matrixed environment Support operational demands with flexibility to work off-hours and overtime as required, aligned with corporate goals and commercial needs Contribute to a culture of innovation by identifying opportunities for process, digital, and operational improvements Operate effectively within a highly technological environment, leveraging digital tools and systems to enhance manufacturing performance 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) 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 As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre-employment check 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 d ... (truncated, view full listing at source)