(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. In this role, you will operate at the intersection of advanced manufacturing, digital systems, and mRNA science—playing a hands-on role in vaccine production that directly impacts patients. You will bring a scientific mindset and strong technical capability to a highly automated, cGMP-regulated environment, where precision and adaptability are essential. Working in a fast-paced and innovation-driven setting, you will contribute to operational excellence while continuously learning and engaging with next-generation manufacturing and digital tools, including emerging Generative AI applications. Here’s What You’ll Do: Practice safe work habits, strictly adhering to Moderna’s safety procedures and guidelines Adhere to gowning procedures and maintain housekeeping of assigned area 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 proficiency and scientific understanding Respond rapidly to, troubleshoot, and resolve routine equipment, process, and digital system issues within a highly technological environment Perform routine basic maintenance activities (including lubrication, mechanical checks, and filter changes) using appropriate hand tools Maintain accurate and up-to-date training records and associated documentation Collaborate closely with Quality Assurance (QA) to ensure timely review and closure of documentation required for batch disposition of commercial products Participate in deviation investigations, including root cause analysis (RCA), and contribute to CAPA (Corrective and Preventive Actions) activities Actively engage in incident investigations and support the development and execution of CAPA plans Proactively identify, escalate, and help resolve compliance, operational, or health and safety issues to Team Leads or Supervisors Apply performance management tools and work collaboratively within a team to achieve operational KPIs aligned with corporate goals and commercial demand Participate in multiple projects and continuous improvement initiatives in a fast-paced, dynamic environment Contribute to process improvements, innovation efforts, and digital advancements within the manufacturing space Operate effectively within a cross-functional, matrixed organization, demonstrating strong collaboration and communication skills Demonstrate flexibility to work off-hours or overtime as required to meet production needs The key Moderna Mindsets you’ll need to succeed in the role: We act with urgency; Action today compounds the lives saved tomorrow. We digitize everywhere possible using the power of code to maximize our impact on patients. Here’s What You’ll Need (Basic Qualifications): 1 years of experience in a GMP manufacturing environment 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 de ... (truncated, view full listing at source)