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Manufacturing Associate II - Shift Position

United Kingdom, Oxford · Job Posted May 03, 2026
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Job Description

We are seeking a skilled Manufacturing Associate and digitally savvy Operator to join our mRNA vaccines production unit. The successful candidate will operate the production equipment, in accordance to cGMP compliance as well as health and safety regulations. The role requires excellent technical skills, a scientific way of thinking, a rapid learning capacity for new technologies in mRNA and meticulousness. The Manufacturing Associate will be expected to demonstrate digital proficiency, be comfortable working in a highly technological environment where their participation in improvements and innovations will be regularly required. This role is central to Moderna’s mission of producing safe, effective vaccines, and requires a balance of scientific understanding, operational skills, collaboration and digital acumen. The ideal candidate is a team player who will maintain meticulous attention to detail and participate actively to operational excellence in our fast-paced and dynamic environment.

Job Responsibility

  • Adhering to Moderna’s safety procedures and maintaining housekeeping of assigned areas to ensure compliance and safety
  • Executing operations activities according to current good manufacturing practices (cGMP), standard operating procedures, and manufacturing documentation
  • Collaborating closely with QA peers for timely closure of documentation related to commercial batch disposition
  • Participating in investigations (RCA) and CAPA tasks to address deviations and compliance issues
  • Utilizing performance tools in collaboration with the team to meet operational KPI objectives
  • Responding to and troubleshooting routine equipment, process, and digital issues rapidly
  • Proactively identifying and reporting compliance or health and safety issues to supervisors
  • Keeping training records and documentation up to date
  • Performing routine maintenance tasks (e.g., lubrication, mechanical checks, filter changes) using hand tools
  • Flexibility to work off-hours and overtime when necessary
  • Contributing to multiple projects and continuous improvement initiatives in a fast-paced environment
  • Collaborating effectively in a dynamic, cross-functional matrix environment

Requirements

  • 3+ years of experience in a GMP manufacturing environment
  • A university degree with a specialization in Pharmaceutical production technology or equivalent
  • 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 values in the workplace

Nice to have

  • Experience with filtration and chromatography, and cold chain management a plus
  • Experience in audit / inspection preparation, understanding Health authority and regulatory guidelines

What we offer

  • 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 support
  • Family building benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

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