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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