We are seeking a skilled Manufacturing Associate and digitally savvy Operator for our mRNA vaccine production unit. The successful candidate will operate production equipment in accordance with cGMP compliance and health and safety regulations. The role requires excellent technical skills, a scientific mindset, rapid learning capacity for new mRNA technologies, meticulousness, and digital proficiency to support continuous improvement and innovation. This shift‑based role requires availability for various roster schedules—including afternoon, night, weekends, public holidays—and adaptation to changing production demands. The Manufacturing Associate will demonstrate operational excellence, collaborate across functions, and maintain meticulous attention to detail in a fast‑paced, dynamic environment. Here’s What You’ll Do Practice safe work habits, adhere to Moderna’s safety procedures and guidelines Adhere to gowning procedures and maintain housekeeping of assigned area for compliance and safety Participate in incident investigation (RCA) and CAPA tasks Responsible for the execution of operations activities following current good manufacturing practices, standard operating procedures, and manufacturing documentation Closely partner with QA peers for closure of documentation required for timely disposition of commercial batches Responsible for applying the performance tools in place while working as a team to meet the objectives of operational KPIs Respond rapidly and troubleshoot routine equipment process and digital issues Proactively identify and report to Supervisor compliance issues/health and safety issues Responsible for keeping training records and associated documentation up to date Perform routine basic maintenance (lubrication, basic mechanical check, filter change) of equipment using hand‑tools Flexibility to work overtime and adjust shift patterns in line with operational demands Participate in multiple projects and continuous improvement in a fast‑paced environment Effectively collaborate in a dynamic, cross‑functional matrix environment Here’s What You’ll Need (Basic Qualifications) Typically, 3‑5+ years of experience in a GMP manufacturing environment A College degree with a specialization in Pharmaceutical production technology or equivalent Aseptic experience and Visual Inspection experience preferred 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 values in the workplace Demonstrated ability and willingness to work across rotating shifts, including afternoon and night shifts, in a 24/7 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 Proficiency in English (verbal and/or written) required due to global collaboration needs As part of Moderna’s commitment to workplace health and safety, this role may be subject to pre‑employment and periodic medical assessments, in line with relevant legal and operational requirements. Pay & Benefits 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 Savingsand investments to help you plan for the future Location‑specific perks and extras Moderna is a smoke‑free, alcohol‑free, and drug‑free work environment. Moderna is committed to equal opportunity in employment and non‑discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements. Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at #J-18808-Ljbffr