Production Engineer at Moderna

Melbourne, Victoria, Australia -

Full Time

Start Date

Immediate

Expiry Date

16 Aug, 26

Salary

0.0

Posted On

18 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Troubleshooting, Root Cause Analysis, Commissioning, Qualification, Validation, cGMP Documentation, PLC/HMI/SCADA, CMMS, Project Management, Technical Support, Equipment Optimization, Interpersonal Communication

Industry

Biotechnology Research

Description

The Role The Production Engineer will provide hands‑on technical support to ensure operability, reliability, and compliance of our mRNA drug‑product manufacturing and fill‑finish equipment. You will support single‑use mixers, parts washer, autoclave, isolator, filling machine, and supporting utilities. You will work closely with Manufacturing, Facilities & Engineering, MS&T, Quality, Production, OEM vendors, calibration teams, and Process Technicians (mechanical and electrical) to troubleshoot, optimize, and sustain critical equipment throughout its lifecycle in a fast‑paced, 24×7 GMP environment. Here's What You’ll Do Daily Operations & Support Ensure in‑scope equipment (single‑use mixers, parts washer, autoclave, isolator, filling machine, utilities) meets compliance, safety, and business requirements. Respond to alarms, OOS, OOT events; perform product impact assessments and initiate containment actions. Tier 1 Operations Meetings Represent Engineering to review and prioritize equipment issues impacting product quality and overall equipment effectiveness (OEE). Track action items, communicate status, and escalate unresolved critical issues. Troubleshooting & Reliability Lead root‑cause analyses (5‑Why, Fishbone) for equipment failures; develop corrective and preventive action plans and supporting change controls. Collaborate with mechanical and electrical technicians to diagnose and resolve failures in drives, valves, sensors, control loops, and utility networks. Commissioning, Validation & Compliance Assist with commissioning, qualification, and validation protocols (URS, IQ/OQ/PQ) for new and modified equipment. Maintain and update cGMP documentation (SOPs, SWPMs, batch records) and support internal/external audits. Original Equipment Manufacturer OEM & Calibration Partnerships Liaise with OEM vendors for installations, commissioning, warranty repairs, and technical escalations. Coordinate with in‑house and third‑party calibration teams to schedule and verify calibration of critical instrumentation. Project Participation & Continuous Improvement Support engineering projects across all phases: user requirements, design reviews, procurement, installation, start‑up, commissioning, and handover. Analyze equipment performance and CMMS data; propose improvements to preventive maintenance strategies and reliability programs. Here’s What You’ll Need (Basic Qualifications) Bachelor’s degree in Chemical, Mechanical, Mechatronics or related engineering discipline. 2–4 years of relevant experience in pharmaceutical or bioprocess manufacturing (GxP/GMP environment preferred). Exposure to drug‑product equipment is preferred (mixers, isolators, filling lines, autoclaves, parts washers, automated inspection and packing machines) . Basic hands‑on troubleshooting of PLC/HMI/SCADA systems, variable‑speed drives, and pneumatic/vacuum loops. Experience assisting with CQV activities and drafting validation deliverables. Familiarity with CMMS, Excel (pivot tables, charts), Word, and PowerPoint. Excellent interpersonal and communication skills; ability to present technical findings and influence cross‑functional teams. Self‑starter with strong problem‑solving skills, adaptability for 24×7 operations, and eagerness to learn under mentorship. Professional demeanour; able to represent Moderna’s interests and policies. 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 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 At Moderna, we believe that when you feel your best, you can do your best work. That’s why our global benefits and well-being resources are designed to support you—at work, at home, and everywhere in between. 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 The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work. About Moderna Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world. By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities. We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S. As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact. If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities. Moderna is a smoke-free, alcohol-free, and drug-free work environment. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply! 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. We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best. 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 leavesandaccommodations@modernatx.com. - Our Mission and Vision At Moderna we are pioneering the development of a new class of drugs made of messenger RNA (mRNA). This novel drug platform builds on the discovery that modified mRNA can direct the body’s cellular machinery to produce nearly any protein of interest, from native proteins to antibodies and other entirely novel protein constructs that can have therapeutic activity inside and outside of cells. We have a clear mission to propel the field of mRNA science forward and deliver new medicines to patients and a unique vision for how to achieve this mission. Our Mission: To deliver on the promise of transformative messenger RNA (mRNA) science to bring new medicines to patients. Our Vision: To unlock the potential of mRNA by establishing an ecosystem of teams and partners that will work together to develop the broadest possible array of drugs, across diverse therapeutic areas and routes of administration, for serious diseases that are not treatable today. Third Party Staffing Agencies Moderna does not accept unsolicited resumes from any source other than directly from candidates. For the protection of all parties involved in the recruiting process, resumes will only be accepted from recruiters/agencies if a signed agreement is in place at the inception of the recruiting effort and authorized for a specified position. Unsolicited resumes sent to Moderna from recruiters/agencies do not constitute any type of relationship between the recruiter/agency and Moderna and do not obligate Moderna to pay fees if we hire from those resumes. Reasonable Accommodation Notice Moderna will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Applicants with disabilities may be entitled to reasonable accommodation under the terms of the Americans with Disabilities Act and certain state or local laws. Please inform the company's personnel representative by calling 617-460-9346 or emailing humanresources@modernatx.com if you need assistance completing any forms or to otherwise participate in the application process. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. Return Home

Responsibilities

Provide technical support to ensure the reliability and compliance of mRNA drug-product manufacturing and fill-finish equipment. Lead root-cause analyses for equipment failures and support commissioning, qualification, and validation activities.