Senior Digital Systems and Automation Engineer
IT, Infrastructure & CybersecurityPosted 20 Jul 2026
Advertised as “Senior Digital Systems and Automation Engineer (GMP)”
Posted 20 Jul 2026
Advertised as “Senior Digital Systems and Automation Engineer (GMP)”
The original posting with the fluff stripped out
Field of studyEngineering, Computer Science, Information Technology (or related)
Study levelBachelor's
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
This role is a permanent, full-time role and is based at our site in Brisbane.
The Senior Digital Systems and Automation Engineer (GMP) owns day-to-day support and leads coordination of lifecycle management and continuous improvement of GMP-regulated digital systems and manufacturing automation platforms at the Brisbane site.
The role provides technical ownership for assigned systems, contributing to system reliability, compliance, and alignment with business needs across Manufacturing, Quality, and Engineering.
The position works across IT and OT environments, collaborating with internal teams and external partners to support integration and performance of systems supporting site operations.
What You'll Do:
Partner with stakeholders to gather and document business requirements (URS/FRS, process documentation)
Support system availability, performance, and compliance with GMP and Data Integrity (ALCOA+) principles
Support and progress incidents, performing root cause analysis and coordinating issue resolution with Global IT and vendors
Conduct audit trail reviews, user access reviews, and periodic system health checks
Support and coordinate activities for plant automation systems including PLCs, HMIs, SCADA, and equipment control platforms
Act as a primary supporting contact for assigned automation systems, working with vendors, system integrators, and engineering teams to progress system changes, upgrades, and issue resolution
Perform and coordinate troubleshooting and issue resolution through appropriate internal and external resources
Support automation platforms such as Rockwell / Allen-Bradley, Siemens, DeltaV / TruBio, and bioprocess systems (e.g. UNICORN, MFCS) or equivalent
Support execution of automation-related activities are executed in accordance with site standards, change control, and validation requirements
Provide subject matter expertise for assigned systems and guide internal stakeholders on best practice use and improvements
Lead lifecycle coordination for assigned systems, operating within Engineering and Automation governance frameworks
Maintain and update enhancement backlogs, supporting prioritization discussions.
Identify and communicate risks related to system obsolescence, compliance, or integration gaps
Provide technical input to site planning discussions.
Contribute to continuous improvement initiatives (PPI)
Coordinate and actively contribute to delivery of approved enhancements, upgrades, and project initiatives in collaboration with engineering and automation leadership
Coordinate and support automation activities across the equipment lifecycle, including design input, commissioning, qualification, and operational handover
Lead site-facing FAT/SAT coordination and readiness activities
Contribute to validation activities including risk assessments, automation impact assessments, IQ/OQ/PQ, and associated documentation
Support digital validation platforms (e.g. Kneat) where applicable
Execute compliance activities in accordance with approved procedures
Author and maintain validation and technical documentation
Support and ensure system and automation changes follow approved change control and governance processes
Participate in internal and regulatory audits
Escalate risks appropriately within established governance frameworks.
Provide guidance on GMP and data integrity expectations for assigned systems
3-5 years’ experience in GMP-regulated manufacturing environments (pharmaceutical, biotech, or similar)
Experience supporting manufacturing automation platform (PLC/SCADA) is required
Experience working across IT and OT environments, with depth in at least one domain
Experience in Computer System Validation (CSV)
Experience supporting commissioning, FAT/SAT, and equipment qualification activities
Strong understanding of GMP, GAMP 5, and Data Integrity principles
Strong troubleshooting, problem-solving, and root cause analysis capability across IT and OT systems
Ability to manage multiple systems and priorities in a complex environment
Strong documentation and change management discipline.
Ability to work effectively in a cross-functional, site-based environment
Continuous improvement mindset with a focus on quality and compliance
Clear written and verbal communication skills
Alignment with Thermo Fisher Scientific 4i Values: Integrity, Intensity, Innovation, and Involvement
This is an on-site role based at the Brisbane manufacturing facility
Occasional off-hours support or project-based flexibility may be required to support critical activities such as commissioning or equipment start-ups
Benefits
Join our team and take advantage of these great benefits! Apply now to learn more about the full range of benefits we offer.
Health & Wellbeing: Join a company that prioritizes your health & wellbeing with comprehensive benefits, wellness programs, and an Employee Assistance Program providing confidential support for personal and work-related issues.
Flexibility: Balance your work and personal life with flexible arrangements.
Extra Leave: Benefit from generous leave policies, including the option to purchase additional leave, paid birthday leave, and company paid parental leave.
Charitable Giving & Volunteering: Make an impact with paid volunteer time to support non-profit organizations that matter to you.
Learning & Development: Advance your career with access to online courses via Thermo Fisher Scientific University Plus and LinkedIn learning, workshops, and mentorship programs for continuous learning and skill development.
Thermo Fisher Scientific Australia WGEA Employer of Choice for Gender Equality
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 125,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.