Free with a WorkJio account: we compare your profile with this job and show what you already meet.
Share with a friend
Start
Not stated
Work mode
On-site
Experience
Some experience
About the role
The Manufacturing team is expanding and looking for an Engineer to act as the technical process and system owner for Central Manufacturing Services (CMS). You will drive continuous improvement, change management and operational reliability across CMS processes and equipment, working with MSAT, Quality, Automation and other cross-functional teams. This role suits someone with a biopharmaceutical manufacturing background who enjoys technical problem-solving and process optimisation.
What you'll do
Own the technical integrity and performance of assigned CMS processes and equipment systems
Serve as technical subject matter expert for CMS operations, supporting troubleshooting and technical decisions
Monitor process performance data and trends to spot improvement opportunities or early signs of drift
Support process parameter definition, control limits and acceptance criteria
Identify and drive continuous improvement initiatives targeting cost, cycle time, robustness and efficiency
Author, lead and manage change controls for process, equipment, procedural or system changes
Apply Lean, OE and Six Sigma methods to reduce waste and variability in CMS workflows
Track and report improvement project outcomes with clear metrics
Work with MSAT and Automation teams on digital tools, data analytics and automation
Drive improvements to equipment and process consistency, reliability and control
Lead or support equipment reliability and asset care improvements, including preventive maintenance optimisation
Conduct process risk assessments such as FMEA
Support equipment qualification, validation and periodic reviews
Recommend equipment or process upgrades to improve reliability and reduce downtime
Lead technical investigation and root cause analysis of deviations, equipment failures and performance issues
Develop and drive corrective actions (CAPAs) to prevent recurrence
Ensure deviations are closed in a timely manner
Track CAPA effectiveness and report outcomes to the Senior Manager, Manufacturing
Ensure CMS technical activities and documentation comply with GMP, EHS and site requirements
Support audit and inspection readiness for CMS
Maintain data integrity and traceability across process documentation and change records
Provide technical process expertise to NPI and process startup activities
Contribute to process risk assessments and readiness reviews for new CMS processes or equipment
Support process data collection, verification and documentation during engineering runs or startup manufacturing
Work with Manufacturing Operations to translate operational challenges into technical improvements
Collaborate with Quality, MSAT and Automation teams on process improvements and system enhancements
Engage with equipment vendors and engineering teams on troubleshooting, optimisation and upgrades
Good to know
Full time position based in the City of Singapore
Reports to the Senior Manager, Manufacturing
Expe
Requirements
Diploma or Bachelor's degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences or a related discipline
3–5 years of experience in biopharmaceutical manufacturing operations, process engineering or technical support in a regulated GMP environment
Demonstrated experience in CMS or related support functions
Proven track record leading or contributing to continuous improvement, change control or process optimisation with measurable outcomes
Strong technical understanding of CMS processes including Media and Buffer preparation, Autoclave operations, Column Packing and Automated Logistics systems
Ability to drive change and lead improvement projects with measurable outcomes
Apply on the company website
You will leave WorkJio. Never pay a fee or share your Singpass password, OTP or bank log-ins to apply.