Engineer I (Biopharmaceutical Manufacturing)

Location: City of Singapore

Company

hirify.global develops medicines and healthcare solutions, with this role supporting biopharmaceutical manufacturing operations.

What you will do

• Own the technical integrity and performance of Central Manufacturing Services processes and equipment, including media and buffer preparation, autoclave operations, column packing, and automated logistics.
• Monitor process performance data, define control parameters, and identify opportunities to improve robustness, cost efficiency, cycle times, and operational reliability.
• Lead change controls, process optimization initiatives, equipment upgrades, preventive maintenance improvements, and asset-care activities.
• Investigate process deviations and equipment failures, perform root cause analysis, and implement sustainable CAPAs.
• Support equipment qualification, validation, periodic reviews, NPI, process startup, engineering runs, and manufacturing readiness activities.
• Collaborate with Manufacturing Operations, Quality, MSAT, Automation, engineering teams, and equipment vendors.

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, process engineering, or technical support in a regulated GMP environment.
• Experience with Central Manufacturing Services or related support functions, continuous improvement, change control, or process optimization.
• Knowledge of GMP requirements, data integrity, process trending, deviation investigations, and root cause analysis.
• Strong technical problem-solving, analytical, writing, communication, and cross-functional collaboration skills.

Nice to have

• Experience with process data analysis, single-use systems, deviation investigation, or equipment troubleshooting.
• Familiarity with Lean, OE, or Six Sigma methodologies.

Culture & Benefits

• Work in a cross-functional manufacturing environment focused on continuous improvement and operational reliability.
• Support GMP, EHS, audit readiness, inspection readiness, and data traceability requirements.
• Contribute to better medicines, outcomes, and science through biopharmaceutical manufacturing.
• Equal opportunity employment is provided regardless of background or protected characteristics.