MSAT Engineer – Pharma Process Excellence & Scale-Up

Amaris Consulting; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

Amaris Consulting is seeking an MSAT Engineer to support commercial-scale pharmaceutical manufacturing in a GMP environment. You will troubleshoot processes, investigate deviations, drive CAPA, and contribute to technology transfer, scale-up, and validation activities with Manufacturing, Quality, and Engineering teams.

You will ensure compliance with GMP, quality, and safety requirements while collaborating across functions in an international, dynamic setting.

Qualifications

• You have experience in pharmaceutical or biopharmaceutical manufacturing within a GMP-regulated environment.
• You have practical exposure to commercial-scale production, process troubleshooting, and deviation investigations.
• You understand GMP requirements and their application within manufacturing operations.
• Experience in process optimization, technology transfer, scale-up, CAPA, or validation would be an advantage.
• You hold a degree in Chemical Engineering, Biotechnology, Pharmaceutical Sciences, or a related discipline.
• You are professionally proficient in English.
• You demonstrate strong analytical and structured problem-solving skills.
• You communicate effectively and collaborate confidently with cross-functional stakeholders.
• You are proactive, detail-oriented, and committed to quality and continuous improvement.

Responsibilities

• Provide technical support for commercial-scale manufacturing operations.
• Troubleshoot process and production issues, identify root causes, and recommend sustainable solutions.
• Support deviation investigations, impact assessments, corrective actions, and preventive actions.
• Monitor manufacturing process performance and identify opportunities for optimization and risk reduction.
• Coordinate with Manufacturing, Quality, and Engineering teams to implement process changes.
• Contribute to technology transfer, process scale-up, and validation activities.
• Prepare and review technical documentation, investigation reports, protocols, and manufacturing records.
• Ensure that all assigned activities comply with GMP, quality, regulatory, and safety requirements.

Skills

GMP knowledge

Process troubleshooting

Deviation investigations

Analytical thinking

Cross-functional collaboration

Problem-solving

Effective communication

Proactivity

Education

Chemical Engineering

Biotechnology

Pharmaceutical Sciences

Related discipline

Job description

Amaris Consulting is seeking an MSAT Engineer to support commercial-scale pharmaceutical manufacturing in a GMP environment. You will troubleshoot processes, investigate deviations, drive CAPA, and contribute to technology transfer, scale-up, and validation activities with Manufacturing, Quality, and Engineering teams.

You will ensure compliance with GMP, quality, and safety requirements while collaborating across functions in an international, dynamic setting.