Downstream Bioprocess Engineer – Associate

Sanofi; Singapore; Sur place; SGD 52 000 - 76 000; Plein temps

Résumé du poste

Sanofi Singapore is seeking an Associate Engineer, Manufacturing – Downstream (Process) to support routine downstream biopharmaceutical operations, including seed train, cell culture, bioreactor operations, and chromatography, ensuring process robustness and GMP compliance.

You will monitor process parameters, analyze trends, support investigations and CAPAs, participate in NPI/startup activities, and collaborate with MSAT and cross-functional teams to drive continuous improvement.

Qualifications

• Diploma or Bachelor’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or related discipline.
• 3–4 years of experience in downstream biopharmaceutical manufacturing, process support, or manufacturing operations in a regulated environment.

Responsabilités

• Routine Manufacturing & Asset Care Support: Monitor parameters, identify deviations, provide day-to-day technical support, act as SME for downstream unit operations, update SOPs/batch records.
• Downstream Process Robustness & Performance: Review data, implement process improvements, collaborate with MSAT and Automation teams.
• NPI & Startup Support: Execute engineering runs, PPQ, startup manufacturing, data collection, readiness handover, and process documentation.
• Deviation, Investigation & CAPA Support: Participate in deviations/investigations and escalate.
• GMP, Safety & Compliance: Comply with GMP/EHS/site requirements and support audit readiness.
• Continuous Improvement: Identify improvements and participate in OE/Lean initiatives.

Connaissances

Downstream processes

GMP & data integrity

Data analysis

Cross-functional teamwork

Structured problem solving

Technical writing

Team player

Formation

Biotech / Bioengineering degree

Description du poste

Sanofi Singapore is seeking an Associate Engineer, Manufacturing – Downstream (Process) to support routine downstream biopharmaceutical operations, including seed train, cell culture, bioreactor operations, and chromatography, ensuring process robustness and GMP compliance.

You will monitor process parameters, analyze trends, support investigations and CAPAs, participate in NPI/startup activities, and collaborate with MSAT and cross-functional teams to drive continuous improvement.