Associate Engineer, Downstream Biopharma Processes

Sanofi Aventis Singapore Pte. Ltd

Singapore

On-site

SGD 56,000 - 89,000

Full time

6 days ago
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Job summary

Sanofi is seeking an Associate Engineer, Manufacturing – Downstream (Process) in Tuas, Singapore. The role supports routine downstream biopharmaceutical manufacturing operations with focus on process robustness and compliance.

You will monitor process performance, analyze trends, and contribute to continuous improvement of downstream robustness, while supporting NPI, startup, and validation activities when needed.

Qualifications

  • Basic understanding of downstream biopharmaceutical processes.
  • Working knowledge of GMP requirements and data integrity principles.
  • Basic data analysis and trending capability.
  • Ability to work effectively in cross‑functional teams.
  • Structured problem solving and analytical thinking.
  • Good technical writing and communication skills.

Responsibilities

  • Support routine downstream manufacturing operations within assigned scope.
  • Monitor critical process parameters and performance indicators to stay within control limits.
  • Identify deviations and escalate issues promptly.
  • Provide day‑to‑day technical support to Manufacturing Operations for downstream processes.
  • Serve as operational SME for assigned downstream unit operations, ensuring safe and compliant performance.
  • Assist updates to SOPs, batch records, and process documentation.

Skills

Downstream processes
GMP knowledge
Data analysis
Cross-functional teamwork
Problem solving
Technical writing
Team player

Education

Biotech/Engineering degree

Job description

Sanofi is seeking an Associate Engineer, Manufacturing – Downstream (Process) in Tuas, Singapore. The role supports routine downstream biopharmaceutical manufacturing operations with focus on process robustness and compliance.

You will monitor process performance, analyze trends, and contribute to continuous improvement of downstream robustness, while supporting NPI, startup, and validation activities when needed.

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