Senior Process Engineer - Drug Substance Lead

Advanced Manufacturing Tech Solutions

Singapore

On-site

SGD 90,000 - 150,000

Full time

14 days+
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Job summary

AMTSOL is seeking a Process Engineering SME / Lead for Drug Substance to drive design and delivery of pharmaceutical process systems. The role requires deep experience in Drug Substance operations with GMP-aligned engineering leadership and collaboration across vendors, C&Q teams, and internal stakeholders.

The candidate will develop URS, DQ and technical specs, review vendor submissions, and participate in HAZOP/LOPA and other risk assessments to ensure safe, compliant, and cost-effective

Qualifications

  • Experience in drug substance manufacturing
  • Strong understanding of GMP and process safety
  • Ability to translate process requirements into design deliverables

Responsibilities

  • Provide technical leadership for Drug Substance / mAbs process systems.
  • Translate process requirements into engineering design deliverables.
  • Develop and review URS, DQ, technical specifications, and equipment package documentation.
  • Support engineering design reviews and Design Assurance activities.
  • Review vendor submissions and support technical equipment selection.
  • Participate in HAZOP, SWIFT, LOPA, and other process risk assessments.
  • Drive value engineering and design-to-cost opportunities while maintaining GMP, safety, and operability requirements.
  • Work closely with engineering contractors, vendors, Work Package Owners, and C&Q teams.
  • Ensure GMP, GEP, SHE, maintainability, and engineering standards are incorporated into the design.
  • Act as the project SME for assigned Drug Substance process areas.

Skills

Process Engineering
GMP Compliance
Pharmaceutical & Biopharma
Risk Assessment

Education

Bachelor's in Chemical/Pharma Engineering

Job description

AMTSOL is seeking a Process Engineering SME / Lead for Drug Substance to drive design and delivery of pharmaceutical process systems. The role requires deep experience in Drug Substance operations with GMP-aligned engineering leadership and collaboration across vendors, C&Q teams, and internal stakeholders.

The candidate will develop URS, DQ and technical specs, review vendor submissions, and participate in HAZOP/LOPA and other risk assessments to ensure safe, compliant, and cost-effective

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