Pharma MSAT/MS&T Engineer: Tech Transfer & Scale-Up

MANTU GROUP SA; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Amaris Consulting is seeking a skilled professional to drive tech transfer and process validation for biologics drug substance in a global setting. You will support scale-up from lab to commercial production and coordinate cross-functional teams to ensure smooth implementation.

The role requires strong GMP knowledge, hands-on chromatography and filtration experience, and the ability to navigate quality and manufacturing perspectives.

Qualifications

• Degree in engineering, life sciences, or related field.
• Experience in commercial-scale GMP manufacturing (biologics drug substance).
• Strong background in tech transfer and process validation.
• Hands-on chromatography and filtration experience.

Responsibilities

• Support and execute technology transfer for drug substance manufacturing.
• Drive scale-up activities from lab to commercial production.
• Collaborate with cross-functional teams to ensure smooth implementation.
• Develop and optimize processes including purification, homogenisation, and cleaning processes for routine operations.
• Provide technical guidance to site teams.
• Lead and support validation activities including cleaning validation, water mixing validation, and risk assessments (e.g. extractables & leachables – E&L).
• Ensure compliance with GMP and regulatory standards.
• Prepare and review validation protocols, reports, and technical documentation.
• Support integration of single-use systems and new manufacturing equipment.

Skills

Tech transfer

Process validation

Chromatography

Filtration

GMP manufacturing

Stakeholder collaboration

English fluency

Problem solving

Education

Bachelor's degree in engineering or life sciences

Job description

Amaris Consulting is seeking a skilled professional to drive tech transfer and process validation for biologics drug substance in a global setting. You will support scale-up from lab to commercial production and coordinate cross-functional teams to ensure smooth implementation.

The role requires strong GMP knowledge, hands-on chromatography and filtration experience, and the ability to navigate quality and manufacturing perspectives.