Pharma Manufacturing Technologist — GMP & Process Ops

ORION PROJECT SERVICES PTE. LTD.; Singapore; On-site; SGD 42,000 - 65,000; Full time

Job summary

Orion Group Life Sciences is seeking a Pharmaceutical Manufacturing Technologist for a multinational biopharmaceutical client in Tuas, Singapore. The role involves hands-on drug product manufacturing, GMP-compliant operations, and real-time documentation on a 12-month contract with potential extension.

You will operate manufacturing equipment, perform in-process controls, and maintain GMP standards across production areas. SIT-based degree and 1–2 years of experience are required.

Qualifications

• Degree in Chemical Engineering or Pharmaceutical Engineering from SIT.
• 1–2 years of manufacturing experience.

Responsibilities

• Execute drug product manufacturing operations including dispensing, blending, granulation, compression, coating, and filling.
• Operate and perform basic maintenance on pharmaceutical manufacturing equipment.
• Complete batch records, logbooks, and GMP documentation accurately and in real-time.
• Perform in-process controls, sampling, and checks as specified in batch records.
• Maintain cleanliness and GMP compliance in production areas.
• Identify and report process deviations, equipment malfunctions, and safety concerns.
• Participate in equipment qualification and cleaning validation activities.
• Attend and apply GMP training programs.

Skills

GMP compliance

Batch records

Equipment operation

In-process controls

Education

Bachelor's degree in Chemical Engineering or Pharmaceutical Engineering (SIT)

Tools

Manufacturing equipment

Job description

Orion Group Life Sciences is seeking a Pharmaceutical Manufacturing Technologist for a multinational biopharmaceutical client in Tuas, Singapore. The role involves hands-on drug product manufacturing, GMP-compliant operations, and real-time documentation on a 12-month contract with potential extension.

You will operate manufacturing equipment, perform in-process controls, and maintain GMP standards across production areas. SIT-based degree and 1–2 years of experience are required.