Senior Pharmatechnologist — GMP Manufacturing Expert

ALLEGIS GROUP SINGAPORE PRIVATE LIMITED

Singapore

On-site

SGD 85,000 - 120,000

Full time

14 days+
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Job summary

Allegis Group Singapore Pte Ltd in Tuas, Singapore, is seeking an experienced Pharmatechnologist III to support pharmaceutical manufacturing operations in a GMP-regulated environment. You will execute drug product manufacturing processes, operate equipment, and maintain documentation to ensure cGMP compliance and production schedules.

The role requires hands-on expertise in dispensing, blending, granulation, compression, coating, or filling, plus strong troubleshooting and communication skills

Qualifications

  • Diploma/Advanced Diploma or Degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or related discipline.
  • Minimum 8 years of experience in pharmaceutical manufacturing within a GMP-regulated environment.
  • Hands-on experience in drug product manufacturing processes such as dispensing, blending, granulation, compression, coating, or filling.
  • Strong understanding of current Good Manufacturing Practices (cGMP).
  • Experience completing manufacturing documentation and batch records.
  • Strong troubleshooting, problem-solving, and communication skills.
  • Ability to work effectively in a fast-paced manufacturing environment.

Responsibilities

  • Execute drug product manufacturing activities including dispensing, blending, granulation, compression, coating, and filling operations.
  • Operate pharmaceutical manufacturing equipment safely and efficiently.
  • Complete batch records, equipment logbooks, and GMP documentation accurately and in real time.

Skills

GMP compliance
Batch records
Troubleshooting
Communication
Fast-paced environment

Education

Pharmaceutical Sciences / related

Job description

Allegis Group Singapore Pte Ltd in Tuas, Singapore, is seeking an experienced Pharmatechnologist III to support pharmaceutical manufacturing operations in a GMP-regulated environment. You will execute drug product manufacturing processes, operate equipment, and maintain documentation to ensure cGMP compliance and production schedules.

The role requires hands-on expertise in dispensing, blending, granulation, compression, coating, or filling, plus strong troubleshooting and communication skills

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