Pharmatechnologist III – GMP Manufacturing

About the role

We are looking for an experienced Pharmatechnologist III to join our GMP‑regulated manufacturing site in Tuas, Singapore. The role will support drug product production, operate specialised equipment and ensure all activities comply with cGMP standards and production schedules.

Key responsibilities

• Execute drug product manufacturing steps including dispensing, blending, granulation, compression, coating and filling according to approved batch records and SOPs.
• Operate and perform routine inspections of pharmaceutical equipment, carry out basic maintenance and report any malfunctions.
• Complete batch records, equipment logbooks and other GMP documentation in real time.
• Perform in‑process controls, sampling and monitor process parameters, reporting deviations promptly.
• Support audit readiness, equipment qualification, cleaning validation and continuous‑improvement initiatives.

Required profile

• Diploma, Advanced Diploma or Degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences or related field.
• Minimum 8 years of hands‑on experience in pharmaceutical manufacturing within a GMP environment.
• Proven experience with drug product manufacturing processes such as dispensing, blending, granulation, compression, coating or filling.
• Strong knowledge of current Good Manufacturing Practices (cGMP) and documentation requirements.
• Excellent troubleshooting, problem‑solving and communication abilities.

Required skills

• Dispensing, blending, granulation, compression, coating and filling operations.
• Equipment operation and basic maintenance.
• GMP compliance and batch record documentation.
• Process validation and root‑cause investigation.
• Quality systems and continuous‑improvement methodologies.