Execute drug product manufacturing activities
Operate pharmaceutical manufacturing equipment safely and efficientl
Complete batch records, equipment logbooks, and GMP documentation accurately and in real time.

Overview

We are seeking an experienced Pharmatechnologist III to support pharmaceutical manufacturing operations within a GMP-regulated production environment. This role is responsible for executing drug product manufacturing processes, operating

production equipment, maintaining documentation, and ensuring compliance with cGMP standards and production schedules.

Location: Tuas, Singapore

Duration: 12 Months

Key Responsibilities

Manufacturing Operations

Execute drug product manufacturing activities including dispensing, blending, granulation, compression, coating, and filling operations.
Perform mnufacturing processes in accordance with approved batch records and standard operating procedures (SOPs).
Support production targets while maintaining product quality and compliance standards.

Equipment Operation & Maintenance

Operate pharmaceutical manufacturing equipment safely and efficiently.
Conduct routine equipment inspections and perform basic maintenance activities.
Identify and escalate equipment malfunctions for timely resolution.

Documentation & Compliance

Complete batch records, equipment logbooks, and GMP documentation accurately and in real time.
Ensure compliance with cGMP requirements, quality standards, and site procedures.
Support audit and inspection readiness activities.

Quality Assurance

Perform in-process controls, sampling activities, and checks as specified in manufacturing instructions.
Monitor process parameters and promptly report deviations or abnormalities.
Assist with investigations relating to production and equipment issues.

Safety & Continuous Improvement

Maintain cleanliness and housekeeping standards within manufacturing areas.
Identify and report safety hazards and process risks.
Participate in equipment qualification, cleaning validation, and continuous improvement initiatives.
Attend and apply GMP and compliance training programmes.

Requirements

Diploma, Advanced Diploma, or Degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or a 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.

Preferred Skills

Pharmaceutical Manufacturing Operations
GMP Compliance
Batch Record Documentation
Equipment Operation and Troubleshooting
Process Validation
Root Cause Investigation
Quality Systems
Continuous Improvement

We regret to inform that only shortlisted candidates will be notified.

Job Reference: R25150511 Cammy Li Xin Hui

Allegis Group Singapore Pte Ltd, Company Reg No. 200909448N, EA License No. 10C4544