- 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
