Full Time Pharmatechnologist Jobs, in TEKsystems - Ricebowl

• 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