Pharmatechnologist

TEKsystems; Singapore; On-site; SGD 90,000 - 130,000; Full time

Job summary

TEKsystems in Singapore is seeking an experienced Pharmatechnologist III to support GMP manufacturing operations in a regulated production environment. You will execute drug product manufacturing processes, operate production equipment, and ensure precise documentation in real-time.

Responsibilities include batch records, SOP adherence, QA support, and continuous improvement initiatives within a fast-paced facility in Tuas.

Qualifications

• Diploma/Advanced Diploma or Degree in Pharmaceutical Sciences or related field.
• Minimum 8 years of experience in GMP pharmaceutical manufacturing.
• Hands-on experience with drug product manufacturing processes (dispensing, blending, granulation, compression, coating, filling).
• Strong knowledge of cGMP and documentation practices.
• Ability to work in a fast-paced manufacturing environment.

Responsibilities

• Execute drug product manufacturing activities including dispensing, blending, granulation, compression, coating, and filling operations.
• Perform manufacturing processes in accordance with approved batch records and SOPs.
• Support production targets while maintaining quality and compliance standards.
• Complete batch records, equipment logbooks, and GMP documentation accurately and in real time.
• Support audit and inspection readiness activities.

Skills

GMP knowledge

Documentation

Problem solving

Communication

Fast-paced environment

Education

Pharmaceutical sciences degree

Job description

• 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