Equipment & Testing Technician I Pharma, Manufacturing #HJN

Recruit Express Pte Ltd; Singapore; On-site; SGD 33,000 - 61,000; Full time

Job summary

Recruit Express Pte Ltd is seeking a candidate to support equipment qualification, validation and related activities in a regulated environment. The role requires collaboration with Engineering, Manufacturing and Quality teams to ensure compliant project delivery.

The ideal candidate has a background in engineering, biotechnology, or pharmaceutical technology and knowledge of GMP, IQ/OQ/PQ processes. Prior experience in regulated manufacturing is advantageous, with strong documentation skills.

Qualifications

• Min Diploma or Degree in Engineering, Biotechnology, Biomedical Sciences, Pharmaceutical Technology or a related discipline.
• Experience in pharmaceutical, biotechnology or regulated manufacturing environments will be an advantage.
• Basic knowledge of GMP, equipment qualification or validation is preferred.

Responsibilities

• Assist in equipment qualification, validation and decommissioning activities in accordance with established procedures.
• Support the preparation and execution of equipment qualification protocols, including IQ, OQ and PQ.
• Perform equipment testing, verification and inspections to ensure compliance with required standards.
• Maintain accurate qualification records, reports and technical documentation.
• Coordinate with Engineering, Manufacturing and Quality teams to support project completion.
• Assist in identifying and documenting deviations, discrepancies and corrective actions.
• Ensure all activities comply with Good Manufacturing Practices (GMP), safety requirements and site procedures.
• Provide technical and administrative support for equipment qualification and validation projects.

Skills

Equipment qualification

Documentation

GMP awareness

Cross-functional coordination

Education

Diploma or Degree in Engineering/Biotech/Pharma

Job description

Job Responsibilities

• Assist in equipment qualification, validation and decommissioning activities in accordance with established procedures.

• Support the preparation and execution of equipment qualification protocols, including IQ, OQ and PQ.

• Perform equipment testing, verification and inspections to ensure compliance with required standards.

• Maintain accurate qualification records, reports and technical documentation.

• Coordinate with Engineering, Manufacturing and Quality teams to support project completion.

• Assist in identifying and documenting deviations, discrepancies and corrective actions.

• Ensure all activities comply with Good Manufacturing Practices (GMP), safety requirements and site procedures.

• Provide technical and administrative support for equipment qualification and validation projects.

Requirements

• Min Diploma or Degree in Engineering, Biotechnology, Biomedical Sciences, Pharmaceutical Technology or a related discipline.

• Experience in pharmaceutical, biotechnology or regulated manufacturing environments will be an advantage.

• Basic knowledge of GMP, equipment qualification or validation is preferred.