Equipment Qualification Technician, MANUFACTURING #HJN

Recruit Express Pte Ltd; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

Recruit Express Pte Ltd is seeking a dedicated engineer to support equipment qualification, validation and decommissioning activities in accordance with established procedures.

You will assist with IQ, OQ and PQ protocols, perform testing and inspections to ensure GMP compliance, and maintain accurate qualification records and documentation while coordinating with Engineering, Manufacturing and Quality teams to drive project completion.

Qualifications

• Degree or Diploma in Engineering, Biotechnology, Biomedical Sciences, or Pharmaceutical Technology.
• Experience in pharmaceutical/regulated manufacturing is advantageous.
• Basic GMP and equipment qualification knowledge 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 GMP, safety requirements and site procedures.
• Provide technical and administrative support for equipment qualification and validation projects.

Skills

Equipment qualification

Validation

Documentation

GMP knowledge

Cross-functional collaboration

Education

Diploma/Degree in Engineering or related

Tools

IQ/OQ/PQ protocols

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.