Biopharma Manufacturing Validation Technician GMP #HJN

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

Job summary

Recruit Express Pte Ltd in Singapore seeks a qualified Equipment Qualification professional to assist in qualification, validation and decommissioning activities in line with established procedures.

You will support IQ/OQ/PQ protocols, perform testing and maintain records while coordinating with Engineering, Manufacturing and Quality teams to ensure GMP compliance and site safety. Prior experience in regulated manufacturing is advantageous.

Qualifications

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

Responsibilities

• Assist in equipment qualification, validation and decommissioning activities according to procedures.
• Support preparation and execution of qualification protocols (IQ, OQ, PQ).
• Perform equipment testing, verification and inspections to ensure compliance with standards.
• Maintain qualification records, reports and technical documentation.
• Coordinate with Engineering, Manufacturing and Quality to support projects.
• Identify and document 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

GMP knowledge

Documentation skills

Education

Diploma/degree in Engineering or life sciences

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.