Biopharma Validation Technician | GMP IQ/OQ/PQ Support

Recruit Express Pte Ltd

Singapore

On-site

SGD 42,000 - 66,000

Full time

14 days+

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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

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.

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