GMP Validation Technician I Manufacturing #HJN

Recruit Express Pte Ltd; Singapore; Presencial; SGD 55.000 - 85.000; Jornada completa

Descripción de la vacante

Recruit Express Pte Ltd in Singapore seeks a qualified engineer to support equipment qualification and validation activities in GMP environments. You will assist in IQ/OQ/PQ protocols and maintain records.

You will coordinate with Engineering, Manufacturing and Quality teams, document deviations, and ensure compliance with GMP and site procedures. Diploma or degree in engineering or related field is preferred.

Formación

• Must have a Diploma or Degree in Engineering or related field.
• Experience in pharmaceutical/biotech or regulated manufacturing is a plus.
• Basic knowledge of GMP and equipment qualification preferred.

Responsabilidades

• Assist in equipment qualification, validation and decommissioning per procedures.
• Support preparation and execution of IQ, OQ and PQ protocols.
• Perform equipment testing, verification and inspections to meet standards.
• Maintain qualification records, reports and technical documentation.
• Coordinate with Engineering, Manufacturing and Quality to support projects.
• Assist in documenting deviations and corrective actions.
• Ensure compliance with GMP, safety rules and site procedures.
• Provide technical and administrative support for qualification and validation projects.

Conocimientos

GMP awareness

Cross-functional teamwork

Educación

Diploma / Degree in Engineering

Herramientas

IQ/OQ/PQ protocols

Descripción del empleo

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.