C&Q Engineer, Life Sciences – Single-Use Systems

Amaris Consulting Pte Ltd; Singapore; Presencial; SGD 70.000 - 120.000; Jornada completa

Descripción de la vacante

Amaris Consulting, Life Sciences team in Singapore, supports commissioning and qualification activities for single-use systems and related materials, contributing to qualification planning, execution, and documentation with technical and quality groups.

You will help ensure equipment and systems readiness, coordinate with Engineering, Manufacturing, Validation, and Quality teams, and uphold GMP standards across assigned activities.

Formación

• Diploma or Bachelor's degree in Chemical Engineering, Biotechnology, Pharmaceutical Sciences, Life Sciences, or related discipline.
• 3+ years of experience in commissioning and qualification in pharma/biotech environments.
• Hands-on experience with single-use systems and materials.
• Experience preparing and executing qualification protocols and maintaining documentation.

Responsabilidades

• Support commissioning and qualification activities for single-use systems and materials.
• Prepare, execute, and review C&Q protocols and supporting documentation.
• Verify that single-use systems and materials meet defined specifications and qualification requirements.
• Document and support investigations and resolution of discrepancies identified during C&Q activities.
• Coordinate with Engineering, Manufacturing, Validation, and Quality teams to deliver C&Q activities.
• Support change-control activities related to single-use systems and materials.
• Ensure activities follow site procedures and GMP requirements.

Conocimientos

Commissioning

Qualification

Single-use systems

GMP understanding

Documentation

Educación

Chemical Engineering

Biotechnology

Pharmaceutical Sciences

Descripción del empleo

Amaris Consulting, Life Sciences team in Singapore, supports commissioning and qualification activities for single-use systems and related materials, contributing to qualification planning, execution, and documentation with technical and quality groups.

You will help ensure equipment and systems readiness, coordinate with Engineering, Manufacturing, Validation, and Quality teams, and uphold GMP standards across assigned activities.