Senior GMP Document Control & Training Specialist

Consortium for Clinical Research and Innovation, Singapore; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A leading healthcare research organization in Singapore is seeking a Senior Quality Document Control & Training Specialist. The role involves overseeing GMP document control processes and managing training records. The ideal candidate will have 3-5 years of experience in a pharmaceutical quality system and a background in science or engineering. This opportunity is pivotal for ensuring compliance and maintaining quality standards in clinical research documentation.

Qualifications

• Minimum of 3 to 5 years of relevant experience in Pharmaceutical Quality System.
• Knowledge of GMP/GDP/HSA/HPRA regulatory requirements.
• Strong understanding of quality management concepts.

Responsibilities

• Lead GMP document control for ACTRIS including creation and management.
• Administer the document control system and ensure compliance.
• Support the GMP training program and maintain training records.

Skills

GMP Document Control

Quality Management Concepts

Regulatory Compliance (GMP/GDP)

Education

Diploma or Degree in Science, Engineering and Life Sciences

Job description

A leading healthcare research organization in Singapore is seeking a Senior Quality Document Control & Training Specialist. The role involves overseeing GMP document control processes and managing training records. The ideal candidate will have 3-5 years of experience in a pharmaceutical quality system and a background in science or engineering. This opportunity is pivotal for ensuring compliance and maintaining quality standards in clinical research documentation.