GMP Document Control & Training Specialist

Consortium for Clinical Research and Innovation Singapore; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading clinical research consortium in Singapore is seeking an experienced professional to manage document control and documentation administration. You will lead the GMP document control process, ensure compliance with quality regulations, and support GMP training activities. Ideal candidates have a degree in Science or Engineering and 3-5 years of relevant experience in the pharmaceutical industry. This is a unique opportunity to contribute to innovative healthcare solutions in a key role.

Qualifications

• 3-5 years of relevant experience in Pharmaceutical Quality System.
• Knowledge of GMP, GDP, HSA, and HPRA regulations.
• Proficient in quality management concepts.

Responsibilities

• Act as the GMP Document Control lead.
• Administer the GMP document control system.
• Support GMP training program administration.

Skills

Document control management

Quality management

Regulatory compliance knowledge

Training program administration

Education

Diploma or Degree in Science, Engineering and Life Sciences

Job description

A leading clinical research consortium in Singapore is seeking an experienced professional to manage document control and documentation administration. You will lead the GMP document control process, ensure compliance with quality regulations, and support GMP training activities. Ideal candidates have a degree in Science or Engineering and 3-5 years of relevant experience in the pharmaceutical industry. This is a unique opportunity to contribute to innovative healthcare solutions in a key role.