GMP Document Control QA Associate

MSD; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical company in Singapore is seeking an Associate Technician in Document Control to manage controlled documents and ensure compliance with GMP standards. The ideal candidate will possess a diploma in a relevant field, have basic GMP knowledge, and 1-3 years of experience in pharmaceutical manufacturing. Responsibilities include document printing and archiving. This temporary position offers an opportunity for those committed to quality improvement and teamwork.

Qualifications

• Minimum ‘O’ level certificate or Diploma in a relevant field.
• Basic knowledge of GMP and pharmaceutical regulatory requirements.
• 1 - 3 years of relevant experience in pharmaceutical manufacturing.

Responsibilities

• Print, issue and reconcile controlled documents.
• Monitor periodic review of all printed controlled documents.
• Archive and retrieve GMP documentation.

Skills

Accountability

Applied Engineering

Biopharmaceutics

Communication

Continual Improvement Process

Failure Mode and Effects Analysis (FMEA)

GMP Compliance

Lean Manufacturing

Life Science

Microsoft Excel

Microsoft Office

Pharmaceutical Manufacturing

Pharmacology

Policy Development

Quality Assurance (QA)

Quality Auditing

Quality Control Documentation

Quality Control Management

Quality Control Tools

Quality Function Deployment

Quality Improvement Programs

Quality Management

Quality Management Systems (QMS)

Root Cause Analysis (RCA)

Education

Diploma in Science/Life Science/Pharmaceutical Science/Engineering

Minimum “O” level certificate

Tools

Microsoft Word

Microsoft Excel

Job description

A leading pharmaceutical company in Singapore is seeking an Associate Technician in Document Control to manage controlled documents and ensure compliance with GMP standards. The ideal candidate will possess a diploma in a relevant field, have basic GMP knowledge, and 1-3 years of experience in pharmaceutical manufacturing. Responsibilities include document printing and archiving. This temporary position offers an opportunity for those committed to quality improvement and teamwork.