GMP Manufacturing QA Lead – Validation & Compliance

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 90,000 - 120,000; Full time

Job summary

A biopharmaceutical company in Singapore is seeking a professional to oversee manufacturing and testing activities ensuring compliance with internal and regulatory requirements. The ideal candidate will have a Bachelor's degree in a relevant field and 8-10 years of experience in production and quality management, including GMP knowledge. Responsibilities include managing production activities, quality oversight, and supporting audits. Strong communication, conflict management, and collaboration skills are essential for this role.

Qualifications

• 8-10 years of experience in production and/or quality management (QA/QC), with minimum 8 years in production QA.
• Familiar with FDA, EMEA, and PICS GMP requirements.
• Experience with biopharma commercial supply preferred.

Responsibilities

• Oversee on-site GMP production and testing.
• Contribute to the quality system establishment and operation.
• Manage quality events including deviations and CAPA.

Skills

Quality oversight

Cross-functional communication

Conflict management

Strong learning ability

Education

Bachelor's degree or higher in Biologics, Pharmacy, Pharmaceutical Engineering, or Bioengineering

Tools

Microsoft Word

Excel

PowerPoint

Job description

A biopharmaceutical company in Singapore is seeking a professional to oversee manufacturing and testing activities ensuring compliance with internal and regulatory requirements. The ideal candidate will have a Bachelor's degree in a relevant field and 8-10 years of experience in production and quality management, including GMP knowledge. Responsibilities include managing production activities, quality oversight, and supporting audits. Strong communication, conflict management, and collaboration skills are essential for this role.