Senior Validation QA Specialist - GMP & Biopharma

WUXI XDC SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A biopharmaceutical company in Singapore is seeking a Validation QA professional. The role involves overseeing manufacturing and testing activities, ensuring compliance with internal and regulatory requirements. Candidates should have a Bachelor's degree in relevant fields and 8-10 years of QA experience in the Biopharma industry. Proficiency in English and skills in Microsoft Office are essential. Strong communication and conflict management abilities are also required. Join us to contribute to the quality system within a dynamic team.

Qualifications

• 8-10 years of relevant QA experience in Biopharma or Pharmaceuticals industry.
• Familiar with FDA, EMEA, and PICS GMP requirements.
• Knowledgeable in biological product manufacturing and related quality control requirements.

Responsibilities

• Provide quality oversight for validation and re-qualification engineering activities.
• Review and approve GMP manufacturing and testing-related documents.
• Authorize the release of facilities, utilities, and equipment for GMP production use.

Skills

Quality oversight

Cross-functional communication

Conflict management

Learning ability

Education

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

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

A biopharmaceutical company in Singapore is seeking a Validation QA professional. The role involves overseeing manufacturing and testing activities, ensuring compliance with internal and regulatory requirements. Candidates should have a Bachelor's degree in relevant fields and 8-10 years of QA experience in the Biopharma industry. Proficiency in English and skills in Microsoft Office are essential. Strong communication and conflict management abilities are also required. Join us to contribute to the quality system within a dynamic team.