GMP Document Control QA Associate

A global pharmaceutical company based in Singapore is looking for an Associate Technician to support the Document Control Center. The role involves managing the printing and issuance of controlled documents, ensuring compliance with GMP standards, and participating in continuous improvement activities. Candidates should have a minimum O level or Diploma in a...

A leading pharmaceutical company in Singapore is seeking an Associate Technician for its Document Control Center. This role involves managing controlled documents and ensuring compliance with GMP standards. Candidates should have a minimum of 'O' level certificate or relevant diploma, experience in pharmaceutical manufacturing, and proficiency in Microsoft...

Responsible for managing, scanning, maintaining, and archiving GMP documents in the factory, ensuring completeness, accuracy, and compliance with GMP and relevant regulatory requirements. Also responsible for managing training materials and maintaining training records. Assist in preparing and supporting documentation for external audits. Key...

A leading biomedical firm in Singapore is seeking a QA Executive to support quality assurance activities within the biotech manufacturing environment. The role involves ensuring compliance with quality standards, managing document controls, and collaborating with cross-functional teams. Ideal candidates should have at least 2 years of QA experience and a...

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...

A leading global biotechnology company in Singapore is seeking a Quality Assurance professional to oversee day-to-day operations at a GMP facility. You will ensure compliance by reviewing and approving various documents and lead quality control initiatives. The ideal candidate holds a Bachelor's degree in a related field, has over 5 years of QA experience,...

A leading life sciences company in Singapore seeks a Quality Assurance Associate to ensure compliance in cell and gene therapy manufacturing. Candidates must hold a Bachelor's or Master's degree in life sciences and have 3-5 years of GMP QA experience. The role involves managing compliance processes, providing real-time support, and engaging in continuous...

Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

Overview At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our...

A leading pharmaceutical company in Singapore is seeking a Validation Officer for a 1-year contract. This role involves supporting validation and quality activities to ensure compliance with GMP and regulatory requirements. Candidates should have a Bachelor’s degree in a relevant field and a minimum of 1-2 years of experience in validation or QA within...