GMP QA Document Control Associate

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 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...

(Senior) Quality Document Control & Training Specialist, ACTRIS Overview The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together seven national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system. The...

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...

Job Description –Validation QA Job Summary Responsible for overseeing manufacturing, testing, validation and NPI activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities Provide quality oversight for validation and re-qualification engineering activities, ensuring validation status is consistently maintained...

Job Description –Validation QA Job Summary Responsible for overseeing manufacturing, testing, validation and NPI activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities Provide quality oversight for validation and re-qualification engineering activities, ensuring validation status is consistently maintained...

A global biopharmaceutical company in Singapore is hiring a Validation QA responsible for overseeing manufacturing, testing, and validation activities. The role requires 8-10 years of QA experience in the Biopharma industry, with a strong knowledge of GMP requirements. Candidates must possess a relevant degree and demonstrate excellent communication, logical...

A biotech and pharmaceutical company in Singapore is seeking a Quality Assurance Specialist to develop, review, and manage Standard Operating Procedures (SOPs) as well as documentation control processes. The ideal candidate should have a solid background in Quality Assurance and GMP manufacturing documentation. Responsibilities include supporting deviations,...