QA OFFICER

Responsibilities:

• Coordination of release system, including the release of incoming raw materials and finished products
• Perform cross funcational investigations and follow-up with CAPA
• Perform internal audits and supplier qualification
• Manage documentation control
• Coordinate test request and sample workflow
• Provide quality assurance checks for manufacturing plants
• Liaise with contract manufacturer on product requirements
• Coordinate stability programme in accordance to regulatory requirements
• Support execution of qualification and validation protocols
• Assist in provision of services as a contract laboratory
• Support regulatory submissions and external audits
• Perform any ad-hoc tasks when required

Requirements:

• A good degree in biotechnology / chemistry / microbiology / pharmaceutical sciences / biomedical science or relevant life sciences
• Meticulous, driven and resourceful with excellent people skills
• At least 3 years of experience in a GMP environment
• Knowledge of qualification / validation is preferred

Please provide the following:

• Reasons for leaving past & present employment
• Last drawn/current and expected salaries
• Your earliest availability

Please email your resumes to jobs@lynkbiotech.com. We regret that only shortlisted candidates will be notified.