- Support quality systems, including On-the-floor quality oversight, deviation management, change control and ensure that the systems are managed in compliance with cGMP expectations
- Review and approve minor deviation, change controls, and other quality records such as electronic batch records, SOPs, logbooks and work orders
- Support in regulatory inspections, and interact directly with regulatory inspectors
- Supporting other QA initiatives/activities such as continuous improvement projects, supplier quality, stability program, product quality review, customer complaint investigation
- Escalate any significant event to Quality management in a timely manner
Requirements:
- Min Diploma/Degree in Quality
- Min 1 – 2 years of Quality experience in Pharmaceutical/Biotechnology
- Good communication and interpersonal skills
- Willing to learn
- Willing to go on shift work - attractive shift allowances
Interested & qualified applicants, please forward your latest CV in MS word format to [email protected]
