- Responsible for establish and direction the implementation of quality system in company activities.
- Responsible for quality of study and testing in the company activities.
- Performing the quality improvement program and quality assurance (QA) program
- Responsible for archiving the QA records.
- Responsible for updating the procedure
- Responsible for the QA audit in the clinical and analytical process
- Monitoring the corrective and preventive action for any non-conformity audit
- Responsible for monitoring in place and review clinical study.
- Conducting computer system validation
- Involve in development new system/application related to data integrity
- Responsible for other additional/special task that assigned by the superior manager
- Pharmacy Degree
- At least 1 year experience as Quality Assurance (QA) in Pharmaceutical Industry
- Willing to learn and understanding principles of GMP, GLP, GCP, GDP, and GXP
- Preferably have experiences in Quality Management System
- Creative, innovative, and self motivated
- English proficiency is preferably
- Fresh graduates are welcome to apply
Equilab International is the leader and the first Contract Research Organization (CRO) that certified by WHO Prequalification and UKMHRA in Southeast Asia region. Equilab International provides services in Bioavailability Bioequivalence Study, Clinical Research, Dermatology Testing, and Contract Analysis. Study Report has been accepted by countries in Europe including UK, Netherland, Poland, Spain, Hungary. Becoming a global player, Equilab International is excited to sow our optimism as we are committed to provide high quality research.