Senior Quality Specialist-Qualification

Responsibilities:

.Lead a small team to execute and carry out the tasks at the client site.

.Will be the point of contact with the client, liaising in term of the project status and etc.

.Ensure that timeline from client on the various stages of the project are met.

.Execute baseline environmental monitoring, and EMPQ for classified cleanrooms (Grade C/D), and clean air devices (Grade A/B/C/D) for manufacturing lines.

.Complete qualification documents during execution of qualification.

.Participate in variation investigation and/or deviations.

.Compliance in project documentation based on required quality level e.g. (but not limited to), completing the record during execution in real time, correction of documentation errors.

Requirements:

.Minimum Diploma in Engineering/Sciences or relevant discipline.

.At least 5 years of relevant working experience in GMP pharmaceutical industry with cleanroom experience.

.Familiar with aseptic techniques/behaviors.

.Experienced in performed environmental monitoring.

.Willing to travel to Tuas.

Contract Duration: 6 months