This role is responsible to coordinate and manage QC samples (receive, retain, shipment), manage and coordinate on-site / off-site archival of QC documents, coordinate equipment maintenance and revision of related operation procedure. Role is also required to coordinate with the other departments to ensure timely delivery of samples/results and equipment maintenance performed.
As a QC-Analyst (Microbiology-Shift) you will support routine QC sampling and testing for environmental and product samples (Eg. bioburden testing, endotoxin testing, etc).
The Career Conversion Program (CCP) training period lasts for 15 months. Structured on-the-job training (OJT) will be provided and conducted at the participating companies to facilitate the application of learning and to ensure that individuals acquire necessary competencies to perform at their job.
The Lead Specialist, Compliance (Audit Management) will support Audit activities in accordance with approved SOPs / Policies for a multi-product, cGxP contract manufacturing facility