Responsibilities:
● Providing support to training team
● Providing support to develop training materials and presentations
● Providing support to the training team in system migration activities
● Manages the day-to-day operations of site-wide learning training credit in LMS system
● Check and review training records meet the data integrity criteria
● Liaises with employees to ensure training records are complete
● Maintaining and organizing files and training records
● Support internal and External documentation such as ISO readiness and certification
● Perform any duties assigned by Supervisor/Manager
About You:
● ITE/Diploma/Bachelor in Engineering, Sciences, Business, Information Systems or equivalent. 1-2 years of experience in documentation DMS/ QA in pharma or biotech facility.
● Proven work experience as a Document Controller or similar role
● Knowledge of Electronic Document Management Systems (EDMS)
● Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a pharma or biotech facility
● Good interpersonal, communication and presentation skills.
● Must be a self-starter, fast learner, curious with strong analytical and organizational skills
● Self-motivated and willingness to learn
● Reliable, Meticulous and Responsible
● Proficient in Microsoft Office and other relevant software
● Able to work independently and as part of a team
● Strong organizational and communication skills
Notes :
Full-time/Part-time options are available
