Assist with the implementation and maintenance of the Quality Management System in accordance with ISO 9001 and 13485 standards, and in compliance with the H.S.A GDP Guidelines.
Provide support for investigation into non-conformances and customer complaints.
Maintenance and Follow-up on Corrective Actions and Preventive Actions (CAPAs).
Provide the trainings and coordinate the trainings for the staff.
Registration of the trainings into the electronic Quality Management System (eQMS) and running of reports.
Assist with the documentation review after an operational activity.
Collection of Temperature Data and Monitoring of the temperature environmental conditions.
Reporting of day-to-day activities.
Take care of and communicate with internal and external contacts.
Control administrational aspects of the facility (e.g. archiving).
Promote a quality culture within the company.
Performing physical checks for GMP and GDP related processes
Job Requirements
Possess at least a Diploma in Pharmacy, Life Sciences or relevant fields.
Possess at least 2 years of pharmaceutical science work experience (or prior Life Science internship experience) is preferable .
Experience with ISO 13485 standards is an advantage.
Knowledge of GMP and/ or GDP guidelines is an advantage.
Able to work in a fast-paced environment
Work well independently/with minimal supervision and with others in a team
Proficient in Microsoft Office especially Excel
Candidate needs to be based in Singapore and comfortable working out of Gul facility
