Job Responsibilities
- 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.
