To gain hands-on experience in quality management systems and regulatory compliance for medical device manufacturing while supporting the QA/RA team in daily operations.
Key Responsibilities:
Assist in preparing, reviewing, and maintaining QA/RA documentation (SOPs, records, reports).
Support activities related to ISO 13485, GMP, and regulatory compliance.
Assist in internal audits, supplier audits, and document control.
Support product registration, licensing, and regulatory submissions.
Participate in quality improvement projects.
Perform administrative tasks as assigned by the QA/RA team.
Qualifications & Requirements:
Open to students who are
looking for an internship placement
(Degree/Diploma in Science, Biotechnology, Engineering, or related field).
Basic knowledge of quality systems and regulatory standards (ISO 13485 is an advantage).
Detail-oriented, organized, and willing to learn.
Good communication skills (English & Bahasa Malaysia).
Interested candidates may drop an email to: hroffice.medisafe@gmail.com
Job Type: Contract
Contract length: 6 months
Pay: From RM600.00 per month
Work Location: In person
Beware of fraud agents! do not pay money to get a job
MNCJobz.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.