Responsibilities
Compile and prepare document of Medical Device File for every Medical device products produced by RLI are in accordance with applicable standard.
Ensure the registration document available and submitted within timeline.
Ensuring compliance for implementation qualification validation in medical device according to with applicable standard requirements and applicable regulations.
Arrange product quality review for medical device that manufactured in RLI facilities.
Qualifications
Candidate must possess at least a Bachelor's Degree in Pharmacy, preferably a licensed pharmacist with a minimum GPA of 3.00 of 4.00
Good knowledge of GMP and QMS
Computer literate and proficient in English
Placement in Padalarang, Bandung