Lowongan Kerja Jakarta Raya Posisi Qa Specialist di Teva Pharmaceutical USA

• Review accurately product data which will be released or rejected based on their specification to certify product that will be released accurate according to specified quality and marketing authorization
• Coordinate execution of product document review according to the priority
• Ensure the completion of product documents for disposition process
• Ensure the archiving of product documentation
• Upload product documentation into the SharePoint
• Perform investigation and risk assessment as required
• Review the implementation of GMP aspects in the shop floor
• Responsible for checking all retained samples based on procedure
• Review the MPPCR and any other related documents prior to use for manufacturing and packaging process

Other tasks:

• Prepare and maintain product documents particularly and other documents generally which deal with team responsibilities according to cGMP, EHS policy and Corporate policy
• Ensure that medicinal products are distributed in accordance with GDP standard
• Implement cGMP, GDP and QEHS policy in the working area
• Consider cost effectively in all department activities so it will not exceed the specified budget