Ensure secondary assembly operations performed per SOP and PIC/S GMP applicable guidelines.
Ensure sufficient PPM inventory level to ensure no disruption to secondary assembly operations.
Responsible in creating Master Batch Packaging Record (MBPR) for Non-Pharmaceutical Products.
Introduce process improvement relevant to second assembly operations.
Housekeeping of redressing area.
Responsible in performing 100% Incoming Quality Inspection for Pharmaceutical Trade Returned Products.
Responsible in performing Sampling Incoming Quality Inspection & reporting based on Principal Artwork (as per Technical Agreement).
Responsible in reporting and follow-up on non-conforming products (Inclusive of Incoming, Outgoing, Returns, 3PL and Redressing).
Responsible in Reporting, monitoring and closing of Customer Complaints.
Responsible in monitoring and verification of warehouse temperature and Humidity Records.
Qualifications
Diploma or Bachelor's degree .
Preferably with certification in ISO 9001 and ISO 13485 standards.
Minimum 1-2 years of experiences in Quality System & Assurance or GMP / GLP will be advantageous
Effective problem-solving skills with a continuous improvement mindset.
Strong interpersonal and communication skills to collaborate effectively across functions and levels.
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