(Pharma Products) Inventory Quality Management Associate (Manage Products Quality/ Regulatory) Up 4K #HJC

SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES

Materials Management

• Manage and ensure products/materials are appropriately stored at the designated locations and lot status correctly assigned in the inventory system.

• Support incoming products/materials inspection activities to ensure conformance to requirements, including preparation of inspection reports.

• Authorize the release of incoming products/materials from the inventory system.

• Execute new material qualifications (eg label component), including preparation of inspection reports.

Operational Activities

• Support 100% inspection activities for potential product issues where applicable.

• Authorize approval of label print setup process in Prisym to facilitate label printing activities.

• Participate in secondary packaging in-process inspection activities to ensure the process conform to the requirements.

Training Programs

• Ensure timely completion of Compliance-Wire assigned SOP training prior to the related work activities execution.

Documentation

• Participate in SOPs development and updates to support EDMS system.

• Manage the site documentation system to ensure effective retrieval and archival of documentation.

Quality System

• Track the quality system performance indicators and establish the trend analysis.

• Participate in quality improvement initiatives assigned by management team.

Other Activities

• Participate in discussion and resolution of potential quality concerns arise in daily operational related activities.

• Report potential inconsistent work practices and non-compliance process activities.

• Participate in review and approval of equipment calibration reports for acceptance.

• Support the non-routine tasks assigned by the management team.

Education and Experience:

• Degree / Diploma preferably in Pharmaceutical or Science disciplines.

• 3+ years’ work experience in Medical / Pharmaceutical related organizations.

• Good knowledge preferably with experience in Regulatory/International Standards (eg. ISO9001, HSA Guidelines, PIC/S Guidelines, etc) will be an added advantage.

TELE me at @jacechooo or WA me at https://wa.me/+6582976283 NOW!

Interested candidates please submit your resume to [email protected]

Jace Choo Oi Kei

Personnel EA License No.: R1875164

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