Job Responsibilities :

• Develop Manufacturing/Operating Instructions and necessary Standard Operating Procedures.
• Develop, maintain and troubleshoot the process control system recipe/Models.
• Ensure adherence to approved procedures and update the procedures as required, including the principles and practices of good data management (ALCOA).
• Accountable for the Good Data Management and Data integrity understanding and performance.
• Report and investigate actions or behaviors that may negatively impact the desired outcome of the GMP process or activity.
• Play an active and impactful role to deliver flawless execution for respective PCTs (e.g. API, MS, QO, Leadership, Engineering) by updating performance against metrics, highlighting & resolving issues with appropriate escalations.

Job Requirements:

• Bachelor's Degree, preferably in Chemical Engineering or degree in science with major in Chemistry
• 3 to 5 years' experience in pharmaceutical (API), with relevant manufacturing environment
• Good organization skills and attention to detail
• Ability to document clearly and concisely.
• Effective written and oral communication

Name: Teoh Xue Ling
Registration No.: R22107190
EA License No.: 02C3423

Shirleen Teoh Xue Ling License No.: 02C3423 Personnel Registration No.: R22107190

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