Job Desciptions:

• Develop Manufacturing/Operating Instructions and necessary SOPs.
• Develop and maintain the process control system models.
• Investigate the findings quality and EHS related issues observed during manufacturing or batch record review.
• Lead safety investigations and execute CAPA after the investigations.
• Implement and monitor robust preventive measures for processing issues.
• Provide operating instruction and process training to operations, process team, quality operations and engineering.
• Own one/multiple equipment/GMP systems in production and present the system overview with evidence compliance to internal and external auditors.
• Accountable for Good Data Management (ALCOA) and Data Integrity.

Job Requirements:

• Bachelor's Degree preferably in Chemical Engineering or degree in science
• At least 5 years' experience in pharmaceutical (API), with relevant manufactuing environment for senior position
• Working knowledge for FDA and GMP

We regret that shortlisted candidates will be notified.
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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