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.: 02C3423Shirleen Teoh Xue Ling License No.: 02C3423 Personnel Registration No.: R22107190Please note that your response to this advertisement and communications with us pursuant to this advertisement will constitute informed consent to the collection, use and/or disclosure of personal data by ManpowerGroup Singapore for the purpose of carrying out its business, in compliance with the relevant provisions of the Personal Data Protection Act 2012. To learn more about ManpowerGroup\'s Global Privacy Policy, please visit https://www.manpower.com.sg/privacy-policy