Jobscope
- Provide assistance to internal customers in support of departmental functions.
- Timely escalation of issues or problems identified to direct supervisor. This includes but not limited to; system inefficiencies, the departure of business processes and/or procedures.
- Ensure timely completion of training tasks assigned in training system to be in compliant and aligned with the company's Right to Operate.
- Perform any tasks as requested or assigned by Management to support Quality oversight activities.
- Perform review and format of word documents in preparation for the approval process in Electronic Document Management System.
- Perform issuance and verification of Shop Packet according to the Process Order (PO) schedule.
- Organize for the safekeeping of site records and other documents in an electronic and physical repository;
- Support the day-to-day aspects of records management for various users, and assisting teams with administrative and/or records aspects related to the site;
- File and cross index records in chronological date-order and document number by system or project name in the records repository;
- Provide administrative support during audits and regulatory inspections.
Requirements
- Bachelor Degree in Science / Chemical Engineering or equivalent with relevant pharmaceutical experience.
- Minimum 1-3 relevant years of experience in QA/QC and GMP Compliance
- Familiar with manufacturing operations applications; six sigma and lean principles and process improvement tools.
- Thorough knowledge of GMP compliance regulations, ICH Q7a Guidelines, Good Documentation Practices and other applicable regulations.
- Proven track record of continuous improvement in quality operations or manufacturing.
All qualified applicants, please send in your resume to:
Tricia Celestine Goh (R1981653)
Recruit Express Pte Ltd | Company Reg. No. 199601303W | EA License Number: 99C4599
