Job Information
Takeda Pharmaceuticals Manufacturing Services Intern in Singapore
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Job Description
Objective:
To provide a meaningful working experience for interns through on-the-job training with the Manufacturing Services (Documentation) team. The takeaway at the end of internship would be to understand the requirements of Data Integrity in the industry, and expectations of a System Administrator. The intern will also be able to participate in tech transfer activities, regulatory/safety audits and understand the end-to-end documentation support required to manufacture batches.
General Responsibilities:
Intern will be responsible for providing administrative support in all aspect of Documentation as follows: -
Master Batch Record (MBR)/Manufacturing Formulation Record (MFR) (Process/ Non-process):
Prepare and issuance of MBR/ MFR packages (include MBR/MFR, and/ or labels)
Attain operating knowledge in internal in-house system such as PRIMR (for Process Monitoring), LIMS (Sample Management) and JDE (Inventory).
Perform data interface with PRIMR but not limited to entry, verification, etc.
Perform JDE transaction
Attain knowledge in troubleshooting and rectification of JDE errors
Perform Inventory Adjustment (Scrap/discard)
Archive completed MBR/MFR
Perform updating of electronic tracking log
Controlled Copy/ Logbook Management
Check/ verify number of the controlled copies that are effective daily
Print controlled copies and replace superseded copies in the manufacturing area
Remove obsolete controlled copies from manufacturing area
Issue and archive logbook timely
Other documentation support
Formatting of Manufacturing and Engineering documents
Issuance of Ad-hoc labels (e.g. Cleaning Monitoring)
Support investigation for event and deviation
Internal/ External Document Archival
Facilitate loan out/ return of internal archived documents
Arrange for documents to be archived externally, and arrange for retrieval
Perform 5S inspection
Administrative support to Manufacturing Standalone equipment (e.g. Casy Cell Counter, BioProfile pHOx, AKTA Explorer, Filter Integrity Tester, Bag Integrity Tester)
Administer user access for Manufacturing Standalone equipment
Perform Annual User review
Routine time synchronization of system
Routine backup and archival of data
Execution of protocol/ test script requiring administrative access
Others
Compile and print JDE Error Report
Perform troubleshooting and resolve documentation related issue
Support investigation for non-conformance in Documentation area.
Actively support continuous improvement initiatives
Actively support implementation of changes to Documentation
Responsibility to adhere to any applicable EHS requirements.
Commitment to a fair and respectful relationship to others and behavior in accordance with Takeda’s Code of Conduct.
Any other duties as assigned by supervisor.
Requirements:
Team player, self-driven and able to work under pressure and good time management
Able to take initiative with problem solving skills
Excellent team player with hands-on attitude
Able to adhere to EHS/GMP requirement
Able to support production demands with adjusted work schedule
Ability to wear appropriate PPE/Cleanroom gowning as per SOP
Locations
SGP - Singapore - Woodlands
Worker Type
Employee
Worker Sub-Type
Paid Intern (Fixed Term) (Trainee)
Time Type
Full time