Takeda
Pharma
QCSpecialist–RawMaterial&PackagingMaterial
Neural analysis suggests this role is
optimal for Junior candidates.
“QC Specialist – Raw Material & Packaging Material at Takeda. Skills: raw and packaging material testing, laboratory investigations, analytical, MS Excel. Schedule incoming material sampling, identification, and testing activities. Verify testing reports to ensure data integrity and compliance with established analytical procedures for raw and packaging material testing. Support activities related to alternating or secondary sources of materials in the QC Laboratory. Support the preparation and a”
Industry & Context.
CAPA; CCR action task
What They're Looking For.
Must Have
Associate's degree/ Bachelor of Pharmacist. Min. 1 year in QC Specialist or or in a closely related position. Have necessary laboratory skills. Good English competency (reading, listening and speaking). analytical, communication and interpersonal skills. Proficient in MS Word, Excel and PowerPoint
What You'll Do.
Schedule incoming material sampling, identification, and testing activities.
Verify testing reports to ensure data integrity and compliance with established analytical procedures for raw and packaging material testing.
Support activities related to alternating or secondary sources of materials in the QC Laboratory.
Support the preparation and availability of registration documents required from the QC Department.
Create and revise specifications for packaging materials and raw materials.
Support the completion of CAPA and CCR action task.
Support the creation and revision of SOPs, conduct periodic reviews of local SOPs, and perform gap assessments against Global SOPs.
Manage laboratory operational activities, including Excel spreadsheet control, routine logbook review, periodic backup of QC instruments, and management of reagents and standards.
Serve as Lead Investigator for laboratory investigations and deviations.
Contribute to the implementation of energy-saving initiatives within the assigned work area.
Ensure EHS rules are properly implemented by teams within their respective work areas, in the capacity of EHS Committee Member and Chemical Occupational Health & Safety (OHS) Officer.
Participate in internal audits as required.
How You'll Work.
Communication Scope
Good English competency
Full Job Description
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s [Privacy Notice](https://jobs.takeda.com/privacynotice) and [Terms of Use](https://www.takeda.com/terms-and-conditions/). I further attest that all information I submit in my employment application is true to the best of my knowledge. ## **Job Description** **Duties & Responsibility** 1\. Schedule incoming material sampling, identification, and testing activities. 2\. Verify testing reports to ensure data integrity and compliance with established analytical procedures for raw and packaging material testing. 3\. Support activities related to alternating or secondary sources of materials in the QC Laboratory. 4\. Support the preparation and availability of registration documents required from the QC Department. 5\. Create and revise specifications for packaging materials and raw materials. 6\. Support the completion of CAPA and CCR action task. 7\. Support the creation and revision of SOPs, conduct periodic reviews of local SOPs, and perform gap assessments against Global SOPs. 8\. Manage laboratory operational activities, including Excel spreadsheet control, routine logbook review, periodic backup of QC instruments, and management of reagents and standards. 9\. Serve as Lead Investigator for laboratory investigations and deviations. 10\. Contribute to the implementation of energy-saving initiatives within the assigned work area. 11\. Ensure EHS rules are properly implemented by teams within their respective work areas, in the capacity of EHS Committee Member and Chemical Occupational Health & Safety (OHS) Officer. 12\. Participate in internal audits as required. **Requirement** • Associate's degree/ Bachelor of Pharmacist • Min. 1 year in QC Specialist or or in a closely related position • Have necessary laboratory skills • Good English competency (reading, listening
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