- Location
- IDN - BEKASI - FACTORY, Indonesia
- Type
- Full-time
- Education
- Bachelor
- Source
- Workday
Description
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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 and speaking)
• Strong analytical, communication and interpersonal skills
• Proficient in MS Word, Excel and PowerPoint
Locations
Bekasi, IndonesiaWorker Type
EmployeeWorker Sub-Type
Fixed Term (Fixed Term)Time Type
Full timeSkills
ExcelCompliance