2,025 Qc Specialist jobs in Indonesia

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*Job Description

Duties & Responsibilities : *

• Responsible as coordinator of stability study activities of finished product, including creating stability protocol, sample request, product sampling from chamber, review testing report, creating stability report, archiving stability study testing report, and monitoring of stability chamber and stability room.
• Responsible as Lead Investigator for Laboratory Event and Deviation.
• Self-inspection coordinator for QC chemical lab.
• Support PQR completion by providing stability data and evaluation as required.
• Support qualification activities of new QC Equipment/ Instrument (support AIQ/CSV).
• Ensure availability of reagenVconsumable/RS/WS for testing purposes as well as its compliance.
• Ensure temperature monitoring in Chemical QC Lab and conduct instrument data backup ex. Manual back up, log tag etc.
• Perform relevant Global SOP Gap Assessment, creating new or revise SOP, perform SOP periodic review at site.
• Ensure5S,GoodDocumentationPracticeanddataintegrityprinciplesareimplementedatQCChemicalLaboratoryarea.
• Support reviewing testing result for Finished Goods according to lead time.

*Requirements : *

• Fresh graduates or minimum has 1 year experience in Quality Control
• Bachelor ofPharmacist or any relevant major
• Good understanding about GMP and GLP
• Have necessary laboratory skills, including knowledge of how to perform analytical chemistry, instrumental analysis and physical chemistry
• Good English competency (reading, listening and speaking)
• Proficient in MS Word, Excel and PowerPoint

*Locations

Bekasi, Indonesia Worker Type

Employee Worker Sub-Type

Regular Time Type *

Full time

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 and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

• Responsible as coordinator of stability study activities of finished product, including creating stability protocol, sample request, product sampling from chamber, review testing report, creating stability report, archiving stability study testing report, and monitoring of stability chamber and stability room.
• Responsible as Lead Investigator for Laboratory Event and Deviation.
• Self-inspection coordinator for QC chemical lab.
• Support PQR completion by providing stability data and evaluation as required.
• Support qualification activities of new QC Equipment/ Instrument (support AIQ/CSV).
• Ensure availability of reagenVconsumable/RS/WS for testing purposes as well as its compliance.
• Ensure temperature monitoring in Chemical QC Lab and conduct instrument data backup ex. Manual back up, log tag etc.
• Perform relevant Global SOP Gap Assessment, creating new or revise SOP, perform SOP periodic review at site.
• Ensure 5S, Good Documentation Practice and data integrity principles are implemented at QC Chemical Laboratory area.
• Support reviewing testing result for Finished Goods according to lead time.

• Fresh graduates or minimum has 1 year experience in Quality Control
• Bachelor of Pharmacist or any relevant major
• Good understanding about GMP and GLP
• Have necessary laboratory skills, including knowledge of how to perform analytical chemistry, instrumental analysis and physical chemistry
• Good English competency (reading, listening and speaking)
• Proficient in MS Word, Excel and PowerPoint

Bekasi, Indonesia

Employee

Regular

Full time

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 and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description:
Duties & Responsibilities :

• Responsible as coordinator of stability study activities of finished product, including creating stability protocol, sample request, product sampling from chamber, review testing report, creating stability report, archiving stability study testing report, and monitoring of stability chamber and stability room.
• Responsible as Lead Investigator for Laboratory Event and Deviation.
• Self-inspection coordinator for QC chemical lab.
• Support PQR completion by providing stability data and evaluation as required.
• Support qualification activities of new QC Equipment/ Instrument (support AIQ/CSV).
• Ensure availability of reagenVconsumable/RS/WS for testing purposes as well as its compliance.
• Ensure temperature monitoring in Chemical QC Lab and conduct instrument data backup ex. Manual back up, log tag etc.
• Perform relevant Global SOP Gap Assessment, creating new or revise SOP, perform SOP periodic review at site.
• Ensure 5S, Good Documentation Practice and data integrity principles are implemented at QC Chemical Laboratory area.
• Support reviewing testing result for Finished Goods according to lead time.

Requirements :

• Fresh graduates or minimum has 1 year experience in Quality Control
• Bachelor of Pharmacist or any relevant major
• Good understanding about GMP and GLP
• Have necessary laboratory skills, including knowledge of how to perform analytical chemistry, instrumental analysis and physical chemistry
• Good English competency (reading, listening and speaking)
• Proficient in MS Word, Excel and PowerPoint

Locations:
Bekasi, Indonesia

Worker Type:
Employee

Worker Sub-Type:
Regular

Time Type:
Full time

Lokasi: Bogor, Citereup

Bertanggung jawab atas perancangan sistem MEP untuk proyek konstruksi bangunan yang sedang berlangsung, termasuk sistem HVAC, perpipaan, drainase, pencegahan kebakaran, dan sistem listrik, memastikan kepatuhan terhadap kualifikasi yang ditetapkan oleh manajemen dan pematuhan terhadap jadwal yang telah ditetapkan.

Anda akan bertanggung jawab atas perancangan sistem MEP dan memastikan kepatuhan terhadap standar kualitas, spesifikasi teknis, dan jadwal proyek.

• Mengawasi seluruh pekerjaan MEP pada proyek serta infrastruktur makro dan mikro, memastikan kepatuhan terhadap standar kualitas dan keselamatan.
• Memastikan pelaksanaan pekerjaan sesuai dengan spesifikasi dan rencana teknis yang ditetapkan.
• Memberikan arahan teknis yang jelas terkait metode kerja, kebutuhan tenaga kerja, dan pengelolaan subkontraktor kepada pihak kontraktor.
• Melaksanakan proses joint commissioning dan full test untuk sistem MEP guna memastikan kelayakan dan kesiapan operasional sebelum serah terima.
• Melakukan supervisi berkelanjutan atas pekerjaan MEP setelah proses Berita Acara Serah Terima (BAST) untuk memastikan kelangsungan fungsi sistem.
• Menyusun dan melaporkan aktivitas harian terkait pekerjaan MEP secara tertib dan akurat, termasuk progres dan potensi masalah.

• Pendidikan minimal S1 Sarjana Teknik Mesin, Teknik Elektro, atau Teknik Sipil dengan fokus pada sistem MEP.
• Dapat berkomunikasi dalam Bahasa Inggris
• Pengalaman kerja minimal 5 tahun di bidang teknik M/E/P, dengan fokus pada proyek konstruksi.
• Memahami prinsip dan implementasi Keselamatan dan Kesehatan Kerja (K3) di lapangan.
• Mampu mengoperasikan AutoCAD, Microsoft Office, dan Google Workspace, terutama untuk keperluan perhitungan teknik elektro/mekanikal.
• Menguasai spesifikasi material dan memiliki kemampuan dalam penyusunan rencana kerja proyek konstruksi.
• Memiliki pengalaman bekerja di perusahaan Konstruksi.

TANGGUNG JAWAB UTAMA

1. Quality & Compliance (Berbasis Prinsip ISO)

• Menyusun, mengimplementasikan, dan memelihara SOP untuk area: procurement, produksi, quality control, logistik, dan digital solution.
• Menerapkan prinsip ISO (dokumen kontrol, corrective action, risk management) secara sederhana dan praktis tanpa perlu sertifikasi formal.
• Memastikan standar mutu diterapkan pada vendor, kontrak, dan syarat & ketentuan kerja sama.
• Melakukan audit internal sederhana (health check) untuk mengidentifikasi ketidaksesuaian (non-conformity).
• Mendorong perbaikan berkelanjutan (continuous improvement) dengan siklus Plan–Do–Check–Act (PDCA).

2. Data & Reporting (Power BI)

• Mengumpulkan dan memvalidasi data operasional dari procurement, produksi, QC, logistik, dan sistem digital.
• Memastikan data yang masuk konsisten dan akurat.

• Membangun dan memelihara dashboard Power BI untuk memantau:

• Kinerja vendor

• Perbandingan order vs. delivery timeline
• Tingkat kelulusan/penolakan QC
• Efisiensi biaya dan utilisasi anggaran
• KPI pelayanan pelanggan
• Menyusun laporan manajemen bulanan/triwulan berbasis Power BI.
• Mengotomatiskan alur data (jika memungkinkan) agar mengurangi input manual.

3. Dukungan Lintas Divisi

• Memberikan pelatihan kepada staf mengenai kepatuhan SOP dan tata cara input data yang benar.
• Bekerja sama dengan tim digital/IT untuk mengintegrasikan data ERP/CRM ke Power BI.
• Menyajikan hasil analisis dan tren kepada manajemen sebagai dasar pengambilan keputusan.

KUALIFIKASI

1. Pendidikan minimal S1 semua jurusan
2. Pengalaman minimal 3–5 tahun di bidang Quality Assurance / Quality Control
3. Memiliki sertifikasi Lead Auditor ISO 9001 (lebih diutamakan bila juga memahami ISO 14001 / ISO
4. Kemampuan memimpin tim, komunikasi, dan koordinasi yang baik.
5. Teliti, detail, analitis, dan mampu memberikan rekomendasi perbaikan yang konstruktif
6. Bertanggung jawab dan memiliki integritas tinggi

TANGGUNG JAWAB UTAMA

1. Quality & Compliance (Berbasis Prinsip ISO)

• Menyusun, mengimplementasikan, dan memelihara
  SOP
  untuk area: procurement, produksi, quality control, logistik, dan digital solution.
• Menerapkan prinsip ISO (dokumen kontrol, corrective action, risk management) secara
  sederhana dan praktis
  tanpa perlu sertifikasi formal.
• Memastikan standar mutu diterapkan pada
  vendor, kontrak, dan syarat & ketentuan
  kerja sama.
• Melakukan audit internal sederhana (health check) untuk mengidentifikasi ketidaksesuaian (non-conformity).
• Mendorong perbaikan berkelanjutan (continuous improvement) dengan siklus
  Plan–Do–Check–Act (PDCA)
  .

2. Data & Reporting (Power BI)

• Mengumpulkan dan memvalidasi data operasional dari procurement, produksi, QC, logistik, dan sistem digital.
• Memastikan data yang masuk konsisten dan akurat.
• Membangun dan memelihara
  dashboard Power BI
  untuk memantau:
• Kinerja vendor
• Perbandingan order vs. delivery timeline
• Tingkat kelulusan/penolakan QC
• Efisiensi biaya dan utilisasi anggaran
• KPI pelayanan pelanggan
• Menyusun laporan manajemen bulanan/triwulan berbasis Power BI.
• Mengotomatiskan alur data (jika memungkinkan) agar mengurangi input manual.

3. Dukungan Lintas Divisi

• Memberikan pelatihan kepada staf mengenai kepatuhan SOP dan tata cara input data yang benar.
• Bekerja sama dengan tim digital/IT untuk mengintegrasikan data ERP/CRM ke Power BI.
• Menyajikan hasil analisis dan tren kepada manajemen sebagai dasar pengambilan keputusan.

KUALIFIKASI

1. Pendidikan minimal S1 semua jurusan
2. Pengalaman minimal 3–5 tahun di bidang Quality Assurance / Quality Control
3. Memiliki sertifikasi Lead Auditor ISO 9001 (lebih diutamakan bila juga memahami ISO 14001 / ISO
4. Kemampuan memimpin tim, komunikasi, dan koordinasi yang baik.
5. Teliti, detail, analitis, dan mampu memberikan rekomendasi perbaikan yang konstruktif.
6. Bertanggung jawab dan memiliki integritas tinggi.

About Us

PT Golden Victory Manufactures, we are part of a big company; stella Group international based in China ).

Currently, we are in the process of establishing a new factory in Pemalang Regency - Central Java, which is engaged in the sports shoe industry

Position : Quality Management

Placement : Central Java, Pemalang

Qualifications :

1. At least an Associate's Degree (D3).
2. Proficient in English, both oral and written.
3. 1–2 years of experience in Quality Assurance/Quality Control (preferably in the footwear/textile industry).
4. Good understanding of basic quality system concepts and product inspection.
5. Skilled and experienced in using Microsoft Office.
6. Detail-oriented, honest, and disciplined.
7. Strong interpersonal skills and adaptability.

Willing to work in Pemalang and attend training in Solo, Central Java

Benefit

1. Competitive Salary
2. Bonus
3. BPJS Kesehatan + BPJS Ketenagakerjaan
4. THR
5. Dormitory
6. Meals

*Noted :

1. Temporary Placement : Surakarta (Solo)
2. Permanent Placement : Pemalang
3. Can Join our team before 20 October 2025

Job Desc

1. Menyusun dan mengimplementasikan kebijakan, sistem, serta target mutu perusahaan.
2. Memastikan proses produksi berjalan sesuai standar ISO atau regulasi terkait.
3. Memimpin tim QA/QC dalam melakukan inspeksi, audit, dan pengujian kualitas produk.
4. Menetapkan prosedur inspeksi bahan baku, proses produksi, dan produk akhir.
5. Mengidentifikasi potensi perbaikan dan menurunkan tingkat defect melalui analisa 5 Why, Fishbone, dan FMEA.
6. Mendorong implementasi program Quality Improvement dan Kaizen .
7. Bekerja sama dengan tim produksi, Engineering, dan supply chain untuk memastikan kualitas di seluruh rantai pasok.
8. Menyusun laporan kualitas dan memberikan rekomendasi strategis kepada manajemen.
9. Melatih dan mengembangkan kompetensi tim QA/QC.
10. Memastikan kepatuhan terhadap standar mutu, regulasi industri, dan audit eksternal.