Lowongan Kerja Bintan Posisi Product Quality Engineer di PT Esco Bintan Indonesia

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Perusahaan	-
Posisi
Tempat
Jenis Pekerjaan
Spesialisasi Dibutuhkan
Gaji Min	Rp. 2.000.000
Gaji Max	Rp. 8.500.000

Esco Lifesciences Group is improving lives through science! Headquartered in Singapore, expanded globally with factories and offices in 43 locations around the world, Esco is building a synergistic ecosystem of life science tools, diagnostics, therapies, and technologies to improve human lives.

With nearly 50 years of history and a strong foundation in Singapore, Esco is a dynamic, fast-growing, mid-sized multinational organization that bridges East and West. We offer a diverse, inclusive, and globally connected environment where you’ll collaborate with top experts and visionary clients worldwide. As we accelerate our global expansion, you’ll have the unique opportunity to grow your career in tandem with the company, driving innovation and shaping a healthier, more equitable, and resilient future.

Key Responsibilities

Product Quality

• Manage product quality from development to mass production.

• Maintain DHF/DMR files and ensure products follow required standards.

• Join product testing and reviews.

• Update quality plans and inspection standards.

• Ensure all quality requirements are met before product release.

Customer Quality

• Lead or support investigations for major customer complaints (8D).

• Work with Service, R&D, Manufacturing, and Technical Support on corrective actions.

• Track field performance and help reduce defect/complaint rates.

Production Quality

• Support Kaizen and quality improvement activities.

• Help improve First Pass Yield (FPY).

• Promote a quality-focused culture in production.

Supplier Quality

• Work with the Supplier Quality team to monitor incoming materials.

• Track and ensure supplier improvement actions are effective.

Engineering Change & Sustaining

• Review quality impact for engineering changes.

• Support design improvements for reliability, manufacturability, and cost.

• Participate in cross-functional problem solving.

Quality Control

• Understand IQ/OQ/PQ validation.

• Create and update SOPs, work instructions, and QC standards.

• Handle non-conformance cases.

Quality System

• Ensure compliance with ISO and medical device QMS requirements.

• Maintain quality documents and support audits.

• Analyse field data and prepare monthly quality reports for management.

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Key Requirements

• Bachelor’s degree in Mechanical, Electrical, Electronics, Biomedical, Industrial, or Chemical Engineering.

• 2–3 years’ experience in Quality Engineering or Manufacturing Engineering.

• Knowledge of root cause analysis (5 Why, Ishikawa, FTA), ISO 9001, ISO 13485, ISO 14971.

• Understanding of electronics, PCBA, sensors, and mechanical assemblies.

• Experience in CAPA, 8D, and control plans.

• Able to read drawings, schematics, and BOM.

• Good communication and documentation skills.

• Able to work with cross-functional teams and train operators/inspectors.

Preferred (Not Required)

• CQE (ASQ), Six Sigma Green Belt, or Internal Auditor certification (ISO 9001/ISO 13485).

Lamar kerja

Deskripsi Perusahaan

Info Perusahaan

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