Quality Control Engineer

Selamat Datang di Situs Lowongan Kerja Indonesia Terbaru 2026 dan Saat ini kami ingin memberitahukan Info Terbaru Mengenai Informasi Loker dari Perusahaan Fapon dengan posisi Quality Control Engineer. Untuk selengkapnya silahkan baca deskripsi lowongan kerja di bawah ini dengan seksama dan teliti, beserta persyaratan minimal lowongan kerja di yang telah tertera dan dijelaskan di bawah ini.

Fapon melalui program rekrutmennya saat ini sedang membuka lowongan kerja untuk posisi Quality Control Engineer di West Java yang bertujuan untuk meningkatkan kinerja operasional di dalam maupun luar kantor Fapon. Perusahaan Tersebut sedang mencari calon tenaga kerja yang siap diterjunkan ke setiap divisi bagian perusahaan yang sesuai dengan posisi, kemampuan dan keahlian para pencari kerja tersebut. Berikut ini adalah detail lengkap persyaratan untuk posisi Quality Control Engineer di West Java Perusahaan Fapon:

Job descriptions :

1.Responsible for the testing of product raw materials, semi-finished products, finished products and retained samples

2. Responsible for workshop environmental monitoring and sampling and microbiological inspection.

3. Responsible for quality control product management.

4. Responsible for laboratory maintenance and management.

5. Responsible for the verification work.

6. Responsible for the experimental analysis and investigation of abnormal quality and customer complaints.

7. To be responsible for the connection of product production transfer, quality standards, technical documents drafting, research and development of transfer technical documents to give review opinions.

8. Responsible for Product stability testing and clinical sample handling

Job requirements :

1. Education & major: Bachelor degree or above on Bioengineering, Health analyst school, biotechnology, or biology-related majors (D3/S1 or above)

2.training record:

◆ Laboratory management-related training.

◆ Biochemical and luminescence technology principle related training experience.

◆ Training of drugs, medical devices, in vitro diagnostic reagents, standards and quality management regulations

◆ Have a blood draw certificate

3.experience:

◆ More than 3 years working in clinical laboratories or similar, able to operate analytical instruments such as:, biochemical, luminous (ELISA, CLIA, etc) related quality testing work experience.

◆ Nucleic acid diagnosis, biochemical, luminescence detection reagent detection experience is preferred.

◆ Theoretical knowledge related to biology, familiar with and master the biological experimental skills, strong practical ability, understand the basic operation and experimental skills;

◆ Establish the quality standard experience according to the product technical standard requirements.

4.basic skill:

◆ Have certain organization, coordination and communication skills;

◆ Proficient in using various kinds of professional office software, biochemical, luminous analysis software.

◆ Practical and willing, strong sense of responsibility, love quality work, good team spirit and cooperation spirit.

◆ Obey the arrangement and management of the company, and complete the temporary tasks assigned by the superior.

◆ Able to speak English actively and professionally