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Manufacturing 🏢 Full Time ⭐️ Terverifikasi

Staff QC - Finish Goods (Sukabumi)

Novell Pharmaceutical Laboratories
Indonesia
Estimasi Gaji
Rp 3.000.000 – Rp 5.000.000
Terbaru
Live Update
13 Juli 2026
Batas Akhir
13 Jul 2027

Deskripsi Pekerjaan

We are looking for a detail-oriented and experienced Staff QC - Finish Goods to join Novell Pharmaceutical Laboratories in Sukabumi. In this pivotal role, you will be responsible for overseeing Quality Control operations to ensure our pharmaceutical products meet rigorous industry standards and regulatory requirements. You will manage the workflow of QC analysts efficiently, troubleshoot technical analysis challenges, and collaborate with the team to ensure the correct application of Standard Operating Instructions (SOI).

Our ideal candidate is passionate about maintaining product integrity and possesses a strong background in laboratory analysis within the pharmaceutical sector. You will play a key role in our manufacturing process, ensuring every batch of finish goods is safe, effective, and compliant before reaching the market.

Tanggung Jawab

  • Oversee and manage the daily tasks of QC analysts to ensure operational efficiency and productivity.
  • Handle complex technical analysis challenges and troubleshoot laboratory issues promptly.
  • Collaborate with the QC team to ensure the correct and consistent application of Standard Operating Instructions (SOI).
  • Perform routine and non-routine testing on Finish Goods to verify quality specifications.
  • Ensure strict compliance with Good Manufacturing Practice (GMP) and company quality assurance policies.
  • Monitor and maintain laboratory equipment to ensure accurate and reliable test results.
  • Document all test results, deviations, and corrective actions accurately in accordance with regulatory standards.

Kualifikasi

  • Degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
  • Experience in Quality Control (QC) or Quality Assurance (QA) within the pharmaceutical or chemical manufacturing industry.
  • Strong understanding of GMP (Good Manufacturing Practice) and regulatory guidelines.
  • Excellent analytical skills with the ability to interpret complex technical data.
  • Proficiency in using laboratory instrumentation and software.
  • Good communication skills to effectively lead and coordinate with the analysis team.
  • Ability to work in a fast-paced environment and adhere to strict safety protocols.

Keahlian yang Dibutuhkan

Quality Control GMP Pharmaceutical Laboratory Testing Data Analysis SOP Finish Goods Regulatory Compliance Chemistry West Java

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