Quality Control Operator – Shift | Teliti & Dokumentasi

Pt Jumbo Power International

Jawa Barat

On-site

IDR 89,280,000 - 133,920,000

Full time

8 days ago
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Job summary

Pt Jumbo Power International invites applications for a Quality Control Analyst to join our Bekasi QA team. The role focuses on ensuring pharmaceutical products meet quality standards through analytical testing of raw materials, in-process samples, and finished products using advanced laboratory equipment.

You will operate instruments such as HPLC, GC, UV-Vis, and dissolution testers, document results meticulously, and participate in CAPAs, method validation, and CoA preparation.

Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
  • Minimum of 2 years of experience in a pharmaceutical Quality Control laboratory setting.
  • Proficiency with analytical instrumentation, particularly HPLC and GC.

Responsibilities

  • Conduct analytical testing on raw materials, intermediate products, and finished pharmaceutical goods according to approved specifications and test methods.
  • Operate and maintain laboratory instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
  • Document all testing activities accurately and meticulously in laboratory notebooks and electronic systems.
  • Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
  • Prepare Certificates of Analysis (CoAs) for released products.
  • Participate in method validation and transfer activities as required.

Skills

Attention to detail
Analytical testing
Documentation
Laboratory work

Education

Bachelor's degree in Chemistry/Biochemistry/Pharmacy

Tools

HPLC
GC
UV-Vis spectrophotometers
Dissolution testers

Job description

  • What Quality Control Operator Shift Teliti Dok...

Showing 73 Quality Control Operator Shift Teliti Dokumentasi jobs in Jakarta Utara

Quality Control Analyst - Pharmaceuticals

Our client is seeking a detail-oriented Quality Control Analyst to join their established quality assurance team in Bekasi . This role is essential for ensuring that all pharmaceutical products meet stringent quality standards before release to the market. You will perform a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment. This position offers the chance to work within a robust quality management system in the pharmaceutical industry , contributing to patient safety and product integrity within a well-respected organization.

About the Role

Our client is seeking a detail-oriented Quality Control Analyst to join their established quality assurance team in Bekasi . This role is essential for ensuring that all pharmaceutical products meet stringent quality standards before release to the market. You will perform a variety of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment. This position offers the chance to work within a robust quality management system in the pharmaceutical industry , contributing to patient safety and product integrity within a well-respected organization.

Key Responsibilities
  • Conduct analytical testing on raw materials, intermediate products, and finished pharmaceutical goods according to approved specifications and test methods.
  • Operate and maintain laboratory instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
  • Document all testing activities accurately and meticulously in laboratory notebooks and electronic systems.
  • Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
  • Prepare Certificates of Analysis (CoAs) for released products.
  • Participate in method validation and transfer activities as required.
Requirements
  • Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
  • Minimum of 2 years of experience in a pharmaceutical Quality Control laboratory setting.
  • Proficiency with analytical instrumentation, particularly HPLC and GC.
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