Pharma QC Analyst - Lab Testing & Equipment QA

PT ASIA MEDIKA NUSANTARA

Kebayoran Baru

On-site

IDR 78,000,000 - 110,000,000

Full time

14 days+
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Job summary

PT Asia Medika Nusantara in Jakarta seeks a Lab Analyst to perform analytical testing on raw materials, in-process and finished products, ensuring compliance with cGMP/GLP standards and company policies. Responsibilities include calibration, maintenance, and qualification of lab instruments, with a focus on timely, accurate results.

The role requires 0–2 years in a pharma setting, familiarity with analytical instruments, and good analytical thinking.

Qualifications

  • Education background from Chemical Analyst High School or Diploma.
  • Preferably 1–2 years as Lab Analyst in multinational company; Fresh graduates are welcome.
  • Capable in QC technical, analytical method and understand cGMP & GLP.
  • Familiar with analytical instruments.
  • Good analytical thinking and attention to detail.
  • General knowledge of Pharmaceutical Industry.
  • Understand English (passive).

Responsibilities

  • Perform analytical testing using approved methods to ensure materials, in-process and finished products meet quality standards.
  • Conduct qualification and requalification (protocols and reports) of chemical laboratory equipment.
  • Perform calibration of laboratory equipment according to schedules to ensure accuracy.
  • Maintain laboratory equipment and instruments to keep assets in good working condition.
  • Drive cost-efficiency in analytical activities while adhering to budgets and guidelines.
  • Implement QEHS procedures within assigned responsibilities.
  • Perform tasks as directed by superiors.

Skills

Analytical thinking
Attention to detail
QC technical
cGMP & GLP understanding

Education

High School Chemistry/Analyst Diploma

Tools

Analytical instruments

Job description

PT Asia Medika Nusantara in Jakarta seeks a Lab Analyst to perform analytical testing on raw materials, in-process and finished products, ensuring compliance with cGMP/GLP standards and company policies. Responsibilities include calibration, maintenance, and qualification of lab instruments, with a focus on timely, accurate results.

The role requires 0–2 years in a pharma setting, familiarity with analytical instruments, and good analytical thinking.

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