Pharma QC Analyst — GMP/GLP Lab, Data & Reporting

MSN Laboratories; Daerah Khusus Ibukota Jakarta; On-site; IDR 55,800,000 - 89,280,000; Full time

Job summary

MSN Laboratories in Jakarta is seeking a QC Analyst to join our pharmaceutical quality control team. The successful candidate will conduct laboratory testing, interpret results and prepare accurate reports, ensuring GMP/GLP compliance.

You should have 1–2 years of pharma QC experience, proficiency with Excel, and the ability to collaborate with Production, QA, and Engineering. Shift availability may be required.

Qualifications

• Minimum education SMA/SMK; preferably Diploma or Bachelor's in Analytical Chemistry or related field.
• 1–2 years of QC/Lab analyst experience in pharma.
• GMP and GLP knowledge.
• Proficient in operating QC lab equipment.
• Ability to perform lab tests, interpret results and prepare reports.
• Knowledge of Excel for data processing.
• Attention to detail with strong analytical skills; able to work independently and in a team.
• Willingness to work on shift when required.
• Good communication and coordination with Production, QA, Engineering and related departments.

Skills

Attention to detail

Analytical thinking

Communication

Team collaboration

Independent work

Shift flexibility

Education

Bachelor's degree in Analytical Chemistry or related field

Diploma or degree in Analytical Chemistry or related field

Tools

Microsoft Excel

QC lab equipment handling

Job description

MSN Laboratories in Jakarta is seeking a QC Analyst to join our pharmaceutical quality control team. The successful candidate will conduct laboratory testing, interpret results and prepare accurate reports, ensuring GMP/GLP compliance.

You should have 1–2 years of pharma QC experience, proficiency with Excel, and the ability to collaborate with Production, QA, and Engineering. Shift availability may be required.