QC Analyst

PT Beacons Pharmaceutical Industries; Kota Semarang; On-site; IDR 78,120,000 - 122,760,000; Full time

Job summary

PT Beacons Pharmaceutical Industries seeks a detail‑oriented analytical support specialist to join the quality control team. You will arrange and execute QSP for raw materials and finished products, assist QC documentation, and validate analytical methods.

You will coordinate with QA to run stability programs, monitor lab equipment and environmental controls, and manage laboratory waste. A D3 in a related field and 1 year of pharma experience are required.

Qualifications

• Diploma (D3) in Analytical Chemistry, Pharmacy, Chemistry or related field.
• Minimum 1 year of working experience in pharmaceutical, traditional medicine, or cosmetics industry.
• Familiar with analytical laboratory instruments such as HPLC, UV-Vis, and dissolution testers.
• Knowledge of analytical method validation/verification and GLP/GMP/EHS is required.
• Able to work independently and in a team; willing to work on a shift if needed.

Responsibilities

• Arrange & execute QSP for Raw Material, Finished Good, etc.
• Help QC Documentation
• Validation of Analytical Method
• Coordinate with QA to conduct stability program
• Monitoring equipment and environment in the lab
• Manage waste of laboratorio

Skills

Analytical method validation

Quality assurance

GLP/GMP/EHS knowledge

Laboratory skills

Team player

Shift work

Education

Diploma (D3) in Analytical Chemistry / Pharmacy / Chemistry

Tools

HPLC

UV-Vis Spectrophotometer

Dissolution Tester

Job description

Arrange & execute QSP for Raw Material, Finished Good, etc.

Help QC Documentation

Validation of Analytical Method

Coordinate with QA to conduct stability program

Monitoring equipment, environment lab

Manage waste of laboratorium

Qualification :

- Minimum Diploma (D3) in Analytical Chemistry, Pharmacy, Chemistry, or a related field.

- Minimum 1 year of working experience in the pharmaceutical, traditional medicine, or cosmetics industry.

- Familiar with analytical laboratory instruments, particularly HPLC, UV-Vis Spectrophotometer, Dissolution Tester, and other relevant instruments.

- Have practical knowledge and experience in analytical method validation and/or verification.

- Good understanding of GLP, CPOB/GMP, and EHS requirements.

- Able to work both independently and as part of a team.

- Willing to work on a shift system (If needed)