QC Analyst: Analytical Method Validation & Lab Compliance

PT Beacons Pharmaceutical Industries

Kota Semarang

On-site

IDR 78,120,000 - 122,760,000

Full time

4 days ago
Be an early applicant

Get more replies from employers

Send a job-specific resume in minutes.

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

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.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

QC Analyst
QC Analyst

PT Beacons Pharmaceutical Industries • Kota Semarang

On-site
IDR 78,120,000 - 122,760,000
Quality Control Staff
Quality Control Staff

PT Mersifarma TM • Sukabumi

On-site
QC Supervisor - GMP/GLP Analytical Lead
QC Supervisor - GMP/GLP Analytical Lead

PT Taisho Pharmaceutical Indonesia Tbk. • Depok

On-site
IDR 290,160,000 - 513,360,000
QC Supervisor
QC Supervisor

PT Taisho Pharmaceutical Indonesia Tbk. • Depok

On-site
IDR 290,160,000 - 513,360,000
QC IPC Analyst
QC IPC Analyst

The Modern Group • Cikande

On-site
IDR 66,960,000 - 100,440,000
Pharma Quality Control Analyst: Equipment & Compliance
Pharma Quality Control Analyst: Equipment & Compliance

Kalbe Farma • Bekasi

On-site
IDR 55,800,000 - 89,280,000
Analytical Lab Specialist | QC & Methods
Analytical Lab Specialist | QC & Methods

Golden Agri Resources • Indonesia

On-site
IDR 167,400,000 - 279,000,000
Physico-Chemical QC Analyst - Sterile & Cosmetics Lab
Physico-Chemical QC Analyst - Sterile & Cosmetics Lab

PT. Daewoong Pharmaceutical Indonesia • Cikarang

On-site
IDR 66,960,000 - 100,440,000
QC Analyst
QC Analyst

Erela • Kota Semarang

On-site
Pharma QC Analyst — GMP/cGMP, Fresh Graduates Welcome
Pharma QC Analyst — GMP/cGMP, Fresh Graduates Welcome

PT Mersifarma TM • Sukabumi

On-site