Quality Control Supervisor: Inspector/Operator Expert

Pt Citra Tubindo Tbk; Batam; On-site; IDR 90,000,000 - 180,000,000; Full time

Benefits offered by this job

Competitive salary

Health insurance

Professional development

Job summary

Pt Citra Tubindo Tbk seeks a Pharmaceutical Quality Control Analyst to perform lab testing of materials and products, analyze results, and report deviations. The role requires GLP-compliant calibration maintenance and active participation in method validation and data review.

The candidate should have a relevant science degree and 2+ years of QC/QA experience, with familiarity in HPLC, GC, UV-Vis, and titration. Batam-based, full-time position.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• 2+ years of experience in pharmaceutical quality control or quality assurance.
• Experience with cGMP and ICH guidelines and regulatory requirements.

Responsibilities

• Perform laboratory tests on raw materials, in-process samples, and finished products using established analytical methods and instrumentation.
• Analyze test results, document findings accurately, and report deviations or out-of-spec results to management.
• Maintain calibration and logs for laboratory equipment in compliance with GLP.
• Participate in method validation and transfer of new analytical procedures.
• Review batch records and QC data to ensure adherence to protocols and regulatory standards.

Skills

Analytical reasoning

Documentation

Attention to detail

Education

Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field

Tools

HPLC

GC

UV-Vis spectrophotometry

Titration

Job description

Pharmaceutical Quality Control Analyst

Location: Batam

Contract: Full-time, Permanent

• Perform a variety of laboratory tests on raw materials, in-process samples, and finished products using established analytical methods and instrumentation.
• Analyze test results, document findings accurately, and report any deviations or out-of-specification results to management.
• Maintain laboratory equipment calibration and performance logs, ensuring compliance with Good Laboratory Practices (GLP).
• Participate in method validation and transfer activities for new analytical procedures.
• Review batch records and quality control data to ensure adherence to manufacturing protocols and regulatory standards.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Proven experience (2+ years) in pharmaceutical quality control or quality assurance.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, and titration.
• Strong understanding of cGMP, ICH guidelines, and regulatory requirements for pharmaceutical manufacturing.
• Excellent documentation skills and attention to detail, with the ability to interpret complex data.

Benefits

• Competitive annual salary commensurate with experience.
• Comprehensive health, dental, and vision insurance plans.
• Opportunities for professional development and training in pharmaceutical quality assurance.
• Paid time off and public holiday allowances.
• A collaborative and safety-focused work environment in Batam.