Pharma Calibration Engineer: Precision & Compliance

Pfizer; Jakarta Pusat; On-site; IDR 240,000,000 - 360,000,000; Full time

Job summary

Pfizer is seeking a Calibration Specialist at the Jakarta site to maintain instrument accuracy and regulatory compliance. You will collaborate with Manufacturing, Packaging, Quality Control, and External vendors to schedule and execute calibration activities, prepare protocols, and document results.

You will support equipment qualification, validation, and related technical tasks while upholding GMP and data integrity principles in a regulated pharmaceutical environment.

Qualifications

• Bachelor’s degree in Automation, Control or Electrical Engineering.
• Basic GMP, Data Integrity and Environmental Health and Safety knowledge.
• Understanding of instrument calibration principles.
• Familiar with validation/qualification processes in pharma.
• Ability to prepare clear, traceable technical documentation.
• Proficient computer skills and electronic records management.
• Strong interpersonal and written communication abilities.

Responsibilities

• Perform calibration activities across Manufacturing, Packaging, Laboratory and QC areas per procedures.
• Prepare, execute, and document calibration protocols, reviews, and final reports.
• Maintain calibration schedules and equipment records using CMMS/EAMS.
• Coordinate calibration with Manufacturing, Quality, Engineering and external vendors.
• Support equipment qualification, validation, commissioning, and related activities.
• Ensure GMP and Data Integrity compliant calibration documentation.

Skills

Calibration principles

Cross-functional collaboration

Documentation

Problem solving

Communication skills

Education

Bachelor’s degree in Automation, Control or Electrical Engineering

Mechanical Engineering or related field

Tools

CMMS

Enterprise Asset Management System

Job description

Pfizer is seeking a Calibration Specialist at the Jakarta site to maintain instrument accuracy and regulatory compliance. You will collaborate with Manufacturing, Packaging, Quality Control, and External vendors to schedule and execute calibration activities, prepare protocols, and document results.

You will support equipment qualification, validation, and related technical tasks while upholding GMP and data integrity principles in a regulated pharmaceutical environment.