Pfizer

Calibration Specialist

Posted Yesterday

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DKI Jakarta, IDN

In-Office

Entry level

Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical

We’re in relentless pursuit of breakthroughs that change patients’ lives.

The Role

Perform and document calibration activities for manufacturing, laboratory, facility, and utility equipment at Pfizer’s Jakarta site. Maintain calibration schedules and electronic equipment records, support qualification, validation, commissioning, cleanroom testing, investigations, CAPA, change controls, and audits. Coordinate with cross-functional teams and external vendors while ensuring compliance with GMP, data integrity, EHS, quality standards, and regulatory requirements.

Summary Generated by Built In

Engineering plays a vital role in ensuring that our manufacturing equipment, laboratories, facilities, and utility systems operate reliably and in compliance with regulatory requirements. By joining our Engineering team as a Calibration Specialist, you will help maintain the accuracy, integrity, and compliance of instruments and equipment that support the manufacture and testing of medicines.
Your technical expertise, attention to detail, and commitment to quality will help ensure that calibration activities are completed safely, accurately, and on schedule. Through close collaboration with Manufacturing, Packaging, Quality Control, Technical Services, Warehouse, and external service providers, you will contribute to reliable operations and help ensure that patients receive the medicines they need.
What You Will Achieve
In this role, you will:

Perform calibration activities for instruments and equipment across Manufacturing, Packaging, Laboratory, Quality Control, Technical Services, and Warehouse areas at the Jakarta site.
Execute calibration activities in accordance with approved procedures, established schedules, applicable regulatory requirements, and Pfizer quality standards.
Prepare, execute, and document calibration protocols, periodic reviews, and final reports accurately and within the required timelines.
Maintain calibration schedules and equipment records using the Computerized Maintenance Management System or Enterprise Asset Management System.
Coordinate calibration schedules and activities with Manufacturing, Quality, Engineering, Technical Services, Warehouse, and other relevant departments.
Support equipment qualification, validation, commissioning, and related technical activities in collaboration with the Technical Services and Engineering teams.
Support the maintenance and verification of manufacturing equipment, laboratory equipment, and cleanroom systems, including HEPA filter integrity testing, air change rate measurement, and air balancing.
Support the development, implementation, and maintenance of calibration procedures, records, and other controlled documentation.
Ensure calibration documentation is complete, accurate, traceable, and compliant with current Good Manufacturing Practices and Data Integrity requirements.
Support the timely execution and closure of Corrective and Preventive Actions, change requests, and other quality commitments related to calibration activities.
Coordinate with qualified external vendors for outsourced calibration services and the purchase, repair, or replacement of instruments.
Follow up on the review and approval of documents associated with calibration activities.
Participate as an auditee and provide the required documentation and technical explanation during regulatory, internal, customer, BPOM, and global audit activities.
Maintain compliance with Pfizer Quality, Environmental Health and Safety, and regulatory requirements while performing all assigned activities.
Contribute to continuous improvement initiatives that enhance calibration effectiveness, equipment reliability, compliance, and operational efficiency.
Organize assigned activities, manage priorities, and deliver individual commitments within agreed timelines.

Here Is What You Need (Minimum Requirements)

Bachelor's degree in Automation, Control or Electrical Engineering. Mechanical Engineering, or another relevant engineering discipline with related experienced are welcome to apply
Basic knowledge of current Good Manufacturing Practices, Data Integrity principles, and Environmental Health and Safety requirements.
Understanding of instrument calibration principles and practices.
Basic understanding of equipment validation and qualification processes within the pharmaceutical or another regulated industry.
Ability to follow approved procedures and prepare clear, accurate, and traceable technical documentation.
Demonstrated computer and technical skills, including the ability to maintain electronic equipment records and schedules.
Effective problem-solving skills and the ability to identify and escalate calibration or equipment-related issues.
Good interpersonal, verbal, and written communication skills.
Ability to collaborate effectively with cross-functional teams and external service providers.
Ability to organize work, manage priorities, and complete assigned commitments within established timelines.

Bonus Points If You Have (Preferred Requirements)

Experience performing calibration activities in the pharmaceutical, biopharmaceutical, medical device, or another regulated manufacturing industry.
Experience working in a current Good Manufacturing Practices environment.
Knowledge of calibration standards, measurement principles, instrument traceability, and calibration documentation.
Experience using a Computerized Maintenance Management System or Enterprise Asset Management System to schedule and document calibration activities.
Experience supporting equipment qualification, validation, commissioning, or periodic review activities.
Experience supporting HEPA filter integrity testing, air change rate measurement, cleanroom testing, or air balancing activities.
Experience supporting investigations, Corrective and Preventive Actions, change controls, and audit commitments.
Experience coordinating calibration activities with external contractors or equipment vendors.
Experience participating in regulatory, customer, or internal audits.
Strong organizational skills and attention to detail.
Ability to work independently while collaborating effectively as part of a cross-functional team.
A proactive, accountable, and continuous improvement mindset.
Ability to adapt priorities in response to operational and business requirements.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Engineering

Skills Required

Bachelor’s degree in Automation, Control, Electrical, Mechanical, or another relevant engineering discipline
Basic knowledge of current Good Manufacturing Practices, Data Integrity principles, and Environmental Health and Safety requirements
Understanding of instrument calibration principles and practices
Basic understanding of equipment validation and qualification processes in pharmaceutical or regulated industries
Ability to follow approved procedures and prepare clear, accurate, traceable technical documentation
Computer and technical skills, including maintaining electronic equipment records and schedules
Problem-solving skills and ability to identify and escalate calibration or equipment-related issues
Good interpersonal, verbal, and written communication skills
Ability to collaborate with cross-functional teams and external service providers
Ability to organize work, manage priorities, and complete commitments within established timelines
Experience performing calibration in pharmaceutical, biopharmaceutical, medical device, or regulated manufacturing industries
Experience working in a current Good Manufacturing Practices environment
Knowledge of calibration standards, measurement principles, instrument traceability, and calibration documentation
Experience using a Computerized Maintenance Management System or Enterprise Asset Management System
Experience supporting equipment qualification, validation, commissioning, or periodic reviews
Experience supporting HEPA filter integrity testing, air change rate measurement, cleanroom testing, or air balancing
Experience supporting investigations, Corrective and Preventive Actions, change controls, and audit commitments
Experience coordinating calibration activities with external contractors or equipment vendors
Experience participating in regulatory, customer, or internal audits
Strong organizational skills and attention to detail
Ability to work independently while collaborating effectively on a cross-functional team
Proactive, accountable, and continuous improvement mindset
Ability to adapt priorities to operational and business requirements

What the Team is Saying

Pfizer Compensation & Benefits Highlights

Healthcare Strength — Health coverage is described as comprehensive across medical, dental, vision, and mental‑health support, with strong plan options and provider networks. Feedback suggests these programs are a clear standout within the total rewards package.
Retirement Support — Retirement programs feature a 401(k) with company matching plus an additional company retirement contribution. Feedback suggests these elements are consistently highlighted as valuable components of overall compensation.
Leave & Time Off Breadth — Paid vacation, holidays, and sick time are often characterized as generous, with some locations offering the ability to purchase additional vacation days. Feedback suggests this breadth contributes meaningfully to work‑life balance.

Learn more about Pfizer's Compensation & Benefits →

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The Company

HQ: New York, NY

121,990 Employees

Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.