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Pfizer

Makes cancer drugs, vaccines and other medicines

Calibration Specialist

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeJakarta, IndonesiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Automation, Control, or Electrical Engineering; Mechanical Engineering or another relevant engineering discipline is also accepted.
  • 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 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.

Responsibilities

  • 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 required timelines.
  • Maintain calibration schedules and equipment records using a 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 Technical Services and Engineering teams.
  • Support maintenance and verification of manufacturing equipment, laboratory equipment, and cleanroom systems, including HEPA filter integrity testing, air change rate measurement, and air balancing.
  • Support 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 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 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 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.

Desired Qualifications

  • 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.

About the Company

Pfizer

Makes cancer drugs, vaccines and other medicines

Pfizer discovers, makes, and sells prescription medicines and vaccines for patients, doctors, and governments worldwide, with large businesses in vaccines, cancer, heart disease, and rare diseases. In 2020, its COVID-19 shot, developed with German partner BioNTech, became the first COVID-19 vaccine authorized in the United States. Its scientists find drug candidates and run clinical trials to prove they are safe and effective, and Pfizer then manufactures approved products in its own plants, earning most of its money from patented drugs before cheaper generic copies arrive. Pfizer was founded in 1849 as a chemicals business in Brooklyn and is based in New York City.

Company size
10,001+
Company stage
IPO
Headquarters
New York City, New York
Founded
1849

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