Pfizer Ltd. Indonesia Posted October 8, 2026

Reliability & MRO Officer

Jakarta, Indonesia Full time
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Pfizer Ltd. Indonesia is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Use Your Power for Purpose

Whether you are managing critical spare parts, supporting maintenance planning, maintaining engineering documentation, or coordinating technical materials, your contributions are essential to keeping our facilities, utilities, and manufacturing equipment safe, reliable, and ready for operation. By collaborating with Maintenance, Engineering, Production, Quality, EHS, Procurement, Warehouse, and our external partners, you will help ensure that the medicines patients need are produced and delivered reliably.

What You Will Achieve

In this role, you will:

Manage the onboarding of MRO spare parts using approved engineering information and create or update part master data in the applicable CMMS/EAMS.

Receive spare parts and verify purchase-order documentation, quantity, technical specifications, and external condition before acceptance.

Ensure that damaged, incorrect, rejected, obsolete, or otherwise nonconforming materials are appropriately identified, labeled, and segregated to prevent unintended use.

Coordinate return-to-supplier activities with Procurement, suppliers, and requestors, including maintaining the required documentation and reasons for return.

Accurately record spare-part receipts, issues, returns, and inventory adjustments in SAP/ERP and CMMS/EAMS, as applicable.

Label and store spare parts in designated locations under the storage conditions specified by the manufacturer.

Issue spare parts against the appropriate work order and process eligible unused parts returned to the MRO stockroom.

Perform cycle counts, inventory reconciliation, and follow-up activities to resolve discrepancies between physical inventory and system records.

Monitor critical-spare availability, stockout risks, lead times, minimum and maximum stock levels, reorder points, safety stocks, and equipment or bill-of-material associations.

Review slow-moving, non-moving, damaged, obsolete, and equipment-specific spare parts, including materials affected by equipment modification or decommissioning.

Maintain accurate part descriptions, manufacturer and model information, storage locations, inventory status, equipment associations, and bills of materials in CMMS/EAMS.

Execute MRO business-continuity activities during planned or unplanned CMMS/EAMS outages, maintain manual transaction records, and restore transactions accurately following system recovery.

Support maintenance planning by reviewing work-order material requirements and preparing spare parts, consumables, tools, vendor support, technical documents, and engineering drawings.

Assist in developing maintenance work packs for preventive maintenance, corrective maintenance, shutdowns, major repairs, and engineering projects.

Support the preparation and updating of mechanical drawings, electrical drawings, wiring diagrams, single-line diagrams, panel layouts, P&IDs, equipment layouts, exploded views, spare-part drawings, and as-built drawings.

Ensure that only current and approved drawing revisions are used, and support field verification and controlled document updates following approved change-management processes.

Support preventive maintenance, corrective maintenance, troubleshooting, inspections, breakdown repairs, and functional checks according to competency, authorization, and operational requirements.

Accurately record completed work, labor hours, parts used, unused parts returned, and functional-test results in the applicable work order or supporting documentation.

Collect equipment specifications, drawings, OEM information, material data, test reports, and other supporting evidence for exact-replacement or like-for-like assessments by qualified Engineering personnel.

Support technical purchasing, quotation clarification, vendor coordination, material-delivery monitoring, repair services, warranty follow-up, and technical-document collection.

Comply with GMP, Good Documentation Practices, data-integrity requirements, EHS requirements, PPE rules, safe material-handling practices, housekeeping standards, and applicable site and global procedures.

Here Is What You Need (Minimum Requirements)

Diploma 3 (D3) or higher qualification in Mechanical Engineering, Electrical Engineering, Automation, Mechatronics, or another relevant technical discipline.

At least 2 years of relevant experience in MRO, spare-parts management, an engineering stockroom, maintenance planning, a technical warehouse, or maintenance operations.

Basic knowledge of GMP, Good Documentation Practices, data integrity, EHS requirements, and record traceability.

Understanding of spare-part onboarding, receipt, storage, issue, return, segregation, cycle counting, and inventory reconciliation.

Ability to use CMMS/EAMS for work-order material transactions, part-master data, equipment associations, and traceable inventory records.

Ability to identify common mechanical, electrical, and automation components and interpret their technical specifications.

Ability to read mechanical drawings, electrical drawings, wiring diagrams, single-line diagrams, equipment layouts, and P&IDs.

Ability to prepare spare parts, consumables, tools, technical documentation, and other materials required to support maintenance activities.

Working knowledge of PPE, safe storage, material segregation, housekeeping, hazard reporting, and applicable site safety procedures.

Strong analytical, organizational, communication, teamwork, and problem-solving skills.

Strong attention to detail and the ability to maintain accurate inventory, transaction, and technical-document records.

Proficiency in Microsoft Office applications, particularly Microsoft Excel, for basic analysis of inventory, consumption, lead time, and stock risks.

Ability to work independently and collaboratively while managing multiple priorities in a dynamic operational environment.

Bonus Points If You Have (Preferred Requirements)

Experience working in the pharmaceutical industry or another regulated manufacturing environment.

Experience using SAP/ERP, CMMS/EAMS, or other maintenance and inventory-management systems.

Experience supporting maintenance planning, preventive maintenance, corrective maintenance, shutdown activities, major repairs, or engineering projects.

Experience with technical purchasing, vendor coordination, quotation clarification, delivery follow-up, repair services, and warranty management.

Knowledge of inventory optimization, critical-spare analysis, minimum and maximum stock levels, reorder points, safety stock, and obsolescence management.

Experience supporting inventory reconciliation, slow-moving and non-moving inventory reviews, or spare-part cost-optimization initiatives.

Ability to perform dashboard preparation, Pareto analysis, and trend analysis related to inventory, material consumption, lead times, or stock risks.

Experience supporting maintenance troubleshooting and hands-on technical activities within the limits of assigned competency and authorization.

Additional training or certification in inventory management, maintenance planning, CMMS/EAMS, CAD or engineering drawings, GMP, data integrity, or safety.

Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support data analysis, problem solving, documentation, and productivity. Demonstrated curiosity in exploring how these technologies can improve maintenance and MRO outcomes, together with an understanding of responsible AI practices, confidentiality, risk management, and ethical use.

Work Location Assignment: On Premise

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

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Jakarta, Indonesia
Employment type
Full time

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3720 comparable Manufacturing & CMC roles across 172 biopharma companies.

3720Comparable roles tracked
3319Currently active
172Companies hiring similar roles
64Countries represented

Salary context

906 of 3720 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $126,575)

Where these roles are based

Top locations among the 3720 comparable roles

United States1724
Germany246
India162
France148
Ireland133
China121

+ 58 more countries

Seniority mix

1647 of 3720 peers have a known seniority level

Senior429
Manager374
Intern/Fellow/Postdoc251
Associate165
Principal134
Director118
Associate Director114
Senior Director53
Executive/VP9

Therapeutic area mix

24 of 3720 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Pfizer Ltd. Indonesia Jakarta, Indonesia
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40%similar
Pfizer Ltd. Indonesia Jakarta, Indonesia
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40%similar
PT Organon Pharma Indonesia Tbk Idn, Indonesia
Same function Same country
25%similar
AstraZeneca New Haven, Connecticut, United States of America
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in Indonesia, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Qualification Engineer
Pfizer Ltd. Indonesia · Jakarta, Indonesia · Seniority not listed
Function Therapeutic area Seniority Country
40%
ES Technician
PT Organon Pharma Indonesia Tbk · Idn, Indonesia · Seniority not listed
Function Therapeutic area Seniority Country
25%
Scientific Director, Process Chemistry - Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
25%
Lab Analytical Automation Scientist
Lilly · Shanghai, Shanghai, China · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.