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Cagents

Utilities Calibration Coordinator

Netherlands

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hirly's read of this role

Seniority
Mid level
Country
NL
Work mode
On-site / unstated
First seen by hirly
10 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

CAI Overview

Are You Ready?

CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field-tested processes, and elite expertise developed over 30 years.

Our approach is simple because our Purpose informs everything we do:

We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.

At CAI, we are committed to living our Foundational Principles, both professionally and personally:

We act with integrity

We serve each other

We serve society

We work for our future

At CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassing expectations. From the beginning, we’ve challenged ourselves to do what others wouldn’t. Not just setting industry standards, but redefining them entirely. We are bold in our thinking and creative in our approach.

We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn’t simply a goal. It’s a way of life. Because tomorrow demands to be at the forefront of today. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement.

We’re not interested in how it used to be done. We’re obsessed with how it will be done.

Job Title: Utilities Calibration Coordinator

Location: Netherlands

Contract Type: Staff or Contract (12-month project)

Job Summary

We are seeking an experienced Calibration Coordinator with strong exposure to pharmaceutical utilities systems, instrument criticality assessment, and validation support. This role will be responsible for managing the calibration programme for GMP-critical utilities and process equipment, ensuring compliance with regulatory requirements and supporting commissioning, qualification, and validation activities.

The successful candidate will work closely with Engineering, Utilities, CQV, QA, and external calibration vendors to ensure all instrumentation is maintained in a validated and compliant state.

Key Responsibilities

Coordinate and manage calibration activities for critical utilities systems.

Ensure all process and utility instrumentation (pressure, temperature, flow, level, conductivity, TOC, etc.) is calibrated in line with GMP requirements.

Schedule, track, and close calibration work orders using a CMMS/EAM system (e.g. Maximo, SAP PM, Blue Mountain).

Support and/or lead instrument and equipment criticality assessments in line with GMP and risk-based approaches.

Classify instruments as direct impact, indirect impact, or no impact to product quality and patient safety.

Ensure calibration strategies align with criticality, risk, and validation status.

Maintain criticality documentation and ensure alignment with site procedures.

Ensure calibration status supports validated state maintenance.

Participate in change control, deviations, and impact assessments related to calibrated systems.

Review and approve calibration certificates and reports.

Support internal audits, regulatory inspections, and site readiness activities.

Investigate calibration failures and out-of-tolerance results, supporting root cause analysis and CAPAs.

Qualifications

Degree or equivalent experience in Engineering, Instrumentation or Utilities in the Life Sciences

Proven experience in a pharmaceutical or regulated GMP environment

Strong exposure to utilities calibration

Experience with instrument criticality assessment

Hands-on experience working alongside CQV / validation teams

Strong documentation and compliance mindset

Experience using CMMS systems

Other Requirements

Must be able to commit to a minimum 40-hour work week, with flexibility based on project needs.

This is a site-based role.

Eligible to work in the EU without the need for visa sponsorship, now or in the future.

Original posting on Cagents's site ↗

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