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Commissioning Engineer

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Onsite

Commissioning Engineer

Panda International

Commissioning Engineer

Skills

Compliance

25 days ago

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Important information


Contract type:

Permanent

Location:

Breda, Netherlands

Work mode:

Onsite

Published on:

2 October 2026

What they need


Overview:

The CQV Engineer will support technical projects under minimal supervision and will report to Sr Manager Validation& Compliance within the site Engineering organization.

The CQV Engineer will demonstrate hands on commissioning/qualification skills, including but not limited to the following: develop, implement and report test strategies for technical solutions in accordance with internal customer requirements and standard CQV procedures. The CQV Engineer will drive the development of system commissioning qualification and validation documentation.

Key Responsibilities:

  • Documentation:

o Develop and Update several Validation documents.

E.g. System Level Criticality Assessments,

Validation, Commissioning, Qualification plans,

Risk assessments,

Test Protocols,

Requirement traceability matrixes

Commissioning, Qualification and Validation summary reports

  • Testing:

o Lead Commissioning, Qualification and Validation activities

  • Technical support

o Deliver guidance to the project group, so the implement technical solution follows the validation plan in order to achieve meeting internal customer requirements, and accordance with Amgen SOPS

Basic Qualifications & Experience:

  • Experienced with Secondary Packaging Systems, including experience with Print and Inspection systems (e.g. Systech, Cognex)

  • At least 3 years experience in executing Commissioning, Qualification and Validation within manufacturing organizations in the pharmaceutical industries.

  • Experienced in Computerized Systems Validation

  • Hands on commissioning and qualification experience within Secondary Packaging Operations.

  • Good understanding of the role of a single document within the bigger picture.

  • Internal and /or external reporting relationships.

Preferred Qualifications & Experience:

  • Experience within a GMP compliance environment regarding practices, policies, procedures, legal requirements and goals of project, develop supporting documentation and monitor activity timeliness / scheduling.

  • Ability to anticipate, evaluate and resolve multiple, simultaneous project issues, delays and problems by utilizing technical and business expertise.

Interested? Apply with your CV or send it directly to Daria at [email protected]

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