Qualification & Validation Specialist – Packaging & Serialization

Akkodis

Eigenbrakel

On-site

EUR 111,000 - 166,000

Full time

10 hours ago
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Job summary

Akkodis is seeking a contingent Qualification & Validation specialist to strengthen our pharmaceutical manufacturing site in Belgium. You will support periodic qualification reviews, execute qualification and validation activities, and lead packaging equipment qualification and serialization projects.

The role requires hands-on experience with CSV, URS, risk assessments, IQ/OQ/PQ, and the ability to work independently.

Qualifications

  • Minimum 5 years of experience in Qualification & Validation.
  • Proven hands-on experience in qualification and validation of packaging equipment and packaging lines.
  • Experience with serialization projects, including implementation and qualification of serialization modules.
  • Mandatory experience in Computerized System Validation (CSV).
  • Experience writing and executing qualification documentation (URS, Risk Assessments, IQ/OQ/PQ).
  • Ability to perform qualification and validation activities independently.
  • Strong problem-solving skills.
  • Autonomous and proactive mindset.
  • Positive attitude and solution-oriented approach.
  • Fluency in French.
  • Ability to read and write technical documentation in English.
  • Availability and commitment for the full duration of the assignment.

Responsibilities

  • Support the periodic review of qualification status and execution of qualification and validation activities.
  • Lead and support packaging equipment qualification projects and serialization module qualification.
  • Perform CSV activities and documentation (IQ/OQ/PQ).
  • Collaborate with stakeholders across qualification/validation processes.
  • Identify issues and propose appropriate solutions; ensure timely execution and follow-up.

Skills

Problem-solving
Autonomous
Proactive
French fluent

Job description

Akkodis is seeking a contingent Qualification & Validation specialist to strengthen our pharmaceutical manufacturing site in Belgium. You will support periodic qualification reviews, execute qualification and validation activities, and lead packaging equipment qualification and serialization projects.

The role requires hands-on experience with CSV, URS, risk assessments, IQ/OQ/PQ, and the ability to work independently.

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