Commission Specialist
2 days ago
Commissioning & Qualification (C&Q) Engineer – Aseptic Manufacturing Line
Attiki, Greece
|
Start:
November 2025 |
Duration:
6 months |
Full-time, on-site (40 hours/week)
Role Overview
We are seeking an experienced
Commissioning & Qualification (C&Q) Engineer
to support the commissioning and qualification of a new aseptic manufacturing line in
Attiki, Greece
. This is a
6-month, full-time, on-site
role requiring solid expertise in pharmaceutical facility qualification and GMP compliance.
Key Responsibilities
- Plan, execute, and document
commissioning and qualification (IQ/OQ/PQ)
activities for equipment, utilities, and cleanroom facilities. - Support the installation, testing, and validation of sterile manufacturing systems.
- Ensure strict compliance with
GMP, GDP, and regulatory guidelines
throughout all phases. - Collaborate with engineering, QA, and operations to troubleshoot and resolve technical issues.
- Prepare and review protocols, reports, and GMP documentation.
- Contribute to risk assessments and PPQ readiness activities.
Requirements
- 5+ years' experience
in commissioning and qualification within the pharmaceutical/biotech industry. - Strong background in
aseptic/sterile manufacturing facilities
. - In-depth knowledge of
GMP regulations
and qualification standards. - Strong organizational, problem-solving, and communication skills.
- Fluent in
English
(written and spoken).
-
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