CQV Engineer: Clean Utilities & Purified Water

Inova Consulting

Basel

Vor Ort

CHF 120.000 - 160.000

Vollzeit

vor 19 Stunden
Sei unter den ersten Bewerbenden
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Zusammenfassung

Inova is seeking an experienced CQV Engineer specialized in Clean Utilities and Purified Water systems to support a pharmaceutical project in the Basel area. You will lead commissioning and qualification activities, focusing on PW generation, storage, and distribution, and collaborate with Engineering, QA, Operations, Automation, and suppliers.

The role requires hands-on CQV execution, strong GMP knowledge, and the ability to coordinate across multi-disciplinary teams for successful handover to

Qualifikationen

  • Degree in Chemical Engineering, Mechanical Engineering, Process Engineering, Biotechnology, Pharmaceutical Engineering or related technical discipline.
  • Minimum 5 years of CQV experience within pharma, biotech, or life sciences.
  • Strong hands-on experience with Clean Utilities and PW systems.
  • Good understanding of pharmaceutical water treatment technologies, sanitary design, instrumentation, piping systems, and automation.
  • Experience executing FAT, SAT, commissioning, IQ, OQ, and PQ.
  • Solid knowledge of GMP, EU GMP Annex 15, risk-based qualification principles, and CQV lifecycle approaches.
  • Familiarity with ISPE Baseline Guides, ASTM E2500, and ASME BPE is a strong advantage.
  • Experience reviewing P&IDs, functional specifications, equipment documentation, and engineering drawings.
  • Strong troubleshooting and problem-solving capabilities in a project environment.
  • Structured, autonomous, and quality-focused working style.
  • Strong communication skills and ability to coordinate with multidisciplinary teams, vendors, and clients.
  • Fluent in English; German is a strong asset.

Aufgaben

  • Plan, coordinate, and execute commissioning and qualification activities for Clean Utility systems with a focus on PW systems.
  • Support the qualification of PW generation, storage, and distribution loops including RO, EDI, ultrafiltration, and sanitization systems.
  • Develop and review CQV documentation (URS, risk assessments, commissioning plans, qualification protocols, test scripts, final reports).
  • Execute and/or supervise FAT, SAT, commissioning, IQ, OQ, and PQ activities.
  • Verify installation and functionality of equipment, instrumentation, piping, automation, alarms, and control systems.
  • Support qualification activities related to water quality, system performance, sanitization cycles, and distribution loop operation.
  • Ensure traceability between user requirements, design documentation, risk assessments, and qualification testing.
  • Review vendor documentation and coordinate qualification activities with equipment suppliers and engineering contractors.
  • Manage deviations, punch-list items, discrepancies, and qualification-related issues through resolution.
  • Collaborate with Engineering, QA, Automation, Operations, Maintenance, and Validation teams.
  • Ensure CQV activities comply with GMP requirements, EU GMP Annex 15, ISPE guidance, and internal procedures.
  • Support system handover, operational readiness, and transition from project execution into routine GMP operation.
  • Contribute to continuous improvement of CQV methodologies, templates, and execution strategies.

Kenntnisse

CQV expertise
GMP knowledge
Cross-functional coordination
Fluent English

Ausbildung

Bachelor's degree in Chemical/Mechanical/Process Engineering or related

Tools

ISPE Baseline Guides
ASTM E2500
ASME BPE

Jobbeschreibung

Inova is seeking an experienced CQV Engineer specialized in Clean Utilities and Purified Water systems to support a pharmaceutical project in the Basel area. You will lead commissioning and qualification activities, focusing on PW generation, storage, and distribution, and collaborate with Engineering, QA, Operations, Automation, and suppliers.

The role requires hands-on CQV execution, strong GMP knowledge, and the ability to coordinate across multi-disciplinary teams for successful handover to

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