For CQV support in the Integral Engineering area.

WHAT MAKES YOU A FIT:

The Technical Part:

- Bachelor’s Degree in Life Science or Engineering, and seven years (7+) of experience in commissioning, qualification, validation, engineering, or related discipline within the pharmaceutical, biotechnology, medical device, or other regulated industry.
- Bilingual (Spanish & English)
- Strong communication, organizational, and problem-solving skills.
- Ability to manage multiple priorities and work effectively in a fast-paced project environment.
- Experience in:
- Coordinating or leading C&Q; activities on pharmaceutical capital projects.
- Facilities, clean utilities, process utilities, HVAC, water systems, process equipment, manufacturing systems, or laboratory systems.
- developing, reviewing, and executing C&Q; documentation and protocols.
- supporting deviations, change controls, non-conformances, and corrective actions.
- engineering contractors, equipment vendors, construction teams, and site operations.

AS A PIECE OF FITS, YOU WILL: (The day-to-day on the job)

- Lead and coordinate day-to-day C&Q; activities for assigned systems and project areas.
- Coordinate C&Q; engineers, subject matter experts, contractors, and equipment vendors.
- Support the C&Q; Manager in developing and maintaining C&Q; plans, schedules, resource requirements, and deliverables.
- Ensure C&Q; activities are incorporated into the integrated project schedule and delivered in line with project milestones.




- Apply risk-based commissioning and qualification principles to assigned systems.
- Coordinate the preparation, review, and execution of commissioning tests, qualification protocols, reports, and turnover documentation.
- Review C&Q; documentation for completeness, accuracy, traceability, and compliance.
- Support the investigation and resolution of deviations, non-conformances, test failures, punch-list items, and other C&Q; issues.
- Coordinate with engineering, construction, quality, operations, maintenance, automation, project controls, and external vendors.
- Provide regular updates on C&Q; progress, risks, issues, and schedule performance.
- Support factory acceptance testing, site acceptance testing, system turnover, operational readiness, and project handover activities.
- Support audits, inspections, and project readiness reviews as required.
- Ensure all activities are performed in accordance with applicable health, safety, environmental, quality, and GMP requirements.

WHO WE ARE: We are a Service Provider company different from the rest. We pride ourselves in how we treat the most important piece of our company's puzzle: you! We integrate Engineering, Construction, Maintenance, Utilities and Specialized Technical services across the Island (and in the US as well!).

Our company is flexible, family-oriented and focused on our resources' well-being, while providing our Pharmaceutical, Medical Device and Manufacturing industry clients with top-notch quality talent. We're FITS!

Are you the Next Piece?

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📌 CQV Lead (Barcelona)
🏢 Flexible u0026 Integrated Technical Services
📍 Barcelona