Store Manager

Therapy Management Corporation; Comunidad Valenciana; Presencial; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

An exciting freelance opportunity awaits in Barcelona for a skilled CQV Lead. This role involves supporting critical commissioning, qualification, and validation activities across pharmaceutical and biotech projects. The ideal candidate will have extensive experience in Clean Room Validation Protocol Execution and be proficient in English, with Spanish as a valuable asset. Join a forward-thinking company and contribute to impactful projects while enjoying the flexibility of a freelance contract. If you are ready to take on this challenge, connect with us today!

Formación

• Extensive experience in Clean Room Validation Protocol Execution is essential.
• Travel flexibility across Europe and the US is required.

Responsabilidades

• Support critical CQV activities in pharmaceutical and biotech projects.
• Collaborate on systems qualification and regulatory compliance.

Conocimientos

Clean Room Validation Protocol Execution

HVAC

Travel across Europe and the US

Proficient in English

Spanish fluency

Experience with pharmaceutical equipment IQ/OQ/PQ

Descripción del empleo

Freelance CQV Lead Opportunity in Barcelona, Spain

We're seeking an experienced CQV Lead for a 12-month freelance role based in Barcelona, Spain. If you're a highly skilled professional in Commissioning, Qualification, and Validation (CQV) with a strong background in Clean Room Validation Protocol Execution, this could be the perfect opportunity for you.

Key Requirements:

1. Clean Room Validation Protocol Execution Experience is a must.
2. HVAC experience is a plus.
3. Must be able to travel across Europe and the US.
4. Proficient in English (mandatory), with Spanish fluency being a strong asset.
5. Experience with other pharmaceutical equipment IQ / OQ / PQ is a great asset.
6. Preference for candidates based in Spain, especially those in or near Barcelona.
7. Freelance (12 months contract).
8. Support critical CQV activities across pharmaceutical and biotech projects.
9. Collaborate on systems qualification, documentation, risk assessment, and regulatory compliance.

If you or someone you know fits these criteria, please reach out. Let’s connect and discuss how you can be a part of this exciting role. Apply Now or Tag a Colleague at ssanchisoptimussearch.com