Cleaning Validation specialist

Cleaning Validation Specialist

Location: Barcelona - On site
Type: Full-time

Are you someone who thrives in regulated environments (GMP) and enjoys making a real impact by ensuring everything runs safely smoothly and compliantly Then you might be the Cleaning Validation Specialist were looking for!

Whats in it for you

Make a real impact: Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma biotech and medical devices

Grow within a community of experts: Benefit from knowledge-sharing mentoring and exposure to diverse challenging assignments that broaden your expertise.

Build a meaningful career: As an ambitious and pioneering company we want to offer you the best possible environment to thrive within the life sciences.

A fair competitive package: We offer tailored transparent compensation aligned with your expertise preferences and local market regulations because your contribution deserves to be valued.

What youll be doing

• You learn to develop and implement validation strategies following internal procedures and industry regulations.

• Drafting and executing cleaning validations protocols (IQ OQ PQ) for manufacturing equipment (reactors mixers tanks filling lines autoclaves refrigerators incubators etc)

• Reporting on validation results and preparing summary reports.

• Contribute to risk assessments related to cleaning procedures and equipment design

• Identify document and investigate deviations; support the definition and follow-up of corrective and preventive actions (CAPAs).

• Participate in periodic reviews and revalidation activities for cleaning procedures.

• You provide support during internal and external audits gaining valuable exposure to industry best practices.

• Uphold a culture of knowledge sharing and continuous learning within the validation team.

What you bring

• Education: Technical background (Chemistry Engineering Biotechnology etc.)

• Experience: At least 1 year of experience in qualification and validation .

• Languages: Good level of English to draft and interpret technical documentation.

Who you are

Our culture is driven by values If this sounds like you youll fit right in:

• Youre resilient and tackle challenges with a positive mindset

• Youre curious and always up for learning something new

• You have a no non-sense approach honest clear respectful

• Youre innovative and bring ideas not just opinions

• And above all youre serious about your work but not too serious about yourself

About us

We support life sciences companies from idea to patient offering tailored solutions in development clinical regulatory compliance production and distribution. With 500 experts across 8 countries we help drive innovation in ATMP biotech medical devices diagnostics digital health and pharma.

We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.

You wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.

Interested Lets talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.