Enhance Quality and Compliance in Life Sciences
A key professional will be responsible for delivering impactful projects in compliance and validation.
The successful candidate will participate in and oversee projects involving the validation of computerized systems across the project lifecycle.
Adherence to industry regulations, including EU GMP Annex 11, FDA 21 CFR Part 11, GAMP 5, and Data Integrity guidelines is essential.
Required Skills and Qualifications :
Bachelor's degree in Chemistry or Engineering
Experience in the pharmaceutical industry, GxP compliance, and computerized systems validation
Multitasking skills and experience in managing multiple consulting projects to meet client needs
Fluency in Spanish and English, with excellent communication skills
What We Offer :
Competitive compensation package
Flexible work schedule, hybrid work model, and flexible hours
Global exposure, opportunities for growth, and leadership development
Dynamic work environment with a young and enthusiastic team
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Senior Consultant • Barcelona, Catalonia, SPAIN