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Validation Technician
Negotiable Salary
Indeed
Full-time
Onsite
No experience limit
No degree limit
Carrer de Sant Josep, 1, 08401 Granollers, Barcelona, Spain
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Description

A leading multinational industrial machinery company located in the Vallés area is seeking to incorporate a Validation Technician for its Quality department (QA). Your mission will be to carry out equipment qualifications according to pharmaceutical quality regulations and internal quality standards, ensuring the conformity/quality of the company's facilities and equipment. Main responsibilities: * Ensure the quality of both internal company projects and those carried out by subcontracted companies. * Draft and execute FDS/DQ, FAT, SAT, IQ/OQ qualifications and protocols. * Coordinate quality assurance activities for assigned projects, both internally performed and supervised subcontracted work. * Collaborate in meeting the qualification task planning schedule. * Gather, negotiate, and reach agreements regarding client requirements in qualification protocols. * Attend the execution of FAT for assigned projects together with the client. * Carry out SAT, IQ, and OQ at the client's site. * Continuously improve validation documentation and update standards adaptable to each project. * Prepare and request quotations for external qualifications. * Support in defining, maintaining, and archiving records of the calibration plan for measurement instruments used in testing. * Apply waste management instructions and reduction measures for energy and material consumption. * Comply with and enforce occupational risk prevention instructions. * Collaborate in the implementation, certification, maintenance, and continuous improvement activities of the company-wide quality management system. Desired skills and knowledge: \- Degree in Chemistry, Chemical Engineering, Industrial Engineering, or Higher Vocational Training in Chemistry. \- Experience in pharmaceutical equipment qualification (both junior and senior levels). \- Knowledge of UNE\-EN ISO 9001:2015 standard. \- Proficiency in Autocad and SolidWorks. \- Advanced level of English. \- Knowledge of international GMP and FDA cGMP regulations is desirable. \- If you are interested in learning more about this opportunity, please send your updated CV to: talent@humact.es

Source:  indeed View original post
David Muñoz
Indeed · HR

Company

Indeed
David Muñoz
Indeed · HR
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