At Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do.What drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference.Above all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution.Are you ready to unlock your full potential?Key ResponsibilitiesParticipate to ensure that the site's Quality System is maintained compliant to regulatory and GxP compliance requirements (pharmaceutical, medical devices, foods and cosmetic products).Participate in the management of the site's Quality Systems Documentation and reviews.Participate in the Quality System Management including management of Non‑Conformances, CAPAs, Change Control, Training, Effectiveness Checks, Risk Analysis report, PQR.Support the Quality Team in the Authorities Inspections,



Clients Inspections and Autoinspections.Revision documentation related to each batch of product and participate in the proposal to the Qualified Person the release of the product (GMP, Medical devices, Food and Hygiene rules)Review the Technical documentation of the CMOs and GDPs previous to release the product to the market.Participation in facilities and equipment qualifications and process validations.Collaboration in Quality postproduction task (complaints, enquiries, preparation of technical information according to the necessities of our clients)Perform other functions and participate in projects not reflected herein based on the needs of the Quality Assurance department.Required EducationBachelor's degree in Pharmacy, Science, Engineering or other education with experience in a similar position in Pharmaceutical CompanyRequired Skills and ExperienceMore than 2 years of experience in Quality in health company, the experience in GxP Pharma Company will positively be assessed.Knowledge in SAP, Veeva, ESKO will be valued will positively be assessed.Required Behaviours and CompetenciesCustomer OrientationResults‑orientedInitiative and proactivityCommunication and teamworkPlanning and flexibilityTransversality and General VisionRequired LanguagesFluent English and Spanish written and spokenWe are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief.#J-18808-Ljbffr

📌 Quality Assurance (Madrid)
🏢 Centrient Pharmaceuticals
📍 Madrid