Quality Assurance Technician

Recordati; Zaragoza; Presencial; EUR 40.000 - 65.000; Jornada completa

Descripción de la vacante

Recordati in Zaragoza, Spain, seeks a Quality professional to maintain the site's Quality System and support regulatory and GxP compliance for pharmaceuticals, medical devices, foods and cosmetics.

The role covers documentation management, CAPAs, change control, training and inspections support, with collaboration across the QA team to ensure batch release readiness and postproduction activities, while upholding our commitment to patient safety.

Formación

• Requires 2+ years of experience in quality within a health/pharma company.
• Knowledge of SAP, Veeva or ESKO is valued.

Responsabilidades

• Maintain the site's Quality System in line with regulatory and GxP standards.
• Manage the site's Quality Systems Documentation and reviews.
• Oversee Quality System Management including Non‑Conformances, CAPAs, Change Control, Training and risk analysis.
• Support Authorities and Client inspections and Auto-inspections.
• Review batch documentation and coordinate release proposals with the Qualified Person.
• Review technical documentation of CMOs and GDPs prior to market release.
• Participate in facilities and equipment qualifications and process validations.
• Collaborate on quality postproduction tasks (complaints, enquiries, technical info for clients).
• Perform other functions and projects as needed by Quality Assurance.

Conocimientos

Quality experience

SAP

Veeva

ESKO

Educación

Bachelor's degree in Pharmacy, Science, Engineering

Herramientas

SAP

Veeva

ESKO

Descripción del empleo

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 Responsibilities

• Participate 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 Education

Bachelor's degree in Pharmacy, Science, Engineering or other education with experience in a similar position in Pharmaceutical Company

Required Skills and Experience

• More 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 Competencies

• Customer Orientation
• Results‑oriented
• Initiative and proactivity
• Communication and teamwork
• Planning and flexibility
• Transversality and Global Vision

Required Languages

Fluent English and Spanish written and spoken

We 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.