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Senior QA Technician and QP Deputy

ID:  2231
Date of Posting:  Feb 19, 2026
Business Area:  Quality
Job Type:  Direct Employee
On site / Remote / Hybrid:  Hybrid
Hub Office: 

Zaragoza, ES

Territory: 
Full-Time or Part-Time:  Full Time
Seniority:  Mid-senior

With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn.

We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries.

At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves.

This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases.

Recordati. Unlocking the full potential of life.

Key Responsibilities

Collaborates to ensure that the site´s Quality System is maintained compliant to regulatory and GxP compliance requirements

Collaborates in the management of the site´s Quality Systems Documentation and reviews.

Collaborates in the Quality System Management including management of Non-Conformances, CAPAS, Change Control, Training, Effectiveness Checks.

Support the Quality Team in the Authorities Inspections, Clients Inspections and Autoinspections

Acts as QP for the Certification of Conformance of the product (pharma, medical devices, food and hygiene products) according to the GMP (Annex 16) and the regulation in reference of these products of the products manufactured in the plant.

Reviews the Technical documentation of the CMOs and GDPs previous to release the product to the market.

Acts as technical provides oversight for the implementation of Regulatory Compliance (Module III) of the products and issues statements required.

Act as a QP deputy before the health authorities due to the absence of the QP

Required Education

Bachelor´s Degree in Pharmacy or training to act as Qualified Person (according to the Spanish Royal Degree 824/2010 art.17)

 

Required Skills and Experience

More than 5 years of experience in GxP pharma company manufacturing operations up of with more than 3 years in Quality Assurance Role

Technical Competencies

Knowledge in SAP, Veeva, ESKO will be valued

Required Languages

Fluent English and Spanish written and spoken

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

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.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

Apply now »