Apply now »
 

 

Quality Specialist 

  
   
   

Purpose

Support the implementation and maintenance of the GMP/GDP Quality Management System in Spain under the guidance of the Country Quality Head (CQH) and Country Cluster Quality Head (CCQH).

Contribute to the execution and documentation of quality processes for commercialized products (pharmaceuticals, medical devices, cosmetics, food supplements) in line with internal and external regulations.

Assist in harmonizing and sharing best practices and procedures at the Europe 3 Cluster level (Italy, Spain, Portugal, Hungary, Ukraine, Romania, Bulgaria, Israel, Greece).

Provide technical support for quality processes and participate in quality-related projects at country and cluster level.

 

Your taks & responsabilities

 

  • Support the maintenance and continuous improvement of the local Quality Management System documentation and records.
  • Assist in the management of quality processes including deviations, complaints, change controls, CAPA, and batch release support.
  • Facilitate day-to-day quality compliance of local commercial operations (e.g., Supply Chain, Customer Service, Regulatory Affairs).
  • Support the preparation and follow-up for internal and external audits, inspections, and self-inspections.
  • Assist in the organization and delivery of quality and GMP/GDP-related training for local employees.
  • Contribute to supplier qualification activities and the maintenance of Quality Assurance Agreements (QAAs) as directed.
  • Support the local implementation of global and cluster quality initiatives and projects.
  • Facilitate communication and share best practices within the Quality function (local, cluster, global).
  • Assist with the management of documentation in quality-related IT systems (e.g., SAP, Dev@Com, Veeva).
  • Provide administrative support for local quality metrics, reporting, and data analysis.
  • Act as a point of contact for quality-related queries from internal stakeholders and external partners.

 

Who you are

 

  • University degree in Pharmacy, Chemistry, Biology, or related scientific discipline.
  • 1–3 years of experience in a GMP/GDP-regulated environment or quality-related function.
  • Knowledge of pharmaceutical/medical device products, quality processes, and relevant regulations.
  • Familiarity with quality management systems (QMS), audit support, and deviation handling.
  • Strong attention to detail and compliance mindset.
  • Effective communication and collaboration skills.
  • Spanish mother tongue
  • Proficient in English
  • Practical experience with quality systems (e.g., SAP, Veeva) is a plus.
  • Ability to analyze data and prepare quality-related reports.
  • Project support and coordination skills.
   
YOUR APPLICATION  
   

This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer. 
 
Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
 

  

 

Location:

Spain : Cataluña : Barcelona  

 

Division:

Pharmaceuticals 

 

Reference Code:

849031 


Job Segment: Medical Device, Compliance, Pharmaceutical, Regulatory Affairs, Supply Chain, Healthcare, Legal, Operations, Science

Apply now »