Senior Manager of Compliance and Quality Excellence

hace 2 meses

Sant Just Desvern, Barcelona, España Laboratorio STADA, S.L. A tiempo completo

About Laboratorio STADA, S.L.

We are a leading international pharmaceutical company dedicated to delivering high-quality products and services to patients, doctors, and pharmacists. Our purpose is to take care of people's health as a trusted partner, and we strive to achieve this through our values of Integrity, Entrepreneurship, Agility, and One STADA.

Our company has a wide range of products, including Generics, Consumer Healthcare, and Specialties, which offer therapeutic options for various medical conditions. We have a team of around 13,000 employees who live our values and work together to achieve our ambitious goals.

Job Summary

We are seeking a Senior Manager of Compliance and Quality Excellence to join our Global Quality team. This role will be responsible for supporting quality strategies for the Specialties department, ensuring compliance with global quality policies and regulations.

Key Responsibilities

  • Support the development and implementation of quality strategies for the Specialties department, aligned with global quality policies and regulations.
  • Provide oversight of quality processes, ensuring compliance with current GMP regulations and internal performance metrics.
  • Monitor and analyze quality performance, identifying areas for improvement and developing mitigation plans.
  • Assist in the implementation of quality and productivity improvement projects in the Quality organizations of the sites in the Specialties department.
  • Provide training and support to Quality employees in the Specialties department, ensuring they have the necessary capabilities to perform their roles effectively.
  • Continuously assess the QA and QC performance of the sites in the department, identifying areas for improvement and working with the SQH to implement remediation plans.
  • Support the development, maintenance, and continuous improvement of Quality processes in the Specialties department.
  • Assess the Compliance level of the sites (internal and external) within the Specialties department, identifying improvement opportunities and assisting in the implementation of remediation plans as required.

Requirements

  • University degree in biologics/biosimilars, pharmaceutical sciences, natural sciences, or a related field.
  • At least 5 years of experience within the pharmaceutical industry as part of a Quality organization.
  • Several years of experience in a related Quality Leader role.
  • Several years of experience with a biologics/biosimilar/specialties manufacturing site.
  • Fluent in English (written and oral).
  • Excellent communication skills.
  • Additional training in Change management, Project Management, 6-Sigma, Lean Processes desirable.

About Us

We offer a competitive environment for personal and professional development in a growing company full of opportunities. Our future project requires dynamic and proactive professionals, capable of adding value in a changing environment. We look forward to receiving your application through our job portal, where you can also find more job opportunities to strengthen our team in line with our growth ambitions.

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