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Quality Compliance Manager

Leo Pharma

France

Sur place

EUR 50 000 - 70 000

Plein temps

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Résumé du poste

A pharmaceutical company located in Auvergne-Rhône-Alpes is seeking a Quality and Compliance Manager to oversee quality systems at its production site. In this role, you will manage a department ensuring compliance with global standards, oversee budgets, and drive continuous improvement. Candidates should have a degree in Chemistry, Biology, or Engineering, plus at least three years of relevant experience in the pharmaceutical industry. Strong communication and teamwork skills are essential.

Qualifications

  • At least 3 years' experience in quality or manufacturing within the pharmaceutical industry, ideally as a quality manager.
  • Previous experience in Compliance QA or Operational QA or in a laboratory.

Responsabilités

  • Manage the Quality Support FR department per company values and principles.
  • Ensure site Quality Systems comply with global and regulatory requirements.
  • Oversee departmental budget, employee performance, training, and development.
  • Provide quality performance data to management and support GMP inspections and regulatory activities.
  • Lead and participate in continuous improvement initiatives.

Connaissances

Strong communication skills
Teamwork skills
Work independently
Adaptability
Diligence

Formation

Degree in Chemistry, Biology, Engineering, or equivalent
Description du poste
Location

Vernouillet - 28 28500, Centre-Val de Loire, France

Contract type

Permanent

Job ID

3741

Role Description

For over 80 years, LEO Pharma has been committed to helping people suffering from skin diseases and thromboses. Each of us, at LEO Pharma, can make a real impact in our daily work, as we strive to provide the necessary support to patients and healthcare providers for many years to come and that's why we need YOU.

As part of the quality team, you will have the opportunity to shape the future and assist individuals suffering from or at risk of venous thromboembolic disease, particularly those with cancer, as well as those with skin conditions like psoriasis or atopic dermatitis, by advancing standards of care.

Being the quality and compliance manager on our production site will involve being the responsible for oversight of quality systems at the site and departmental strategy execution, personnel and departmental budget management, compliance with regulatory requirements in quality systems and lead and coordinate for third-party inspections and continuous improvements.

Main tasks
  • Manage the Quality Support FR department per LEO Pharma values and principles.
  • Ensure site Quality Systems comply with global and regulatory requirements.
  • Oversee departmental budget, employee performance, training, and development.
  • Provide quality performance data to management and support GMP inspections and regulatory activities.
  • Lead and participate in continuous improvement initiatives.
Qualifications

To succeed in this role, you will need:

  • Degree in Chemistry, Biology, Engineering, or an equivalent qualification.
  • At least 3 years' experience in quality or manufacturing within the pharmaceutical industry, ideally as a quality manager.
  • A previous experience in Compliance QA or/and Operational QA or in a laboratory.

You must also possess strong communication and teamwork skills, as well as the ability to work independently, demonstrate adaptability, and be diligent.

About Your Team

You will join a dynamic team of 7 people in the quality department at LEO Pharma. This team is a key partner for the rest of the organization, working closely with MSAT, Maintenance, Utilities, Projects, Control Lab, Automation, and IT.

At LEO Pharma, We Innovate Together

At LEO Pharma, we are dedicated to improving the lives of patients suffering from skin diseases in the field of dermatology. Our knowledge, collaborative spirit, and curiosity drive us to explore advancements in dermatology. LEO Pharma is at the forefront of science in developing new medications.

Moreover, LEO Pharma is a leader in the field of thrombosis, with a particular focus on cancer-associated thrombosis. Leveraging our expertise in venous thromboembolic diseases, we continue to engage the medical community while supporting education and training in this specific area of care. At LEO Pharma, we prioritize patients in everything we do, and that's what sets us apart! For us, pioneering together means continuously improving and expanding what is possible for others, our company, and our patients.

At LEO Pharma, we welcome and value applications from all qualified candidates because we believe that our diverse perspectives, experiences, and approaches enable us to make the best decisions for LEO Pharma and meet the needs of the markets in which we operate.

For certain positions, LEO Pharma may conduct third-party background checks.

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