Presentación
As part of the Quality Assurance team, you will play a key role in ensuring compliance with regulatory requirements in relation to the company’s worldwide licensing, contract manufacturing, and distribution of pharmaceutical products. This is a cross-functional position, supporting multiple departments and engaging with key players in the pharmaceutical B2B sector. Your responsibilities will include maintaining quality standards, promoting a quality mindset, and driving continuous improvement across company operations.
Organización
You will work at a prominent Italian pharmaceutical company with a global presence and a solid track record of over 130 years in the industry, located in Badalona. With a team of more than 700 professionals in Spain, they are among the top 15 pharmaceutical companies in the country. Their current focus covers key areas such as cardiovascular risk, respiratory, analgesia, male sexual health, and the digestive system. Additionally, they are committed to research and development of new products in various therapeutic areas, including oncology.
Función
Key Responsibilities – Ensure daily activities comply with company and Menarini Group procedures. – Manage quality complaints related to the company’s product portfolio. – Support the maintenance and improvement of the local Quality Management System (QMS), including SOP development, documentation review, and record-keeping. – Define and review quality/technical agreements related to the manufacturing and distribution of active substances and medicinal products. – Review commercial agreements to ensure regulatory compliance. – Serve as a contact point for affiliates, third parties, and internal departments on quality-related matters.
Requisitos
Requirements: – A Master’s degree in Life Sciences (a degree in Pharmacy is preferred). – 3-4 years of experience in Quality Assurance within the pharmaceutical industry. – Strong knowledge of EU GMP and EU GDP quality management systems. – Experience in wholesale distribution of pharmaceutical products under EU GDP regulations. – Proven experience in managing pharmaceutical quality/technical agreements. – Fluency in English (written and spoken) is essential; knowledge of French and/or German is a plus.
Oferta
The process will be managed from the global talent adquisition deparment.