Brenntag, the global market leader in the distribution of chemicals and ingredients, supports customers and partners with high-quality technical, commercial, and logistical solutions. To strengthen our Pharma Business Unit, we are looking for a Regulatory Affairs Specialist
Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
We are looking for Stakeholder Engagement Intern to join our Sustainable Development Team based in Milan. How you make the difference This internship is key to strengthening Bolton’s stakeholder engagement and ESG governance. The role supports
We are looking for a Legal Trainee to join our Group Legal team for the Food Business Unit based in Milan. How you make the difference This position is important because the Legal Trainee supports the
THE INTERNSHIP In this role you will join the Clinical Development & Operations team in our offices based in Milan. You will support operational and scientific set-up, execution, and delivery of the clinical trials at the
Summary We are currently seeking a Junior Product Compliance Engineer to join our global Product Compliance Team, composed of four professionals and operating within the Legal & Regulatory Affairs Department. This role will support regulatory, safety, and
QUALITY MANAGER Role Purpose The Qualified Person (QP) is responsible for ensuring that medicinal products are manufactured, tested, certified, and released in full compliance with applicable GMP regulations and regulatory requirements. The role acts as a
Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South
Why Orthofix? Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want
Apex Analytica Ltd. is a premier corporate advisory firm specializing in global market business development and high-level strategic advisory services. We help multinational clients navigate complex international landscapes, seize growth opportunities, and manage geopolitical risks across
Sei pronto per entrare a far parte di una società di consulenza leader mondiale nellindustria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie
A leading agricultural company seeks a Regulatory Affairs Project Manager in Milan, Lombardy. This full-time role involves managing regulatory activities for product registrations in Italy and Malta. Candidates should have a relevant degree and a minimum of
ZEISS Sun Lens is seeking a Regulatory Affairs Expert in Castiglione Olona, Varese, for a permanent full-time role (3 days on-site, 2 days smart working). The role focuses on ensuring lens products meet EU and international regulatory requirements,
Alfasigma is seeking a Regulatory Affairs Specialist to support local Italian product regulatory strategies, including new MA and lifecycle management. You will prepare dossiers, interact with AIFA, and ensure compliant submissions for local and global brands. You
Res Novare s.r.l. cerca un/a Regulatory Affairs Specialist da inserire nel team tecnico-scientifico per gestire la conformità normativa di formulazioni cosmetiche e progetti internazionali. La risorsa lavorerà a Busnago, collaborando con formulatori, project manager e clienti, redigendo
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global
ZEISS Group in Castiglione Olona, Italy is seeking a Regulatory Affairs Expert to ensure products meet safety, labeling, and legal requirements across the EU and other markets. The role emphasizes collaboration with global teams and regulatory authorities. You
Chiesi Farmaceutici, in collaboration with IQVIA, seeks a Global Rare Disease Regulatory Affairs Specialist EU/INT to join a dynamic, international team. Under supervision, you will prepare regulatory documents for submissions, coordinate lifecycle management, and liaise with partners to
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for a Global
On behalf of our Client, Chiesi Farmaceutici, one of the top 50 pharmaceutical companies in the world with more than 80 years of experience in the pharmaceutical and biotechnology industry, IQVIA is looking for this global,