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
Area Iberia, Italy & Malta is part of DNV Maritime, Region West Europe. The Area includes all maritime business activities and consists of ~60 employees in 11 locations. The Area operates with two Service Lines: Newbuilding
Area Iberia, Italy & Malta is part of DNV Maritime, Region West Europe. The Area includes all maritime business activities and consists of ~60 employees in 11 locations. The Area operates with two Service Lines: Newbuilding
Area Iberia, Italy & Malta is part of DNV Maritime, Region West Europe. The Area includes all maritime business activities and consists of ~60 employees in 11 locations. The Area operates with two Service Lines: Newbuilding
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
Now is an amazing time to join Nozomi Networks as we build the future of OT and IoT cybersecurity. We defend some of the world’s largest organizations and critical infrastructure in more than 68 countries and
Now is an amazing time to join Nozomi Networks as we build the future of OT and IoT cybersecurity. We defend some of the world’s largest organizations and critical infrastructure in more than 68 countries and
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
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
Director – Regulatory CMC Are you a CMC regulatory expert with experience across product development, submissions, and lifecycle management? This is an opportunity to lead on CMC regulatory strategy for a biopharma organisation advancing innovative therapies across multiple modalities.
Date: 10 Feb 2026 Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Senior Manager, CMC Regulatory Affairs, Global Rare Diseases About us Chiesi is
With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro
A leading biopharmaceutical group is seeking a Senior Manager in CMC Regulatory Affairs to support their Global Rare Diseases portfolio. The role requires extensive Regulatory CMC experience, particularly in Biologics, along with leadership in maintaining regulatory documents and
Sia is a next-generation, global management consulting group born digital, augmented by data, enhanced by creativity, and driven by responsibility. We partner with clients to resolve challenges and capitalize on opportunities. We believe that in today’s
Sia is a next-generation, global management consulting group born digital, augmented by data, enhanced by creativity, and driven by responsibility. We partner with clients to resolve challenges and capitalize on opportunities. We believe that in today’s
Sia is looking for a CMC Project Scheduler in Lombardia, Italy, to support project scheduling for CMC product development. The ideal candidate will have at least 2 years of experience in the biopharmaceutical industry, with a strong proficiency
Sia is seeking a CMC Technical Project Manager in Lombardy, Italy, responsible for operational management of CMC development projects. The ideal candidate will have at least 2 years of biopharmaceutical industry experience, including project management responsibilities. Strong skills
A global pharmaceutical company in Turbigo is seeking a Regulatory Affairs CMC Specialist to manage dossier preparations for regulatory submissions. This role requires a degree in chemistry, pharmacy, or biotechnology, and at least 3 years of experience
OverviewIn this role you will serve as the operational hub for CMC project teams, guiding day‑to‑day management of CMC development and tech transfer efforts within the Life Sciences and Healthcare unit. You collaborate with multidisciplinary teams and external
Experteer OverviewIn this role you drive the preparation and management of CMC dossiers for regulatory submissions worldwide. You work with cross‑functional teams to translate technical reports into submission‑ready Module3 content and assess regulatory impact of changes. You