Experteer Italy is seeking a qualified candidate for a global technical reference role in Respiratory, Orals & Small Molecules. The successful candidate will ensure robust manufacturing tech throughout the product lifecycle, leading validation and lifecycle management initiatives.The position
Experteer OverviewIn this role you act as the global technical reference for Respiratory, Orals & Small Molecules, ensuring robust, compliant manufacturing tech throughout the product lifecycle. You’ll contribute to industrialization strategies within R&D Product Teams and lead validation
Adecco italia spa is looking for a major client in pharmaceutical industry anExternal Manufacturing Small Molecule Sterile Technical Operations Specialist.The position is fully remote. We offer a six months fixed-term contract for maternity leave.The ExM Small Molecule Sterile Technical Operations
Adecco Italia spa cerca un Tecnico Specialista delle Operazioni Sterili in ambito farmaceutico. La posizione è completamente remota e prevede un contratto a tempo determinato di sei mesi per maternità. Il candidato fornirà supporto tecnico per
Adecco Spa is seeking a contractor for a fully remote position in Sterile Technical Operations, supporting drug product manufacturing across Europe. The role involves ensuring optimal production runs and providing technical support to external partners. The
Adecco Italia spa cerca un Tecnico Specialista delle Operazioni Sterili in ambito farmaceutico. La posizione è completamente remota e prevede un contratto a tempo determinato di sei mesi per maternità. Il candidato fornirà supporto tecnico per
A biopharmaceutical group is seeking a global technical reference for Respiratory, Orals & Small Molecules in Parma, Italy. The role demands a strong background in drug product manufacturing and requires leadership in lifecycle management and process validation. Candidates
Date: Mar 16, 2026 Job Type: Direct Employee Business Area: Industrial Operations & HSE Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more
An international pharmaceutical company based in Parma is seeking a Subject Matter Expert in Process Validation and Life Cycle Management. The role involves providing technical support for respiratory products, managing process validation activities, and collaborating on
Oxygen, nitrogen, hydrogen, and many other essential small molecules are the invisible pillars of our world and our lives. They have been at the core of the Group’s activities since its creation in 1902. A world leader in
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
Oxygen, nitrogen, hydrogen, and many other essential small molecules are the invisible pillars of our world and our lives. They have been at the core of the Group’s activities since its creation in 1902. A world leader in
Oxygen, nitrogen, hydrogen, and many other essential small molecules are the invisible pillars of our world and our lives. They have been at the core of the Group’s activities since its creation in 1902. A world leader in
Oxygen, nitrogen, hydrogen, and many other essential small molecules are the invisible pillars of our world and our lives. They have been at the core of the Group’s activities since its creation in 1902. A world leader in
Job Description Our Small Molecule API Chemical Technical Operations Unit is seeking a highly motivated individual to fill an open Technical Lead position to support drug substance tech transfer and commercial manufacture within our External Manufacturing Network. This
Oxygen, nitrogen, hydrogen, and many other essential small molecules are the invisible pillars of our world and our lives. They have been at the core of the Group’s activities since its creation in 1902. A world leader in
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
Date: 20 Apr 2026 Business Area: Industrial Operations & HSE Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT Subject Matter Expert Process Validation & Life Cycle Management – Respiratory Orals & Small Mol. This is
BSP Pharmaceuticals S.p.A is a Contract Development and Manufacturing Organization (CDMO). The BSP campus hosts 2 segregated facilities to serve the clients with development from pre-clinical GLP to cGMP manufacturing for clinical and commercial supply of
Experteer OverviewAs VP, Head of Project Toxicology, you will define and lead Evotec’s safety assessment strategy across the drug discovery and development portfolio, enabling science‑driven decisions from concept to regulatory submission. You will be the key