GMP Documentation

Hikma Italia S.p.A. cerca una risorsa per il team di Quality Assurance presso il sito di Pavia. La risorsa gestirà la documentazione GMP, emissione, revisione e archiviazione di produzione, confezionamento e qualità. Responsabilità principali includono la revisione di batch record di confezionamento e sperlatura, gestione della documentazione GMP,...

Hikma Italia S.p.A. cerca una risorsa per il team di Quality Assurance presso il sito di Pavia. La risorsa gestirà la documentazione GMP, emissione, revisione e archiviazione di produzione, confezionamento e qualità.Responsabilità principali includono la revisione di batch record di confezionamento e sperlatura, gestione della documentazione GMP, supporto...

Hikma Italia S.p.A. cerca una risorsa per il team di Quality Assurance presso il sito di Pavia. La risorsa gestirà la documentazione GMP, emissione, revisione e archiviazione di produzione, confezionamento e qualità.Responsabilità principali includono la revisione di batch record di confezionamento e sperlatura, gestione della documentazione GMP, supporto...

Join the Future of Regenerative Medicine Multiply Labs is a robotics company on a mission to solve a significant bottleneck in modern medicine: the manufacturing of life‑saving cell therapies. Currently, cell therapies are produced through manual, labor‑intensive processes. This keeps costs astronomical—often exceeding $1M per patient —and...

Overview In this role, you support sterility and aseptic processing activities within CAI’s life sciences and mission-critical projects. You will apply microbiological methods, ensure compliance with GMP and Good Documentation Practices, and contribute to sterile manufacturing initiatives. The role collaborates with cross-functional teams to execute...

Overview In this role you lead technology transfer and industrialization efforts for small molecule products, ensuring robust technical oversight across internal and external manufacturing sites. You will coordinate cross-functional teams to drive project execution, manage risks, and support supply continuity. You help shape scalable processes and maintain...

Overview As a Computer Systems Validation (CSV) Engineer at CAI, you design and execute validation protocols for GMP environments, ensuring compliant, data-grade systems. You will craft and review GxP and 21 CFR Part 11 documentation and guide resolution plans with cross-functional teams. This role connects advanced validation practices with biotech and...

Overview In this role you drive quality assurance across healthcare projects, ensuring a robust QMS aligned with ISO 9001, ISO 13485, EU GMP, and EU GDP. You’ll coordinate QA activities, support audits, risk assessments, and change controls, and partner with internal and external stakeholders to deliver compliant, efficient project outcomes. You will lead...

Overview In this role you drive analytical development for gene editing and nucleic acid-based therapeutics within the GRD CMC team. You lead method development and control strategies for complex modalities, including ATMPs and LNP-based products, collaborating across functions from candidate selection to clinical development and launch. You oversee...