217 English-speaking jobs in Emilia-Romagna

Oversee external manufacturing operations across contract partners, ensuring product availability while balancing service, inventory, and cost. Drive supply risk management and coordinate manufacturing commitments in a regulated pharmaceutical environment.

Lead Statistical Programmer responsible for SAS programming for clinical and safety data systems. Develop work plans, ensure data integrity, and create CDISC-compliant deliverables for regulatory submission.

Senior Process Scientist needed for gRNA process development. Lead process development and manufacturing oversight for gene therapy programs, focusing on in vivo LNP programs. Expertise in gRNA, synthetic nucleotide manufacturing, and GMP transfer is required.

Manage training and documentation across Global TechOps & Supply. Responsibilities include EDMS management, user training, compliance monitoring, and supporting system implementation. Requires a scientific degree and 5+ years in pharma QA.

Manage training and documentation for Global TechOps & Supply. Responsibilities include GMP course organization, system governance, and supporting new document management system implementation. Requires a scientific degree and 5+ years in pharma QA/Production.

R&D Bioinformatician Lead drives hands-on bioinformatics analyses for target identification and translational research. This role requires methodological ownership, expertise in R/Python, and experience with biological/clinical datasets.

Senior Manager to drive R&D digital transformation by designing and implementing end-to-end, data-driven processes using platforms like Veeva Vault. This role connects business processes, data, and technology to enhance efficiency across the drug development lifecycle.

Manage pharmacovigilance operations for interventional clinical trials, ensuring compliance with PV legislation. Responsibilities include data collection, process ownership, CRO oversight, and audit support. Requires a Master's degree and 3+ years in Pharmacovigilance or Clinical Research.

Lead R&D GRAPS Affiliate and Partnership Oversight. Manage partner/affiliate relationships regarding patient safety and global regulations. Serve as SME for SDEAs and Intracompany Agreements. Requires Master's in life sciences and 5-7 years in international Pharmacovigilance.

GCP Specialist in R&D Auditing manages GCP CAPAs, quality metrics, and executes first and second party audits. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Ensure pharmacovigilance quality system compliance with regulatory requirements. Manage deviations, monitor CAPAs, and review SOP/WIs. Requires Life Sciences degree and 3-5 years in pharmacovigilance/QA.

Lead Scientist role driving industrialization and lifecycle management of upstream bioprocesses. Responsibilities include process insourcing, scale-up, and validation, ensuring robust, compliant manufacturing. Requires 10+ years in biologics CMC.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Requires 7+ years of Regulatory CMC experience, 3+ in Biologics/Biopharmaceuticals, and advanced knowledge of global CMC regulations.

Ensure GCP compliance within project teams as the QA reference person. Responsibilities include reviewing clinical study documents, managing deviations, and writing SOPs. Requires 3+ years in clinical QA or related roles.

IT Application Manager & Functional Business Analyst for Finance and PPM Tools. Partner with Finance stakeholders to translate business needs into IT solutions, managing application lifecycles and defining future processes.

Senior GDP QA Specialist supports the Good Distribution Practice Quality Management System. Responsibilities include managing deviations, change control, complaints, and risk assessments to ensure regulatory compliance.

The Export Area Supervisor implements brand distribution activities and contributes to sales objectives. Responsibilities include leading the sales team, managing customer portfolios, developing market opportunities, and finalizing contracts.

Metal Fabrication Technologist needed to set technical standards for carpentry, welding, and machining. This role leads process design, manages documentation, and drives continuous improvement in manufacturing. Requires a Mechanical Engineering degree and experience in relevant technologies.

Senior Analytical Scientist specializing in LNP/RNA analytics. Drive analytical development and control strategy for gene editing products, including mRNA-LNP modalities, using advanced techniques like UPLC, DLS, and NGS.

Provide legal support to Staff and Global R&D functions, including contract drafting, negotiation, and risk evaluation. Requires a Master's in law and 2-3 years of experience in pharma or a top law firm.