187 English-speaking jobs in Emilia-Romagna

Project Manager - End-of-Line automates secondary packaging lines for pharma, cosmetics, and food. Manage projects from planning to FAT, ensuring adherence to customer requirements and timelines. Requires 3-5 years in automatic machinery/industrial sectors.

Mechanical Designer 1 role involves defining layouts, designing components, and developing mechanical aspects of new functions for packaging machines. Requires a Mechanical Engineering degree and approximately 5 years of experience.

Sales Engineer to plan and develop sales activities for automated packaging lines in e-commerce. Requires technical degree and 5+ years in B2B sales, preferably with machinery. Fluent English is required.

Electrical Hardware Designer needed for IMA ACTIVE Division. Design and select hardware for electrical and automation systems of new machine functions, ensuring regulatory compliance. Requires 5-10 years in industrial automation and EPLAN knowledge.

Manage QMS, inspections, and site compliance ensuring GMP adherence to FDA and EU regulations. Develop procedures, analyze quality data, and drive continuous improvement in pharmaceutical manufacturing.

Senior Technical Leader, GRD CMC, manages CMC development and IMP supply strategy for rare disease projects. Requires 10+ years in pharma, expertise in drug substance/product development, and experience with EMA/FDA regulatory interactions.

Senior Clinical Project Manager coordinates operational management of clinical trials to develop compounds. Responsibilities include managing CROs, budget adherence, and ensuring compliance with SOP and GCP standards. Requires 3+ years of experience.

Drive global supplier quality oversight and lifecycle management for APIs, packaging, and critical GxP suppliers. Define strategy, governance, and performance monitoring across the supply chain.

Lead global post-marketing pharmacovigilance operations, ensuring data quality, compliance, and integrity across the portfolio. Oversee safety data collection, literature review, and regulatory adherence.

GCP Specialist in R&D Auditing responsible for ensuring compliance and managing GCP CAPAs. Duties include executing first and second party audits, managing quality metrics, and finalizing audit reports. Requires 3+ years in Pharma/CRO QA with strong GCP knowledge.

Clinical Partnership Manager to optimize governance and operations of strategic partnerships with CROs. Develop trust-based vendor relationships, manage performance, and ensure high-quality clinical trial delivery. Requires 8-10 years in Clinical Operations.

Principal Statistician for Global Rare Diseases. Provide statistical expertise for drug development programs, clinical trials, and regulatory submissions. Requires PhD/MSc in Statistics and 10+ years in clinical trials.

Senior Manager, CMC Regulatory Affairs, Global Rare Diseases. Direct experience in post-approval CMC activities to support the GRD portfolio worldwide. Responsible for authoring/reviewing CMC sections for global submissions.

Senior GDP QA Specialist to strengthen the Good Distribution Practice Quality Management System. Responsibilities include managing deviations, change control, audits, and temperature excursions while ensuring regulatory compliance.

This role ensures control and validation of software systems in GXP processes, managing computerized system validation. Responsibilities include drafting validation documentation and managing change control. Requires 5+ years in CSV within the pharmaceutical industry.

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. Requires 7+ years of experience.

Senior Technical Leader for Protein Biologics Development in GRD CMC. Lead CMC strategies for recombinant protein therapeutics, covering expression, upstream/downstream process development, and quality attributes.

Senior Technical Leader in GRD CMC with end-to-end responsibility for CMC strategy, execution, and risk management. Expertise includes analytical method development, validation, and control strategy for biological products.

Senior Manager to shape R&D digital transformation by designing data-driven processes using platforms like Veeva Vault. This role orchestrates process excellence, digital innovation, and change management across the drug development lifecycle.

Support Chiesi's Global Workplace and Real Estate strategy across affiliates. This role manages workplace standards, office transformations, location evaluations, and real estate portfolio visibility. Requires a Master's degree and 3-6 years of relevant experience.