106 English-speaking jobs in Parma

Global Category Lead for Research & Preclinical services. Responsible for defining and executing category strategy, acting as a strategic business partner, managing supplier relationships, and ensuring cost predictability and risk mitigation. Requires a university degree and 6+ years of experience in pharmaceutical/biotech procurement, with expertise in Preclinical Outsourcing or Category Management. Fluency in English is required.

The Planner/Scheduler implements project planning, scheduling, and progress measurement strategies. Responsibilities include developing Work Breakdown Structures, Cost Breakdown Structures, and progress reports. The role requires expertise in project controls, time/schedule management, and project scheduling tools (Primavera P6 preferred).

Junior HSE Specialist to support the development and improvement of the HSE Management System. Responsibilities include ensuring compliance with HSE standards, preparing documentation, participating in audits, and promoting a strong safety culture. Requires a Bachelor's degree in Engineering, 5+ years of experience, and fluency in English.

Junior Proposal Engineer supports the preparation of technical and commercial proposals for bids and tenders. Assists in drafting, reviewing documents, gathering data, and collaborating with internal teams. Requires a degree in Engineering, fluency in English, and 1-2 years of experience in similar roles.

Leads all Drug Substance Process & Analytical Development activities, setting strategy and ensuring organizational goals are met. Responsible for defining and executing the strategy for biologics CMC development, including process development, analytical sciences, and regulatory readiness. Manages CDMO partnerships and external development packages.

The IT Application Manager & Functional Business Analyst – Logistics partners with Logistics and Supply Chain teams to translate business needs into IT solutions. The role focuses on functional analysis, application ownership, and solution evolution within a regulated pharmaceutical environment. Responsibilities include acting as a trusted IT partner, collecting and analyzing business requirements, managing logistics applications, and collaborating with internal and external teams.

Provides support for chemical and biological risks assessments at CHIESI sites, including application of EU regulations. Assists in the development and implementation of risk assessments and occupational hygiene studies.

The Global Health Execution Intern will support the implementation and operational execution of Chiesi's Global Health strategy. The role supports cross-functional activities to enable sustainable and inclusive access to essential medicine in low-income countries.

The Global Commercial Effectiveness Manager ensures a robust, data-driven customer engagement strategy built on the omnichannel go-to-market model. Responsibilities include leading global coordination of affiliates in the definition and execution of the Customer Engagement Impact Plan (CEIP), defining and maintaining application success, customer success, and engagement effectiveness metrics, and acting as the global data owner for Customer Engagement data. The role requires at least 5 years of experience in Commercial Excellence, Business Intelligence, Digital Marketing, Omnichannel or Customer Experience roles (preferably in pharma or healthcare).

Support Talent Management and Employee Experience initiatives within a global HR environment. Assist with data consolidation, talent review processes, employee engagement surveys, and learning and development initiatives. Provide operational support, coordination, and execution excellence.

The Legal Confidentiality Assessment Assistant will support confidentiality assessments, draft decisions, and coordinate with stakeholders. Requires excellent English (C1 level), experience in Food Law, Transparency Regulation, and European Law.

Lead a team, drive sales, and deliver exceptional customer experiences as a Skechers Store Manager. Manage daily operations, inventory, and motivate employees to achieve goals. Previous managerial experience and strong leadership, communication, and problem-solving skills are required.

The Training & Documentation Coordinator manages training and documentation for Global TechOps & Supply. Responsibilities include analyzing training needs, organizing GMP courses, managing the documentation system, and supporting projects to improve training processes. Requires a degree in scientific subjects and at least 5 years of experience in pharmaceutical manufacturing.

Project Controls Specialist to manage change management processes for capital projects in the pharmaceutical or high-tech manufacturing industry. Responsibilities include managing change logs, developing procedures, and supporting project execution. Requires a bachelor's degree and proven experience in project controls change and/or risk management.

The Senior Director, Global Quality Integration & Alliances defines, leads, and executes global quality integration activities for mergers, acquisitions, divestments, strategic partnerships, and growth initiatives. This role ensures acquired or partnered entities are integrated into the global Quality Management System in a compliant, risk-based, and business-enabling manner. Provides global quality governance oversight for external partners and alliances.

The R&D Data Elaboration Head leads a team focused on data elaboration and visualization to support R&D activities and product development. Responsibilities include translating stakeholder needs into data solutions, driving the digital transformation of R&D, and overseeing the lifecycle of data models and visualizations. The role requires a PhD or Master's degree in a relevant field and 5+ years of experience leading data elaboration/computation modeling in the pharmaceutical/biotech/medtech industry.

The Global IBP Manager supports the execution and continuous improvement of the global Sales & Operations Planning process, ensuring transparency and alignment between Demand, Supply, and Finance. The role prepares, structures, and facilitates the S&OP cycle, addressing risks and misalignments.

Subject Matter Expert for process validation and technical maintenance activities supporting industrialization, product technology transfer, and life-cycle management for respiratory, oral, and small molecule products. Provides technical support to R&D, Operations, Quality, and external stakeholders. Responsible for participating in technology transfer processes, collaborating on technology transfer documents, and finalizing the industrialization of new products.

Leads Data Management, Biostatistics, and Statistical Programming functions within Global Clinical Development. Drives data strategies across all drug development phases, ensuring scientific rigor, operational efficiency, and regulatory compliance.

Provides data-driven insights and long-term projections to support Chiesi Governance Bodies and Senior Management. Analyzes pipeline value, composition, timelines, costs, resource demand, and probability of success. Supports cross-functional alignment on project assumptions and contributes to R&D strategy definition. Manages project cards for internal project evaluation and coordinates the update of project Probability of Technical and Regulatory Success (PTRS). Prepares quantitative projections on pipeline and R&D costs and resources. Supports R&D headcount planning based on workload projections. Collaborates with Finance R&D Planning and Control to ensure consistency between short and long-term cost projections. Supports the maintenance and improvement of R&D long-term planning processes and tools. Supports qualitative R&D strategy definition and refresh cycles. Elaborates quantitative projections on R&D pipeline to support Pipeline Reviews and R&D strategy definition. Ensures relevant long-term projections are uploaded to the FP&A system (BOARD). Keeps aligned with business needs and manages standardized project cards to evaluate R&D pipeline business cases. Supports the Head of unit and the R&D Portfolio and Resource Management Sr Director in the design and execution of XRC meetings to align cross-functional teams