129 English-speaking jobs in Parma

Material Planning Specialist will define stock policies, collaborate with teams to manage material flow, and ensure timely deliveries. Requires a Master's degree, 3+ years of experience, and proficiency in SAP and MS Office.

Provides technical support to sales teams in managing complex offers for structured customers and key accounts, focusing on Verona Tunnel Machines. Supports value selling by guiding teams in proposing solutions based on customer needs and priorities. Ensures quotations meet technical requirements and contribute to successful project outcomes.

Field Service Engineer specializing in mechanics needed. Responsibilities include testing, evaluating, and ensuring equipment performance at customer sites, troubleshooting mechanical systems and HMI, and preparing technical reports. Requires a Bachelor's degree in Engineering, fluency in English, and at least 5 years of field service experience, preferably in the beverage industry. Willingness to travel up to 90% of the time is required.

The BI Analyst will develop and maintain BI dashboards and reports to support commercial, marketing, and cross-functional teams. Responsibilities include designing and optimizing SQL queries, data models, and ETL workflows to ensure accurate data delivery. The role requires a BS/MS degree in a quantitative or scientific field and 2+ years of experience in a commercial function as an analyst, BI developer, or dashboard designer. Strong technical skills in SQL, BI tools (Power BI, Tableau, or Qlik), and ETL development are essential.

Senior Mechatronic Engineer to drive innovation in motion and motors technologies for next-generation equipment. Lead the exploration, evaluation, and integration of new motion technologies, including track and planar linear motor systems. Design and optimize mechatronic architectures, develop control algorithms, and define protocols for real-time synchronization.

Process, Governance & Tools Expert (QtC-E) manages governance frameworks, business tools, and user support for QtC-E execution across regions. The role requires 5+ years of project management experience, proficiency in MS Office, Project, and ERP/SAP, and fluency in English.

Senior Project Manager will develop and update integrated cross-functional project plans, coordinate project teams, and track project progress. Responsibilities include defining project objectives, scope, and milestones, managing budgets, and identifying and mitigating risks. Requires a degree in Life Sciences, Economics, or Management/Engineering, an International Project Management certification, and 5+ years of experience in product development.

Global Category Lead for Research & Preclinical services. Define and execute category strategy, act as a strategic business partner, manage supplier relationships, and ensure cost predictability and risk mitigation.

Industrial Designer to lead the design system for filling lines. Responsible for creating modular, production-ready designs emphasizing ergonomics and hygienic design. Experience in beverage/food machinery and strong CAD skills required.

Packaging Operator needed for a rotating 12-hour schedule (2-2-3) at a pasta manufacturing facility. Operates packaging machinery, inspects products, and maintains quality and safety standards. Previous manufacturing experience is preferred but not required.

Leads and coordinates technical teams, laboratories, and equipment to support formulation and manufacturing process development for MDIs and liquid dosage forms, including technology transfer. Ensures compliance with GMP/cGMP and HSE requirements.

Leads and coordinates technical teams, laboratories, and equipment to support formulation and manufacturing process development activities from laboratory to industrial scale for MDIs and liquid dosage forms, including technology transfer. Ensures compliance with GMP/cGMP and HSE requirements.

Senior Algorithm Engineer will design and refine algorithms for visual recognition and analysis tasks. Responsibilities include building deep learning models, using computational geometry methods, and collaborating with engineers to integrate work into automated data labeling systems.

Lead clinical pharmacology science for assigned Clinical Development Programs, incorporating quality pharmacokinetics and pharmacodynamic analysis. Contribute to the development and application of clinical trial methodologies. Work with other members of the pre-clinical and clinical development matrix to steer clinical pharmacology study science. Keep abreast of developments in the field of clinical pharmacology and ensure colleagues are kept up-to-date. Acts as leader of the Early First In Human (FIH) Study Team, delivering the execution plan for FIH trials. Responsible for the design of outlines relative to the assigned Project Development Plan(s) and for securing timely and quality execution of the plan. Provides expert input to the design of the Clinical Pharmacology protocols relative to the assigned Project Development Plan(s). Ensures application of enhanced, up to date trial designs by partnering with all relevant disciplines, as well as of Company standards, SOPs and achievement of agreed KPIs. In cooperation with the study team, understands and interrogates data. Works on Statistical Analysis Plan with the statistician and interprets statistical analysis results. Be responsible to plan and perform the population PK and PK/PD analyses (safety and efficacy) on a continuous and live basis as the project progresses. In collaboration with study team and modeling and simulation experts plan

The Clinical Program Leader leads the strategic planning and execution of clinical development programs, ensuring scientific rigor and alignment with regulatory and business objectives. They provide clinical leadership within the Core Team, designing and executing a global clinical development strategy from Phase 1 through Phase 4. The role requires significant experience in designing and executing a comprehensive clinical research & development plan and a Medical Doctor Degree.

Senior clinical development leader responsible for shaping and executing global clinical development strategy for Bronchiectasis, Pulmonary Hypertension, and Interstitial Lung Diseases. Leads a team of Clinical Development professionals and oversees clinical trial design, execution, and regulatory submissions. Requires 8-10 years of experience in pharmaceutical R&D with a track record of driving programs from early development through approval. MD required, board certification in pulmonology preferred. Fluency in English required.

The Operational Excellence Manager leads and implements initiatives to drive continuous improvement, enhance operational efficiency, and ensure high-quality standards across pharmaceutical manufacturing processes. This role involves collaborating with cross-functional teams, managing projects, and fostering a culture of excellence and innovation.

Leads the creation of semantic layer, data model, and ontologies for Chiesi's R&D data ecosystem. Defines and implements data governance framework, policies, and standards for data stewardship. Manages product backlog and roadmap for data sets delivered by the engineering team. Establishes R&D data quality frameworks and integrates data quality checks into pipelines. Communicates the value of data governance and semantic initiatives to stakeholders.

The Global Commercial Analytics & Customer Insights Manager generates, collects, and analyzes business, customer, and commercial data to drive strategic value. This role acts as the global source of truth for commercial data, enabling data-driven decisions across Chiesi brands and markets. Responsibilities include developing analytics solutions, leading customer insights projects, and supporting strategic decision-making. The ideal candidate has 5-7+ years of experience in commercial analytics, customer insights, or BI within global healthcare organizations.

Leads the Clinical Trial Documentation & Records Management Unit, ensuring alignment between organizational and technical requirements for clinical trial documentation and records. Drives compliance with regulatory and business standards, guaranteeing inspection readiness across the R&D Clinical trial technology ecosystem. Manages strategic vendors for clinical trial technology and oversees the adoption, setup, and maintenance of clinical trial technologies.