53 English-speaking jobs in Parma

GCP specialist for the R&D Auditing Department will manage CAPA plans, quality metrics, and Trackwise, Suppliers, and Audit workflows. Responsibilities include executing first and second party audits, finalizing audit reports, and writing/reviewing SOPs. Requires at least 3 years of experience in pharmaceutical Quality Assurance with knowledge of GCP and the pharmaceutical development process.

Ensures GCP compliance within project teams, acting as QA reference person. Reviews clinical study documents and manages deviations. Supports preparation and follow-up of GCP inspections. Requires at least 3 years' experience in clinical QA or clinical studies.

The R&D Process Excellence & Digital Solutions Senior Manager designs and implements end-to-end, data-driven processes enabled by digital platforms to enhance efficiency, quality, and speed across the drug development lifecycle. This role translates business needs into functional requirements, orchestrates the functional design of digital solutions, and contributes to enterprise transformation programs.

Manages external manufacturing operations across a portfolio of contract manufacturing partners, ensuring product availability while balancing service levels, inventory, and operational efficiency. Oversees production planning activities, drives supply risk management, and coordinates logistics and transportation strategies. Collaborates with internal stakeholders to support supply chain strategy and execution for new product launches, product lifecycle management, and external manufacturing network optimization.

This internship within the Global Finance FP&A team provides support for monthly closing and reporting, planning and forecasting activities, business performance analysis, and process improvement. The intern will collaborate with various finance teams and contribute to projects at the Group, Regional, and Country levels.

This senior leadership role is responsible for driving the industrialization and lifecycle management of upstream biopharmaceutical processes. The position leads process insourcing, technology transfer, scale-up, and validation activities, ensuring robust, scalable, and compliant manufacturing. The role requires strong scientific and technical expertise in upstream biologics, combined with hands-on leadership in pilot and commercial environments.

This internship supports the management and development of corporate travel activities within a global pharmaceutical environment. The intern will collaborate with global and local teams, assisting in the coordination of suppliers, travel agencies, and internal stakeholders.

The Consolidated Financial Statement Senior Analyst prepares the Group Consolidated Financial Statements, applying IFRS operative guidelines. The role supports the Senior Manager in managing the Intercompany Reconciliation process, Financial Consolidation process, and preparation of the Group Annual Report. The analyst leads the IAS 19 – Pension Funds actuarial process, manages relationships with external providers, and coordinates related consolidation activities.

The Principal Regulatory Writer will author, review, and manage regulatory documents for global health authorities. Responsibilities include drafting CTD Module 1 and 2 documents, responses to regulatory questions, and post-approval lifecycle management documents. The role requires a relevant life science degree, experience authoring regulatory documents, and fluency in English.

Develop data visualizations to communicate insights to stakeholders. Responsibilities include data analysis, visualization design, tool development, and collaboration with data scientists and analysts. Requires a Bachelor's or Master's degree in a related field and strong skills in data visualization tools, programming languages, and data manipulation. Experience with Tableau or Power BI in the pharmaceutical industry is preferred.

The Learning and Digital Workplace Intern supports the design, implementation, and management of digital solutions within the HR function, focusing on learning technologies, digital workplace platforms, and AI-powered solutions.

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 Specialist, Labelling & Compliance Regulatory Affairs will contribute to labelling and compliance activities for the Global Rare Diseases portfolio. Responsibilities include maintaining RIMS records, tracking regulatory obligations, and supporting inspection preparation. The role requires a degree in a life science field or IT, experience in Regulatory Affairs, and proficiency in RIMS and document management systems.