86 English-speaking jobs in Parma

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.

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.

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.

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 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.

Senior Strategic Buyer Manufacturing responsible for selecting and purchasing quality products. Requires 5+ years in procurement, engineering degree, and strong negotiation skills.

Support distributors and partners in commercial activities for UK & international markets. Requires initial training in Wales, followed by relocation to Italy. Travel is approximately 50%.

Senior Clinical Project Manager coordinates operational management of assigned projects to develop compounds. Manages 1-3 clinical trials, CROs, and ensures adherence to scope, timelines, and budget. Requires 3+ years of experience and a Life Sciences degree.

Maintenance Engineer organizes and optimizes maintenance activities. Responsibilities include developing maintenance plans, defining material needs, and creating shutdown work packs. Requires 5 years of Oil & Gas operational experience.

Own the EU Indirect & Services spend portfolio, leading regional sourcing strategy and supplier relationships. Responsibilities include commercial negotiations, spend management, and ensuring compliance and risk mitigation.

Manage QMS, inspections, and site compliance ensuring GMP adherence to FDA and EU regulations. Develop procedures, analyze quality data, and investigate issues within the biopharmaceutical sector.

Senior Architect to lead design and development for the Expo 2030 project. Responsibilities include Revit modeling, BIM coordination, and mentoring junior staff. Requires 5-8 years of experience and advanced Revit proficiency.

Seeking an IT Sourcing Manager to drive RFQ processes, cost optimization, and contract value enhancement across the IT perimeter. This role requires strong experience in IT sourcing, commercial negotiations, and financial analysis.

IT Sourcing Manager needed to drive RFQ processes, cost optimization, and contract value enhancement across the IT perimeter. This role requires strong experience in IT sourcing, commercial negotiations, and delivering measurable savings.

Global Regulatory Affairs Manager for maternity cover. Contributes to and executes aligned EU and global regulatory strategy. Manages Health Authority interactions and leads regulatory sub teams for filings. Requires 3-4 years in International Regulatory Affairs.

Technical Sales Manager for Beverages & Beer Portfolio. Empower sales networks by accelerating growth with solutions like Regular Fillers, Combi, and Super Combi. Responsibilities include training, market intelligence, and supporting product development. Requires experience as a Business Development Manager or in Sales/Account Management.

Senior Process Engineer to lead commissioning and start-up of a new state-of-the-art plant. Responsibilities include monitoring KPIs, implementing Lean improvements, and creating process specifications. Requires an engineering degree and 5 years of manufacturing experience.

The Operational Excellence Manager leads continuous improvement initiatives in pharmaceutical manufacturing. Responsibilities include implementing Lean/Six Sigma, managing projects, and monitoring KPIs to enhance efficiency and quality.

Contract Administrator role supporting business initiatives, including commercial agreements and contractual management. Requires a Bachelor's or Master's degree in Engineering, strong communication, and a detail-oriented approach.

Global Category Lead for Research & Preclinical services. Define and execute category strategy, manage supplier relationships, and ensure operational excellence for early-stage R&D activities. Requires relevant procurement experience.