Training & Documentation Manager (Parma, IT)

Biopharma Careers; Parma; In loco; EUR 55.000 - 85.000; Tempo pieno

Vantaggi offerti da questo lavoro

Healthcare benefits

Relocation support

Flexible working arrangements

Remote work options

Tax assistance for foreign colleagues

Descrizione del lavoro

Chiesi, headquartered in Parma, Italy, is seeking a Training & Documentation Coordinator for Global TechOps & Supply. You will manage GMP training and documentation, coordinate a system-wide document management upgrade, and ensure compliance with EU/FDA guidelines across the Parma plant.

The role requires a degree in scientific subjects, 5+ years in pharma manufacturing, GMP expertise, and fluent English. Relocation and a comprehensive benefits package are offered.

Competenze

• Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering)
• At least 5 years of experience in manufacturing sites within the pharmaceutical/biopharmaceutical sectors (QA, Production, Process Technology)
• Excellent knowledge of pharmaceutical guidelines (EU and FDA)
• Specialized expertise in GMP compliance improvement processes
• Fluent English (written and spoken)

Mansioni

• Analyze and gather the training needs of Parma Plant personnel with respect to GMP topics
• Organize general GMP courses for TechOps staff, directly or with external consultants
• Issue the TechOps training programme and prepare the related annual report
• Participate in governance team for the training management system and ensure regulatory alignment
• Support projects aimed at improving TechOps training processes
• Manage the documentation system in compliance with GMP and regulatory bodies
• Participate in governance team for the current document management system
• Contribute to the implementation project for the new document management system
• Supervise and support TechOps QA archive management
• Provide support during Corporate Quality audits and regulatory/customer audits
• Evaluate and authorize access requests to computerized systems in TechOps
• Monitor training and documentation KPIs

Conoscenze

GMP compliance

English fluency

Quality Assurance

Formazione

Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering)

Descrizione del lavoro

About us

Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet. This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas. Discover more here.

At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose. This fosters a culture of reliability, transparency, and ethical behaviour at every level. As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.

Diversity and inclusion are at the heart of who we are. We believe our differences make us stronger. We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.

Global Technical Operations & Supply

Global Technical Operations & Supply (Global TechOp&S) is Chiesi’s global manufacturing and supply area, responsible for ensuring consistent, outstanding quality, service and value across our end‑to‑end supply chain. Global TechOp&S oversees the entire lifecycle of the drug: from process optimization and industrialization, to manufacturing, engineering, quality oversight, and supply chain management. Throughout this journey, Operational Excellence drives continuous improvement. This end‑to‑end model is powered by our four manufacturing sites - Parma (IT), Blois (FR), Santana de Parnaíba (BR), and Nerviano (IT) - together with our Virtual Plant network of external partners.

This is what you will do

The Training & Documentation Coordinator is responsible for managing training and documentation across the entire Global TechOps & Supply area. Both training and documentation are managed using dedicated systems, which require governance oversight and/or development. A new project has been launched to replace the current document management system; this will require the involvement and coordination of the Training & Documentation Coordinator for its future implementation at the site.

You’ll be responsible for:

• Analysing and gathering the training needs of Parma Plant personnel with respect to GMP topics
• Organising general GMP courses for TechOps staff, either directly or in collaboration with external consultants
• Issuing the TechOpstraining programme and preparing the related annual report
• Participating in the governance team for the training management system, ensuring it remains updated and aligned with regulatory requirements
• Supporting projects aimed at improving TechOps training processes
• Managing the documentation system in compliance with company guidelines, GMP requirements, regulatory authorities, and certification bodies
• Participating in the governance team for the current document management system
• Participating in the project team for the implementation of the new document management system
• Supervising and supporting the management of the TechOps QA archive
• Providing support during Corporate Quality audits, as well as audits conducted by regulatory authorities and customers
• Evaluating and authorising requests for access to computerised systems within the TechOps area
• Monitoring training and documentation KPIs

You will need to have

• Degree in scientific subjects (Chemistry, Pharmaceutical Chemistry and Technology, Engineering)
• At least 5 years of experience in manufacturing sites within the pharmaceutical and biopharmaceutical sectors, specifically in Quality Assurance, Production, and Process Technology departments.
• Excellent knowledge of pharmaceutical guidelines (EU and FDA regulations)
• Specialized expertise in GMP compliance improvement processes
• Fluent English (both written and spoken)

We would prefer for you to have

• Ability to establish strategies for managing multiple projects efficiently and effectively
• Strong teamworking skills, contributing positively and constructively to achieving goals
• Capacity to analyze technical issues and find shared solutions, evaluating related risks

Location

Parma

What we offer

No matter where your path starts at Chiesi, it leads to inspiring possibilities. Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way.

We provide top-class benefits, including comprehensive healthcare programs, work-life balance initiatives, and robust relocation support. Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive.

Chiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business. All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination.