ph3About us /h3pChiesi 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. /ppAt 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 Agevolazioni Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact. /ppDiversity 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. /ph3Chiesi Research Development /h3pOur RD team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, RD project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China). /ph3Who we are looking for /h3h3This is what you will do /h3pTo verify and ensure the compliance and the correct application of Good Clinical Practices (GCP) being primarily responsible for the management of all the GCP CAPAs, preparation of the quality metrics,



KPIs supporting the compliance inside Global RD Departments, management of Quality Documents and by execution of first and second party audits. /ph3You will be responsible for /h3ulliManagement of CAPA Plans from GCP audits /liliManagement of the requests for the collection of quality metrics, KPIs supporting Global RD Departments /liliManagement of Trackwise, Suppliers and Audit workflows /liliSupport the management of external consultants supporting the Auditing Supplier Qualification Unit. /liliFinalization of Quality Documents supporting the Auditing Supplier Qualification Unit. /liliWrite/Review SOPs relating to audit and qualification of clinical service providers /liliEnsure training on relevant activities and procedures /liliEnsure good documentation and traceability /liliExecution of GCP first and second party audits /liliFinalization and management of the GCP audit reports /li /ulh3You will need to have /h3ulliAt least 1 year of experience in Pharmaceutical, Consultancy Companies or Contract Research Organization in the Research Development environment Quality Assurance with knowledge of GCP supporting clinical trials and knowledge of compliance /liliKnowledge of GCP requirements and quality system /liliKnowledge of the pharmaceutical development process supporting clinical trials /liliKnowledge of training technique /liliScientific degree /liliGood knowledge of English.



/li /ulh3We would prefer for you to have /h3ulliKnowledge of auditing technique to be considered an added value /liliISO auditor Certification to be considered an added value /li /ulh3Location /h3pThe position is based at our headquarters in Parma and offers a flexible hybrid working arrangement. /ph3Compensation Range /h3pThe minimum salary for this role is € 39.000, aligned to our established salary framework. The final offer will reflect the candidate’s skills, experience, qualifications and internal equity considerations. /ppThis role is eligible to participate in an annual bonus scheme, subject to company and individual performance. /ppIn addition, we offer a comprehensive benefits package including pension, private medical insurance, wellbeing programme, flexible benefits programme and more. /ph3What we offer /h3pNo 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. /ppWe 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. /ppChiesi 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. /p /p #J-18808-Ljbffr

📌 GCP specialist R&D Auditing Department - Temporary (Parma, IT)
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