R&D Qa Gcp Manager
Pubblicato il 22-08-2026 - Chiesi Group in Parma
ppChiesi 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.
/p pAt 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.
/p pDiversity 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.
/p h3Chiesi Research Development /h3 pOur 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).
/p h3Who we are looking for /h3 h3This is what you will do /h3 ul liEnsure the GCP compliance within the project teams, acting as QA reference person in the clinical project teams.
/li liEnsure the implementation and maintenance of the quality system in the GCP areas.
/li /ul h3You will be responsible for /h3 ul liActing as QA GCP reference person in the clinical project teams, both related to organic and inorganic growth, providing QA inputs and supporting the clinical study teams in the design, execution and reporting of clinical studies.
/li liReviewing the documents related to clinical studies (protocol/amendment, patient information sheet/Informed consent form, CTS label, CTS instruction for use, CSR).
/li liManaging the Suspected Serious Breaches /li liSupporting the preparation, management and follow-up of GCP inspections from Regulatory Authorities.
/li liManaging the GCP deviations.
/li liWriting the SOPs and working instructions related to the activities performed by RD QA GCP /li liReviewing the SOPs and working instructions related to the clinical studies, in order to ensure the compliance with the current regulations.
/li /ul h3You will need to have /h3 ul liPreferably: At least 3 years' experience as clinical QA, in pharmaceutical companies or clinical CROs.
/li liAlternatively: At least 3 years' experience in clinical studies working as CRA or Project Manager, in pharmaceutical companies or clinical CROs.
/li liScientific degree, Pharmacist or Life Sciences /li liEnglish deep knowledge, both oral and written /li /ul h3Technical Skills /h3 ul liKnowledge of GCP regulations /li liUse of common computer tools (e.g. Office) /li /ul h3Location /h3 pBased in Parma,
with the possibility of a hybrid working arrangement.
/p h3Compensation range /h3 pThe minimum salary for this role is €******, aligned to our established salary framework.
The final offer will reflect the candidate's skills, experience, qualifications and internal equity considerations.
/p pThis role is eligible to participate in an annual premio scheme, subject to company and individual performance.
/p pIn addition, we offer a comprehensive benefits package including pension, private medical insurance, wellbeing programme, flexible benefits programme, tivcket restaurant and more.
/p h3What we offer /h3 pNo 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.
/p pWe 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.
/p pChiesi 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.
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