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
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
Experteer Italy is looking for a Regulatory CMC Specialist to manage CMC regulatory activities within Chiesi’s Global Rare Diseases portfolio. This role requires collaboration with various teams to ensure compliance and timely deliverables. The ideal candidate will have
Chiesi Farmaceutici S.p.A. in Parma is currently seeking a Senior Manager for CMC Regulatory Affairs within their Global Rare Diseases unit. This role is critical for managing regulatory submissions across various markets for biopharmaceutical products. The ideal
THE COMPANY This pioneering biopharmaceutical company is committed to transforming patient outcomes through cutting‑edge science in ophthalmology, neuroscience, and rare diseases. Operating globally, the organisation integrates R&D, regulatory, and manufacturing excellence to bring novel therapies from
Singular: Building Brilliant Biotechs is seeking a Director – Regulatory CMC to lead regulatory submissions and compliance initiatives. You will ensure timely and accurate submissions, engaging proactively with health authorities throughout the regulatory process. Ideal candidates will
Experteer Overview In this role you will support Chiesi’s Global Rare Diseases portfolio by managing CMC regulatory activities across submissions and lifecycle. You will collaborate with Core teams, GCST, and external CMOs to ensure compliance and timely
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Chiesi is an international research-focused biopharmaceutical
Job Grade: PT12F Hiring Manager: Ana Lúcia Vasconcelos Internal Posting Date: - Referral Bonus: 500.00 EUR Professional | Permanent | Full-time | Hybrid Our people in Manufacturing & Global Operations share two priorities: getting things done
Grünenthal Group is seeking an experienced professional for a permanent position in Bardi, Italy. The role focuses on regulatory CMC documentation, requiring a strong background in pharmaceutical sciences and at least 5 years of industry experience. The
Chiesi Farmaceutici S.p.A. in Parma is currently seeking a Senior Manager for CMC Regulatory Affairs within their Global Rare Diseases unit. This role is critical for managing regulatory submissions across various markets for biopharmaceutical products. The ideal
Scope of the role This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. It ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global
Alfasigma S.p.A. is seeking a highly experienced professional for a key role in defining global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC). The ideal candidate will have over 15 years of regulatory experience with a deep
Experteer Overview As Regulatory CMC Lead at Alfasigma, you define and execute global regulatory strategies for CMC across product life cycles. You will influence development, registration, and lifecycle management, collaborating across functions to align with product strategies. You
Alfasigma S.P.A. is seeking a highly experienced professional for a key role in defining global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC). The ideal candidate will have over 15 years of regulatory experience with a deep
Scope of the role This position is responsible for defining and executing global regulatory strategies for Chemistry, Manufacturing, and Controls (CMC) across the product lifecycle. It ensures robust regulatory CMC strategies, submission generation, compliance, and alignment with global
A leading biopharmaceutical group is seeking a Senior Manager in CMC Regulatory Affairs to support their Global Rare Diseases portfolio. The role requires extensive Regulatory CMC experience, particularly in Biologics, along with leadership in maintaining regulatory documents and
Date: 10 Feb 2026 Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, IT Senior Manager, CMC Regulatory Affairs, Global Rare Diseases About us Chiesi is
Experteer Overview As Regulatory CMC Lead at Alfasigma, you define and execute global regulatory strategies for CMC across product life cycles. You will influence development, registration, and lifecycle management, collaborating across functions to align with product strategies. You
Experteer Italy is seeking a Regulatory CMC Lead to define and execute global regulatory strategies for CMC across product life cycles. This role will involve collaboration with global health authorities and alignment of CMC regulatory approaches. The ideal candidate