Offerte di lavoro cmc – Genova

Select how often (in days) to receive an alert: 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 group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy....

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines, with remote options across Europe. You will collaborate with manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance across variations, renewals, and market expansions.The role...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval CMC activities for biologics and vaccines. You will collaborate with manufacturing, QA, QC and regulatory teams to shape submission strategies and support variations, renewals and market expansions, with remote options across Europe.Responsibilities include developing...

Parexel is seeking a Senior Regulatory Affairs Associate to lead post-approval CMC activities for biologics and vaccines. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.This role offers remote options in several European locations and focuses on variations, renewals, and...

Chiesi Farmaceutici S.p.A. in Parma, IT, seeks an experienced senior CMC leader for protein biologics drug substance development within GRD CMC. You will lead upstream/downstream development, analytical control strategies, comparability, and lifecycle management for recombinant protein therapeutics. The role requires deep CMC expertise, leadership of...

Thermo Fisher Scientific seeks an experienced Regulatory Affairs professional to support EU/EEA regulatory assessments of changes for clinical trial documentation and related CMC activities. The role focuses on coordinating regulatory change control, SoC preparation and interaction with cross-functional teams.The candidate will review SmPCs, labels,...

Parexel is seeking a Senior Regulatory Affairs Associate focused on CMC for biologics and vaccines. The role involves post-approval regulatory activities, worldwide submissions, and close collaboration with manufacturing, QA, QC, and regulatory teams to drive submission strategies and risk mitigation.This position supports variations, renewals, and market...

Chiesi Farmaceutici S.p.A. in Parma, IT, seeks an experienced Senior Technical Leader for Analytical Method Development and Validation in GRD CMC. You will lead analytical strategy, development plans, and lifecycle activities for biologics, partnering with CDMOs, CROs, and internal teams. You will guide method development, qualification, validation, and...

Chiesi Farmaceutici S.p.A. is seeking a GRD Technical Leader to manage budget, strategy, and execution for CMC development and IMP supply. The role directs ETT workstreams, collaborates with CT and product teams, and leads external partners to drive development milestones and regulatory approvals. The candidate will lead technical reviews, ensure...

Parexel is seeking a Regulatory Affairs Consultant - CMC vax/bio in Caserta, Italy, offering home or office based work. You will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products within a regulatory team.You will collaborate across manufacturing, QA, QC, and regulatory groups to ensure compliant...

Parexel is seeking a Senior Regulatory Affairs Associate to drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance.Responsibilities include developing post-approval CMC submission...

Parexel is seeking an Regulatory Affairs Consultant - CMC for post-approval activities related to vaccines or biological products. The role collaborates across manufacturing, QA, QC, and regulatory groups to ensure compliant submissions and timely regulatory outcomes.You will support worldwide regulatory activities, manage regulatory information systems, and...

Chiesi Farmaceutici S.p.A. is seeking a GRD Technical Leader to manage budget, strategy, and execution for CMC development and IMP supply. The role directs ETT workstreams, collaborates with CT and product teams, and leads external partners to drive development milestones and regulatory approvals. The candidate will lead technical reviews, ensure...

Select how often (in days) to receive an alert: Senior Technical Leader, Analytical Method Development and Validation, GRD CMC Date: 12 Aug 2026 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 group with 90...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join our global Regulatory Affairs team in a client-dedicated role supporting commercial medicinal products used in clinical trials, including comparator and auxiliary medicinal products. This highly client-facing position combines EU/EEA regulatory assessment, CMC and labelling...

In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional input for regulatory dossiers. The position emphasizes collaboration across manufacturing, QA,...

Select how often (in days) to receive an alert: 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 group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma,...

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 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...

As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions, delivering...

Chiesi Farmaceutici S.p.A. in Parma, IT, seeks an experienced senior CMC leader for protein biologics drug substance development within GRD CMC. You will lead upstream/downstream development, analytical control strategies, comparability, and lifecycle management for recombinant protein therapeutics. The role requires deep CMC expertise, leadership of...