We're sorry, the job you are looking for at Chiltern on EuroPharmaJobs has expired.
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
Rhythm is looking for a Sr Manager QA to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical and...
Manages the process to verify, through risk-based independent audit, compliance of PV activities with national/international regulations and guidelines on Good Pharmacovigilance...
You will be responsible for leading global, complex extractables and leachables (E&L) projects with internal and external laboratories. You will work with site and global teams to...
Ensuring clinical studies are conducted according to the study protocol, SOPs, ICH/GCP regulations, and study-specific manuals and procedures; Participating in the development of...
Develop and maintain excellent thought leader relationships in the field of rare disease specifically Fabry Disease, Pompe Disease and Batten Disease; Lead on medical initiatives...
Responsible for managing GCP and GVP Quality Management Systems of Research and Development activities in accordance with applicable legal, regulatory and other Quality standard...
Moderna is seeking a talented, experienced, and motivated Senior Scientist to join the Immuno-Assays group to serve as a scientific expert and point of contact for the oversight of...
The External Manufacturing Manager plays a pivotal role in overseeing and managing all aspects of drug product manufacturing operations. This role requires a strategic leader with...
As the Senior Project Engineer, you will be responsible for supporting the manufacturing of products produced externally. You will develop, implement, and maintain methods...
Activities include but are not limited to, quality control of PV tasks fulfilled by DSE (EU headquarter office), EU affiliates, CROs and license partners and proactively monitors...
Support the analysts with technical input during performance of analytical determinations on active drug substance, raw material, intermediates and final drug product in agreement...
The Senior Clinical Scientist will lead the scientific and operational elements of the clinical development plan for one of the ProQR pipeline projects, proactively engaging key...
Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual...
Ensure systems, processes and products are in compliance with cGxP, MDR and current regulatory requirements. Ensure all quality monitoring as audits, are proactively in place for...