Responsibility for the release of medical devices as legal manufacturer (Merckle), Securing that the manufacturing and testing of 3rd Party products, is in compliance with...
The role will have responsibility for escalating high-risk issues to management while providing support to the wider organisational team. The position will also support Teva Global...
Management of operational QA aspects within the daily collaboration with CMOs during CMC development and GMP manufacturing of early and late stage projects in close coordination...
Establish the regulatory strategy and understand the regulatory requirements for submission of marketing applications globally as part of LCM Plan, review, prepare and submit CMC...
The Neurology Account Manager will work across Switzerland to develop commercial relationships with relevant stakeholders and decision makers in order to maximize product access...
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Proactively manages regulatory CMC aspects of projects, including overseeing preparation and submission of CMC regulations appropriate to the phase of...
Responsible for organizing and supervising the Commercial QA unit (Quality Assurance Unit for the commercial unit, that is, the Teva Group's sales laboratories in Spain, and the...
Act as project champion for customer project within Lonza Drug Product Services. Support proposals team concerning potentially new projects as well as preparing amendments and...
The Senior GMP Quality Auditor will report to the Global Audit Manager of Insud Pharma and the primary role of this position will be to perform GxP audits in Europe and the Rest of...
The position will be responsible for pre-formulation studies, formulation and process development, optimization, scale-up and manufacturing, including the for each phase relevant...
Preparation of the project planning taking into account the personnel and production capacities. Offer preparation for supplements. Management of project execution, both internally...
Responsible for regulatory submissions and approvals for worldwide market expansions and renewals, Provide regulatory CMC strategy and expertise to cross-functional teams such as...
As a member of Incyte Global Quality, QP develops and maintains a strong collaboration with external partners and Incyte cross-functional teams to support implementation of Incyte...
Working as part of the Quality Assurance team on site ensuring products are manufactured, in accordance with cGMP, to ensure that all work carried out is in compliance with the...
As the Regulatory Affairs Team Leader you will lead the Site Regulatory CMC team (up to 10 members) supporting products marketed globally. Product range includes oral dosage forms,...