GRA CMC Manager - Bern
vor 1 Monat
Job summary
We are looking for a GRA CMC Manager to lead strategic and operational CMC regulatory activities across product development clinical submissions registrations and lifecycle management.Responsibilities
- Drive global CMC strategies for clinical trial applications new product licenses and post approval changes.
- Assess CMC facility equipment and plasma related changes and manage regulatory submissions in coordination with regional teams.
Stellenbeschreibung
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Zugang zu allen hochrangigen Positionen und den Job Ihrer Träume erhalten.
Ähnliche Jobs
We are looking for a GRA CMC Manager to lead strategic and operational CMC regulatory activities across product development, clinical submissions, registrations, · and lifecycle management. · ...
vor 1 Monat
We are committed to saving and improving lives by unlocking the power of the immune system. We excel in R&D innovation, manufacturing, and commercialization—working every day to protect people's health and quality of life.The role is for a Medical Officer providing medical leader ...
vor 1 Monat
We're looking for an experienced Medical Officer providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP), Epidemiology, Medical Affairs, and Medical & Process Compliance. You will guide patient safety and benefit–risk. · Lead and develop high-perform ...
vor 1 Monat
We are committed to saving and improving lives by unlocking the power of the immune system. Our commercial portfolio includes market-leading vaccines against smallpox/mpox, rabies, tick-borne encephalitis, typhoid fever, and cholera. · We excel in R&D innovation, manufacturing, a ...
vor 1 Monat
The Senior Engineer will bring new Drug Delivery Systems through development. · Planning and execution of projects for evaluation. · Cross-functional interaction with Quality Assurance, Regulatory Affairs, Packaging... · ...
vor 1 Monat
In this role you will be responsible for bringing new Drug Delivery Systems through the development process. · Responsible for the planning and execution of projects for evaluation, selection, improvement and implementation of new or existing primary packaging materials medical d ...
vor 1 Monat
We are looking for an experienced Regulatory Affairs Manager for our complex and highly regulated environment in Switzerland.The successful candidate will take their place within the engaged and knowledgeable Thermo Fisher Regulatory Community of 70+ regulatory professionals with ...
vor 1 Monat
We are seeking an innovative and experienced Program Manager to lead strategic initiatives in the Technical Operations organization. · The scope of this role will include cross-functional management of continuous improvement efforts across process development MSAT manufacturing Q ...
vor 4 Wochen
This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Director, CMC Regulatory Affairs in Switzerland. · Lead CMC regulatory strategy for investigational and early commercial biological products across global teams · Advise cross-func ...
vor 1 Woche
As a Regulatory Affairs Manager at Thermo Fisher Scientific in Lengnau, Switzerland, you will be responsible for ensuring compliance with Swiss regulations and trends impacting the local business. You will work closely with the regulatory community of 70+ professionals to enhance ...
vor 1 Monat
We are looking for a SPM Group Lead to manage a team of six Site Product Managers within the Aubonne MSAT team. The role involves overseeing project execution, ensuring compliance with regulatory standards, and driving continuous improvement initiatives within the team. · Lead an ...
vor 1 Woche
We are looking for a skilled Program Manager · to join our team at Thermo Fisher Scientific Inc. As a Program Manager,you will be responsible for ensuring flawless project execution while maintaining exceptional standards. · ...
vor 3 Wochen
We are seeking an MSAT Manager capable of driving projects in the Contract manufacturing Organization. · ...
vor 4 Wochen
We are seeking an MSAT Manager capable of driving projects in the Contract manufacturing Organization.The ideal candidate will have late-stage process development expertise preferably aseptic processing and technical project management experience. · ...
vor 4 Wochen
Senior Director, Regulatory Compliance, Large Molecule
Nur für registrierte Mitglieder
This role leads a team of compliance professionals and is part of the IM Compliance Leadership Team. The Senior Director is the GMP compliance leader for Large Molecule Biologics across the Platform and is accountable for inspection readiness, audit programs, supplier/CMO support ...
vor 1 Monat
We are looking for an Industrial Lead Bio Drug Substance who is proactive, · strategic, and quality-oriented to join our Industrialization & Network Planning team. · Develop long-term industrial plans for Bio Drug Substance manufacturing · Manage strategic project portfolios and ...
vor 1 Monat
The Lead Process Excellence is responsible for supporting DePuy Synthes separation and standardization of our core business processes and products across Plan, Source, Make, Quality, Deliver streams. · The Lead Process Excellence has knowledge of Manufacturing, Planning, Procurem ...
vor 2 Wochen
The Lead Process Excellence is responsible for supporting DePuy Synthes separation and standardization of our core business processes and products across Plan, Source, Make, Quality, Deliver streams. · ...
vor 1 Woche
We seek an MSAT Manager to drive projects in Contract manufacturing Organization. · Cross-functional management of new product introductions and continuous process improvement initiatives. · ...
vor 1 Woche
+Job summary · We are looking for an Industrial Lead Bio Drug Substance who is proactive, strategic and quality-oriented to join our Industrialization & Network Planning team. · +Develop long-term industrial plans for Bio Drug Substance manufacturing · Manage strategic project po ...
vor 3 Wochen