Les résultats de la recherche: 42 offres d'emploi
Das sind deine Aufgaben:
Du verantwortest regulatorische Fragestellungen rund um Energie und verfolgst die politische und regulatorische Entwicklung
Aus deinen Analysen leitest du Handlungsempfehlungen ab, erstellst Risikobewertungen, unterstützt die Strategiedefinition...
Suggéré
Travail à domicile
...About the role
As Regulatory Affairs Manager, you will be responsible for all drug regulatory affairs matters for the assigned indication group and will act as an interface between global Regulatory Affairs departments and Swissmedic to obtain new marketing authorizations...
Suggéré
Temps plein
Das sind deine Aufgaben:
Du verantwortest regulatorische Fragestellungen im Rahmen der Strom- und Gasversorgungsgesetzgebung und verfolgst die politische und regulatorische Entwicklung
Aus deinen Analysen leitest du Handlungsempfehlungen ab, erstellst Risikobewertungen...
Suggéré
Travail à domicile
Das sind deine Aufgaben:
Du verantwortest regulatorische Fragestellungen im Rahmen der Strom- und Gasversorgungsgesetzgebung und verfolgst die politische und regulatorische Entwicklung
Aus deinen Analysen leitest du Handlungsempfehlungen ab, erstellst Risikobewertungen...
Suggéré
...Description
About the role:
The Senior Director, Global Regulatory Strategy, Therapeutic Area Lead in Global Regulatory Affairs is... ...of regulatory submissions including Investigational New Drug (IND) and New Drug Applications (NDA)/centralized Marketing Authorization...
Suggéré
Temps plein
...modernsten Dienstleistungen ein wirklich persönliches Kundenerlebnis schaffen.
Ihr Aufgabengebiet
Als IT Business Analyst Regulatory & Investment Compliance arbeiten Sie an der Schnittstelle zwischen der Bank und der IT. In dieser abwechslungsreichen und verantwortungsvollen...
Suggéré
...requires careful consideration. In most cases, the therapies investigated in clinical trials are not yet approved by regulatory agencies like the Food and Drug Administration (FDA) in the United States. The benefits and risks of taking investigational drugs are not...
Suggéré
...working practices within the matrix structure.
Support the regulatory teams, Market Access and Reimbursement activities in the EPM markets... ...Doctor degree is mandatory.
Proficient in all aspects of drug development, GCP and regional regulations - including the...
Suggéré
...Act as Responsible Person (RP) delegate for Commercial Biologics Drug Substances (DS), Parenteral Drug Products (DP), Parenteral... ...compliance.
Experience in clinical products manufacturing and/or regulatory is an asset. Knowledge of medical device regulations and...
Suggéré
...portfolio of innovative medicines.
Enabled by our proprietary drug discovery platform, Deciphera has developed a diverse pipeline... ...within the UK.
Provide medical expertise in all regulatory, early access and reimbursement approval processes.
Partner...
Suggéré
Temps plein
Temporaire
...accountabilities, for providing hands-on legal commercial support to medmix Drug Delivery business segment and provide corporate and governance... ..., including preparing the Annual General Meeting, address regulatory aspects of Swiss listed companies.
~ Demonstrated ability to...
Suggéré
Temps plein
...assessments
Possess and maintain knowledge of current global GMP regulatory requirements and industry trends to ensure compliance at... ...is preferable.
At least 5 years of experience working with drug substance/drug product manufacturing, Quality Control and/or Quality...
Suggéré
Temps plein
...curiosity meets purpose
Neuroscience
Connecting the dots in neuroscience
Science & Innovation
Multiple modalities in drug development
See all Stories
Disease Areas
We believe no other disease area holds as much need or promise for medical...
Suggéré
...interested in
Responsibility
Increasing diversity in clinical trials: A collaboration with Tufts Center for the Study of Drug Development
Multiple Sclerosis
The hidden face of MS
Lupus
Living with lupus: Hazura’s story
2021 Year in...
Suggéré
...Solid knowledge of cGMP requirements, EU/FDA regulations and compliance.
Experience in clinical products manufacturing and/or regulatory is an asset. Knowledge of medical device regulations and manufacturing is a plus.
Ability to develop effective working relationships...
Suggéré
Recrutement immédiat
...classification under applicable law. Thomson Reuters is proud to be an Equal Employment Opportunity/Affirmative Action Employer providing a drug-free workplace.
We also make reasonable accommodations for qualified individuals with disabilities and for sincerely held...
Temps plein
...coordination with the content manager, subject matter experts, and project teams
Ensures that quality targets, timelines, and regulatory requirements are respected
After translation, creates target language versions of deliverables (in all appropriate formats)...
Temporaire
...inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines.
Enabled by our proprietary drug discovery platform, Deciphera has developed a diverse pipeline of wholly-owned drug candidates. QINLOCK® (ripretinib) is Deciphera’s...
Temps plein
Temporaire
Recrutement immédiat
Remote job
...Engineer III will be leading, facilitating, or coordinating all activities pertaining to tech transfer within the Switzerland internal drug substance manufacturing site. Also, this person will lead technology transfer assignment and prioritization for drug product...
Temps plein
...English & German
Proficiency in accounting software (Infoniqa) and MS Office (proficient in Excel)
Familiarity with GAAP and regulatory requirements and with IFRS experience being highly beneficial
Strong attention to detail analytical and able to work on...
Temps plein
Horaire flexible