Regulatory submission Jobs
126-150 von 165 Jobs
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- Innerhalb der letzten 24 Std. 30
- Innerhalb der letzten 7 Tage 133
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Clinical Data Standards Manager
argenx Zürich, Zürich
...submission, interpret published data standards guidance documentation and perform impact assessments to decide on a strategy for implementationIn support of...
vor 11 Tage in WhatjobsMelden -
Device & Packaging Senior Expert – 6650 ADA
neu CTC Resourcing Solutions Basel, Basel-Stadt
...regulatory, QA and GMP aspects Experience with test and verification, including development of methods and equipment Understanding of Human Factors...
vor 1 Tag in LifeworQMelden -
Senior Packaging and Delivery Specialist
Proclinical Staffing Bern, Bern
...regulatory aspects. Knowledge of mechanical/industrial engineering, product design, and test/verification methods. Understanding of Human Factors...
vor 4 Tage in LifeworQMelden -
R&D Engineer
The Biopôle Lausanne, Waadt
...and detailed drawings using CAD software. Lead and support process validation activities, including IQ, OQ, and PQ, to ensure all processes meet regulatory...
vor mehr als 1 Monat in JobleadsMelden -
Medical Science Liaison (MSL)
Mundipharma Basel, Basel-Stadt
...will join the Medical Affairs team with a focus on the pre-launch activities of an Anti-Infective product in the Swiss market to ensure successful submission...
vor 4 Tage in LifeworQMelden -
Device & Packaging Senior Expert
CTC Basel, Basel-Stadt
...Regulatory, QA and GMP aspects, Mechanical / Industrial engineering in general Product design / Design for manufacture Test and verification, incl...
vor 5 Tage in LifeworQMelden -
Scientist Lab Technician Assay Development (m/f/d)
Gi Group SA Zug, Risch-Rotkreuz, Zug
...studies, stability studies, and technical performance verification studies; and documentation of analytical performance for product labeling and regulatory...
vor mehr als 1 Monat in Arca24Melden -
Device & Packaging Senior Expert
Novartis Basel, Basel-Stadt
...Regulatory, QA and GMP aspects Mechanical/Industrial engineering foundations (design for manufacture, test and verification, etc) Understanding of Human...
vor 5 Tage in LifeworQMelden -
Device & Packaging Senior Expert (6650)
neu CTC Resourcing Solutions Basel, Basel-Stadt
...regulatory environments Experience with complex projects/programs; knowledge of FDA 21 CFR 820, EU MDR/Medical Device Regulation Experience in technical...
vor 1 Tag in LifeworQMelden -
Manager, Country Safety Lead Switzerland / Liechtenstein
Biogen Baar, Zug
...submission (as applicable) of Individual Case Safety Reports (ICSRs) for Company products from any source. Managing and triage of Emails received in the...
vor mehr als 1 Monat in JobleadsMelden -
Senior Packaging and Delivery Specialist
neu Proclinical Staffing Basel, Basel-Stadt
...regulatory aspects. Knowledge of mechanical/industrial engineering, product design, and test/verification methods. Understanding of Human Factors...
vor 1 Tag in LifeworQMelden -
Principal Engineer - Device Process
Real Basel, Basel-Stadt
...regulatory, QA, and GMP aspects Background in mechanical/industrial engineering: product design/DFM, test and verification, and equipment development...
vor 2 Tage in LifeworQMelden -
CAPEX Program Project Consultant
Consultys Suisse Bern, Bern
...regulatory submission requirements Experience to manage high level project budgets Ability to handle many tasks simultaneously and integrate project planning
vor 5 Tage in LifeworQMelden -
CAPEX Program Manager
Proclinical Bern, Bern
...CMC and facility regulatory submission requirements Experience in managing high level project budgets Ability to handle many tasks simultaneously and integrate
vor 5 Tage in LifeworQMelden -
Engineering Project Manager – Focus on Safety (6621)
CTC Resourcing Solutions Bern, Bern
...submission requirements Experience to manage high level project budgets Ability to handle many tasks simultaneously and integrate project planning efforts...
vor 5 Tage in LifeworQMelden -
Drug Product Peptide Launch Expert
Roche Basel, Basel-Stadt
...regulatory CMC source and submission documents, with a demonstrated ability to assess program and submission risks from a drug product formulation and
vor 29 Tage in JobleadsMelden -
Hardware Engineer
illumicell AI Zürich, Zürich
...and deliver the mechanical and electrical backbone of our point-of-care imaging system—turning requirements into a robust, manufacturable, and regulatory-ready...
vor 4 Tage in LifeworQMelden -
Global Program Clinical Head - Rheumatology/Gastroenterology
neu Novartis Basel, Basel-Stadt
...an industry environment spanning clinical activities in Phases I through III/IV, including submission dossiers required Immunology disease expertise, ideally
vor 1 Tag in LifeworQMelden -
Clinical Development Director (Neuroscience)
Novartis Basel, Basel-Stadt
...(regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups) and internal stakeholders (CTT...
vor 4 Tage in LifeworQMelden -
Device & Packaging Senior Expert
WillHire Basel, Basel-Stadt
...regulatory dossiers Leading Risk management activities Managing and monitoring Human Factors Engineering activities Monitoring of design verification...
vor 3 Tage in LifeworQMelden -
Isotope Project Lead (Associate Director S&T)
neu Novartis Basel, Basel-Stadt
...Regulatory aspects). Sound experience of data handling and applied statistics. Strong understanding of risk assessment and risk management...
vor 1 Tag in LifeworQMelden -
Senior Medical Writer
Incyte
...regulatory documents. Review other documents associated with the assigned project(s) (eg. Protocols and Statistical AnalysesPlans), as appropriate May...
vor mehr als 1 Monat in JobleadsMelden -
Full Stack Engineer
illumicell AI Zürich, Zürich
...Full-Stack Software Engineer to build production-grade code across edge devices, cloud services, and lightweight UIs as we move toward FDA 510(k) submission...
vor 5 Tage in LifeworQMelden -
Device & Packaging Senior Expert (6650)
CTC Resourcing Solutions Dagmersellen, Luzern
...regulatory dossiers Leading Risk management activities Managing and monitoring Human Factors Engineering activities Monitoring of design verification...
vor 5 Tage in LifeworQMelden -
Junior Specialist Complaint Management
BIOTRONIK Bülach, Zürich
...submission of Medical Device Reports (MDRs) to the U... Food and Drug Administration (FDA). General administrative and assistance tasks as required...
vor 5 Tage in LifeworQMelden
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