Kezdő állások, munkák egészségügy, gyógyszeripar területen

• Development new formulations: contribute to design of studies, perform experiments and prepare reports
• Develop analytical methods (e.g. HPLC)
• Prepare and characterize large number of formulations following DOE
• Assist in the development of methods to characterize formulations or raw materials

• Start date:
• Latest Start Date:
• Planned duration: 6 months
• Extension: not likely (maternity leave)
• Max. Bill Rate: CHF (Depends on the experience)
• Workplace: Basel
• Workload: 100%
• Home Office: No
• Travel: No
• Team: 5-10 people
• Working hours: Standard

IHR PROFIL Abgeschlossene Ausbildung als Kosmetikerin, Beauty- oder Spa-Therapeutin Erfahrung in Maniküre & Pediküre UNBEDINGT ERFORDERLICH und idealerweise auch in Make-Up Freude am Verkauf sowie an individueller, persönlicher Beratung Gepflegtes Erscheinungsbild und ein herzliches,...

Collaborate closely with Translational Science Leads (TSL), Clinical Operations, Biostatistics/Bioinformatics, and Data Management teams to execute translational science strategies in clinical trials....

• Global pharmacovigilance product responsibility for the medicinal products
• Monitoring of the benefit-risk profile
• Signal management: signal detection, signal validation, signal evaluation
• Risk management: preparation of risk management plans, supervision of risk minimization measures

Gyógyszerforgalmazással kapcsolatos teendők ellátása: gyógyszerek és egyéb forgalmazott termékek kiadása pénztárhasználat, gyógyszerek átvétele, rendelés leadása beérkező anyagok bevizsgálása, számlák feldolgozása leltározási feladatokban segítségnyújtás Ellátja az állattulajdonosokat a háziállatuk...

• Support development projects at transfer or validation level by executing laboratory work
• Perform immunological tests using various platforms (e.g., Flow Cytometry, ELISA, PETIA, etc.)
• Conduct studies to establish and optimize kit reagents and protocols

• Az intézmény gyógyszerkészletének feltöltése
• A gyógyszerforgalom előírás szerinti pontos vezetése, negyedévente történő leltározása
• Lejáratos szavatosságú gyógyszerek, eszközök selejtezése, a selejtezési jegyzőkönyv pontos vezetése, a keletkezett veszélyes hulladék elszállíttatása

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....

• Batch record review for API and bulk product for monoclonal antibody prefilled syringes
• Assessment and documentation of product deviations, OOS, and changes
• Quality oversight for relevant service providers, including CMO's, laboratories, technical operations and supply chain

Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e.g. KPIs, PSMF)...

• Working with high throughput lab – analyzer
• Routine lab work with infectious samples and leading of own experiments including the analysis of them
• Plan and execute different work packages for the development of molecular diagnostics test

• Welcome guests upon their arrival at the Spa
• Provide facial treatments in accordance with our Spa program
• Perform various massages, body scrubs, and wraps in line with Spa standards and our selected treatment menu
• Promote Spa treatments and products by offering professional advice to guests

Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e.g. KPIs, PSMF)...

• Provide guidance on regulatory and quality requirements, including MDR and FDA requirements, for our in-house and our customer software projects
• Create technical documentation for our industry projects together with our software development teams

You develop, maintain, and continuously improve the Quality Management System in accordance with ISO 13485, MDR, and other applicable regulatory requirements...

• Working with high throughput lab - analyzer
• Routine lab work with infectious samples and leading of own experiments including the analysis of them
• Plan and execute different work packages for the development of molecular diagnostics test

• Páciensek manuálterápiás kezelése és gyógytornák tartása
• Szakmai tanácsadás és támogatás a gyógyulás folyamatában
• Kiváló kommunikáció a páciensekkel, hogy mindenki otthon érezze magát

• Play an important role within in a multidisciplinary team in the development of new and complex products / segments / features and in the management throughout the entire life cycle
• Create product visions and/or strategies independently for complex products / segments / features

• Drive innovation by evaluating and continuously advancing therapies through aerosol inhalation
• Communicate scientific insights effectively and foster strong interdisciplinary collaborations to ensure successful translation into clinical practice