No et perdis res!
Uneix-te a la comunitat de wijobs i rep per email les millors ofertes d'ocupació
Mai no compartirem el teu email amb ningú i no t'enviarem correu brossa
Subscriu-te araTransport i Logística
1.187Comercial i Vendes
1.052Informàtica i IT
1.045Administració i Secretariat
913Comerç i Venda al Detall
611Veure més categories
Enginyeria i Mecànica
515Desenvolupament de Programari
502Educació i Formació
399Indústria Manufacturera
388Màrqueting i Negoci
329Dret i Legal
307Instal·lació i Manteniment
257Publicitat i Comunicació
154Sanitat i Salut
139Disseny i Usabilitat
135Art, Moda i Disseny
121Arts i Oficis
108Construcció
101Recursos Humans
99Alimentació
86Comptabilitat i Finances
82Atenció al client
56Hostaleria
51Turisme i Entreteniment
48Cures i Serveis Personals
44Producte
42Banca
32Farmacèutica
32Immobiliària
28Social i Voluntariat
22Seguretat
18Energia i Mineria
13Esport i Entrenament
7Assegurances
6Telecomunicacions
4Editorial i Mitjans
1Agricultura
0Ciència i Investigació
0Scientist (Percutaneous Absorption)
14 de febr.Kymos Group
Cerdanyola del Vallès, ES
Scientist (Percutaneous Absorption)
Kymos Group · Cerdanyola del Vallès, ES
We are hiring a Scientist for our Percutaneous Absorption department.
Under the supervision of the Department Manager, the Scientist will carry out the following activities:
- Conduct in vitro release studies of dermal/topical products from the development to the final stages.
- Perform in vitro permeation studies through biological membranes from the development to the final stages.
- Be responsible and accountable for the execution and oversight of the assigned IVRT/IVPT projects.
- Preparation of study protocols and reports.
- Knowledge in the use of equipment for sample analysis generated from the in vitro studies, mainly HPLC.
- Equipment maintenance and qualification operations.
- Writing and update of specific Standard Operational Procedures of the department.
- Ensuring compliance with timelines and quality of the studies.
- Work under GLP/GMP standards.
- If you join us, you will enjoy:
- Working in a dynamic company with a highly qualified growing team
- Professional development and collaborative environment and a culture of empowerment.
- Flexible Working Hours and intensive schedule on Friday.
- Access to the employee benefits flexibility platform.
- 23 vacation days per year plus 24th and 31th of December.
- Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
- Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.
- Degree in chemistry, biotechnology, pharmacy or biology.
- Experience in transdermal or in semi-solid products.
- In depth knowledge in working in a GLP/GMP environment.
- Able to work and lead studies autonomously.
- Good communication and interpersonal skills.
- Good planning, organization and problem-solving activities.
- Proactive, adaptable and energetic approach.
- English – Level B2.
Analista Revisor de Calidad Interno
7 de febr.Kymos Group
Barcelona, ES
Analista Revisor de Calidad Interno
Kymos Group · Barcelona, ES
Estamos contratando un Analista Revisor de Calidad Interno para nuestro Departamento de Control de Calidad de Biológicos. El analista será responsable de las siguientes funciones:
- Revisar auditar los datos primarios del departamento
- Colaborar en la mejora interna de procesos de registro de datos
- Tareas administrativas generales (gestión de compras, gestión de laboratorio, archivo de documentación,…)
Review audit departmental primary data
Collaborate in the internal improvement of data recording processes
General administrative tasks (purchasing management, laboratory management, documentation archiving,...)
Requisitos:
Requisitos
- Ciclo formativo Análisis Químico, Control de calidad, Auxiliar de farmacia, Análisis clínico o similar
- El candidato debe tener conocimientos de Técnicas de Control de Calidad y Análisis en Productos Farmacéuticos y de la normativa GMP.
- Para este puesto se requiere un nivel medio de inglés escrito.
Training Cycle Chemical Analysis, Quality Control, Pharmacy Assistant, Clinical Analysis or similar
The candidate must have knowledge of Quality Control and Analysis Techniques in Pharmaceutical Products and GMP regulations.
An intermediate level of written English is required for this position.