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 araInstal·lació i Manteniment
1Màrqueting i Negoci
1Publicitat i Comunicació
1Sanitat i Salut
1Administració i Secretariat
0Veure més categories
Agricultura
0Alimentació
0Art, Moda i Disseny
0Arts i Oficis
0Assegurances
0Atenció al client
0Banca
0Ciència i Investigació
0Comerç i Venda al Detall
0Comercial i Vendes
0Comptabilitat i Finances
0Construcció
0Cures i Serveis Personals
0Desenvolupament de Programari
0Disseny i Usabilitat
0Dret i Legal
0Editorial i Mitjans
0Educació i Formació
0Energia i Mineria
0Enginyeria i Mecànica
0Esport i Entrenament
0Farmacèutica
0Hostaleria
0Immobiliària
0Indústria Manufacturera
0Informàtica i IT
0Producte
0Recursos Humans
0Seguretat
0Social i Voluntariat
0Telecomunicacions
0Transport i Logística
0Turisme i Entreteniment
0Top Zones
Sabadell
8Granollers
5Parets del Vallès
5Palau-solità i Plegamans
4Barberà del Vallès
3Caldes de Montbui
1Llagosta, La
1Lliçà de Vall
1Montornès del Vallès
1Santa Perpètua de Mogoda
1Top Ocupacions
Netejador/a
1Noucor
Palau-solità i Plegamans, ES
Junior Clinical Quality Associate (R&D)
Noucor · Palau-solità i Plegamans, ES
. QA Office
Do you want to be part of a team with a real impact on global health?
At Noucor, a chemical and pharmaceutical company, we offer you the opportunity to lead projects that reach more than 100 countries worldwide 🌍.
We are currently looking for a Clinical R&D Quality Assurance Technician to join Noucor’s Quality team.
Main Tasks:
- Ensure that all processes related to clinical trials are performed in compliance with GCP (Good Clinical Practice) and applicable quality standards.
- Provide QA support to clinical trial activities, including documentation review and quality oversight of internal teams and external partners (CROs, service providers).
- Evaluate and manage quality issues, deviations, CAPAs, change controls and complaints related to Clinical Trials.
- Support quality activities related to Investigational Medicinal Products (IMPs) in collaboration with Pharmaceutical Development and Analytical Development.
- Maintain awareness of applicable quality regulations and compliance requirements impacting clinical development and R&D activities.
Requirements:
- Degree in Pharmacy, Chemistry, Biology, or similar.
- Fluent in English and Spanish.
- Experience in Good Clinical Practices (GCP); knowledge of GMP requirements for IMPs in clinical trials (formerly Annex 13).
- Good command of MS Office.
- High willingness to learn and take on new challenges and responsibilities.
- Motivation, teamwork, and good communication skills.
We Offer:
🤩 Work within a great team of professionals with a very good work environment.
⚙️ Innovative work environment focused on continuous improvement.
🚀 Continuous learning and development.
💼 Competitive benefits package and flexible schedule.
📍 Offices in Palau-solità i Plegamans.
💰 Competitive salary.
Interested in joining us?
At Noucor, we believe in the value of diverse teams. We therefore welcome and consider all applications regardless of gender, age, background, sexual orientation, gender identity, or any other personal characteristic.
If you meet most of the requirements and are motivated by the project, we would be pleased to hear from you.