capa

This role as quality specialist – Clinical QP needs to assess and strengthen the Quality Management System in alignment with applicable EU GMP requirements. The function supports inspection readiness and the Manufacturing Import Authorization project by identifying gaps, defining actins, and enabling compliant processes for clinical product...

About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis...

About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis...

About Akkodis Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis...

Senior Pharmacovigilance Quality & Compliance Lead (AD Level) Summary This is a strategic leadership role focused on ensuring the effectiveness, compliance, and continuous improvement of the global Pharmacovigilance Quality Management System. You will oversee audit and inspection readiness, PV agreements, training programs, quality processes, and...

IntroductieApply below after reading through all the details and supporting information regarding this job opportunity.Solid Talent is een expert in flexible & temporary staffing gespecialiseerd in technische specialisten voor sectoren zoals energie, petrochemie, metallurgie, bouw en infrastructuur, life sciences, logistiek, opslag en transport. We...

Position SummaryThe Director, External Manufacturing Regulatory Compliance Oversight, provides independent regulatory compliance oversight, risk visibility, inspection-readiness support, governance, and organizational learning across the Innovative Medicine External Manufacturing network. The role partners with External Manufacturing Operations, Quality,...

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and...

Want to join a growing company in the biotech industry ? Do you enjoy hands-on, structured work while participating in a variety of tasks ? Willing to be part of a company advancing health and improving lives ? At LaCAR, we are advancing health and improving lives. LaCAR is continuing to grow and we are looking for a Production Scientist who is passionate...

About Cellistic Cellistic is an iPSC-first CDMO helping bring the next generation of cell therapies from innovation to the clinic. Based in Mont-Saint-Guibert, Belgium, we provide integrated services from iPSC cell line development and process development through GMP manufacturing and release testing. Combining deep iPSC expertise with our proprietary...

Johnson & Johnson Innovative Medicine in Beerse, Belgium seeks a Quality Assurance Associate – Clinical Supply Quality (CSQ) to join the CSQ Post-Certification team. You will help ensure the quality, safety, and compliance of investigational medicines used in clinical trials worldwide, working across Quality, Supply Chain, Clinical Development, and...

NOUVELLE OPPORTUNITÉ – SECTEUR BIOPHARMA / GMPPlease read the information in this job post thoroughly to understand exactly what is expected of potential candidates.Manufacturing System Quality PartnerSecteur : Braine-l'Alleud (Belgique)Régime : Temps plein (8h/jour)Vous souhaitez rejoindre un acteur majeur de l'industrie biopharmaceutique et contribuer...

NOUVELLE OPPORTUNITÉ – SECTEUR BIOPHARMA / GMPPlease read the information in this job post thoroughly to understand exactly what is expected of potential candidates.Manufacturing System Quality PartnerSecteur : Braine-l'Alleud (Belgique)Régime : Temps plein (8h/jour)Vous souhaitez rejoindre un acteur majeur de l'industrie biopharmaceutique et contribuer...

Functie Maken of assisteren bij het schrijven van testprotocollen/rapporten, change requests, CAPA’s, rootcause analyses en technische documentatie met bijhorende rapportage Opvolgen van de beoordeling van de opgestelde Sharp documenten binnen het eigendom Beheer van testen, changes en CAPA actionlists en het garanderen van de noodzakelijke vooruitgang...

Functie - Maken of assisteren bij het schrijven van testprotocollen/rapporten, change requests, CAPA’s, rootcause analyses en technische documentatie met bijhorende rapportage - Opvolgen van de beoordeling van de opgestelde Sharp documenten binnen het eigendom - Beheer van testen, changes en CAPA actionlists en het garanderen van de noodzakelijke...

Functie - Maken of assisteren bij het schrijven van testprotocollen/rapporten, change requests, CAPA’s, rootcause analyses en technische documentatie met bijhorende rapportage - Opvolgen van de beoordeling van de opgestelde Sharp documenten binnen het eigendom - Beheer van testen, changes en CAPA actionlists en het garanderen van de noodzakelijke...

pVous êtes passionné(e) par l'Assurance Qualité et souhaitez rejoindre un environnement GMP où votre expertise fera réellement la différence ? /pbrLike the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description.brpDans le cadre du renforcement de son département...

Functie - Maken of assisteren bij het schrijven van testprotocollen/rapporten, change requests, CAPA’s, rootcause analyses en technische documentatie met bijhorende rapportage - Opvolgen van de beoordeling van de opgestelde Sharp documenten binnen het eigendom - Beheer van testen, changes en CAPA actionlists en het garanderen van de noodzakelijke...

Functie - Maken of assisteren bij het schrijven van testprotocollen/rapporten, change requests, CAPA’s, rootcause analyses en technische documentatie met bijhorende rapportage - Opvolgen van de beoordeling van de opgestelde Sharp documenten binnen het eigendom - Beheer van testen, changes en CAPA actionlists en het garanderen van de noodzakelijke...

Senior Pharmacovigilance Quality & Compliance Lead (AD Level) Summary This is a strategic leadership role focused on ensuring the effectiveness, compliance, and continuous improvement of the global Pharmacovigilance Quality Management System. You will oversee audit and inspection readiness, PV agreements, training programs, quality processes, and compliance...