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Adviseur Brand- en Omgevingsveiligheid

Schiphol Group - Schiphol
voornamelijk op de Omgevingsveiligheid. Er wordt nauw samengewerkt met de andere adviseurs binnen de HSE Office en afgestemd met collega’s binnen de afdelingen Assetmanagement, Operations en de Brandweer. Bij alles wat we doen is er
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Operator Drug Products

Luba - Amsterdam
Over het werkAls operator speel je een cruciale rol in het productieproces van bloedplasma en gerelateerde producten. Je voert verschillende productiehandelingen uit volgens strikte kwaliteitsnormen en gestandaardiseerde proc
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QA Operations Manager

Grafton Recruitment - Amsterdam
compliant microbial-based production of recombinant proteins, vaccines, and live microbials as drug substances and products. We are currently seeking a Manager Quality Assurance Operations to join our expanding team.Job Overview The
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Site Research Assistant

Iqvia via Talent - Ede
expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Nijmegen
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Groningen
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Breda
expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the
CONTRACTOR

Deputy European Union (EU) Qualified Person for Phar...

Lilly via Talent - Utrecht
effectively in a multi-cultural environment, team structure and independentlyCurrent awareness of product safety regulatory environment; ability to communicate and translate into company processesBroad knowledge of drug development and

Senior Pharmacovigilance Consultant, QPPV Office

ProPharma Group 760507 via Magnet.me - Leiden
suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. The Role The Senior Pharmacovigilance (PV) Consultant, QPPV implements and maintains QPPV
FULL_TIME

Responsible Person GDP & Responsible Person for Info...

B. Braun
promotional activities Responsible for the information provided by his company Ensures compliance of regulations on « premiums or advantages » Deputy Local Safety Officer for pharmaco-, and veterinary vigilance To review
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Brand manager benelux sunstar

Hillary Step - Naarden
ORGANISATION SUNSTAR is a leading Japanese family company operating in the business sectors of oral care, health and beauty, safety , and environment. SUNSTAR strives to provide products and services that help people
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Electrical Engineer Wacker

Wacker via Jobsonline - Amsterdam
on the GMPcompliant microbial based production of recombinant proteins, vaccines and live microbials as drug substance and drug product. To strengthen our team in Amsterdam, we are looking for you as a(n) Electrical
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