Jobs

Do you have (micro)biology background? And do you want to work in safety? 2M and Thermo Fisher Scientific are looking for you! For our client, we are looking for an Environmental, Health and Safety specialist.

De functie van Monstercoördinator is ondergebracht in het Service Laboratorium Delft (SLD) met in totaal circa 50 medewerkers. Het SLD heeft als werkgebied microbiologische, biochemische, chemisch/fysische of chromatografische analyses en voert standaardanalyses uit volgens bekende voorschriften.

The QESH Advisor, as a member of the DBC QESH team, informs, advises, coaches, challenges and supports the DBC organization on Safety, Health, Quality, Environment (QESH), in order to secure a healthy and incident-free working environment, today and tomorrow.

The Contract Manufacturing Organisation planner (CMO planner) serves as the primary point of contact for CMO’s for demand and supply day to day activities. The CMO planner is responsible for the coordination of order demand and supply planning (API order and delivery, consumption of API at CMO, the production planning in alignment with customer contracts). Deals with issues related to the production of FDF and takes mitigating actions, in alignment with CMO manager, when necessary. The CMO planner is responsible for reporting and administrating relevant production-related data (e.g. SAP) and KPI reporting for the CMOs assigned to the portfolio. For this position cross-functional cooperation is essential and the CMO planner is a core team member of the cross-functional CMO teams.

Royal DSM is a global, purpose-led, science-based company active in Nutrition, Health and Sustainable Living. DSM’s purpose is to create brighter lives for all. DSM addresses with its products and solutions some of the world’s biggest challenges while simultaneously creating economic, environmental and societal value for all its stakeholders – customers, employees, shareholders, and society at large.

We offer a family of solutions that benefit our customers and make lives brighter. But what sets us apart is our unique scientific approach – what we really provide are commercially attractive answers to the greatest challenges facing our world; how to feed everyone and keep them healthy and happy, tackle climate change and enable a restorative bio-based, circular economy.

In deze rol ondersteun jij verschillende afdelingen op logistiek gebied. Het kan zijn dat je de ene dag binnen de afdeling Transport werkt en de andere dag binnen de afdeling Distributie. Een zeer afwisselende en uitdagende logistieke functie.

Voor onze klant Centrient Pharmaceuticals in Delft zijn wij per direct op zoek naar een procesoperator met Vapro B. In de rol van procesoperator staat het controleren en beheersen van delen van productieprocessen in de fabriek centraal. Dit moet zodanig gebeuren dat de producten worden geproduceerd binnen de gestelde normen ten aanzien van kwaliteit, GMP, milieu en veiligheid tegen de laagst mogelijke kosten en binnen de afgesproken planning.

For this role, 3D PharmXchange works exclusively with 2M International Recruitment. 
Our client 3D PharmXchange is hiring a CMC professional to strengthen their dedicated CMC Consultancy team! 3D-PharmXchange is a Dutch Life Sciences consultancy and operational support firm with offices in Tilburg and Oss.  There’s a dedicated team of Drug Development experts covering the key areas of pre-clinical, clinical, CMC, regulatory affairs and project management. In addition, 3D-PharmXchange provides out-licensing and interim management support. Their clients are mainly early phase biotech, but they also support leading big pharma companies.

Our Client, Centrient Pharmaceuticals, is looking for a Regulatory Affairs Lead in its Rijswijk offices. 

Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics and a provider of next-generation statins and anti-fungals. We produce and sell intermediates, active pharmaceutical ingredients, and finished dosage forms.

Consultant non-clinical development

Our client 3D-PharmXchange is a Dutch Life Sciences consultancy and operational support firm located in Tilburg and Oss. We are dedicated to the development of (bio-)pharmaceuticals and diagnostics. Our team of experts covers the key areas of pre-clinical, clinical, CMC, regulatory affairs and project management. In addition, we provide out-licensing and interim management support. Our clients are leading big pharma companies as well as innovative biotech start-ups.