Do you want to develop your team lead skills and be responsible for managing accounting processes, ensuring financial integrity, and supporting strategic decision-making by delivering reports? Symeres is looking for a detail-oriented and enthusiastic Finance Lead to manage accounting operations for our Dutch entities. You will report directly to the Group Financial Controller, based in Nijmegen. You will be part of an international and autonomous team of professionals, where you can drive your own career path. Here, you help shape the future of medicine development.
For more information, check the vacancy text.
For our Weert site, we are looking for a talented Process Engineer. The primary focus of the Process Engineer comprises scale-up and commercial cGMP manufacturing activities in the Manufacturing Department. The work is carried out on (extended) dayshifts and is done in the multipurpose facilities at the Kilogram Lab and the Pilot Plant.
For more information, check the full vacancy text.
For our Weert site, we are looking for an enthusiastic QC Analyst. The Quality Control department is responsible for analytical method validation, testing of raw materials, In-
Process Controls, Intermediates, Active Pharmaceutical Ingredients (APIs), and stability testing.
For more information, check the full vacancy text.
Symeres is looking for an entrepreneurial Global Director Quality who is responsible for managing and further developing Quality Assurance and Quality Control within the organization. With a focus on managing the QA/QC departments at our biggest API GMP manufacturing site in Weert, The Netherlands, the Global Director Quality will be responsible for setting up and maintaining a coherent global Quality Assurance and Quality Control framework covering all activities of Symeres.
For more information, check the full vacancy text.
Symeres komt graag in contact met een gemotiveerde Team Leader Facility die zijn ervaring, kennis en kunde wil inzetten bij onze Groningen site.
Voor meer informatie, lees de vacature tekst door hier te klikken.
Word de drijvende kracht achter onze technische operaties!
Ter versterking van het maintenance team in Weert zijn wij op zoek naar een ervaren en gemotiveerde Maintenance Engineer.
Voor meer informatie, lees de vacature tekst door hier te klikken.
Do you want to contribute to the development of new medicines? We are recruiting for an Analytical Chemist in Groningen. In this role, you will closely work with synthetic chemists to analyze and purify molecules. Through comprehensive training and hands-on experience with diverse techniques, you will grow into a confident, skilled, and adaptable analytical chemist.
For more information, check the full vacancy text.
In this senior role, you will not only execute advanced analytical work but also take responsibility for scientific problem-solving, mentoring of junior colleagues, and acting as a key discussion partner for both internal teams and clients. You will operate with a high degree of independence, managing your own projects and ensuring quality and timely delivery of results.
For more information, check the full vacancy text.
In deze functie geef je leiding aan ons HR Services-team, bestaande uit twee ervaren HR-assistenten. Samen met je team en onze externe payrollpartner bouw je aan een solide basis en stimuleer je procesverbetering en digitalisering. De functie vereist hands-on leiderschap. Je begeleidt de dagelijkse operatie, coacht je team en leidt initiatieven die HR-diensten optimaliseren, de medewerkers-ervaring verbeteren en de groei van de organisatie ondersteunen.
Voor meer informatie, lees de vacature tekst door hier te klikken.
DGr Pharma, a member of the Symeres group, is a young and dynamic consultancy company with a very strong client base. DGr Pharma is specialized in guiding drug development programs from end lead selection to Phase II clinical development. To expand and strengthen our support in drug development, we are searching for a senior Quality Assurance Manager, with a focus on GxP in general and GLP/GcLP in detail.
To expand and strengthen our support in clinical drug development, we are searching for an organized Clinical Trial Manager to implement and oversee projects, and to ensure quality of trials.
The QA Projects Officer ensures compliance with current Good Manufacturing Practice (GMP) guidelines, corporate policies, and site standard operating procedures. The QA team provides quality oversight for the production and analysis of Active Pharmaceutical Ingredient (API) batches for our customers. You will be part of a dedicated team of five QA professionals based at our Weert site.
For more information, check the full vacancy text.
As Principal Scientist, you will serve as a scientific authority in early phase small molecule Drug Development, bridging solid-state chemistry with pre-clinical formulation development and developability risk assessments. You’ll provide strategic, scientific and experimental leadership to ensure that our clients’ drug candidates move efficiently from discovery to toxicological and clinical studies.
For more information, check the full vacancy text.
