31 jobannoncer matcher din søgning 31 jobannoncer fundet

QA Assistant, GS-5, QAC

This position is embedded in the Quality Assurance Centre (QAC), where teams have coreresponsibilities around quality assurance and quality control of supply processes and the productswe procure and deliver.

The incumbent will beresponsible for assisting the Quality Assurance Specialist (non-pharma) in the management of all aspects of Pre-Delivery Inspection (PDI) arrangements for non-pharma items from initial request tofinal invoice certification.

Global Regulatory Specialist, Plant Health (temporary position)

As Regulatory Affairs Specialist you will be part of the Global Regulatory Affairs team, with around 18 team members across the globe. You will work closely with stakeholders in the Plant Health industry and support the execution on regulatory strategies globally.

You will interact with cross-functional product and project groups and maintain close interaction with stakeholders in biotechnology, other parts of R&D, sales, marketing and with strategic customers and authorities.

Formulation Scientist

Are you looking to use and grow your experience in formulation development in a broad role with independent responsibilities? Do you want to drive formulation projects and contribute to the strategic development of future products?

In this role, your overall focus will be formulation development of drug products. Your responsibilities will cover formulations used for toxicology and clinical studies through the development phases and all the way to the commercial drug product.

Senior Operation Engineer

This is a unique opportunity to take an active part in the development of a green industry and to have a very independent position with a high degree of personal responsibility and a variety of work tasks, both practical and desk-work.

This is not just a job, but a career you can take an active role in the industrial energy transition. We believe carbon capture is essential to reach the goals of the Paris Agreement. We value the feeling of belonging, and this role will be crucial in supporting Aker Carbon Capture to help the industry meet its carbon capture obligations.

Experienced Scientist for validating QC methods in Novonesis

Do you want to work in an environment where great collaboration is valued as highly as scientific excellence?

Working as Scientist in our team, you will be responsible for validating and optimizing analytical methods for Human Health products in our QC labs. You will work closely with other scientists and laboratory technicians to plan and implement efficient microbiological methods.

QA Specialist for Environmental Support

In this role, you will join Bavarian Nordic's QA Organization as a QA Specialist tasked with establishing strong relationships with stakeholders, effectively communicating GxP requirements, and handling crucial Quality Events in the Quality Management System (QMS).

This is in the context of environmental monitoring, aseptic performance, and sterile & low bioburden processes in Drug Substance and Drug Product Production. Additionally, you will contribute to the ongoing improvement of QA processes to elevate overall quality standards.

Microbiologist

You will contribute to the testing and release of vaccines against critical diseases. QC Microbiology is responsible for performing analyzes of routine samples and validations of new products.

You will be part of a workplace with a high pace and many different types of tasks e.g.: Approval of sample results, write deviations and change requests, and write validation protocols and reports.

QA Ext. Manufacturing Specialist

Would you like to work in one of the most interesting, complex, and dynamic areas in Bavarian Nordic? Are you ready to engage, support, and mobilize colleagues in a growing international business environment where we focus on saving lives every day?

As a QA Specialist, you will be responsible for daily support, QA oversight, and GMP guidance to Contract Manufacturing Organizations (CMOs) to ensure that our products are manufactured according to current GMP and our marketing authorizations.

Manufacturing Process Engineer

Are you a results-driven problem-solver, eager to positively change the world? Do you believe that climate change is the biggest issue facing us today?

You are primarily responsible for primary process tracking, deviation tracking and reporting, as well as process transfer and optimization for our pilot plant and larger manufacturing systems.

Process and Innovation Lead

We are hiring a Process and Innovation Lead for our factory in Odense, where we produce detergents under our strong Home Care brands such as Neutral, Biotex, and OMO.

In this position you will be the owner of our fabric wash manufacturing processes in the factory. A critical part of this role will be ensuring an effective link with R&D, planning, and factory for innovation, capacity, and project delivery. You will be responsible for mapping potential sustainability projects.

Single Use Systems Professionals

Som Single Use Systems Professional arbejder du med at forbedre Drug Substance produktionens Single Use systemer. Det kan eks. være i forbindelse med en eksisterende item, der ikke fungerer optimalt eller udgår. Du skal derfor søge efter brugbare erstatninger på markedet og kommunikere med leverandørerne og i samarbejde med processpecialisterne designe nye løsninger.

Du bliver en del af en afdeling på i alt 14 kolleger og i dette team er der 7, hvor alderen ligger omkring 30-45 år. Som ny medarbejder bliver du sidemandsoplært og kommer til at følge interne kurser. Du får også en Buddy fra teamet, som du kan støtte dig til.

Kemiker til QC med GMP-erfaring

Syntese A/S søger en erfaren kemiker med kompetencer og interesse for analytisk kemi og GMP. Stillingen er en udvidelse af nuværende team.

Dine primære opgaver er at indgå i afdelingens daglige drift, hvor du supporterer og godkender analyser i et tæt samarbejde med dine kollegaer i teamet. Du udarbejder afvigelser, opdaterer SOP´er og vedligeholder kvalitetssystemerne.

Manufacturing Supporter

We are looking for a talented Manufacturing Supporter for the Drug Substance Production to join the DS Documentation and Support Department in Hillerød.

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) has never been more important—and we are looking for talented candidates to join us.

You will be part of a team, consisting of 14 people, with a great sense of humor and a high willingness to support where needed.

Drug Substance CIP Process Supporter

Are you passionate about pharmaceutical CIP? Do you know processes and optimizing production?

As a CIP Process Supporter (Cleaning In Place), you will have a cross-functional role as a link between production, support teams, and technical support.

Your primary focus will involve optimizing our vaccine production and ensuring robust operation in line with CIP requirements and regulations. Additionally, you will play a vital role in daily troubleshooting, collaborating across diverse professional groups to ensure a streamlined production process.

Senior QA Specialist

You will be part of our QA Business Support Team, consisting of 12 QA Specialists and Senior QA Specialists, allocated to projects including innovation projects, capacity projects and strategic QA/QC projects. We participate in projects both as quality and compliance experts to ensure compliance with the requirements for Class III Medical Devices.

We are driven by improving patient outcomes and we take our values to work every day – we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions.

PhD scholarship in digitalization of polymer-based battery electrolyte development - DTU Energy

If you have the ambition to build your scientific career at the forefront of cutting-edge research and contribute to accelerating green transition via digitalization, we have a perfect PhD opportunity for you.

You will work on a project to design fluorinated polymers prepared through light-induced polymerization. The design space for finding the optimal composition and synthesis conditions for polymer electrolytes is too vast to explore manually. Therefore, we are combining self-driving labs, high-throughput atomic scale simulations, and AI to transition to digitalization-based automation of electrolyte development.

Graduate – Software Automation Program

Cognizant Denmark is currently seeking applications from Graduate Engineers for our Graduate Program in 2024 based in Hillerød, Denmark.

Successful candidates will be part of the Global Graduate Program.

This Program is an intensive 8-week Training Program that consists of Classroom Training, Workshops, Theory, Practical Training, and a Simulation Project.

Nyuddannet laborant til QC-afdeling

Brænder du for kvalitets- og laboratoriearbejde, og vil du være med til at sikre driftssikkerhed og kvalitet af analyser indenfor medicin- og fødevareindustrien?

Vi søger en laborant på fuldtid til vores QC-laboratorie i Birkerød, hvor du vil komme til at indgå i et team af 8 laboranter, 5 kemikere og 1 laboratorieleder.

Afdelingen er kendetegnet ved at have et godt samarbejde, være fagligt dygtige og meget lydhøre overfor forbedringer i arbejdsgange omkring analyse.

QA Specialist

We are seeking a competent new colleague to join our QA team in a dynamic and growing company.

You will be part of our highly dedicated team consisting of 5 colleagues working with a broad range of QA tasks such as batch review, processing of complaints, deviations and change requests as well as validation and ad hoc projects.

Laborant til mikrobiologisk team

Har du lyst til at være med til at sikre vacciner til forebyggelse af infektionssygdomme?

Bavarian Nordic er i en rivende udvikling og derfor søger vi en laborant til det mikrobiologiske team i Kvistgaard. Du vil i stillingen bidrage til test og frigivelse af vacciner mod kritiske sygdomme. QC-mikrobiologi har ansvaret for at udføre analyser af rutine prøver og valideringer af nye produkter. Desuden yder vi support til vores produktion.