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.

QA-assistent til international producent af kosttilskud og lægemidler

‎Trives du med at arbejde i et GMP-reguleret miljø, og vil du gerne bidrage til at opretholde den høje kvalitet?

Vi tilbyder et alsidigt job i et åbent og dynamisk arbejdsmiljø med muligheder for faglig og personlig udvikling.

Du kommer til at indgå som en del af et tæt tværfagligt samarbejde med bl.a. laboratorie-, kemi- og kvalitetssikringsafdelingen. Du vil være tilknyttet kvalitetssikringsafdelingen, hvor der vil være gode muligheder for udvikling.

Opgaverne kan bl.a. bestå i:

• Gennemgang, kontrol og frigivelse af råvarer, færdigvarer eller emballagedele.
• Arkivering af dokumentation og referenceprøver.
• Supportfunktion for øvrige afdelinger i form af certifikater og øvrig dokumentation.

Senior Engineer Device Manufacturing

Are you passionate about cutting-edge medical technology? Do you thrive in a collaborative environment where innovation drives patient care?

Amgen, a global biotechnology leader, is expanding its device development capabilities in Denmark and is seeking a talented Senior Engineer to join our Device Engineering group.

Nanofabrication Technician to state of the art laboratory

We are looking for a Nanofabrication Technician for our client’s brand new, state of the art, semiconductor and fabrication laboratory in Copenhagen. The lab is among the largest in Europe and you get to work with cutting edge technology in a highly dynamic environment of scientist, researchers and engineers trying to push the boundaries of computing.

Material science and fabrication are the foundation and the enablers of qubit devices. In their research, our client deals with complex stacks of different materials, combined at the nanoscale, and require high repeatability of fabrication processes.

Senior Compliance Professional

Do you have a broad experience with compliance-related matters within root cause investigations and systematic problem-solving in a pharmaceutical Engineering or Manufacturing organization?

You will participate in improving our systematic problem-solving skills and systems to prevent recurrent deviations and deliver compliance support for the Utility-, Metrology-, Maintenance- and Automation- specialists.

You will be part of a team with a focus on well-being, and achieving our goals, and where there is room to have fun along the way.

Specialist til API-produktion i København - Vær med, når vi redder liv

Du vil lede root cause-analyser, koordinere kvalitetsopgaver, være ansvarlig for kvalificeringer/valideringer af procesændringer, følge op på produktionsdata samt overvåge processerne. Arbejdet foregår i tæt samarbejde med kvalitetsafdelingen og den tekniske afdeling. Du vil ligeledes opleve operatører, teknikere, specialister og API-ledelsen som vigtige interessenter.

I stillingen vil dit primære ansvar og dine opgaver være:

• teknisk sparring og processupport til produktionen
• håndtering af kvalitetssager

Kvalitetschef, QP/RP

Vil du gøre en forskel for den enkelte patient og bringe alle dine farmaceutiske kompetencer i spil?

Som Kvalitetschef vil du både arbejde i dybden med QA-opgaver og samtidig drive og udvikle kvalitetsområdet gennem dine medarbejdere.

Du vil sikre, at godkendelser og certificeringer altid er ajourførte, og at alle forretningsgange imødekommer gældende krav og regler.

Nyuddannet proces, - eller industrioperatør til fermentering i medicinalproduktion hos Xellia

Er du teamplayer af natur og parat til nye udfordringer?

Som operatør vil dine primære arbejds- og ansvarsområder være:

• fyldning, sterilisering, podning, fermentering og høst
• overvågning og betjening af procesanlæg
• overvågning og betjening af forsyningsanlæg, herunder vandanlæg og nedbrydningsanlæg

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.

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.

Project Manager

Som Project Manager på fabrikken i Hobro vil dit job være opdelt i en projektlederrolle, og en rolle der dækker daglige driftsopgaver.

Du både deltager i og leder selvstændigt større projekter relateret til fabrikkens anlæg og udstyr - fx lokaleombygning, installation af ventilationsanlæg, dokumentation etc. Du skal planlægge og udføre projekter fra start til slut, herunder sikre at tidsplaner og budgetter overholdes, være primær kontakt til myndigheder og eksterne samarbejdspartnere samt udføre, lede og koordinere arbejdet i projekt teamet, så projekterne kommer godt i mål.

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.

QA Assistant

Motiveres du af en stilling, hvor du har fokus på systemer og kvalitet? Og vil du arbejde med fremstilling af pakkematerialer til den farmaceutiske industri?

Du vil få daglig sparring med operatører, specialister og ingeniører i vores produktionsenhed i Horsens – som årligt producerer ca. 2,5 milliarder enheder.

Vi tilbyder en spændende stilling med mulighed for at sætte dit personlige præg på måden, tingene fremadrettet skal gøres på.

Senior Medical Writer

Do you want to work in a global context and according to the highest standards of current practice to provide new products to patients with unmet medical needs?

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.