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Senior Specialist, Visual Inspection
Er du interesseret i at blive en del af en nystartet fabrik under hurtig udvikling? Har du erfaring med visuel inspektion inden for lægemiddelindustrien? Hvis ja, så er der en fremragende mulighed for at blive en del af vores eventyr hos Bavarian Nordic.
Vi er på udkig efter en specialist i visuel inspektion til at indgå i vores back office team inden for produktionssupport. Du vil spille en central rolle i håndteringen af vores proces for visuel inspektion.
Manager Virus Production
Do you want to play a central and important role in Bavarian Nordic´s manufacturing strategy by setting directions and ensuring smooth daily operation in our production facility?
Our newly established Drug Substance Facility in Kvistgaard will soon start production ramp-up, and we therefore need to strengthen our leadership. You will become responsible for the day-to-day shopfloor management of 15-20 operators.
Senior Project Manager
Are you motivated by being the driver of the implementation of new equipment/facilities or complex upgrading projects) up to EUR 15 million?
You will be responsible for and ensure project execution of all phases in your projects including scope definition, identifying the solution, and mitigating risks, time, budget, and quality. We primarily work with the stage gate model for our larger projects.
Drug Substance Production Supporter
Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. In Virus Production Support team your main area of responsibility will be:
- Trouble shooting in production
- Process confirmation to ensure your processes are running according to written procedures
Specialist QA Record Management
Do you have solid experience with electronic Document Management Systems (EDMS), Data Integrity, and record-keeping policies and systems?
Our vaccines make a real difference to people, and no matter your role we all contribute to protecting lives every day. This is how your work matters:
- Act as process manager for the Record Management process
- Responsible for how our EDMS systems work
- Responsible for how our physical paper archive system works
Manager
Are you ready to take the lead and guide a team of competent project managers and talented specialists to new heights of success?
We are seeking a passionate people Manager to join our dynamic project and process team for this new role in Drug Product technical support at our manufacturing site in Kvistgård. You will report to the Director of Drug Product Production Support and have seven/eight direct reports.
Tech Transfer Scientist
Do you want to play a central role in ambitious projects? Are you motivated by cross-organisational tasks? Would you like to join a fast-moving international company with state-of-the-art technologies within vaccine production?
In this position you will be responsible for the transfer of Drug Product manufacturing processes, like formulation, filling, and freeze-drying.
As a scientist you will work closely together with the colleagues in the Manufacturing Science & Technology department as well as colleagues across the organization
Regulatory Affairs Manager
Are you an experienced regulatory affairs professional who is looking for a new and exciting challenge as a next step in your career?
Your main responsibilities:
- Ensure compliance with food legislation for Denmark (mainly waters).
- Being the trusted subject matter expert within EU and local food legislation for waters/drinks.
We offer a career in a purpose driven and fast-moving international company.
Regulatory Affairs Assistant – Farmakonom eller tilsvarende
Vi søger en farmakonom med RA-erfaring, der har mod på afvekslende opgaver i en dynamisk virksomhed. Der er gode udviklingsmuligheder, og da det er en nyoprettet stilling, kan du selv være med til at præge stillingen.
Stillingen indeholder en god blanding af selvstændige og også mere rutineprægede opgaver:
- Indtastning af data og sikring af, at produktinformationerne er opdaterede
- Efter en oplæringsperiode selvstændigt at kunne udarbejde og indsende både standard-variationsansøgninger og nationale tekster for nye lanceringsprodukter til myndighederne
Utility Engineer
Er du klar til at blive en del af en innovativ, international vaccinevirksomhed, som den tekniske specialist?
I rollen vil dine primære arbejdsopgaver være support til teknikere og brugere, herunder hjælp til fejlsøgning på anlæg og udstyr, samt at sikre:
- Robusthed af anlæg ved kontinuerligt at have styr på vedligehold
- At GMP og regulatoriske krav er overholdt
Senior Specialist Clinical Safety and Pharmacovigilance (CSPV)
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system.
The global team consists of subject matter experts for vaccine safety who work either from our site or remotely in Denmark and globally. Together they constantly collect and assess data for the life cycle benefit risk management across our vaccines whether authorized or still in clinical development.
You would add your clinical safety and pharmacovigilance expertise as your depth knowledge of the PV legislation to the team.
Serialization Process Specialist
Are you an experienced project manager and have experience with serialization and aggregation in pharmaceutical packaging?
You will design and set the direction for the serialization & aggregation strategy. You will become a role model throughout the organization and be recognized as an expert within the field of expertise.
We offer an inclusive and professional workplace with a strong focus on personal and professional development and welcome all people who share our passion for saving lives.
Nordic Regulatory Affairs & QA Manager
Med reference til virksomhedens General Manager vil du få ansvaret for det regulatoriske arbejde og QA for Virbac i Danmark, Sverige, Norge og Island.
Dit hovedansvar kan beskrives således:
- Ansvarlig for at Virbac overholder gældende lovgivning i henhold til GDP, veterinære lægemidler, foder samt markedsføring af veterinære produkter (petcare) i Danmark, Norge, Sverige og Island
- Ansvarlig for kvalitetsstyringssystem
- Ansvar for gennemførelse af audits. Både på lægemidler (lægemiddelstyrelsen) og foder (fødevarestyrelsen)
Production Lead – Food Ingredients
Foodjob Nordic is looking for a strong food industry professional for an attractive Production Lead role. Our client, Agrain, is a food-tech company specialized in the upcycling of spent grains. We turn spent grains into nutritious, versatile and aromatic functional flours.
The position is a new role based on the need of strengthening the technical competence and knowledge in the scale-up phase of operations. The right candidate’s strength and know-how is focused on production, technical support, equipment scoping and installation within the food or feed industry.
Senior Environmental Professional
Som vores nye miljøsupporter vil du blive involveret i den daglige drift, og vi vil sikre at du får de rigtige kompetencer til at løse dine opgaver, så du nemt kan supportere vores vaccineproduktion med:
- Support til vores procesfolk i aseptisk produktion
- Håndtere dagligdags udfordringer i vaccineproduktionen
- Evaluering af data for miljømonitorering for proces og renrum
Quality Assurance Specialist
Do you want to help secure products for the market from our Production Facility? Are you motivated by a diverse everyday life characterized by new challenges and problem-solving? Are you challenged by ensuring the quality of Batch documentation?
We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and welcome people who passion for saving lives. Working from home is an option, when it fits into the needs of the department.
Senior QA Professional for Environmental Monitoring
You will become a part of the QA for ENV team, working alongside two experienced QA specialists and a QA professional, and reporting to the QA Manager for the EQ and ENV team.
In this team, everyone helps and is always available for each other. We promote a quality mindset throughout the organization.
We offer an inclusive and flexible workplace with a strong focus on personal and professional development, and we welcome people who share our passion for saving lives.
Regulatory Affairs Assistant
Are you keen on processing documents, checking texts, and managing various databases, and do you actually enjoy paperwork?
Then you could be exactly what we are looking for as our Regulatory Affairs Assistant.
The role will involve, but not be restricted to, the following activities:
- Proofreading of artwork, SmPC, PIL, and labelling text
- Updating SmPC, PIL, labelling in connection with variations
Zentiva offers an opportunity to learn the newest approaches in managing creative and highly adaptive business organizations.
QC Scientist for Stability
Are you ready to be part of an innovative, international vaccine company committed to making a real difference by protecting lives every day?
At our fast-growing company, we're dedicated to protecting lives every day through the development and production of essential vaccines. As a QC Scientist for Stability, you´ll play a crucial role in ensuring the quality and efficacy of our products.
Lead Automation Engineer til Pharmadivisionen
Har du en god procesforståelse og erfaring med at arbejde i pharmabranchen, kan du måske se dig selv som Lead Automation Engineer i Pharmadivisionen.
Vi søger to nye kollegaer med en stærk automationsfaglig erfaring og kendskab til at arbejde med sterile processer. Du bliver en del af afdelingen: C&Q/Automation – en nyere afdeling som vi er godt i gang med at opbygge. På nuværende tidspunkt består den af syv dedikerede medarbejdere, der arbejder med commissioning, automation og test af anlæg. Her vil du indtage en central rolle som specialist på automationsområdet, og du vil få rig mulighed for at være med til at udvikle C&Q/Automation-afdelingen.