33 job matcher din søgning
Unique Human Capital recruiting on behalf of Ascendis Pharma A/S in Hellerup
Make a difference in an exciting and entrepreneurial Danish biopharmaceutical company
As Senior Quality Manager, Quality Management Systems and Compliance at Ascendis Pharma you will drive the continual improvement and maintenance of a flexible and robust quality system that supports development activities as well as the upcoming commercial activities (GMP, GLP, GCP).
With direct report to the Senior Director of Quality Systems and Compliance, you will become part of a newly established and very dedicated team.
Your main tasks are:
- Define, design, implement and maintain easy to comply and easy to follow QM processes
- Support regulatory compliance across company sites
- Guide inspection readiness at Ascendis and the CMOs
- Monitor and drive improvement of KPIs
- Challenge status quo and continuously seek out more efficient ways of working
Chr. Hansen A/S, Hørsholm
For our global QA organization, we are looking for a Senior QA Product Quality Specialist to be globally responsible for the QA setup in our product range of Food Cultures for primarily Meat & Processed Foods and Wine & Fermented Beverage applications.
You will be responsible for managing the quality of the product ranges from end-2-end i.e. across Innovation, Operations, Logistics, Commercial Development and Sales.
Your main responsibilities will be to:
- Support in defining product requirements for quality and product safety in Innovation projects and in associated HACCP framework in relation to product application
- Define specification framework and needed product surveillance/analysis programs to support claims and ensure performance in the market
Hartmanns A/S søger for RAMCON A/S i Birkerød eller Vejle
For RAMCON søger Hartmanns en produktspecialist til salg af laboratorieudstyr inden for molekylærbiologi og in vivo imaging-systemer samt køleskabe og frysere til medicinsk brug og forskning.
Din hverdag er præget af tæt samspil med dine kolleger, og selvom du arbejder selvstændigt og selv planlægger din dag, får du solid support fra din leder samt dine kolleger, så I sammen udgør den foretrukne samarbejdspartner for kunden. Du tilbydes grundig træning i produkterne og i salgskompetencer.
Fra kontorerne i Vejle eller Birkerød vil du dække hele Danmark. Inden for produktområdet vil du have fokus på forretningsmuligheder i pharma-industrien samt hospitalerne og universiteterne.
Chr. Hansen A/S, Hørsholm
We are looking for an additional engineer for our Pilot Plant in Hørsholm within the field of fermentation and downstream process development.
Collaborating with external stakeholders such as subcontractors, it will be your responsibility to make sure that user requirements are fulfilled. You will also collaborate and interact with the internal stakeholders from maintenance, engineering and the users. It will be your responsibility to make decisions based on the divergent interests of stakeholders. Further you will:
- Participate in equipment tests at subcontractors manufacturing facilities making sure that the equipment is compliant to our requirements.
- Write, review and approve documentation, e.g. during FAT/SAT and CV/PV.
Bavarian Nordic A/S, Kvistgård
To strengthen our Project Office in Kvistgaard, we are searching for an experienced Project Manager to drive projects within Bavarian Nordic throughout the whole value chain.
In the role as Project Manager/Sr. Project Manager you will have 1-3 projects at any given time - depending on the projects complexity, scale, timeframe etc.
As Project Manager/Sr. Project Manager you develop project charter, plans and secure stakeholder buy-in at all times. You visualize clear objectives, deadlines and progress, all while securing regular project team and Steering group meetings. Continuously predicting and risk mitigating problems is natural for you as meeting success criteria, deadlines and individual project budget - in close cooperation with Finance. When requested you develop, facilitate and document workshops.
Do you have profound experience with regulatory CMC for biopharmaceuticals? Would you like to share your experience and be part of building up expertise within biopharmaceuticals across Lundbeck? Then you might be the new colleague we are looking for.
Lundbeck has traditionally worked with small molecules, but we are now also aiming to develop the competences necessary to be a key player in development of biopharmaceuticals (such as monoclonal antibodies). You will have a key role in this new strategy.
In your new job, you will be:
- Responsible for all Regulatory CMC activities on biopharmaceuticals development Projects
- Responsible for developing the Regulatory CMC strategy for assigned Projects
The Center for Microbial Secondary Metabolites, CeMiSt, is a Center of Excellence funded by the Danish National Research Foundation. The Center started 1st of January 2018 and will run for six years with an option for a four-year extension.
We are looking for an ambitious mycologist with a broad experience in fungal ecophysiology, genetics and secondary metabolite production.
You will get a unique possibility to work on fungal (and bacterial) ecosystems focusing on how secondary metabolites of terrestrial fungi affect microbial diversity and functionality in both natural and engineered systems.
Arla Foods, Viby J.
Are you passionate about Food Chemistry? If so, join the Food Chemistry Team in Arla Foods. We have a global role in Arla R&D and are based in our Innovation Centre in Aarhus, Denmark.
You will be a key partner in innovative science projects and tasks with focus on protein chemistry. In this role you will combine your strong scientific skills with a business mindset. To be a success in this job you drive the protein chemistry link to a number of research and innovation projects and make sure they meet the expectations as to deliverables, time and resources.
In this job you will together with our R&D laboratory technicians maintain and develop our analytical competencies through method development and optimisation.
Albright Life Sciences A/S recruiting on the behalf of AJ Vaccines in Copenhagen
Would you like to challenge yourself and daily see the value and impact of your deliverables through building key customer relations and sales through distributors delivering high quality vaccines that fulfil a global public health mission? Then come join the Sales & Marketing Team as Regional Sales Manager.
Your main responsibility will be to build customer relations and sales through distributors operating in a tender-based and special permit market while supporting, training, motivating and developing them and their sales teams to meet strategic growth- and revenue goals.
Our Sales and Marketing Department currently employs 10 people. Our activities cover all aspects of Sales, Marketing and also includes Shipping. Travelling: 50-60 days yearly is expected.
Foodjob Nordic, Birkerød or Sverige
As Business Manager you will be responsible for a highly motivated team consisting of 4 Area Sales Manager and 3 Back-office employees. Further you will be managing a few key customer accounts within the FOOD department and working closely with the Managing Director and the Business Manager for the Health Care unit to target areas of growth and new product opportunities.
The objectives for the Business Manager include:
- Manage, coach and develop the FOOD team in order to secure a sustainable growth
- Pro-actively drive forward sales and gross margin within the sectors by managing all aspects of the customer relationship
- Responsible for the total customer interface, maintaining and growing existing business with current customers
Foodjob Nordic recruiting on behalf of Alsiano in Birkerød
Foodjob Nordic is looking for an Area Sales Manager for Alsiano’s Healthcare business.
Alsiano Healthcare offers a broad range of ingredients and raw materials for the nutraceutical and healthcare industry in Denmark, Sweden, Norway and Finland, working together with leading manufacturers of ingredients and bioactives. The product portfolio comprises among other ingredients; fibres and coating systems, plant extracts, bioactives and proteins.
Reporting to the Business Manager for Healtcare you will be part of the team of 6 dedicated colleagues. The healthcare team is covering pharmaceutical, health & personal care and this will be the industries you will work in. Further you will work very closely together with the FOOD business unit.
Y-mAbs Therapeutics A/S, Hørsholm
A new position is now open! Y-mAbs Therapeutics A/S (Y-mAbs) is looking for a CMC Project Manager. You will primarily focus on CMC activities associated with our late stage biologic development programs, and you will work with close interfaces to other functional groups within Y-mAbs. A good understanding of the outsourcing process, from quotations and contract negotiations to follow-up and troubleshooting with our CMC partners is a key competence as all manufacturing is outsourced.
It is key that you have in depth expertise within one of the following areas:
- Specific knowledge about drug product development in late stage development programs including commercial launch
- Formulation development of biologics – knowledge about sub-cutaneous formulations will be an advantage
- Solid experience in working with CMO/CRO's and international regulatory bodies like FDA and EMA
Brænder du for environment, health, safety & sustainability? Og er du god til at prioritere, tage action på udfordringer og drive løbende forbedringer i et multikulturelt og uformelt miljø, så er stillingen som tekniker hos Umicore Danmark måske noget for dig.
Vi tilbyder en spændende stilling i en international virksomhed. Du bliver tilknyttet et team på 6 medarbejdere fordelt i Lyngby og Frederikssund, der bl.a. arbejder med fremstilling af vores næste generation af produkter, som skal sikre miljørigtige løsninger til dieselbiler.
Din primære opgave bliver at fremstille katalysatorer til dieselbiler fra bunden. Arbejdet kommer til at foregå i laboratorie-, pilot- og fuld produktionsskala i samarbejde med forskere, ingeniører og andre teknikere af international topklasse fra Umicore.
We are looking to add a new Senior Specialist with strong experience within upstream process development and manufacturing to our CMC Biologics team. The team is responsible for the strategic and technical leadership of pharmaceutical development activities in support of our biologics pipeline – spanning from pre-IND stage through process validation and launch.
As a Senior Specialist, you will join focus teams responsible for the development for our biopharmaceutical drug candidates and you will work closely with colleagues responsible for the development of drug substance, drug product and analytical methods with the aim of achieving project objectives and global registrations for our biopharmaceutical drug candidates.
Haldor Topsøe A/S, Frederikssund
Har du gennem en årrække arbejdet inden for arbejdsmiljø med områder som fx ulykkesforebyggelse, arbejdsmiljøledelsessystemer og maskinsikkerhed med gode resultater? Så er det dig, vi har brug for i QEHS-afdelingen hos Haldor Topsøe i Frederikssund.
I jobbet som ’Senior Health and Safety Professional’ får du mulighed for at bringe både dine faglige og personlige kompetencer i spil, når du støtter konkrete afdelinger i den daglige drift ved rådgivning og sparring.
Derudover kommer du til at drive og medvirke i en række faglige udviklingsprojekter for at forbedre sikkerhedskulturen generelt, men også for at styrke indsatserne på en række specifikke områder som maskinsikkerhed, ATEX, ulykkesforebyggelse, ændring af processer m.m.
LEO Pharma, Ballerup
You will be Lead Auditor and will plan, perform, report and follow-up on audits. Are you a structured and systematic team player, who dream of a job with major responsibility and the license to impact decisions, you might be just the person we are looking for.
As our new Principal Quality Auditor, you will perform audits of LEO Affiliates, Regions and at our GXP regulated third parties. Audits is performed within GDP/GMP, PV and RA areas. LEO Pharma has more than 30 Affiliates in Europe, North America, South America, Middle East/Mahgreb, Asia and Australia. Each Affiliate/Region has GXP responsibilities towards QMS, distribution, pharmacovigilance, medical information and regulatory. It is LEO Pharmas responsibility from a corporate level to oversee the GXP compliance level through audits.
LEO Pharma, Ballerup
LEO Pharma has embarked on a very ambitious journey to become the world’s preferred dermatology care partner – and that is why we need you. If you can assure quality for clinical trials in order to safeguard subjects’ safety and well-being, you are the one we are looking for.
You will be GCP Lead auditor and will plan, perform, report internal and external audits and follow-up on audits. Are you a structured and systematic team player, who dream of a job with major responsibility and the license to impact decisions, you might be just the person we are looking for. As our new Principal Quality GCP auditor you will perform audits of clinical sites, laboratories and CRO’s located worldwide and be able to travel minimum 40 days per year worldwide.
Hartmanns A/S recruiting on behalf of Maersk Container Industry (MCI) in Tinglev
Maersk Container Industry (MCI) is looking for a Post-Harvest process owner to manage and drive new projects in the field of post-harvest for their Refrigerating R&D department.
The concepts will rely on data analysis and data exchange (Cloud), so you will be the one to link the process to refrigeration machine, overall cloud architecture and not at least the customer.
This is a key position in the R&D department and you will be part of a highly engaged team working with one of the most advanced products in the industry, the Star Cool (SC) Refrigeration machine. You will be part of MCI that oversees a fleet of over 260.000 Star Cool® reefer machines in operation around the world.
DuPont Nutrition Biosciences ApS, Copenhagen
You will be responsible for leading a team of 50 regulatory professionals located in 20 countries. The team is responsible for the regulatory approval of food, dietary supplement and pharmaceutical excipient products as well as influencing regulations, legislation and industry protocols to the benefit of company interests.
- Provide strategic regulatory direction on the overall regulatory plan, regulatory requirements for clinical studies and marketing approval, development plans and study designs, risk assessments, critical issue management.
- Drive regulatory leadership to support product development and ensure successful implementation and execution of regulatory plans to support product approval and commercialization.
LEO Pharma, Ballerup
Would you like to play a key role in the development of our growing portfolio together with a Global, friendly, ambitious and professional team of Clinical Trial Supply Professionals?
As a Clinical Trial Supply Sr. Professional you will join a very dedicated team, who is responsible for managing IMP outsourced related activities in connection with the conduct of Clinical Trials Phase I-IV. You will be working according to given LEO Pharma procedures and relevant GMP, GCP, GDP and regulatory requirements. You will also:
- Create SOP´s and keep them updated.
- Participate/lead in cross-functional optimizing Projects
- Present at Investigator/CRA meetings