47 job matcher din søgning
You will be part of an application specialist group of five persons who all strive to help our technical sales persons succeed when visiting our customers, by developing solutions based on experience and knowledge. The job is both practical and theoretical as you will both be carrying out trials in our application center and evaluating samples.
Furthermore, you will try to link the observed properties of the samples to the processing and the functional ingredients in the recipe. You share the gained experience and knowledge with colleagues in the R&D department, technicians, specialists and the sales force.
You have an in-depth theoretical and practical knowledge of food technology. You probably hold a degree in Dairy Science or Food technology at Master level and your professional experience has been gained within the food ingredients’ sector or in the food industry.
Pharmacosmos A/S, Holbæk
Registreringsafdelingen er ansvarlig for nye ansøgninger om myndighedsgodkendelse af vore humane og veterinære produkter samt vedligeholdelse af eksisterende godkendelser. Registreringsafdelingen arbejder globalt og stillingen indebærer en bred kontaktflade såvel internt som til partnere og myndigheder i mere end 40 lande.
Stillingen omfatter administrative opgaver inden for registrering. Vi arbejder fleksibelt i teamet indenfor et bredt spekter af opgaver, og du vil få en varieret arbejdsdag.
Registreringskoordinatorens arbejdsområder vil bl.a. være:
- Forberedelse og indsendelse af dokumenter til myndigheder og partnere, herunder udarbejdelse af elektroniske ansøgninger (eCTD)
- Legalisering af dokumenter
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to join us in a challenging position as design control specialist? We offer a challenging and exciting job in an international company with great development possibilities, an entrepreneurial and open work environment, where your contributions will be valuable and make a difference.
Your main focus is to work within the device development projects as responsible for the design controls from project initiation until successful design verification, validation and transfer. The position is an opportunity to contribute to the development and documentation aspects of the device part of drug delivery projects including responsibility for the risk management activities, as they move from project initiation to clinical studies, manufacturing, global submission and commercialization.
Movianto Nordic, Greve
Movianto Nordic's Quality team is looking for an experienced and dedicated QA associate who possess strong analytical skills with an eye for details. Our new team member has the ability to work effectively, independently as good as in team work cross-functionally both for local business but also within European structure.
It is a requirement you have a relevant background as pharmacist and can become qualified person. Preferably you have experience from GMP/GDP environment.
- Maintaining and improving QMS – compliant to regulations
- QP release of compassionate use products
- QP release of repacked medicinal products
Do you have solid qPCR technical knowledge and a commercial background? Do you have the passion and drive to succeed in a challenging environment, and would you like a chance to develop a fantastic career in a world-renowned company, and Europe’s market leader in qPCR? Then this may be the right opportunity for you.
The role will involve significant travel activity – at least 50% of the time – predominantly within the Nordics (DENMARK and NORWAY), but also outside the region.
Your responsibilities among others will include:
- Develop and implement account specific strategic plans with the other sales teams in Bioscience Division and Research and Safety Division
- Develop and maintain effective business relationships, at all levels within assigned accounts to influence purchasing decisions
Jakob & Partners ApS, Copenhagen
Pharmaceutical sciences, biotechnology, medical devices
If you want to work for a highly successful company providing research and analyses of markets within the pharmaceutical and biotechnological industries, you should consider this position in Jakob & Partners. You will be part of a highly qualified team with expertise within life and pharmaceutical sciences, market insights and economics.
Your job will be exciting and challenging and will demand a high degree of flexibility. You will become part of a highly qualified, truly international and top performing team. You will be working on a range of projects within different therapeutic areas and develop a unique insight of the pharmaceutical and biotechnological markets through training courses and interactions with internal and external experts.
Unique Human Capital recruiting on behalf of Zealand Pharma in Glostrup
Work with QA in a fast growing and exciting biotech company
As QA Manager – CMC at Zealand Pharma you will become a part of the QA organization overseeing all activities and delivering professional quidance to ensure GxP compliance within all areas. You will be responsible for the overall QA oversight for one of the current phase 3 products applying your knowledge within GMP. The department is headed by the Vice President, Head of QA, and in addition to this position, encompasses 7 QA colleagues. You will be reporting directly to the Vice President, Head of QA.
Your key responsibilities
- Employ GxP QA expertise during the development providing GMP compliance guidance to internal stakeholders
- Influence the compliance of projects and programmes
- Review and approve internal and external documentation
Gubra ApS, Hørsholm
At Gubra we are looking for an experienced Group Leader to head our Histology Group currently consisting of 7 scientists and 4 laboratory technicians. The focus of the histology group is to deliver high quality data within diabetes, obesity, and related metabolic disorders.
Gubra is a very dynamic and data driven company. Our research activities are focused within the metabolic space where many of our disease models and technologies are interconnected.
Your tasks as Group Leader of the Histology Group are varied, but include:
- Daily management of the entire group of scientists and technicians ensuring personal development and a high level of information
- Help scientists prioritize resources, maintain efficiency and timeline adherence in complex research projects without compromising quality
- Participation in relevant cross-functional meetings ensuring a smooth collaboration on internal and external projects
We are offering a job opportunity for a motivated professional to join a small team, which supports Global Pharmacovigilance & Clinical Development (GPCD) and ensures that we stay in compliance with internal and external requirements. Are you ready to bring your GCP knowledge and skills to an analytical level ensuring that our organisation is supported and maintains a high level of Regulatory compliance?
Fields of responsibility
- Provide GCP and other relevant Regulatory advice and support to GPCD
- Support GPCD with maintenance and continuous improvement of the QMS and the training system
- Act as project manager on relevant updates to the QMS and support GPCD where relevant in writing Quality Documents.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
High degree of influence in an exciting and fast growing biotech company
The Process Manager will work closely with the Global Clinical Development team leading/supporting the process changes, updates and compliance, and R&D operation's strategic directives. You will do that by ensuring the development and management of processes that enable compliance and standards across departments and apply best in class methodologies.
You will also drive global process improvements projects and support ongoing evaluation. You will lead the creation and maintenance of our processes – including but not limited to SOPs, guidelines, written instructions and other documentation processes. You will also ensure adherence to applicable guidelines/regulations.
As Process Manager, you will be responsible for effective implementation and creation of training sessions.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within drug development - and are you passionate about the voice of patients and their caregivers?
Lundbeck’s focus is first and foremost on the patients suffering from Alzheimer’s Disease, Parkinson’s Disease, depression and schizophrenia, for whom we develop innovative medical treatments. In the Medical & Regulatory Science business unit, we strive to integrate patient perspectives in our activities.
Your job will be at the center of this, helping us to develop and operationalize patient and caregiver insights linked to the regulatory and medical aspects of our drug development strategies. We would therefore expect you to have a passion for patient focused drug development combined with the skills and educational background to understand and navigate medical and scientific data.
Are you looking for the next step to kick-start your transition from being a student to becoming a young professional within Clinical Pharmacology in an international pharmaceutical company? Then we have the Graduate Programme just for you.
As part of your two-year graduate journey at Lundbeck you will be exposed to various parts of the business and encounter many exciting challenges cross functionally. The learning curve will be steep and we expect a lot from you, but in return we offer a programme that will empower you to grow both on a professional and personal level.
We are searching for a graduate who can support Quantitative Pharmacology in the daily work and help us in our mission to become a world class pharmacometric service provider for Lundbeck.
Symphogen A/S, Ballerup
The position as (Senior) Drug Product Scientist offers a unique possibility to take part in the de-velopment of Symphogens antibody products. You will mainly be responsible for drug product process development and manufacture from early stage IMP manufacturing and later stage manufacturing including process validation strategy.
You will collaborate closely with staff from our CMC group and in project teams, to ensure de-velopment progress of Symphogen’s antibody lead candidates.
Tasks and Responsibilities:
- Tech transfer of manufacturing processes to CMOs
- Technical responsible for drug product manufacturing documentation
- Ensure implementation of drug product manufacturing strategy between projects
Manpower søger for Agilent i Glostrup
Manpower søger på vegne af Agilent en laboratorie opvasker, med start hurtigst muligt, til laboratorie opvask i medicinalindustrien i Glostrup.
Arbejdet består af betjening af halv- og fuldautomatiske industriopvaskemaskiner, indsamling af opvask og levering af rengjort opvask. Du får en stor kontaktflade blandt laboratorie- og produktionspersonalet. Det er din vigtigste opgave, at leve op til de høje hygiejne- og kontrolkrav, der er forbundet med opvask af laboratorieudstyr.
Grundig og kvalitetsbevidst
- Du har muligvis erfaring med laboratorie opvask fra enten medicinalbranchen eller et hospital og har et godt praktisk håndelag
- Kendskab til GMP/GDP/GLP er en fordel
- Du skal kunne dansk i skrift og tale og have brugerkendskab til PC-arbejde
LEO Pharma, Ballerup.
Do you have a strong quality mind-set? Do you have interest in and experience with Packaging Materials within the pharmaceutical industry? Do you have experience with cooperation with 3rd parties? Then you may be the Senior Quality Professional we are looking for in Patient Supply and Suppliers Quality.
The PSSQ department is a global department at LEO Pharma, responsible for handling of all GPS suppliers of API’s, packaging materials, raw materials, and excipients. Furthermore, the department is responsible for supporting Distribution Management, including 3PLs and freight forwarders, and Customer Order Management.
As our new Senior Quality Professional your primary responsibilities will be:
- Planning, performing and follow up on audits of all primary and secondary packaging materials
- Establish and maintain Quality Agreements (primary and secondary packaging materials)
Erhvervsakademi Aarhus, Viby J
Vi søger en ny kollega til de videregående uddannelser miljøteknolog og professionsbachelor i fødevareteknologi.
I undervisningsfunktionen kommer du til at arbejde med forskellige aspekter af undervisning fra klasseundervisning til laboratorie- og teknologiøvelser, herunder:
- Planlægning af undervisningen
- Udarbejdelse af undervisningsmateriale
- Forberedelse og afholdelse af lektioner, såvel teoriundervisning som praktiske øvelser
Vi arbejder tæt sammen i teams af 2-3 personer om hvert fag og forbedrer sammen undervisningen løbende. I perioder vil der også være udviklingsopgaver f.eks. i forbindelse med opdatering af fag og udstyr eller nye uddannelser.
How often do you get to work with a new idea that may change the world?
In order to further strengthen our team, SaltPower is looking to hire a process engineer who will be responsible for running the demonstration unit and help further develop and scale up the technology. SaltPower is a small company with less than 10 employees, but we have teamed up with several large partners.
We are looking for a new colleague who can operate and help further develop the demonstration unit. Your main responsibilities will be:
- Operate the demonstration unit. This include going out in the field to set up and commission the system at the test sites, troubleshooting and handling unforeseen errors.
- Optimize performance of the SaltPower power plant to improve energy generation. This will be through optimization of the operating parameters at each test site where conditions will be different.
Hansen Toft A/S recruiting on behalf of Medicom Innovation Partner in Struer
To manage the complex development projects your responsibilities as a senior project manager are:
- Secure continuous progress and quality of projects with strong focus on agreed timeline and economy
- Ensure the profitability of a project
- Close communication and reporting with internal and external stakeholders
- Facilitate and document project meetings
- Follow-up on project finances and contractual implications to the project
As a Senior Project Manager, you will be responsible for one or more projects with budgets ranging from single to double-digit millions of EUR. Typically, you will manage activities ranging from the early sales process, concept development, detailed device development and transfer to final production.
Unique Human Capital recruiting on behalf of Genmab in Copenhagen
Work in the CMC Regulatory Affairs area within an exciting and fast growing biotech company
Genmab has a robust pipeline of innovative human antibody therapeutics and a number of strategic partnerships are already in place with international blue chip companies.
As CMC Regulatory Affairs Manager, you will be responsible for operational and strategic regulatory input with an emphasis on CMC matters to support worldwide development and commercialization of the Genmab pipeline. You will be part of the operational teams directing and coordinating international regulatory submissions supporting the conduct of clinical trials. Furthermore, you will be supporting marketing authorization submissions to EMA and other regulatory health authorities.
Badenoch & Clark søger for Lely Nordic i Fredericia
Lely Nordic søger en ny kollega til deres tekniske support-team. Den nye medarbejder skal bistå i teknisk support og træninger til teknikere, som udfører installation og service hos slutkunder.
Teknikerne er ansat hos Lely Center, der er dedikerede forhandlere af Lelys teknik til mælkeproduktion. Lely Nordic er bindeled mellem Lely Center og Lelys udviklings- og produktionsfaciliteter. De dækker primært de nordiske lande dvs. Danmark, Sverige, Norge, Finland, Estland og Island. Derudover er der et tæt samarbejde med et andet Lely Team, som varetager Østeuropa.
Du bliver en del af et teknisk support-team som p.t. er på 10 personer. Teamet varetager alle Lelys produkter, hvoraf Barn & Feeding er det produktområde som indeholder fodringsudstyr og udstyr til rengøring af stalde.