82 job matcher din søgning
Flügger A/S, Rødovre
Leder du efter nye udfordringer og en afvekslende hverdag? Brænder du for kemikalielovgivning og formidling? Er du personen, der kan styre implementeringsprojekter? Så læs endelig videre.
Du vil få en spændende og udfordrende hverdag, hvor du vil være ansvarlig for planlægning og udførelse af egne opgaver, samtidig med at du kommer til at bidrage til projekter. Opgaverne er mangeartede, og dagligdagen vil være afvekslende, og der er stor mulighed for personlig udvikling. Dine primære arbejdsopgaver vil være at:
- fortolke lovgivning og drive implementeringsprojekter
- aktivt holde dig opdateret med lovgivningen på området
- foretage produktvurdering af nye og eksisterende produkter og råvarer i forhold til gældende regler.
Anticimex Innovation Center A/S, Helsinge
Vi vækster fortsat og søger derfor til nyoprettet stilling en Regulatory Affairs Manager.
Med direkte reference til den Adm. Direktør har du ansvaret for alle forhold i virksomheden, der vedrører generel lovgivning, godkendelser samt kvalitets- og miljøledelse.
I jobbet vil du have en bred berøringsflade, da ansvarsområdet går på tværs af alle afdelinger.
Jobbet indebærer bl.a.
- Implementere og varetage det ledelsesmæssige ansvar for kvalitets- og miljøledelsessystemer for hele virksomheden.
- Varetage kontakten til relevante myndigheder og interesseorganisationer.
- Etablere og vedligeholde et digitalt dokumentstyringssystem for alle aktiviteter i virksomheden.
Radiometer Medical ApS, Brønshøj
This job is your opportunity to impact regulatory aspects and compliance related to the development and product life cycle of several medical devices.
Our previous maternity cover has recently accepted a permanent position internally in Radiometer and this has reopened this position in our Regulatory Immunoassay Department.
Now you have the chance to quench your thirst for knowledge by applying for this role and learn all about how we combine complex technology consisting of software, hardware, electronics, chemistry and mechanics for important usage in the healthcare industry.
Your future colleagues, many of whom has been in Radiometer for several years, look forward to work with you because you are passionate and persistent. We need your ability to deliver quality on time and your attitude that ensures that what you don’t know today, you will learn tomorrow.
LEGO System A/S, Billund
In this position, you join our Legal, Compliance and Risk Management department (LCR) alongside 90 highly skilled colleagues in 8 global locations. Rooted in the EMEA legal team and based in Billund, Denmark, you provide legal services to business units within the Product and Marketing Development area of the LEGO Group. Here, you keep abreast of relevant legislation in various legal areas such as data protection law (GDPR) and marketing law, primarily regarding consumer-engaging initiatives. More specifically, your role is to:
- Identify and build working relationships with leaders and decision-makers at all levels as well as business areas and units – all with a digital focus
- Build and/or maintain best-in-class legal knowledge and skills relevant to digital business
- Provide focused and enabling legal advice relative to digital LEGO opportunities and experiences
©2018 The LEGO Group
Ferring Pharmaceuticals A/S, Copenhagen
Would you like to be part of a great, growing team responsible for global safety surveillance of Ferring’s portfolio within reproductive health and gastroenterology? Do you thrive in an international environment of great change where you can influence the surroundings? Do you like to work both with post-marketing and clinical activities?
We are looking for a permanent, experienced Pharmacovigilance Manager with good drive and positive energy.
As Senior Pharmacovigilance Manager you will play an important role in leading drug safety for a key area of Ferring’s portfolio working as an integrated member of a highly motivated and dedicated team collaborating with clinical development, regulatory affairs, affiliates and partners for assigned products/projects.
Arla Foods, Viby J.
Can you lead and inspire a knowledgeable team? And would you like to influence the strategy of a global leader in industrial food ingredients?
In collaboration with Sales, you become globally responsible for driving and implementing our value add product and sales strategy, just as you set the focus for our documentation strategy in collaboration with our team of nutrition scientists. In more detail, you:
- Act as an inspiring, coaching and motivating manager who actively support the strategy execution for our products, market segments and business area
- Help your team utilise their nutritional and technical knowledge surrounding our products to facilitate the strategic value-added sales
- Make sure your team can support all geographies and customers and travel 30-40 days a year to visit trade shows and customers yourself
Dansk Flygtningehjælp, Copenhagen
The position as Donor Focal Point serves to facilitate and support DRC’s engagement with two of DRC’s core donors: Danida and UNHCR.
The primary deliverables of the function are to:
- coordinate DRC’s partnership engagement grant with Danida
- to increase DRC’s capacity to engage with UNHCR under the UNHCR Framework for Implementing with Partners (FIP) and the Project Partnership Agreements (PPAs)
- advise DRC operations globally and in HQ on Danida and UNHCR donor compliance
- to develop and provide trainings, webinars, and written guidance on donor compliance
Novartis Healthcare A/S, Copenhagen
Do you want to work for a Global Pharmaceutical company where you will be recognized for your contribution and commitment? Look no further, apply today for Head Market Access & External Affairs Denmark.
The Head Market Access & External Affairs Denmark (MAX & EA) has overall responsibility for securing market access of Novartis’ oncology products in Denmark. He or she leverages on a deep understanding of Danish political environment, healthcare structure and regulations to devise innovative MAX & EA initiatives that will provide a sustainable competitive advantage in a given business environment.
The Head MAX & EA Denmark ensures patient access to Novartis’ pharmaceuticals and therapies, and in collaboration with other functions influences and develops health political legislation, regulations and reimbursement systems.
LEO Pharma, Ballerup
As Principal Regulatory Specialist your overall focus is to contribute to bringing products to the market by facilitating smooth approvals of Marketing Authorisation Applications. You will unfold your skills in cross-functional teams, where you will provide strategic and operational regulatory CMC input for biological development projects. As such, you will create results via a close dialogue with team members, affiliates and stakeholders. Your primary tasks will be to:
- Provide strategic and operational regulatory CMC input for biological development projects
- Participate in preparing global regulatory strategies and CMC strategies for biological products in development
- Identify documentation needed for simultaneous submissions in the major markets worldwide
Kevin Murphy Europe A/S, Copenhagen
Reporting to the Global Director of Procurement, the Global Regulatory Affairs Manager will be responsible for leading activities of the Regulatory Affairs Department with an emphasis on global regulatory strategy and the preparation, review and submission of documents to any regulatory authorities at a global level.
Oversees the regulation process for products requiring governmental approval, including filing necessary applications and handling all government interactions in the geographical areas where KEVIN.MURPHY Group products are marketed. Coordinates inspection of the organization and contract facilities and develops procedures to ensure regulatory compliance. Requires a Master's degree in the area of specialty.
Novo Nordisk A/S, Bagsværd
Are you looking for an opportunity to work in drug safety and use your skills as a scientific communicator? Do you build strong relationships with stakeholders and enjoy putting plans into action? Join us as a Safety Medical Writer and use your skills to ensure patient safety and best practice.
As a Safety Medical Writer in Safety Surveillance Reporting at Novo Nordisk, you will be responsible for planning and managing document preparation of Development Safety Update Reports [DSURs], Periodic Safety Update Reports [PSURs] and Clinical Risk Management Plans [RMPs] in a cross-functional environment and ensuring high quality scientific writing.
You will work in close collaboration with Safety Surveillance Advisers, Medical Specialists from Global Development, Medical Advisers from Medical Affairs, Project Managers from Regulatory Affairs, and Safety Publishers.
Ambu A/S, Ballerup
Are you looking for independence in your job and a working day characterised by exciting new challenges? Would you like to be part of Ambu’s new product development groups and ensure that we meet all regulatory requirements? And are you looking for an international job? Then Ambu might be your next career move…
As Senior Regulatory Affairs Professional, you will be responsible for ensuring compliance with regulatory requirements for products and processes.
Your primary responsibilities will be to:
- Participate in development projects as a regulatory professional sparring partner.
- Contribute to Ambu successfully implementing new EU medical device regulations.
- Have fully updated knowledge about regulatory requirements.
ROCKWOOL International A/S, Hedehusene
Are you an expert in the fire area able to communicate complicated matters into simple concepts, to create consensus and motivate people towards fruitful collaboration? Are you familiar with standardization systems or with implementation of Third Party Researches?
As part of Group Marketing and Communications (GMC), the Regulatory Affairs teams aim is to influence future directives, laws, fire regulations, insurance rules, as well as standards that may have a significant impact on the ROCKWOOL Group’s long-term business.
Moreover being part of the Technical Knowledge Centre, you will also have the chance to translate your knowledge into contents for boosting and supporting the daily activities of your Marketing and Communications colleagues.
Bristol-Myers Squibb, Virum
Er du et politisk menneske og/eller et kommunikativt talent, og kunne du tænke dig at bruge dine evner til fulde for en førende, global biofarmavirksomhed? Government Affairs-teamet hos Bristol-Myers Squibb (BMS) Danmark søger to ambitiøse og selvstændige praktikanter med stærke faglige kompetencer inden for politik og kommunikation til et udfordrende praktikophold i efterårssemestret 2018 med start i august 2018.
Du vil blive udfordret inden for mange forskellige områder af Government Affairs såsom policy-udvikling, advocacy og kommunikation. Som praktikant inden for politik eller kommunikation kan du forvente at:
- Skrive policy-papers – briefingmaterialer, taler, præsentationer samt artikler
- Beskæftige dig med projektledelsesopgaver samt strategiske opgaver
- Beskæftige dig med intern og ekstern kommunikation
Studerer du kommunikation eller samfundsforhold på kandidatniveau? Og vil du have en praktikplads i én af Danmarks største virksomheder, hvor du bliver introduceret til en bred palette af kommunikationsopgaver?
Læringskurven er stejl, og du får mulighed for at prøve kræfter med alle kommunikationsfelter i vores afdeling. Det inkluderer blandt andet at levere research til at understøtte public affairs, CSR og branding, vores pressearbejde, håndteringen af sociale medier, samt leder- og medarbejderkommunikation.
Det vigtigste for os er, at du kommer med en smittende energi, en utvivlsom læringslyst og er klar til at levere en stor arbejdsindsats.
Arla Foods, Viby J.
Are you a regulatory affairs professional, with the skills to work on a global agenda?
Your overall objective is to support different business units in AFI on strategic and legal requirements. This covers areas such as Product Management, TPM, Quality Assurance, R&D, Sales and Supply Chain in order to secure AFI has the right knowledge with a proactive approach to regulatory affairs.
Reporting to the Director of Global Regulatory Affairs, your area of responsibility will be within food regulatory affairs with emphasis on quality assurance, new product development, product standards and regulatory support to current submissions for product marketing.
ABACUS MEDICINE A/S, København
Har du lyst til at arbejde i en ambitiøs og innovativ virksomhed med højt fokus på personlig udvikling? Her er en enestående mulighed for at blive en del af Abacus Medicine A/S og spille en nøglerolle i udviklingen af firmaets produktportefølje.
I din rolle som analytiker vil dit hovedfokus være på produktlanceringer, herunder at identificere og validere hvilke markedsføringstilladelser der skal ansøges fra et økonomisk perspektiv. I processen vil du, udover Product Development teamet, arbejde tæt sammen med vores afdelinger, der beskæftiger sig med salg, Business Development og Regulatory Affairs.
Vi er teamet der får enderne til at mødes på tværs af flere afdelinger i bestræbelserne på at videreudvikle og øge vores portefølje. Vi er et ungt team, med et højt drive og ambitionsniveau i en omskiftelig hverdag, hvor der ikke er langt fra idé til handling.
FMC Corporation, Hørsholm
As the BioSolutions Registration Manager you will report to the Director, Regulatory Affairs, EMEA Region. You will be responsible for defining and managing the implementation of the registration strategy for key biological crop protection and plant health compounds working in collaboration with global regulatory scientists and regulatory affairs managers.
Your principal duties and responsibilities
- Define and manage the EMEA registration strategy for key compounds
- Develop, in collaboration with the Biologicals Team, plans and timelines for when and how testing activities will be implemented
- Coordinate and identify data and studies required to support and defend registrations
LEO Pharma, Ballerup
Do you want to take on global responsibility for one of LEO Pharma’s best-performing brands? Does high complexity and navigating in cultural preferences motivate you?
You will become part of Region INTERNATIONAL, one of three business critical regions in LEO Pharma. You will report into the newly established “Established Portfolio Department”, working closely with the managing Director, three Marketing colleagues with responsibility for other therapy areas and a Pricing/Access Manger.
We have set ambitious goals for LEO Pharma towards 2025. Among others to help more than 125 million people suffering from a skin condition. As Senior Global Marketing Manager, you will hold global responsibility for driving one of LEO Pharma’s best-performing brands, by leading the creation of the global commercial plan for the franchise in alignment with the LEO 2025 strategy.
Radiometer Medical ApS, Brønshøj
Imagine opening a box full of technologically advanced medical devices designed to help caregivers make diagnostic decisions that save lives. You immediately feel the curiosity to learn more about the functions, designs and ideas behind these inventions. Now you can open that box and begin a professional journey in Radiometer Medical, a successful medical device company. This job is your opportunity to impact regulatory aspects and compliance related to the development and product life cycle of several medical devices.
You have most likely always known that you would love to work with products like ours. Finally, the combination of complex technology for usage in the healthcare industry. Your future colleagues, many of who has been in Radiometer for several years, look forward to work with you because you are passionate and persistent.