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Bupa Danmark, Copenhagen
This is a diverse and skilled customer facing role where you will be responsible for resolving all customer queries to the customer’s complete satisfaction without the need to refer the customer on. This will include resolving and case managing complex and challenging situations from all customer groups – individual, Corporate and Intermediaries.
You will be a customer service champion, putting the customer at the centre of everything you do and putting forward ideas for the continual improvement of the customer experience
- Taking end to end ownership for the resolution of all customer enquiries and contacts. Manage all queries through to resolution
- Case management of complex cases
Jobindex A/S søger for Cook Medical i Bjæverskov
Vil du sammen med dine kolleger på tværs af Cook Medicals internationale organisation sikre, at vores labels lever op til både nuværende regulativer og den nye medical device regulation fra 2020? Så er jobbet her måske noget for dig.
Som vores nye projektleder arbejder du på store projekter, hvor du udvikler teamets samarbejde med resten af organisationen. Din første store opgave bliver at gå forrest og komme med input til handling, så vi skaber en overordnet praksis omkring labeling, hvor vi lever op til nuværende og fremtidige regulativer.
Det er nemlig dig, der har det daglige overblik over vores labeling af medical devices – både i dagligdagen og når vi skal udvikle vores arbejdsmetoder. Det giver dig en hverdag, hvor du både holder overblikket over projekter og sikrer, at vores nye processer lever op til alle krav samt er hands-on i at opsætte og kvalitetssikre vores enkelte produkter.
Symphogen A/S, Ballerup
The position as Senior Downstream Scientist offers a unique possibility to take part in the CMC development of Symphogen´s products and participate in shaping the path for late stage development of our antibody mixture products in the Purification and Product Supply Team.
The Senior Downstream Scientist will be responsible for execution of process development of our products in clinical development including tech transfer to external CMO. In particular, the main tasks will be the downstream scientific lead for late stage development including process characterization and process validation activities for Symphogens most advanced projects.
In this position it is possible for the right candidate to participate in defining the late stage development platform and collaborate closely with staff from our CMC group and with the project team, to drive development progress of Symphogen’s antibody lead candidates.
Maersk Line, Copenhagen
- Are you a 2nd engineer, preferably with a Chief Engineer license, ready for a new challenge on shore?
- Have you sailed on Triple E-, 14K-, 19K-, WAFMAX-, Winter Palace-class vessels?
- Do you thrive in a dynamic and everchanging environment?
This is a unique opportunity to join the progressive and competent Maersk Line Fleet Management & Technology team.
We offer an exciting role with the world’s largest and most efficient container vessel operator, part of a dynamic and international organisation with the possibility to continuously apply and develop your competencies.
Paranova Pack A/S, Herlev
Du vil sammen med vores 5 øvrige farmaceutstuderende indgå i vores regulatoriske team. Som en del af det regulatoriske team vil du være medansvarlig for udvidelse og vedligeholdelse af vores portefølje af parallelimporterede lægemidler som forhandles på det danske, svenske og finske marked.
Hvad skal du lave
- Håndtering af produktreklamationer.
- Korrekturlæsning af indlægssedler og emballage.
- Gennemgang af nye produktresuméer og styring af tilhørende emballage.
Arla Foods, Viby J.
Do you have what it takes to communicate product benefits with consumers based on unique product formulations?
As Senior Specialist, you will support the business in building the necessary knowledge and procedures related to food regulatory affairs worldwide. Your overall objective will be to provide assistance to the business units on regulatory requirements related to production, new product development and communication – including food labelling, use of claims, evaluation of new technology and product standards etc.
More specifically, it will be your task to:
- Proactively develop, maintain and apply your deep regulatory expertise
- Identify upcoming regulatory changes and coordinate implementation of regulatory changes
Saxo Bank A/S, Hellerup
Located at our Headquarters in Hellerup (DK), you will mainly participate in the development of our existing Financial Risk framework, over time you will drive the risk framework committee and analyse the impact to the Financial Risks area of regulatory changes etc.
You will also be a part of solving daily risk management issues especially related to credit and market risk, as well as participate in on-going risk related projects. You will be working closely with a team of specialists, responsible for controlling and analysing the Groups market, credit, client, model, valuation and trading algo risks.
As a person you are curious and in possession of a high degree of integrity. You are methodical and detail oriented taking pride in delivering high quality work in everything you set yourself to.
Pharma Nord, Vojens
– myndighedsanmeldelser og godkendelser af kosttilskud og lægemidler.
Pharma Nord søger en ny medarbejder til vores regulatoriske afdeling i Vojens. Som medarbejder i afdelingen deltager man i at sikre godkendelse af nye produkter samt vedligeholdelse af eksisterende produkters tilladelser. Dette sker i samarbejde med interne og eksterne kolleger i Danmark, virksomhedens datterselskaber i udlandet samt i tæt kontakt med diverse myndigheder.
Du vil primært beskæftige dig med:
- Kontakt og samarbejde med lægemiddelstyrelsen, fødevarestyrelsen og andre relevante myndigheder i Danmark og i udlandet.
- Udarbejdelse af produktdokumentation.
- Analyse, fortolkning og implementering af diverse EU-love på området.
Hvad kan vi tilbyde:
- Et job i en international virksomhed med fokus på dokumenterede produkter.
- Gode personlige og faglige udviklingsmuligheder.
- Stor berøringsflade i en organisation med mange dygtige kolleger.
Satair A/S, Kastrup
For Satair’s headquarters in Copenhagen we are looking for a Contract Risk Manager to support our operations worldwide, mainly within risk management and mitigation related to international contracts; contract management activities and support of compliance initiatives.
Reporting to our Legal Officer you will become part of a Legal & Compliance department consisting of three Legal Counsels providing legal advice on all matters of relevance to Satair. The team is reporting directly to the Executive Management and works very closely with other central functions within Satair, including Customer Solutions, Business Development, Product Management and Marketing. Furthermore, Legal is part of the international Legal & Compliance team within Airbus consisting of approx. 300 people.
Scandinavian Tobacco Group A/S, Søborg
We are looking for a new colleague to join the Legal & Public Affairs department located in our head office in Søborg, Denmark. You will be part of a dedicated team of highly competent people which supports our colleagues around the world, fulfilling the Scandinavian Tobacco Group business strategy.
You will look after Scandinavian Tobacco Group’s interests via the international associations in the tobacco business (such as the European Cigar Manufacturers Association, Cigar Association of America, the European Smoking Tobacco Association etc.) as well as through the national manufacturers’ and trade associations where the local Scandinavian Tobacco Group sales subsidiaries are represented.
You will be cooperating with and assisting our local managing directors and other Scandinavian Tobacco Group colleagues in their tasks in these international and national associations.
Bavarian Nordic A/S, Kvistgård
Do you like to take great professional responsibility and always ensure your process is in compliance and ready for operation? Maybe it's you who we're looking for right now!
Bavarian Nordic is looking for a specialist to handle the professional responsibility for introducing new products on our small scale fill & finish line at Bavarian Nordic. This entails that you implement new products through and through, and you take charge of ensuring that our equipment is compliant with regulatory standards.
This includes full descriptions of handling and risk assessments, ensure right trending and fully describe all CPP's in the process to keep the process in control, support smoke study and aseptic process simulation were needed, generate and keep updating process description in SOP, training of operators.
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?
As 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.
Your essential tasks include case processing, post-marketing safety surveillance, safety reports and safety handling in clinical trials in collaboration with Pharmacovigilance Physicians.
Coloplast A/S, Humlebæk
You will be involved in long-term and high-business-impact projects where you develop globally recognised clinical documentation accepted by key markets and payers but also in daily operational tasks.
You will gain a broad role, both in terms of tasks and in terms of organisational interfaces. You will be part of one or more R&D project groups, being responsible for preparing and fulfilling clinical strategies, providing scientific and clinical advice and potentially preparing publications. Furthermore, you will support Marketing and Market Access within claiming, questionnaires and post market studies.
Your key responsibilities will be to:
- Prepare literature reviews, clinical evaluation reports, data-on-file documents, clinical data presentations and clinical investigation reports
- Create clinical strategies that support our ambition of strong clinical evidence on innovative products for regulatory and marketing purposes
Coloplast A/S, Humlebæk
You will become an expert on one of our product groups, e.g. Ostomy Care, Continence Care or Wound Care. You will be involved in change projects where you use your regulatory knowledge to evaluate and communicate the impact of changes to product components.
You will be working on multiple projects in close collaboration with specialists in marketing, clinical operations, supply chain and R&D, as well as our subsidiaries. To do so, you need to be comfortable communicating, coordinating and collaborating across functions and cultures, applying your proactive mind-set to plan, execute and meet deadlines.
- Participate in cross-functional projects for product modifications to ensure regulatory compliance
- Prepare regulatory files, clarify procedures and create or approve relevant documentation
- Communicate regulatory requirements across Coloplast
Coloplast A/S, Humlebæk
Join Coloplast to become part of a global company that makes a difference every day.
You will work from our Headquarter in Humlebæk, Denmark. Here, you as a senior specialist will ensure appropriate and compliant biocompatibility documentation for Coloplast products applying your insight into regulations and industry trends. You will help grow the team by acting as a mentor through guidance and coaching of junior colleagues, especially with respect to scientific and professional aspects of evaluation of biocompatibility and toxicology.
In addition, you will provide expert toxicological support to the business, initiating and monitoring biocompatibility testing in-house as well as with our suppliers. Supporting cross-functional activities related to biosafety, you will influence our policies, guidelines and attitudes regarding environment and safety for our customers.
LEO Pharma, Ballerup
Har du nogle års erfaring fra en koordinatorrolle, og drømmer du om et job, hvor du virkelig kan udfolde alle dine evner og udvikle dig selv? Så behøver du ikke lede videre. Du kommer til LEO Pharma på det måske mest spændende tidspunkt i virksomhedens historie.
Grundlæggende handler dit job om at supportere Global Regulatory Affairs med en meget bred vifte af opgaver. Det er dig, der får en hel masse vigtige processer og opgaver til at glide. En væsentlig del af opgaverne er funderet i vores IT system GLOBE, som du derfor bliver superbruger af. Du skal:
- Blive superbruger og derfor også supportere kolleger på vores IT-system GLOBE
- Supportere ledelsen med komplekse Purchase Orders og kontrakter etc.
- Supportere ledelsen ved planlægning og afvikling af store events, møder m.m.
LEO Pharma, Ballerup
LEO Pharma har sat det meget ambitiøse mål at blive verdens førende lægemiddelvirksomhed inden for behandling af hudlidelser. Derfor er vi i gang med at transformere hele virksomheden på tværs af systemer, processer, produktionsapparat, organisering… Og det er her, at du kommer ind i billedet.
Dit fokus bliver koordination og support til vores tværorganisatoriske projekter, der involverer rigtig mange interessenter og har overlappende deadlines etc. På den vis er kommunikation et helt afgørende omdrejningspunkt og værktøj. Du skal kunne formidle dine budskaber enkelt og tilgængeligt med forståelse for vidt forskellige typer af modtagere med vidt forskellige faglige og kulturelle baggrunde.
LM Wind Power, Lunderskov
As EHS coordinator you will set and communicate requirements, guidelines and good practices ensuring that our Workshops and Laboratories are safe, healthy and environmentally desirable.
You will be based in our Technology Center in Lunderskov, where the Workshops and Laboratories are located. You will report to the Operations Manager, and work closely together with the Test & Validation Center’s EHS manager and the working environmental organization to improve our safety culture.
We offer a challenging, international position in an organization of professional and highly qualified leaders and colleagues, where you will have ample opportunity of gaining experience and working for the wellbeing of our employees and the organization. For the right applicant, the job offers possibilities of career progression and personal development.
FMC Corporation, Hørsholm
We are seeking an experienced Sourcing Manager within Tolling Services/Contract Manufacturing responsible for developing and implementing sourcing strategies and management of key supplier relationships. In this position, you serve as an important partner to our Operations teams in EMEA and deliver value by managing risk, quality and cost as defined by the business and regulatory groups.
You will have the responsibility for the Toller Services/Contract Manufacturing for Agricultural active ingredients, intermediates and formulated products in EMEA region with an annual spend of approximately $50 million but growing. In this role, you will occasionally be required to support the North America region and to assist in the sourcing of materials outside the normal scope of this category.
Trustpilot A/S, Copenhagen
Join Trustpilot's Legal team in Copenhagen as a Corporate Counsel if you are ready to be a part of a great company, have fun and take advantage of real opportunities for growth in a fast-paced environment.
As our Corporate Counsel you will be joining our Legal team where you will play a key role in supporting our business. The Legal team consists of 9 people with different backgrounds and nationalities. They are dedicated, hard-working and have the best team-spirit you could ever hope for. The team is constantly growing together with the company overall.
You will play a key role in supporting our European offices with legal assistance and taking lead on corporate matters, including drafting and negotiating vendor contracts. You will be based in our Copenhagen office and will be reporting to our SVP Legal & Compliance.