Lundbeck

Gem
Lundbeck Student Assistant

Lundbeck, Copenhagen

We are currently looking for a structured and detail-oriented Student Assistant for Lundbeck’s Non-Clinical Documentation and Submission Management team in Copenhagen.

The Non-Clinical Documentation and Submission Management team is amongst many other things responsible for ensuring submission readiness of relevant nonclinical documentation and that all systems and processes involved in this are available and sufficient.

We belong to the Drug Safety division under Non-Clinical Safety Research, which is responsible for safety assessment of biologicals and small molecules. Drug Safety consist of 25 experienced employees with various backgrounds, and our working environment is characterized by an open, collegial, and collaborative atmosphere.

Gem
Lundbeck Research Scientist

Lundbeck, Copenhagen

We are looking for a highly motivated Research Scientist with experience and a strong interest in molecular biology techniques and in vitro/ex vivo cellular assay development to join our efforts in developing novel medicines against CNS disorders in the Department of Functional and Cellular Pharmacology.

Together with the rest of the Neuroscience organization we represent biological research at Lundbeck and are focused on generating the necessary pre-clinical data and knowledge for advancing both early drug discovery as well as late-stage projects. We focus our efforts in four dedicated biology clusters: Synapse Biology and Neuronal Circuits - Hormonal and Neuropeptide Signalling - Protein aggregation, folding and clearance - Neuroinflammation and Neuroimmunology.

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Lundbeck CMC Technical Writer

Lundbeck, Copenhagen

Join our community of specialists and take part in the journey towards restoring brain health

You have a unique opportunity to join our CMC Biologics team as an experienced CMC technical writer This new position will require a high level of collaboration with stakeholders including the Regulatory CMC group.

As Technical writer you will lead the authoring, review and approval of various regulatory documents including the CMC sections of regulatory submissions, briefing documents and information request responses to support multiple biologics products in the clinical and commercial stages of development.

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Lundbeck R&D Finance Director

Lundbeck, Copenhagen

Are you looking for a unique opportunity to become a trusted business partner for Research & Development at Lundbeck?

As our new Head of R&D Finance, you will secure the solid financial management of the R&D organization by being a proactive and trusted advisor R&D Management, Group Finance and a variety of senior stakeholders in the company, including Executive Management.

In your new role, you will have ownership of all the key financial processes for R&D (long-term financial planning, budgets, estimates, etc.), and you will secure full transparency of the financial impact of our R&D pipeline.

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Lundbeck Director BD&L Search & Assessment

Lundbeck, Copenhagen

We currently have an outstanding opportunity to join our Corporate Business Development & Strategy (CBDS) team as Director, Search & Assessment to support the development of Lundbeck’s R&D pipeline and find new growth platforms.

You will become part of an experienced business development team and be responsible for leading cross-functional teams that evaluate business opportunities from early to late stage independent of deal structure.

You will scout for external opportunities; lead scientific due diligences; conduct global commercial assessments; build internal and external relationships and be an ambassador with respect to executing Lundbeck’s growth aspirations to become ’the partner of choice’ for neuroscience within the biopharmaceutical industry.

Gem
Lundbeck Process Technician

Lundbeck, København

Hvis du motiveres af tekniske udfordringer og kan arbejde struktureret med problemløsning så, søger vi en dygtig tekniker gerne med erfaring fra Pakkelinjer og en GMP reguleret produktion. I Finished Goods Production - Packaging har vi klare ambitioner om at blive endnu bedre, samt at tage digitalisering til næste niveau på vores højt teknologiske pakkelinjer.

Dine primære opgaver består af fejlsøgning, reparationer af maskinel samt vedligeholdelse i produktionsområdet. Du vil derudover bidrage til implementeringen af projekter og forbedringer som skal løfte produktionen op på næste niveau. Derudover skal du sikre god kommunikation mellem dine kollegaer men også til managers og projektledere om aktuelle problemstillinger og indgå i de daglige tavlemøder. Da der arbejdes i et GMP-miljø er udfyldelse af dokumentation så som, job-kort og afskrivninger af reservedele, en naturlig del af jobbet.

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Lundbeck Records Manager

Lundbeck, Copenhagen

Are you passionate about structuring complex data and want to work in an environment where quality and regulatory requirements are in focus, this is a great opportunity to join H. Lundbeck A/S, Valby.

You will be working in the Regulatory Central Archive with records management of GLP, GCP and GMP records supporting Lundbeck products covering both Lundbeck’s physical archive and electronic document management systems. Your job role will involve strategic planning but also daily routines as archiving, cataloguing and retrieval of records.

You will participate in process optimization initiatives and be involved in system upgrades and development of records management procedures, training material, including eLearning’s. Further you will be involved in tasks and projects within Records & Information Management responsibility areas.

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Lundbeck Senior Process Engineer

Lundbeck, Lumsås

Vi har nu en enestående mulighed åben hos os, for dig der gerne vil arbejde med implementering af vores CAPEX projekter i Lumsås. Hvis du vil være med til at installere og validere vores fremtidige produktions udstyr, så har vi en spændende stilling til dig som Senior Process Engineer i Chemical Engineering (CE).

Som Senior Process Engineer vil du sammen med dine øvrige kollegaer i teamet, skulle installere og idriftsætte nyt udstyr i produktionen. Sammen med dine kollegaer i teamet vil du skulle sikre at Lundbeck installerer udstyr der modsvarer de krav der sættes af produktionen, og samtidigt kigge visionært på udstyret og derigennem sikre, at vi installerer det bedst egnede udstyr i vores produktionsafdeling.

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Lundbeck IT Specialist

Lundbeck, Copenhagen

We are looking for a focused and motivated IT Specialist with Danish whose knowledge and expertise in IT will support our employees with their daily IT challenges, as well as long-term IT projects. We will also consider applicants with less IT experience, but highly motivated to learn and gain new experience with our guidance. If it sounds like you, why don’t you join Lundbeck, a certified Great Place to Work and Poland’s Best Employer, and get your brain in the game?

As IT Specialist with Danish, you will join the international IT Service Desk team whose main goal is to provide IT support to our Lundbeck employees; as well as participating in migration and optimization projects of our IT platforms.

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Lundbeck Manager Regulatory Data & Submission Management

Lundbeck, Copenhagen

If you have significant experience in regulatory operations, preferably data or packaging management, and have some leadership experience, this is a great opportunity to join Lundbeck’s journey as our new Manager of the Regulatory Data and Packaging Change Management Section.

The RIS team plays a pivotal role in ensuring global operational compliance within Regulatory Affairs, but even more so now that Lundbeck is embarking in the IDMP readiness journey, where many technical and operational questions will have to be answered in close collaboration with several areas across the company.

As line manager for the RIS and PCR teams, you will be responsible for:

  • Setting business objectives in alignment with overall company and area strategic goals.
  • Ensuring processes and systems are in compliance with applicable global and internal requirements.