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You will be part of a department with highly skilled engineers that support the Finished Goods Production within the SVP area ‘Pharmaceutical Production’. The area has the ambition to take our effectiveness to the next level of performance.
In this position you will be one of the main drivers on troubleshooting and implementing improvements to ensure the strategic targets are met which implies that Lundbeck succeeds with this journey going forward. This means, handling improvements, upgrades and expansion of production equipment, take Process ownership and working closely with our Technicians and Operators. Your tasks will amongst others be:
- Identify and drive improvement projects on Production lines
- Use systematic problem solving and a LEAN mindset to solve production issues related to your field – Mechanical and/or Automation
- Collaborate across many functional areas and with people from different backgrounds
Er du kvalitetsfokuseret, positiv i forhold til forandringer og tager selvstændig initiativ til løsninger? Så er du måske vores næste kollega i et meget velfungerende team.
Dine primære arbejdsopgaver vil være at bestille, forberede og kontrollere de varer, der skal bruges i pakkeriet. Du inspicerer fysisk materialerne på de paller, pakkeriet skal bruge og sørger for at sætte dem på den interne transportvogn. En stor del af arbejdet foregår ved PC, hvor den visuelle inspektion af materialer skal dokumenteres i SAP. Vi arbejder efter GMP-regler og har stor fokus på at levere høj kvalitet til tiden. Du skal derfor kunne arbejde koncentreret med fokus på detaljer.
Du er god til at prioritere på tværs af arbejdsopgaver, og du har vist at være i stand til at pege på, hvor der er størst behov. Det er en forudsætning, at du er god til at omstille sig til nye prioriteter i løbet af dagen.
Are you passionate about Procurement and within this defining and executing category strategy across CAPEX (construction and equipment), Distribution and Facility Management (FM)? Do you bring extensive market and category knowledge to Lundbeck and does curiosity and innovation within this space describe you? Do you thrive in a busy environment where you will impact core business success by taking on a strong business partner role maturing and facilitating strategic sourcing initiatives globally?
Our new (Senior Category) Manager will join a team of 3 Category Managers, 2 Associate Category Managers and 4 Category Negotiators within the department of Indirect Category Management. We work individually as well as in teams where sparring and mutual support are key in the way we interact. We are a homogeneous team of highly professional and ambitious colleagues who also realize that a workday needs to be fun and social.
Are you passionate about Procurement and within this facilitating and executing category strategy across CAPEX (construction and equipment), Distribution and Facility Management (FM)? Do you thrive in a busy environment where you will impact core business success by leading complex technical sourcing projects in close collaboration with colleagues around the world?
As an Associate Category Manager, you work closely with the Category Manager CAPEX, FM & Distribution who sets out overall category strategies just you take on ownership of specific sub-categories driving and executing strategy within these.
We work individually as well as in teams where sparring and mutual support are key in the way we interact. We are a homogeneous team of highly professional and ambitious colleagues who also realize that a workday needs to be fun and social.
As a Senior Global Brand Manager, you will be a brand ambassador and directly influence the development and execution of the global brand strategy in close collaboration with affiliates, partners and internal stakeholders.
The SGBM is accountable for the successful development and implementation of assigned tasks, aiming to increase the competitive advantage for the brand through translating insights into strategic initiatives and concepts. The Senior Global Brand Manager provides strong commercial input into R&D projects to ensure the development of differentiated products.
We are looking for an experienced Clinical Pharmacology Senior Specialist to join our Clinical Pharmacology department.
The department is part of the Experimental Medicine organization, where we are responsible for translating pre-clinical research into early clinical development strategies and for generating the clinical data that support the further global development of both small molecules and biologics.
You will contribute both scientifically and strategically to Lundbeck research and development projects:
- Serve as an expert within clinical pharmacology and early clinical development in the department and in cross-functional R&D project teams
- Develop and execute strategies for early clinical development, including responsibility for clinical pharmacology input to global clinical development plans
Are you passionate about category management within Research & Development, specifically about Medical & Regulatory Affairs and/or Pharmacovigilance? Are you motivated by managing a wide array of business-critical procurement projects in close collaboration with core business on a global scale?
The Medical & Regulatory Affairs & PV category is global and complex in nature and requires a Category Manager with a good level of experience within this space to ensure that category strategies and execution contribute positively to overall business priorities.
The role requires strong business partnering skills and an ability to equally support and challenge the business to drive the right short- and long-term sourcing decisions. Complex commercial and legal contracting is a central part of day-to day business and the right candidate should be no stranger to fronting legal negotiations.
Are you passionate about toxicology? If so, Lundbeck is now looking for 2 toxicologists with expertise in development of mainly large molecular products to join the Department of Regulatory Toxicology & Safety Assessment.
The successful applicants will be important players in a department that participates in the full development process of pharmaceuticals from early research to post-marketing commitments. When ready you will join cross-functional Global Project Teams (GPTs) as the non-clinical representative.
As GPT member you will be leading the non-clinical project team responsible for all non-clinical safety activities in the project. Also, you will join the NCSR Biologics Team that oversees all biologics projects and participates in due diligences.
We are expanding our portfolio and therefore looking for experienced International Study Managers.
As an International Study Manager, you are overall responsible for leading a global cross-functional study management team consisting of participants from relevant functions within Clinical Research & Development.
We conduct our studies in close collaboration with CROs and as International Study Manager, you are responsible for the management of the CROs, and their deliverables in collaboration with your Lundbeck colleagues and CRO teams, you are responsible for delivering high quality study execution within timelines and budget.
Lundbeck Neuroscience is looking for a technician or senior technician highly motivated by the outlook of discovering new treatments for diseases in the central nervous system.
The main responsibility is to identify and validate drug targets, develop and support drug discovery with cell and animal-based readouts needed for compounds or biologics to be developed into drug candidates.
You will be part of the Departments ‘misfolded proteins’ team contributing to develop in vitro/in vivo disease models and cell-free assays based on induction of protein misfolding. Your key tasks will be to produce and characterize protein aggregates from recombinant source and tissue, and to run fluorescence-based aggregation assays to detect presence of misfolded proteins in biofluids.