Head of Exploratory Toxicology Would you like to lead an experienced scientific team at the interface of drug discovery and non-clinical safety? Help shape early safety strategies and build capabilities that support Lundbeck's next generation of treatments for brain disorders.

Does it excite you to shape regulatory strategies for early-stage metabolic health projects, and do you have experience leading global regulatory strategy and health authority interactions? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.

Medical Writing Senior Specialist, Medical Documentation Requisition ID: 8250 Location: Copenhagen, Danish Capital Region, DK Medical Writing Senior Specialist, Medical Documentation Do you want to shape the clinical, regulatory documents that advance the development and approval of medicines for people living with brain disorders? We are looking for a senior specialist (equivalent to Associate Director level) regulatory medical writer with extensive submission experience to lead complex documents, advise cross-functional teams, and contribute to the continued development of our authoring practices and technologies. You will bring a proven track record of leading the authoring documents for major regulatory submissions.

Join Pharmacosmos in a newly established function, in a role combining people leadership with direct involvement in clinical processes, compliance and continuous improvement. Build and lead a new Clinical Administration & Compliance function As Director, Clinical Administration & Compliance, you will report directly to the Senior Director, Head of Clinical Operations, Trine Kolding, and take on a key role combining leadership with hands-on responsibility for clinical trial administration, processes and operational GCP compliance.

Does it excite you to work with complex inventory flows, including cross-border movements and transactions, and the indirect tax implications, such as VAT, that follow them? Do you also bring broad accounting experience, especially within inventory, tax and VAT, bank and treasury, and intercompany accounting? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague. ​ 

Does it excite you to work with shaping the equity story of a peptide-based biotech company and strengthening relationships with investors and analysts across Europe, and do you have experience with investor relations and corporate communications in biotech or pharma? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.

Does it excite you to shape digital products and AI-enabled solutions that make regulatory data flow reliably across the enterprise and on to EMA and FDA, and do you have experience with Veeva Vault RIM? If this sounds like you, and you are ready to take on a broad area of responsibilities, then you could be our new colleague.

Biograil is expanding its Pharmaceutical Research organization and is seeking an experienced Analytical Scientist to drive analytical development and CMC activities for our proprietary BIONDD™ oral delivery platform for peptides and biologics. You will play an important role in analytical development across drug substance, drug product, and combination product development, supporting our ambition to advance next‑generation orally delivered biotherapeutics.

Join a leading international life science company in an exciting role and assume end-to-end responsibility for a high-impact role at the intersection of operational strategy and execution.

Vil du kombinere din sundhedsfaglige viden med en selvstændig og udadvendt salgsfunktion? Hos TIMIK får du frihed til at drive salget af Point of Care-løsninger på Sjælland i tæt dialog med kunderne.

Lead complex Analytical Development across a growing development pipeline As Principal Analytical Development Chemist at Pharmacosmos, you will serve as the Analytical Lead across CMC development programs, driving analytical development, characterization, control strategies, and regulatory readiness from early-stage development through commercialization to lifecycle activities.

As our Senior Specialist, Drug Product, you will execute DP activities across the development lifecycle, from early clinical development through regulatory approval and commercial handover. You will also act as a technical expert in late-stage development, Process Characterization (PC) and Process Validation (PV), helping to establish best practices and supporting colleagues across the portfolio. You will apply this expertise directly in your own projects, leading process design, control strategy, technology transfer, PC and PPQ to establish robust, registration-ready aseptic fill-finish processes.

Bliv en del af IBSA Nordic som Nordic Product Manager og få ansvaret for lokale kommercielle indsatser, kampagner og salgsunderstøttende aktiviteter inden for urologi- og reumatologiområdet.

oin IBSA Nordic as Operative Business Specialist and play a key role in operational support and commercial execution within the Dermo Aesthetics business.

PharmaRelations is the Nordic market leader in talent services for the life science industry. We specialize in partnering with some of the most innovative and successful organizations across the Nordic life science sector. We create value for both clients and candidates through our consultancy services, outsourcing solutions, and recruitment of specialists and leaders. We are a Nordic organization with over 200 colleagues and with offices in Sweden, Norway, Denmark and Finland. PharmaRelations is headquartered in Solna, Sweden.