On-site jobs in Belgium (8), Bulgaria (1), Croatia (4), Denmark (6), France (18), Germany (10), Greece (4), Hungary (1), Ireland (19), Italy (3), Multiple Countries (11), Netherlands (7), Poland (8), Portugal (2), Romania (2), Slovenia (1), Spain (3), Sweden (1), Switzerland (8) and United Kingdom (28).
The role will provide scientific and technical leadership for analytical development at various stages of drug development both internal and external through CDMO with particular emphasis on research and early development (pre-DP0) including material
This role is accountable for defining the vision, operating model, and multi-year strategy for internal QC to support Genmab’s evolving pipeline and transition to a fully integrated, commercial-stage biotechnology company. The role will shape future QC
You will be a contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance including electronic pharmacovigilance system, adverse drug experience (ADE) reports, trending reports, ADE
Ensure commercial Drug Product batches are manufactured and released in time to guarantee continuous supply to all global markets. Ensure a timely arrival of Drug Substance shipments and allocate Drug Substance to the Drug Product batches, taking into
The scientific and strategic leader of oncology drug discovery programs, accountable for driving projects from early concept to Preclinical Candidate (PCC) nomination, in alignment with Oncology Therapeutic Area and R&D strategy. As the integrator of
Lead the planning, development and implementation of integrated marketing strategies and associated tactical plans. Such activities will also include performance and tracking metrics for plan evaluation, as well as managing the marketing budget.
The QC Lab Manager is integral to managing a team responsible for QC testing, ensuring adherence to product specifications, quality, and safety goals. This role involves overseeing laboratory operations, including analytical testing for API and OSD
Responsible for establishing and execution of work plans for their protein science area. Accountable for protein science project delivery from early drug discovery projects in their area of expertise, across modalities and therapeutic areas
Understands and keeps updated with the pre-clinical, clinical pharmacology and data relevant to the molecule of interest. Knowledge on antibody is a plus; Critically reads and evaluates relevant medical literature with deep understanding of the data and
This role provides expert scientific leadership across Lonza’s global Biologics network, supporting technical challenges and driving the implementation of strategic technology programmes across the network. The position leads complex,
Create expert medical and scientific inputs for biosimilar products and programs; Maintain general scientific expertise, including up-to-date knowledge of international guidelines and requirements for biosimilars; Prepare and deliver high-quality internal
This Expert Level role provides on‑site regulatory leadership with a strong manufacturing focus, ensuring regulatory considerations are embedded early into site initiatives and day‑to‑day operations. This leader interacts closely with global and
Play a key role in the design, execution, and evaluation of Phase 1, 2, and 3 clinical trials, providing subject‑matter expertise in pediatric viral infectious diseases. This role will support the development and registration of novel therapies for
Manage a team of Scientists, Senior Research Associates and Research Associates within the EDS Bioconjugation team. This includes performance review, goal setting, implementation of personal development plans and provide timely constructive feedback.
Your tasks include project management of interdisciplinary teams (leadership, team building, goal achievement) tasked with Chemical R&D and Manufacturing activities. Structuring and coordinating project specific activities including risk and time
Define and execute the scientific strategy for of the Pole of Activity, ensuring alignment with the broader Unit goals and the R&D vision, to discover and develop high therapeutic value drugs for patients. Leverage structural biology and biophysical
Accountable for assessing, establishing and operationalizing the regulatory strategy and execution plan for assigned IVD performance studies and for clinical trials that use IVDs, ensuring that study conduct and IVD use are compliant with the EU IVDR
Lead and develop the gastroenterology medical team, setting direction and fostering a culture of medical excellence. They will define and implement medical affairs therapeutic area (TA) strategy for gastroenterology, aligned with affiliate
We are looking for a motivated and detail-oriented Scientist with hands-on experience in biochemical and biophysical assays to support our drug discovery projects. This role combines experimental work with data analysis and offers the opportunity to
In this senior leadership role, you will lead an interdisciplinary Analytical Development team responsible for the implementation, development, optimization, and validation of analytical methods for small‑molecule products in a GMP‑regulated
Play a pivotal role in advancing next-generation purification technologies. This is a hands-on scientific role where you will drive innovation in downstream processing and contribute to the development of intensified, scalable purification solutions for
A senior scientific and strategic leadership role responsible for shaping and executing the R&D strategy within the I&I therapeutic area. Reporting to the Head of Therapeutic Areas, this role drives innovation, identifies high-impact opportunities, and
Lead, motivate and mentor your team to maximize their effectiveness by clearly communicating task details and goals to your team members, allowing them to work effectively. Foster a positive progressive culture within the lab that focuses on EED&I
The role assures that project output meets combination product regulatory requirements. This position assists in the development and implementation of site/Global QMS GMP policies and procedures. Additional responsibilities will ensure departmental
Provide strategic medical leadership across CEE in alignment with global and regional priorities; Lead and inspire regional medical team; Drive CEE regional medical strategy and execution in alignment with Sobi’s global and brand priorities