On-site jobs in Austria (2), Belgium (5), Bulgaria (1), Croatia (2), Cyprus (2), Czech Republic (2), Denmark (9), France (14), Germany (16), Greece (4), Hungary (3), Ireland (14), Italy (7), Multiple Countries (7), Netherlands (5), Poland (13), Romania (1), Spain (5), Sweden (1), Switzerland (24) and United Kingdom (20).
Leading our global investigative toxicology efforts with operations in Boston, Paris and Montpellier and with Senior Scientific Advisors serving as global safety experts in various toxicology disciplines based in multiple countries (France, US and
Providing scientific/medical leadership, strategy, and support for Teva products in the migraine area. Leading integrated strategic medical & brand planning, GTMAP, and execution of all medical activities and projects for the migraine product within
Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. The pharmacoepidemiology
You will play a crucial role in driving the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials studying TransCon C-type natriuretic peptide (CNP). This is an exciting opportunity to work in a fast-paced environment,
Lead and perform Quality and compliance specific tasks including but not limited to processing product complaints, review of information about secondary packaging/redressing, ensure proper labelling of products at the distributor, and product recall
Responsible to supervise and lead the Laboratory release function including Raw Materials, Intermediates, DPI and API’s (including the stability program) and In Process Control and provide core technical support in areas of chromatography,
Laboratory testing of household chemical products and raw materials, in a regulated environment where GMP/GLP standards apply. Formulation of laboratory samples for stability and consumer testing. Participation in industrial trials, supervising compliance
Lead a team of MSAT Experts who are tasked with technology transfers (process implementation and transfer) and timely process implementation at our aseptic fill&finish line. Manage the MSAT team with full responsibility for all aspects of human resource
Responsible for providing Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsible for preparing and managing CMC regulatory
Responsible for developing and overseeing a robust Quality Assurance strategy focused on the transfer of New Product Introduction (NPI) QC methods to manufacturing sites and Third-Party Laboratories. This role supports the Test Method Gate Review process,
Develop, implement, and maintain the quality management system applicable to R&D activities (SOPs, work instructions, standards, etc.). Ensure compliance of R&D projects assigned to CMO Office with relevant regulations (e.g., GCP, GVP, GMP, GLP, ISO, ICH,
Overseeing the overall end to end COE Research group covering pDNA, mRNA & Delivery (including Lipids discovery, associated synthesis) research teams and capabilities supporting Sanofi ambition in the field of therapeutic and prophylactic approaches
We are looking for a seasoned R&D leader to spearhead a newly established global initiative focused on cardiovascular technologies. This position will oversee cross-functional teams across multiple international locations and play a pivotal role in
Plays a role in establishing and maintaining partnerships with biopharma drug development translational and clinical biomarker teams. As such, this individual will participate in customer facing meetings to provide technical
Are you an experienced manager and an inspirational leader seeking a new challenge within Quality? Do you want to make a meaningful impact in a company dedicated to advancing cancer diagnostics and improving patient outcomes? If so, we invite you to
Leading the development and manufacture of inhaled drug delivery systems, including dry powder inhalers and pressurised metered-dose inhalers (pMDIs); Inputting into manufacturing processes strategies from concept through scale up to commercialisation;
In this role, you will contribute to the design, synthesis, and characterization of novel payloads, bioconjugation technologies, and linkers that enable innovative therapeutic modalities. You will work in a multidisciplinary environment
Primary responsibilities will include designing and planning of synthesis of novel chemical entities, analyzing structure-activity relationships (SAR), and optimizing lead compounds for potency, selectivity, and pharmacokinetic properties. Close
Lead the development & qualification of analytical methods (HPLC/CE related). Serve as project representative for pharmaceutical product development on cross-functional project teams. Transfer of analytical methods to quality control (QC) or external
You will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with
A strategic role that drives enhanced compliance throughout the PV domain to support the obligation of the Marketing Authorization Holders and appointed QPPV, to maintain and improve a Global PV system in accordance with international regulations. He/She
This role is pivotal in ensuring regulatory compliance, operational excellence, and continuous improvement within a cGMP environment. You will manage a team of 17, fostering a culture of accountability, adaptability, and technical expertise while
Lead, plan, and coordinate daily cell and tissue culture activities in compliance with GMP standards. Supervise and mentor a team of (Senior) Biotech Associates, ensuring quality and efficiency in manufacturing. Initiate and follow up on deviations,
In this exciting role, you will be part of a highly driven team responsible for developing innovative workflow solutions for the CliniMACS Prodigy® and Plus® platforms—from initial concept to market launch. These solutions enable automated, fully
Validate performance of new Agilent Automated Electrophoresis instrumentation and assays; Support quality of current products through corrective and preventative action (CAPA) investigations and continuous product improvement projects according to the
Provide expert advice on GVP compliance and regulatory matters, acting as quality partner to PV Operations (US/DK) and the EU QPPV. Author and maintain GVP Quality procedures and support implementation of new or updated GVP requirements.
In this role, you’ll provide global scientific and technical leadership, contribute to innovation strategies, and act as a thought leader - both within Lonza and the wider biopharmaceutical industry. Guide development of mammalian USP/DSP processes for
In this global role, the Industrial Lead Drug Product will bring a strategic vision and leadership in the industrialization of our late-stage development and commercial products (NBE and NCE). You will develop cutting-edge industrialization strategies,
Act as key point of contact for TPM on all operational aspects - equipment, performance, cycle time, yield etc. Build solid relationships with first tier TPM’s and drug linker TPM’s to monitor manufacturing performance weekly through the application
Responsible for all tasks and resources including cross functional co-ordination required to complete relevant QC microbiology activities within regulated environment in the required timeframe. Management of QC Microbiology team to carry out tasks.
Lead and manage a senior scientific team of up to 5 Hcs, including experts in fields of oral formulation, pulmonary drug delivery, long acting and modified release dosage forms, solubilization and bioavailability enhancing technologies, formulation of
Lead key projects in mammalian cell line development, while spending the majority of your time (~80%) performing hands-on lab work; Mentor and support junior scientists within the team, fostering skill development and knowledge sharing; Contribute to the
As a functional expert within a small, innovative group, you will play a pivotal role in advancing our clinical development programs. In this highly collaborative environment, you will provide strategic guidance on pharmacokinetics (PK), pharmacodynamics
In this role, you will coordinate and track regulatory submissions, partnering with the Regulatory Lead to prepare high-quality global submissions and ensuring timely delivery to health authorities worldwide. You will provide operational support to
Lead the full lifecycle of complex programs from contract signature to delivery. Act as the single point of contact for customers and advocate for their needs on-site. Ensure delivery on time, within budget, and to the highest quality standards.
In this role, you will be responsible for applying biology knowledge in an engineering environment to support product development of novel systems used in biopharmaceutical development. This involves working in a multidisciplinary team to achieve the
You will oversee a team responsible for managing the end-to-end regulatory artwork process for pharmaceutical and non-pharmaceutical products across Europe. In addition to your leadership responsibilities, you’ll remain actively involved in daily