OneLab Laboratory Team Leader

Job description

Title: OneLab Laboratory Team Leader Company: Ipsen Innovation (SAS) About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavor every day to bring medicines to patients in 88 countries. We build a workplace that champions human-centric leadership and fosters a culture of collaboration, excellence and impact. At Ipsen, every individual is empowered to be their true selves, grow and thrive alongside the company’s success. Join us on our journey towards sustainable growth, creating real impact on patients and society! For more information, visit us at https://www.ipsen.com/ and follow our latest news on LinkedIn and Instagram. Job Description: Job Title: OneLab Laboratory Team Leader Division / Function: Early Development/Clinical Pharmacology, DMPK & Pharmacometrics Manager’s Job Title: Director, Immunogenicity and Immunoanalysis (IMA) Ipsen Job Profile: Principal Scientist Location: Dreux Laboratories WHAT - Summary & Purpose of the Position The Early Development (eDev) department plays a critical role in advancing Ipsen’s portfolio of products of biologics and small molecules across all therapeutic areas, from early non‑clinical development to Proof of Concept in humans. eDev is organized around three interconnected functions: Non-Clinical Drug Safety (NCDS); Translational Sciences (TS) and Clinical Pharmacology/DMPK, BioAnalysis (BioA)/ImmunoAnalysis (IMA)/OneLab, and Pharmacometrics. Together, these functions provide comprehensive expertise in evaluating safety, efficacy, and pharmacological profiles of drug candidates prior to clinical development. The newly established OneLab laboratory in Dreux provide state‑of‑the‑art capabilities to design, develop, and execute experimental work supporting the entire Ipsen R&D pipeline. Within this environment, the OneLab Laboratory Team Leader plays a dual and strategic role: OneLab Laboratory Team Leadership: Ensure the effective management of OneLab activities through day‑to‑day coordination of teams (TS/IMA, BioA, NCDS), optimal resource allocation, and oversight of laboratory planning, execution, documentation, and continuous improvement. The Team Leader also holds the hierarchical responsibility for all technical staff and postdoctoral researchers within the OneLab TS/IMA teams. In Vitro Pharmacology Lead (Translational Sciences): Provide technical guidance and scientific oversight to TS staff and postdoc fellow ensuring alignment with project objectives and scientific rigor and contributing to translational science plans across the portfolio by defining the in vitro strategy to answer key scientific questions and design/monitor outsourced in vitro studies. This position requires strong experience in laboratory operations, team management, and translational science in immuno‑oncology models, combined with demonstrated leadership, organizational excellence, and the ability to drive high‑quality scientific output in a dynamic and multidisciplinary environment. WHAT - Main Responsibilities & Technical Competencies ONELAB LABORATORY TEAM LEAD (50% OF TIME) OneLab Laboratory Management Functional management of all OneLab teams (NCDS / TS / IMA / BioA). Act as the representative for all OneLab teams based in Dreux (TS/IMA, BioA, NCDS) to ensure efficient interactions with:EHS teams (e.g., BSL2 lab representative, human material authorization requests, biological sample listings, quality audits) IT services (e.g., network access for new equipment, platform updates, maintenance) Facility Management (e.g., equipment and infrastructure maintenance). Anticipate needs and ensure centralization and sharing of information and actions required for optimal laboratory operations. Manage equipment investment requests (CAPEX). Enforce EHS regulations, promote a safety culture, conduct safety inspections, and ensure mandatory EHS training for lab staff, newcomers, students, interns, and postdoctoral researchers. Ensure proper organization of OneLab team documents in shared spaces (SharePoint, Teams, eLN). Identify, develop, and coordinate synergies between OneLab and PharmDev teams on the Dreux site. Attract, develop, and retain laboratory staff to maintain scientific excellence. Manage trainees, PhD students, and postdoctoral fellows. Hierarchical Management of OneLab TS/IMA Teams and all Postdocs Directly manage a team composed of postdocs, scientists, and research assistants. Adjust and coordinate experimental workload and planning based on project strategies defined by TS and IMA Leads to ensure high-quality deliverables within timelines. Provide technical support and expertise for experimental activities and equipment use/maintenance. Ensure detailed and accurate reporting of experimental activities for TS/IMA teams. Occasionally contribute to wet lab activities to support experimental work. Conduct performance evaluations for team members. Participate in scientific and technological monitoring in TS/IMA domains. Environment, Health & Safety (EHS) Comply with current EHS regulations and procedures. Contribute to site EHS performance by reporting risks, malfunctions, or improvement opportunities. Participate in mandatory EHS training sessions. IN VITRO PHARMACOLOGY LEAD (TS TEAM) WITHIN THERAPEUTIC PROJECTS (50% OF TIME) Identify gaps related to in-vitro pharmacology and propose mitigation plans. Define study protocols based on scientific questions raised by the project, following the translational plan; propose appropriate protocols integrating current scientific knowledge and literature data. Participate in meetings with in vitro leads and TS subteams to define in-vitro plans; interact with TS lead, in vivo lead, biomarker lead, and study coordinator to ensure project success. Assess feasibility of conducting assays internally or outsourcing; if outsourced, manage CRO studies (CRO identification, study design, contract generation, report validation). Coordinate, perform, and supervise in vitro/ex vivo analyses on study samples (e.g., flow cytometry, Luminex, ELISA, Western blot, IHC, PCR, immunofluorescence) internally or externally. Review and perform QC of reports provided by partners/CROs. Prepare QC reports for activities conducted internally at Dreux laboratories. Conduct literature reviews to understand context and integrate data. Perform critical data analysis, record data in ELN, and draft reports. Contribute to drafting, reviewing, and editing regulatory documents (FIHSA, IND) and reviewing documents provided by CROs or internal preclinical writing leads. Ensure all regulatory requirements are met before initiating internal and/or external studies. HOW - Behavioural Competencies Required Competency Competency Behavioural Markers Explanation of Choice References to Job Description Excellence in Execution • Approaches priority setting and setting the stage through the lens of execution • Establishes clarity about the goals, accountabilities, timelines, and next steps; can identify/spot opportunities for real impact on patient and society • Able to be focused and performance‑driven with clear KPIs • Plans and aligns effectively (steps, resources, timelines etc.) • Displays a commitment to best practice sharing and setting • Promotes single point of accountabilities This role is responsible for planning, coordinating, and delivering a high volume of laboratory work across TS/IMA, NCDS, and BioA. The position requires excellent operational rigor, prioritization, and consistent delivery of high‑quality scientific outputs aligned with project timelines and regulatory expectations. Ensure the effective management of O