Site Logistics Manager H/F
Vue: 145
Jour de mise à jour: 01-12-2023
Localisation: Dreux Centre-Val de Loire
Catégorie: Direction Production/Opération
Industrie: Pharmaceutical Manufacturing
Type d’emploi: Full-time
le contenu du travail
TitleSite Logistics Manager H/FCompanyIpsen PharmSciences SASJob DescriptionClinical distribution responsibilities- For each asset and each clinical study, define the clinical distribution strategy and ensure alignment with clinical needs and internal capabilities,
- Define clinical distribution plans (short, mid and long term) for Ipsen assets (small molecules and toxins) according to clinical forecasts and timelines to ensure on-time in full supply to patients,
- Anticipate and assess the impact of changes in clinical studies on the distribution plans, proactively propose alternatives when possible to streamline the activity and reduce costs,
- Perform prioritization exercise when needed,
- Act as a key interface with the Global Clinical Supply Management team,
- Represent his/her function in cross-functional project meetings to support clinical study launch,
- Perform the make vs buy assessment for the distribution activities,
- Manage transporters: set up contracts and Quality Technical Agreements, organize regular meetings and steering committees, monitor performance through KPIs, control the budget,
- Develop/maintain a network of efficient transporters to ensure his / her activities,
- Maintain good collaboration with our Importers of Record,
- Ensure the on-time availability of the documents and packaging materials required for his/her activities,
- In collaboration with the Operational Quality Assurance team, support quality events management in line with defined KPIs,
- Ensure the follow-up of the quality management system related to its perimeter (KPIs, risk analysis, self-evaluation, internal audit, etc.) in close collaboration with the Quality Department,
- Be the contact person for his / her perimeter during visits, audits or regulatory inspections and lead the preparation of such visits with his / her team,
- Ensure technical and regulatory surveillance related to his / her scope,
- Guarantee adequate communication and alignment within the Drug Product Development department, the CMC workstreams and more broadly within Pharm Dev.
- Follow and communicate on team performance through relevant KPI,
- Manage reception, shipment and storage areas and define appropriate CAPEX plans.
- Ensure the reception of all incoming goods in PharmSciences site,
- Manage the delivery of the packages to the recipients in the adequate buildings,
- Develop and maintain an intermediary store for shared materials and ensure stock availability for PharmSciences collaborators and laboratories,
- Ensure mail distribution within the site,
- Manage storage areas and define appropriate CAPEX plans.
- Lead a team in a matrix environment,
- Maintain staff by recruiting, selecting, orienting employees,
- Define the annual objectives of his/her group in alignment with the objectives of Pharmaceutical Development & R&D. Lead his/her team by mobilizing it around its objectives and evaluates the outcomes,
- Provide effective and continuous feedback, through employee recognition, rewards, performance appraisal and development discussions,
- Define and propose the training/development plan for his/her team, ensure its implementation and carry out the follow-up. Develop, monitor and guide the levels of expertise of his/her team in terms of knowledge and know-how. Ensure continuous professional development of its employees,
- Anticipate any resource needs to ensure that his / her team provides deliverables in time, with the expected quality.
- Contribute to continuous improvement projects within the Formulation, Process and Clinical Supply Department and/or wider Pharmaceutical Development,
- Be a promoter of continuous improvement processes and guarantee the method.
Date limite: 15-01-2024
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