Industry Lead Emplois | Theodo (Paris)

Nouveau

Coordinateur Supply Chain

Votre rôle en tant que Coordinateur Supply Chain consiste à piloter et suivre ac...

Emplacement

France , Val-de-Reuil

Salaire:

44000.00 - 45000.00 EUR / Année

Randstad

Date d'expiration

30 septembre 2026

Exigences

Bac+5 with minimum 4 years experience in industry (operational or Supply Chain functions: planning, execution monitoring, demand management)
Rigorous, autonomous, proactive in challenging the status quo
Excellent communicator able to collaborate transversally with multiple functions
Mastery of Excel, Power BI and use of an ERP (ideally Ishift)
Professional English

Responsabilités

Pilot and actively monitor the availability of batches to meet validated commitments and ensure optimal customer satisfaction
Rigorously monitor the execution of flows and provide regular reporting to internal and external clients
Manage end-to-end flow execution from stock entry to product release using FaCT Kanban board and FaCT DA tools
Ensure the realization of the availability plan on the current horizon, alert, prioritize and communicate to effectively implement client priorities
Ensure the reliability of commitments on your products by updating planned end dates based on information from End to End flow instances
Consolidate indicators needed for flow and production plan monitoring
Evaluate cycle time performance of steps under your responsibility in collaboration with Production and Quality departments
Alert in case of deviation and contribute to defining remediation plans
Summarize risks and opportunities related to availability commitments, propose and lead continuous improvement actions
Provide visibility on one year of workload for the Quality Capacity Management process

Temps plein

RWE Data Scientist

Real-World Evidence Data Scientist. The overall purpose and main responsibilitie...

Emplacement

India , Hyderabad

Salaire:

Non fourni

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

PhD in quantitative field such as Statistics, Biostatistics, Applied Mathematics or related field with 6 years of industry or academic experience
Relevant Master’s Degree, with 10 years of related industry or academic experience.
Strong oral and written communication skills
ability to work and collaborate in a team environment
Excellent knowledge of English language (spoken and written)

Responsabilités

Provide a high level of expertise in employing cutting-edge analytical & computational approaches to drive evidence-based pharmaceutical product development
provide scientific and technical leadership in machine learning and AI
work closely with other disciplines across Sanofi including Business Units, Digital, R&D, Biostatistics, Information Technology Systems and other Data Science partners to deliver cutting edge analysis to key business questions.
Act as a subject matter expert in machine learning, statistical and/or modelling working on team projects
Work with internal and external study lead to execute Advance Analytics projects and studies.
Implement and execute computational and statistical methodologies in Advanced Analytics for RWE
Provide expertise and execute advanced analytics for solving problems across R&D, Medical Affairs, HEVA and Market Access Strategies and Plans
Apply a broad array of capabilities spanning machine learning, statistics, mathematics, modelling, simulation, text-mining/NLP, data-mining to extract insights and be able to communicate and champion these efforts across the company
Plan and deploy methodological standards, standardized processes, demos, and POCs for the company’s highest priority business needs
Contribute to the design, development, and implementation of Sanofi’s data science architecture and ecosystem to guide decision-making and building foundational capabilities

Temps plein

Medical Director, Dermatology

Join the team transforming care for people with immune challenges, rare diseases...

Emplacement

United States , Cambridge; Morristown

Salaire:

178500.00 - 257833.33 USD / Année

Sanofi

Date d'expiration

24 août 2026

Exigences

Advance degree in life sciences or pharmaceutical sciences (PhD, PharmD, PA, NP or MD with relevant experience)
Minimum 5 years of relevant experience in Medical Affairs
Strong track record in developing and executing medical strategies in the US
Clinical or medical affairs experience in Dermatology and/or Immunology strongly preferred
Industry experience in Medical Affairs and/or Clinical Development, with significant experience in Medical Affairs Launch and Life Cycle Management activities
High degree of knowledge of relevant healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends to accurately identify key issues and develop strategies
Sound scientific and clinical judgment, including an in-depth understanding of the scientific method and clinical applications based on medical, scientific, and practical rationale
In-depth understanding of how to conceptualize, design, and conduct clinical trials. Experience in clinical trial design and execution preferred
Ability to disrupt status quo with innovation while remaining pragmatic and focused on priorities
ability to translate innovative strategies or solutions into actionable plans.

Responsabilités

Develop strategy and tactics for an integrated Medical Plan (Medical Science Liaisons, Medical Education, Medical Communications and Publications, Health Outcomes, Safety, and Clinical Research including Phase IIIB-IV and Investigator Sponsored Trials) and annual budget for assigned Dermatology products
Execute the Integrated Medical Plan to ensure on-time and on-budget delivery of all tactical activities and deliverables
Communicate the details and Progress of the Medical Plan to Management, the Core Team, and all parties responsible for execution
Provide relevant data evidence to ensure that strategy is clearly defined and consistent with clinical development and commercial strategic objectives
Support the generation and communication of scientific and medical insights to internal stakeholders, develop/execute strategic and tactical Medical Engagement Plans
Provide impactful medical strategy and expertise to Clinical, Commercial, Market Access, and Regulatory partners
Ensure strategic and cross-functional alignment across the organization and any joint ventures to achieve the medical mission of supporting safe and appropriate use of Dermatology products, cultivating a culture of teamwork and collaboration to ensure the delivery of key priorities
Provide medical leadership and expertise to sales, marketing, legal, and regulatory functions for marketed products and drugs in development
Pro-actively provide guidance and collaborate with field team, marketing, HEVA, Market Access, and sales teams
Support the generation and communication of scientific and medical insights to internal stakeholders, develop/execute strategic and tactical Medical Engagement Plans, and manage MSL resources and budgets.

Ce que nous offrons

high-quality healthcare
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

Temps plein

Field Reimbursement Manager, Pulmonology and Gastroenterology - Kansas, North Missouri

The Field Reimbursement Manager (FRM) will be the field subject matter expert re...

Emplacement

United States

Salaire:

Non fourni

Sanofi

Date d'expiration

03 août 2026

Exigences

BA/BS Degree required
Minimum 5+ years in the pharmaceutical/healthcare industry or other relevant experience
Ability to travel to meetings/trainings/programs as necessary - additional travel will be required within the assigned geography
Demonstrated success of cross functional teamwork and working in a matrix and co-promote
Must be energetic and driven to succeed
Interpersonal skills including managing and resolving conflict and building strong working relationships
Obtain ability to adapt to change and react constructively in a high-energy and fast paced environment
Excellent strategic thinking, analytical, and communication skills required
Achieve and maintain compliance with all applicable Sanofi policies and procedures, regulatory and legal requirements, and help to monitor compliance during cross functional team interactions
Valid driver's license

Responsabilités

Be subject matter experts on Dupixent MyWay support programs, access issue resolution, financial assistance and alternative funding options provided by our Patient Support Program
Act as a point of contact for Patient Support Services (Dupixent MyWay), and communicate and collaborate cross-functionally to lead Dupixent pull through efforts assisting the ABM as appropriate
Support field in education of office personnel on prior authorization and appeals processes, reimbursement support through Dupixent MyWay, free drug programs and financial assistance programs
Plan and implement geographic business plans to support appropriate access to Dupixent
Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for Dupixent
Establish positive and productive working relationships with all key customer segments (internal and external)
Partner with Alliance colleagues to create a culture of respect and customer focus
Develop working relationships with state societies, associations, and advocacy groups, as needed, to support patient access and raise overall awareness for the Alliance, Dupixent MyWay and Dupixent
As needed, conduct HCP office visits to facilitate pull through efforts and problem solve escalated issues as a HIPAA compliant contact
Work compliantly to reduce cycle time and increase conversion rate for patients prescribed Dupixent

Ce que nous offrons

high-quality healthcare
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

Temps plein

Global Safety Officer

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-po...

Emplacement

United States , Cambridge, Massachusetts; Morristown, New Jersey

Salaire:

178500.00 - 297500.00 USD / Année

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

M.D. Degree or equivalent
For MD, Board Certified/Board eligible, or equivalent, is preferred
Minimum 3 years' total experience in international pharmacovigilance, or equivalent relevant industry experience (e.g. clinical development) with relevant clinical experience considered. Exceptionally, candidates may be considered if they have proven excellence in a similar prior position, even if they have less than 3 years international PV experience
Excellent clinical judgment
Capability to synthesize and critically analyse data from multiple sources
Ability to communicate complex clinical issues and analysis orally and in writing
Able to develop and document sound risk assessment
Demonstrates initiative and capacity to work under pressure
Demonstrates leadership within cross-functional team environment
Excellent teamwork and interpersonal skills are required

Responsabilités

Provide PV and risk management expertise to internal and external customers
Safety expert for product
Maintain knowledge of product, product environment, and recent literature
Maintain PV expertise, and understanding of international safety regulations and guidelines
Lead cross functional Safety Management Teams (SMTs) and GPE internal Safety Analysis Teams (SATs)
Communicate with and represent PV position within project/product teams, with external partners, key opinion leaders, and Health Authorities, and during internal and external negotiations
Provide strategic and proactive safety input into development plans
Support due diligence activities and pharmacovigilance agreements
Responsible for signal detection and analysis
Collaborate with Center of Excellence for Signal Detection and Data Mining and Safety Epidemiology group

Ce que nous offrons

high-quality healthcare
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

Temps plein

Director of Purchasing and Supply Chain

A Strategic Role at the Heart of Our Operations. We are seeking a strategic lead...

Emplacement

Canada , Boisbriand

Salaire:

Non fourni

Plaisirs Gastronomiques

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Ten (10) years of experience in procurement management within the food manufacturing industry
Five (5) years of experience managing teams
Excellent command of both French and English is required to communicate effectively with our English-speaking suppliers
Bachelor's degree in Business Administration or another field relevant to the position
Strong negotiation skills
Proven experience working with an ERP system (SAP experience is considered an asset).

Responsabilités

Define and implement the overall procurement strategy for all raw materials, ingredients, and packaging materials
Ensure the availability of critical materials while optimizing costs, quality, lead times, and inventory levels
Develop and maintain a strong network of local and international suppliers to support the company's growth
Identify, qualify, and onboard new strategic partners to mitigate supply risks and enhance the company's competitiveness
Continuously monitor market trends to anticipate price fluctuations, supply challenges, and business opportunities
Negotiate pricing, commercial terms, supply contracts, and long-term agreements
Identify and implement cost-reduction initiatives while maintaining quality and service standards
Monitor supplier performance through measurable key performance indicators
Actively support new product launches in collaboration with product development, production, and sales teams
Oversee the entire procurement process to effectively meet short-, medium-, and long-term production requirements

Ce que nous offrons

Salaire compétitif
Conciliation travail-famille et travail-études
Emploi permanent, stable et à temps plein
Quarts de travail stables
Possibilité de travail à temps partiel avec horaire sur mesure
Avantages sociaux compétitifs (congé mobile et de maladie, primes selon années de service, vacances adaptées et bonifiées avec années de service)
Régime d'assurance collective adapté
Rabais aux employés sur les produits
Espace de stationnement gratuit et accès au transport en commun
Uniformes fournis pour postes en usine

Temps plein

Gestionnaire de l'engagement

Le ou la gestionnaire de l'engagement agit à titre de principal intermédiaire en...

Emplacement

Canada , Montreal

Salaire:

Non fourni

MaintainX

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Minimum 5 years of experience in professional services, consulting, or client implementation roles in SaaS or technology industries
Demonstrated ability to clearly and effectively communicate complex technical or procedural concepts to executive and operational audiences
Strong presentation, facilitation, and relationship management skills
Proven experience in client expectation management and alignment of multiple stakeholders
Good knowledge of project management methodologies and frameworks
Experience in manufacturing, maintenance, or industrial technology sectors (an asset)
Knowledge of Industry 4.0 principles and their application in maintenance engineering, smart manufacturing, or digital transformation initiatives
Bachelor's degree in business administration, engineering, or a related field (MBA or PMP certification considered an asset)

Responsabilités

Acts as the primary intermediary between MaintainX sales and service delivery teams, ensuring enterprise clients fully understand the implementation and integration process
Collaborates with the sales team during the pre-selection process to represent MaintainX's professional services organization and explain the client onboarding methodology
Participates in discovery sessions with clients to understand their business needs and uses this information to propose clear, realistic implementation plans that demonstrate MaintainX's structured approach to success
Once the client is committed, leads the transition from sales to implementation, ensuring all stakeholders understand the project scope, timelines, responsibilities, and deliverables
Acts as a trusted advisor and single point of contact during this critical period, helping the client navigate each stage of the integration process with confidence and clarity
Throughout the engagement, monitors delivery progress, facilitates communication between MaintainX teams and the client, and proactively manages any changes or issues that may arise
Overall success is measured by client understanding and adherence to the integration process, rigorous expectation management, and the confidence the client demonstrates during the successful implementation and adoption of the solution

Ce que nous offrons

Competitive salary and significant equity opportunities
Health, dental, and vision coverage
401(k)/RRSP program
Take the time off you need
Work culture that reflects MaintainX values: Smart, Humble, Optimistic
Meritocracy where ideas and efforts are publicly celebrated

Temps plein

Head of Quality Assurance Operation Unit (APU) & Sterility

Nos équipes produisent et livrent chaque année plus de 4 milliards de médicament...

Emplacement

China , Beijing

Salaire:

Non fourni

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

5+ years' experience in quality control and/or quality assurance
3 years management position
3 years of experience in sterility assurance and microbiological control in the medical device, pharmaceutical, biotechnology, or related industry
Good communication
Able to burden pressure
Think strategically
Make decisions
Good leadership
Must be a committed 'quality' professional with knowledge of regulated quality systems within the pharmaceutical or related industry
Knowledge of analytical chemistry and microbiology

Responsabilités

Assist site quality head to ensure that product is manufactured and controlled under cGMP condition and marketing authorization
Develop quality system to be in alignment with local cGMP, industry standards, regulatory expectations and Sanofi requirements
Keep on developing the quality system and establish or update the related SOP according to the global quality standard / cGMP and other local requirements together with other departments
Ensure the cGMP compliance of the calibration, utilities, systems, production processes (raw materials, in process product, finished products) and control procedures
Make decision of batches, materials and quality event in compliance with the registered specifications and cGMP requirements
Review the batch manufacturing / packing master records and review the annual products quality
As the Lead of operation QA to respond to operational business
Establish procedures and ensure continuous improvement of the PCU quality oversight and GMP documentation
Provide quality assurance oversight by performing routine walk-throughs and inspections on production, laboratory, warehouse, engineering deportment and other areas assigned
Ensure the plan in place

Temps plein

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Industry Lead

Description du poste

Responsabilités

Exigences

Souhaitable

Ce que nous offrons

Looking for more opportunities?

Industry Lead

Coordinateur Supply Chain

RWE Data Scientist

Medical Director, Dermatology

Field Reimbursement Manager, Pulmonology and Gastroenterology - Kansas, North Missouri

Global Safety Officer

Director of Purchasing and Supply Chain

Gestionnaire de l'engagement

Head of Quality Assurance Operation Unit (APU) & Sterility

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