Global Pharmaceutical Product Manager Emplois

Senior Scientist Drug Product

Within the Synthetics platform of Sanofi's Global CMC organization, we are offer...

Emplacement

Allemagne , Francfort-sur-le-Main

Salaire:

79104.00 - 105472.00 EUR / Année

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Ph.D. in pharmaceutical or related natural sciences
Strong scientific background in formulation development
Experience in biopharmaceutical experimentation and modelling
German: spoken with confidence to ensure proper communication with lab staff
English: excellent written/oral communication and presentation skills

Responsabilités

Act as formulation expert and representative in global R&D project teams for pre-clinical and clinical formulation development
Provide formulation strategies/solutions and early biopharmaceutical risk evaluations to project teams enabling proper candidate profiling, selection and development
Responsible for the supply of various pre-clinical studies
Evaluation, interpretation and presentation of data and Progress
Manage close interaction and exchange with global CMC functions, pharmacokinetics, pre-clinical safety, medicinal chemistry and the therapeutic areas
Contribute to the continuous evolution of methods, analytics, way of working and formulation strategies as part of the DP Design team
Laboratory management – including equipment and documentation
Instruction and training of technicians

Temps plein

Pharmacovigilance Manager II

Mettez votre curiosité au service d’une équipe où l’immunoscience de pointe renc...

Emplacement

Brésil , São Paulo

Salaire:

Non fourni

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Experience in Pharmacovigilance or related pharmaceutical disciplines (Medical Affairs, Quality Assurance, Regulatory Affairs), with progressive experience in managerial roles
Demonstrated expertise in pharmacovigilance systems and safety-related product management, with proven proficiency in developing high-quality safety documentation including RMPs, PBRERs, signal detection reports, and benefit-risk assessments
Strong leadership capabilities in building and directing multidisciplinary teams (example: hands-on experience implementing risk minimization measures)
Established track record of effective stakeholder engagement and regulatory liaison with national and international regulatory agencies
Proven leadership capabilities with demonstrated ability to build strategic networks and drive collaboration across international, cross-functional teams while championing diversity and cultural inclusion
Results-driven professional with strong problem-solving skills, strategic thinking, and ability to act with appropriate urgency
Excellent communication skills with the ability to convey complex information clearly to diverse audiences
Strong influencing and negotiation abilities, adept at building consensus and driving alignment across stakeholders
Extensive experience operating effectively in global, matrix, and cross-functional team environments
Advanced analytical skills with expertise in interpreting clinical and post-marketing data, translating insights into strategic recommendations and actionable communications

Responsabilités

Supports the Country Safety Head (CSH) in ensuring all local PV activities comply with PSPV policies and global/regional/local regulations, enabling safe and appropriate use of Sanofi products in Brazil, while ensuring effective collaboration with in-country functions to execute and monitor PV activities
Builds and maintains strong cross-functional collaboration with PSPV stakeholders, CSHs, and local teams (Medical, Regulatory, Quality, Commercial, Legal, etc.), representing PSPV in local decision-making bodies for assigned products
Supports product submissions and launches by preparing safety documents (e.g., RMPs) and ensuring implementation of appropriate post-launch risk management strategies
Leads local implementation of Risk Management Plans (RMPs), including defining and executing aRMM strategies, adapting to local context, and training stakeholders in collaboration with Risk Management Experts and cross-functional teams
Supports the Global Safety Officer (GSO) in local safety surveillance, contributing to signal detection, defining and executing local surveillance strategies, monitoring safety communications, and ensuring timely escalation to PSPV, global PV, health authorities, and partners
Manages local periodic reports (e.g., PSRs) end-to-end, including planning, development, coordination with Medical, Regulatory and vendors, and submission
additionally reviews safety sections of product information, contracts, and medical programs when applicable
Participates in due diligence for acquisitions/divestments by assessing safety profiles and reviewing SDEAs, and provides oversight of local medical safety activities, including acting as Local Safety Officer (LSO) when required, leading safety analyses, documentation (PSRs, RMPs, benefit-risk, signals), and defining risk minimization actions
Promote the culture of Ethics and Business Integrity in your team by serving as a role model by ensuring appropriate knowledge and adherence to the principles of ethics and integrity, Sanofi policies and codes of conduct that regulate the pharmaceutical market
Comply with and promote Sanofi Health, Safety and Environment (HSE) policies in relation to the team it manages, which includes the Road Safety Program (Road Safety) with the purpose of preventing accidents, avoiding health risks, promoting the well-being of employees, and reducing environmental impacts resulting from the execution of their work activities

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

Medical Education & Training Manager

Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are ...

Emplacement

Thaïlande , Bangkok

Salaire:

Non fourni

Teoxane

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Bachelor’s degree in Medicine, Nursing, Pharmacy, Life Sciences, Dentistry, Aesthetic Medicine, or related healthcare / science field
Minimum 4 years of experience in medical education, clinical training, customer education, medical affairs, clinical specialist, or sales training roles
Prior experience in HA injectables, aesthetic medicine, dermatology, medical devices, or pharmaceutical training is strongly preferred
Strong understanding of facial anatomy, HA fillers, treatment planning, product selection, injection technique, patient safety, and aesthetic clinic workflows
Experience developing and delivering HCP training programs, faculty-led activities, in-clinic education, workshops, speaker programs, or advanced anatomy training
Experience recruiting, engaging, developing, or supporting faculty, trainers, KOLs, clinical advocates, or clinical specialists is strongly preferred
Strong familiarity with the Thai aesthetics market, including KOLs, faculty, key accounts, clinics, and injector education needs, is strongly preferred
Working knowledge of regulatory, medical, and marketing compliance policies involving dermal fillers
Strong presentation, facilitation, coaching, and stakeholder management skills
Hands-on, credible with doctors, commercially aware, well-organized, and comfortable working in a fast-moving market environment

Responsabilités

Develop and execute TEOXANE Thailand’s medical education and training plan, translating global and regional strategies into effective local programs
Implement TEOXANE’s educational framework (ATP, anatomy, facial assessment, treatment planning, product selection, injection techniques, and patient safety)
Assess HCP capabilities, identify training gaps, and segment audiences to build structured learning pathways from foundation to advanced levels
Design and deliver high-quality education programs that improve injector confidence, product understanding, ATP adoption, and safe, consistent clinical practice
Recruit, develop, and manage local faculty and trainers, leveraging global and regional expertise to strengthen capability, governance, and training quality
Plan and manage the full training calendar, including workshops, masterclasses, in-clinic training, congresses, and internal/distributor education
Support advanced programs (e.g., cadaver courses, anatomy-based training, partnerships with academic and training institutions)
Leverage the TEOXANE Regional Academy (Bangkok) and digital platforms to deliver hybrid learning and enhance training impact
Drive KOL, clinic, and key account engagement through targeted education, coaching, and case-based discussions
Train distributor and field teams on HA science, product differentiation, ATP, and compliant scientific messaging

Sr. Associate – Evidence Synthesis

Sanofi Business Operations (SBO) is an internal Sanofi resource organization bas...

Emplacement

India , Hyderabad

Salaire:

Non fourni

Sanofi

Date d'expiration

Jusqu'à nouvel ordre

Exigences

5+ years of experience in Health Economics and Outcomes Research (HEOR) for the pharmaceuticals industry, CRO consultancy or academia
Stakeholder management, writing/communication skills, external engagement and ability to work independently and within a team environment
Strong analytical skills to translate clinical and economic information and messages into payer evidence strategies
Understands reimbursement decisions to determine value drivers and how evidence is used in decision making and how it impacts various payers (e.g., providers, patients, health systems)
Knowledge of methods and principles of health economics, health technology assessment (HTA) reviews
Advanced degree in life sciences/pharmacy/similar discipline or medical degree
Excellent knowledge of English language (spoken and written)

Responsabilités

Support HEVA/Medical team in assigned therapy area portfolio to plan and generate robust health economics and value based evidence to maximize the value propositions from both a global and US perspective working within the Market Access tripod
Seek opportunities to innovate HEVA/Medical value identification, evidence generation and dissemination process/plan to increase the relevance and impact of HEVA/Medical evidence to ensure reimbursement decisions and optimal access
Develop and maintain therapeutic area (TA) expertise
Support and maintain effective relationships with key stakeholders
Work effectively with global HEVA/Medical teams across various time zones
Support in the HEVA/Medical evidence generation plan: Develop research plan for pre-launch, launch and post-launch evidence for investigational and marketed drugs
Evidence generation plan includes burden of illness studies, epidemiology, literature reviews, meta-analysis, retrospective, and prospective observational studies, economic evaluations, development and analysis of patient-reported outcomes
Provide strategic support with individuals and institutions, which may serve as resources for evidence generation purpose, etc.
Support execution of approved HEVA/Medical study(s) and manage ongoing study(s) if required: Supports the HEVA/Medical product lead to manage and execute research studies to support the clinical, economic and humanistic value of products
Support development of core value dossier (CVD) and Academy of Managed Care Pharmacy (AMCP) dossier and provide strategic direction

Temps plein

Chef(fe) de Produit Marketing Global Urologie

Contribute to the development and drive marketing strategy and/or the developmen...

Emplacement

France , Tarn (81)

Salaire:

Non fourni

Pierre Fabre

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Formation supérieure en sciences (Pharmacien, Ingénieur…) complétée par une spécialisation en école de commerce, vente ou marketing
Expérience de 2 ans minimum sur un poste similaire
Maîtrise de l'anglais à l'oral et à l'écrit impérative
Capacités analytiques
Créativité
Excellentes compétences en communication, à l'oral comme à l'écrit

Responsabilités

Contribute to the development and drive marketing strategy and/or the development of products/services and associated omni-channel content to stimulate the growth and profitability of products in your area
Constantly analyse trends, competitors, market developments, studies, consumer needs, patients, distributors, and KOL in relation to markets and put forward innovative ideas
Communicate key brand/franchise strategies to the countries/territories concerned by product/product line specialities and make sure they are adopted
Contribute to defining positioning, commercialisation, communication and development strategy for products in your product lines
Ensure implementation of the marketing strategy
Drive product portfolio performance and be responsible for its optimisation (sales objectives, costs/costing, marketing and media costs, pricing, profitability, obsolete products and budget management and tracking)
Participate in drawing up and monitoring the budget and key performance indicators for your area
Ensure strategic alignment in respect to regulatory compliance, R&D, and Market Access (for products concerned)

Ce que nous offrons

13ème mois
bonus
intéressement
participation
actionnariat salarié avec abondement
mutuelle
prévoyance
16 jours de RTT
CET
CE

Temps plein

Nouveau

Technicien Chimiste Purification

Le Technicien Chimiste Purification effectue en autonomie toutes les activités r...

Emplacement

Belgium , Lessines

Salaire:

41600.00 - 57200.00 EUR / Année

BioLife Plasma Services

Date d'expiration

Jusqu'à nouvel ordre

Exigences

Bachelier Scientifique (Spécialisation Chimie/Biotechnologie/Agronomie) et/ou formation équivalente
Une expérience en tant que technicien chimiste de production est un atout
Horaire en pause matin/Après-midi
Maîtrise de soi face à des situations de stress
Maîtrise des operations arithmétiques fondamentales
Ecriture soignée, rigueur documentaire
pHmètrie, conductivimètrie, spectrophotomètrie
Chromatographie
Filtration frontale, tangentielle
Test point bulle

Responsabilités

Effectuer toutes les opérations de production nécessaires à la fabrication d’une solution dérivée de plasma sanguin
Effectuer toutes les opérations de cleaning nécessaires au maintien en état des équipements et locaux de production
Effectuer les mesures in-process nécessaires au contrôle des opérations de purification
Documenter rigoureusement des opérations effectuées pour garantir la traçabilité des opérations effectuées
Appliquer les procédures de santé, sécurité en vigueur au sein de la société afin de garantir sa sécurité et celle d’autrui
Appliquer les procédures environnementales en vigueur au sein de la société afin d’assurer le traitement adéquat des déchets liés aux activités de production
Appliquer les procédures de bonnes pratiques de fabrication afin de garantir la fabrication d’un produit pure, sure et efficace
Appliquer les standards déployés par l’organisation dans le but d’atteindre « l’excellence opérationnelle »
Participer à l’encadrement et à la formation des nouveaux techniciens
Participer à des activités relatives à des projets et nécessitant une expertise « bulk »

Ce que nous offrons

20 jours de congés payés et 12 jours de repos compensatoire
Assurances santé et hospitalisation complètes
Bilans annuels à partir de 45 ans
Soutien pour les soins de santé préventifs
Congés maternité, paternité et adoption
Espaces dédiés
Accès à un catalogue de formations
Cours de langue
Opportunités de mobilité interne et internationale
Contributions pour les transports publics

Temps plein

Nouveau

Electricien industriel

Prêt·e à transformer des défis électriques complexes en solutions industrielles ...

Emplacement

France , St Lin

Salaire:

13.00 EUR / Heure

Randstad

Date d'expiration

30 septembre 2026

Exigences

Formation initiale CAP/BEP/BAC Pro Électrotechnique et bonne maîtrise des appareils de mesure
Expérience minimale de 3 mois sur machines agricoles ou matériel roulant
Compétences en lecture de schémas électriques et automatisme
Capacité à travailler en équipe et assurer la maintenance de premier niveau

Responsabilités

Analyse et interprétation de schémas électriques et automatisés, avec recherche d'ordres de fabrication et de numéros de pièces
Réalisation méthodique des opérations de montage en suivant strictement les consignes, plans et schémas fournis par l'entreprise
Participation active aux formations en matière de sécurité et métiers, tout en maintenant un environnement de travail ordonné et sécurisé

Ce que nous offrons

Avantages CSE
Indemnité kilométrique
Prévoyance santé
Primes et intéressements
Restaurant d'entreprise
Fast TT

Temps plein

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Global Pharmaceutical Product Manager

Description du poste

Responsabilités

Exigences

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