All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. + Demonstrates strong teamwork capabilities to collaborate effectively and compliantly across the organization to address customer inquiries and advance Pfizer objectives. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives.$29k-39k yearly est.5d ago
Fullstack Engineer
There will be a close collaboration required with Levi's Global Product, and Technology Teams in San Francisco, but also with the specialists in the US and European region.The successful candidate will have a winning combination of technical skills, passion and interest for SEO, collaborative mindset and an entrepreneurial spirit. From my perspective: its an SEO engineer role (SEO, SEM, Web Analytics) with some programming implementation in VueJS and possible substitution with ReactJS. ChatGPT SEO Engineer will be responsible executing technical enhancements based on business growth objectives and in collaboration with key business partners.$133k-170k yearly est.5d ago
Senior Manager, LSCC Manufacturing Program Support
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. But working at Bristol Myers Squibb is anything but usual.$119k-152k yearly est.3d ago
Représentant-Santé et Sciences, Soins primaires / Health and Science Representative, Primary Care (Rive-Nord de Québec)
Date de fin d'affichage : le 2 juin 2023
Posting closing date: June 2, 2023
Statut : Temporaire à temps plein (15- 18 mois)
Status : Temporary full time (15 - 18 months)
Endroit: Rive-Nord de Québec
Location: Quebec North Shore
(English to follow)
Représentant-Santé et Sciences, Soins primaires
Fonctions:Relevant du Chef, Affaires régionales, le Représentant - Sciences de la santé est responsable d'atteindre les objectifs de vente du plan d'affaires établi pour son territoire.Responsabilités:Le titulaire du poste vise à atteindre les objectifs de vente établis pour son territoire en faisant la promotion de produits auprès des professionnels de la santé conformément à la stratégie de ciblage relative aux différentes marques. Le représentant(e) - activités pharmaceutique rend visite aux médecins de famille, omnipraticiens et pharmaciens cibles. Par ailleurs, il lui incombe d'organiser des symposiums, des présentations de vidéos, des expositions ainsi que d'autres activités d'éducation médicale continue; d'élaborer et de mettre en œuvre un plan d'action pour l'équipe territoriale; de signaler toute manifestation indésirable; d'entretenir des relations professionnelles conformément à la politique de l'entreprise; et de maintenir en bon état le matériel que l'entreprise lui fournit dans le cadre de ses fonctions : voiture, échantillons, matériel promotionnel, etc.
Responsabilités en matière de pharmacovigilance: Veiller à la reconnaissance et à la déclaration des manifestations indésirables et des plaintes relatives aux produits, conformément aux normes de l'entreprise, dont la formation intitulée Responsabilités en matière de pharmacovigilance Principales Responsabiltés:
Participer aux congrès, notamment coordonner et réaliser les programmes EMC.Engagement avec client en face à face et dans un environnement virtuel .Travailler en collaboration avec les collègues interne et les partenaires d'affaires externes.Adopter les valeurs et les comportements de leader de Pfizer, notamment en respectant les politiques et les procédures ainsi que le Code de pratiques de commercialisation des MNC et de Pfizer.
Le candidat idéal possède les qualifications suivantes :Le candidat idéal compte au moins cinq années d'expérience comme représentant pharmaceutique et possède une bonne connaissance des produits et des soins visés par les fonctions de son poste. Il est titulaire d'un baccalauréat en administration des affaires ou en sciences. Il possède des aptitudes supérieures en vente et est capable d'utiliser efficacement les tirés à part et d'organiser des programmes de conférences EMC. Avoir des aptitudes de ventes supérieur avec une expertise dans l'utilisation des études ainsi qu'au niveau organisationnel au niveau des FMC (Formation Médical Continue) tant en présentiel qu'en virtuel. Une connaissance du territoire serait un atout.Autres Qualités
Aptitude à communiquer efficacement sur le plan professionnel Bilinguisme - le ou la titulaire du poste doit pouvoir bien communiquer en anglais, car ses fonctions exigent des interactions avec des intervenants et collègues se trouvant à l'extérieur du Québec ou du Canada.Connaissance de la micro-informatique Aptitude manifeste à atteindre ou à dépasser des objectifs de vente stratégiques
Conditions pré-emploi :
Être entièrement vacciné contre la COVID-19. *Doit posséder un permis de conduire valide Conscients de notre responsabilité en tant que leader mondial de l'industrie biopharmaceutique à l'avant-plan du combat contre la COVID-19, nous sommes fiers de déclarer que nous attendons des employés de Pfizer qu'ils soient adéquatement vaccinés. Entièrement vacciné signifie avoir recu la thérapie à dose complète d'un vaccin contre la COVID-19 approuvé par Santé Canada depuis plus de 14 jours.
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Health and Science Representative, Primary Care
Scope of the position:Reporting to the Regional Business Manager, the Health and Science Representative is accountable for achieving the sales results for their territory as approved in the territory business plan.Duties & Responsibilities:The Health and Science Representative is responsible for achieving sales objectives for their territory by promoting products to healthcare professionals in accordance with the brand targeting strategy. The HSR provides effective coverage of targeted family, general practitioners and pharmacists. Other responsibilities include: conduct symposia, audio and video conferences, exhibits and other Continuing Medical Education activities; develop and implement a Business Plan; report on adverse drug reactions; provide professional public relations in accordance with approved Company policy; as well as maintain all company property, including car, samples, promotional supplies, etc., in a satisfactory manner Responsibility to Report: Identifies and reports adverse events and product complaints as per Corporate procedure, including Your Reporting Responsibilities (YRR) training.Primary Responsibilities include:
Establish strong relationships with the key customers Engage customers in both a face to face and virtual environment Attending congresses including coordinating and executing CME programs Work collaboratively with internal colleagues and external business partners Demonstrating Pfizer Values and Leader Behaviors including adherence to Pfizer policy and procedure as well as the IMC code and guidelines.
The ideal candidate possesses the following qualifications:The ideal candidate possesses a minimum of five years pharmaceutical sales experience, superior product and therapeutic knowledge specific to the position's focus as well as a bachelor's degree in business or science. Have superior selling skills with expertise in reprint use and CME organization of both live and virtual events. A knowledge of actual territory will be a huge asset.Further Qualifications Include:
Excellent communication skills (oral and written) experience communicating at a professional level Networking skills Computer proficiency
Pre-employment requirement:
Be fully vaccinated against COVID-19*Must have a valid driver's license Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies that is at the forefront of the fight against COVID-19, Pfizer is proud to declare that it expects its employees to be fully vaccinated. Fully vaccinated is defined as receiving the full dose therapy of a Health Canada approved COVID-19 vaccine at least 14 days post the completion of the required dose regimen.
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Pfizer encourages women, Aboriginal people, persons with disabilities and members of visible minorities to apply. Pfizer will accommodate the needs of applicants with disabilities throughout all stages of the selection process. Should accommodation during the recruitment process be required, please advise your Talent Acquisition representative.
Pfizer est un employeur qui invite les femmes, les Autochtones, les personnes handicapées ainsi que les membres des minorités visibles à soumettre leur candidature. Pfizer s'adaptera aux besoins des candidats handicapés pour chaque étape du processus de sélection. Si des mesures d'adaptation sont nécessaires pendant le processus de recrutement, veuillez en aviser votre représentant du recrutement.
Sales
#LI-Remote #LI-PFE$115k-202k yearly est.2d ago
Medical Affairs Scientist (m/w/d) Gastroenterologie, in der Region Süd-Ost (Bayern, BW, Thüringen) - befristet auf 24 Monate
Unsere Mitarbeitenden profitieren auch au erhalb der Arbeitszeit von einem umfangreichen Betrieblichen Gesundheitsmanagement "Pfizer in Balance". Medical Affairs Scientist (m/w/d) - Gastroenterologie Als Arbeitgeber setzt sich Pfizer daf r ein, diese Vielfalt in all ihren Formen zu f rdern. Weiterf hrende Informationen erhalten Sie jederzeit auf unserer Website unter: Arbeiten bei Pfizer Deutschland Weltweit arbeiten die Mitarbeiter von Pfizer gemeinsam daran, die Gesundheit eines jeden Einzelnen berall zu verbessern.$76k-105k yearly est.Easy Apply2d ago
Représentant Spécialisé - Sciences de la Santé, Oncologie (région de Montréal) / Specialty Health and Science Representative, Oncology (Montreal)
Diffuser de l'information aux sp cialistes locaux et r gionaux de l'oncologie ainsi qu'aux partenaires r gionaux, s'il y a lieu, afin de promouvoir le recours optimal aux protocoles et aux m dicaments, en s'appuyant sur les donn es factuelles portant sur l'emploi des produits d'oncologie de Pfizer. Communiquer avec les oncologues et les membres des quipes multidisciplinaires de son territoire afin de promouvoir les produits de Pfizer, et cela, conform ment la fr quence et la port e demand e. Assurer la formation d'experts des produits d'oncologie de Pfizer par la mise sur pied de programmes r gionaux de perfectionnement des conf renciers et des experts.$103k-145k yearly est.2d ago
Director, Drug Product Lead, Seasonal mRNA Vaccines
Pfizer Global Supply (PGS) is at the heart of fulfilling Pfizer's purpose as we work to make sure customers and patients have the medicines they need, when they need them. Pfizer's purpose is to deliver breakthroughs that change patients' lives. As the Drug Product Lead, you will build and maintain strong matrix relationships with key partners in GTE, Supply Chain, Manufacturing Sites, Launch Excellence, PGS Sites, Biotherapeutics Pharm Sci, Quality, Procurement, and Regulatory CMC. As the Director, Drug Product Lead seasonal mRNA Vx for Vaccines in Biotech and Sterile Injectable Technology, you will be accountable for the seasonal mRNA Vx Drug Product (DP) processes lifecycle and leading the matrix DP teams for Pfizer's seasonal mRNA vaccine assets (Ex: mRNA Flu).$86k-121k yearly est.2d ago
Manager, Software Validation Specialist
Working in close collaboration with scientific, technical, and QA teams, the Manager, Software Validation role in R&D Solutions will manage the validation and compliance of software solutions in accordance with FDA GxP, 21 CFR Part 11, and EMEA regulations and guidances, and Pfizer Digital policies. By building a talented community of colleagues that align with our patient-focused purpose and core values, Pfizer has improved global health and impacted more than 780 million patients around the world. Pfizer's digital and data first' strategy focuses on implementing impactful and innovative technology solutions across all functions from research to manufacturing. The Pfizer Tampa site has constructed an atmosphere that fosters interaction and prioritizes colleague health and wellness. Located in Heights Union, the Pfizer Tampa site offers a modern industrial design, the latest in innovative technology, and close proximity to Downtown with views of the Tampa Riverwalk and access to the Channel district and Bayshore Boulevard. This year, Pfizer launched a new initiative that we call Log In For Your Day where a majority of colleagues can arrange with their manager to work remotely two or three days a week while still maintaining the ability to collaborate regularly in person at our sites. With so many diverse and highly-skilled colleagues supporting multiple functions and services across the organization, Pfizer Tampa offers ample opportunity to engage in newer ways of working that enhance, simplify, and transform how we deliver treatments to our patients. Additionally, to achieve breakthroughs that change patients' lives, Pfizer is revolutionizing and evolving how colleagues work today. For more than 170 years, Pfizer has continuously worked to make a difference by delivering innovative therapies that improve the lives of our patients. In 2021, Pfizer expanded its global footprint to Tampa, establishing a strategic powerhouse that brings together multi-disciplinary, professional services including Finance, Accounting, Treasury, Digital, HR Services, Sourcing, Commercial and Project Management into a single, centralized location.$81k-107k yearly est.2d ago
The CTA-SM may be assigned as a Hub Submission Manager to meet business demands. Manager Drives global submission management activities for their assigned assets. Provides an interface to Regulatory and GPD partners within designated Business Units, offering project leadership and expertise in the logistics involved with execution of regulatory CTA submissions to regional partners and selected Health Authorities.The CTA Submission Manager (CTA-SM) is accountable for working with contributing business lines to lead operational submissions execution for designated CTAs.$108k-145k yearly est.2d ago
Director - Process and Innovation Lead
Product License Maintenance Data Sciences (PLMDS) is a multi-functional organization in Global Regulatory Operations/Global Regulatory Sciences.
The PLMDS Process and Innovation Lead is responsible for a range of research, development, business and process-related initiatives across the PLMDS organization.
The role is broad, covering a wide range of supportive disciplines, and colleagues within the role will specialize in one or more areas depending on business need:
The role is a key driver of innovative thinking in PLMDS, helping create a virtual culture of risk-taking and creativity, and works closely with the Head of PLMDS Functional Leads, PLMDS Managers and CDM Managers to execute cutting edge innovations and transformative projects.
Leadership of large and medium scale projects to improve efficiency, quality or cost, with equal focus on effective implementation of these projects, using advanced change management and knowledge management techniques.
Subject matter expertise in general business process, this role will have awareness of a local regulations. The role sponsors, coordinates and directs process forums and associated continuous improvement efforts to ensure PLMDS processes are efficient and globally consistent.
Championing data quality, verification, connectivity and governance to facilitate understanding and contextualize areas of opportunity. The role has expert knowledge of PLMDS metadata and systems, and their relationship to wider business process and policies, and acts as a facilitator to other support lines to leverage expertise into PLMDS to resolve challenges.
Development of products, services or approaches which support the smooth functioning of PLMDS and wider business value. Such support may include partnership with Business Operational functions to facilitate full transparency of capital opportunities across the organization, predictive analytics which enhance forecasting ability, and practical return-on-investment (ROI) calculation techniques to support PLMDS. This support is highly integrated and tailored to meet the needs of PLMDS functions so that the model is optimized to meet customer needs.
Acting as a Mentor/Coach to peers/colleagues delivering projects including project management, advanced change management and knowledge management techniques.
He/She will have a global view of PLMDS functions, is comfortable working across a range of deliverables from early research investigations, through project design/management, to effective implementation. The incumbent is both an advocate for innovation as well as a champion for quality and delivery.
In addition, this role may include monitoring trends and policy positions in the global regulatory environment that impact PLMDS. Partners with Policy Intelligence to provide seminal analyses of these regulatory trends and communication to internal stakeholders.
JOB RESPONSIBILITIES
Program management of multi-regional technological, behavioral and process change activities, with particular emphasis on transformational projects.
Leads selected roadmap projects, working with other functions to ensure effective implementation of final solutions.
Participant/lead on Steering groups across selected geographies (Americas, Europe, Asia, Emerging Markets) to progress strategic change related to Labeling processes
Where appropriate acts as subject matter expert on development of standards supporting Industry associations, regulatory agencies (as support to PPLS teams), vendors, and in-licensing partners
Accountable for associated PMO activities for selected roadmap projects including but not limited to provision of metrics dashboards, ROI calculations, Hypothesis testing, predictive modelling, and impact assessments.
Review draft and final regulatory agency regulations, guidelines and regulatory policies. Identify the strategic impact of these regulatory documents to PPLS.
Development of effective knowledge management and communication techniques to organize and deliver training either personally or via network of trusted experts
Prepare environmental analyses to identify emerging regulatory trends and likely future scenarios resulting from emerging trends. Educates PPLS and stakeholders on key priorities, trends, and changes in the regulatory environment.
Promotes innovation and takes appropriate risks to challenge the status quo, resulting in enhanced processes; takes appropriate risks to develop innovative ideas/ processes/products.
Fosters an environment that thrives on curiosity
Identifies innovative concepts, translates into processes within PPLS and recommends courses of action to senior leaders that impact PPLS and the wider business.
Working with the PLMDS LT, develops vision, strategy, and performance objectives for the end-to-end processes.
Acts as SME Point of Contact with Information Management (IM), Business Operations Center of Excellence (CoE), Regulatory Policy and other functions on behalf of PPLS.
Exercises foresight and judgment utilizing comprehensive breadth of knowledge and prior work experience
Acts independently on self-initiated projects and leverages knowledge from others related to overall objectives, strateg
y, critical issues and policy matters
QUALIFICATIONS / SKILLS
Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications and other job-related technical and managerial skills.
Proven fluency with the use of soft skills and ability to adapt core project management skills successfully within a dynamic line environment.Extensive business experience at required level to enable thorough understanding of the responsibilities associated with strategic pursuit and tactical application of evolving business processes Ability to transform ambiguous situations/discussions into structured outcomes Management of change in partnership with key stakeholders Proven leadership and delivery to time and quality driving highly complex projects to meet evolving business needs.Mastery of processes, tools and techniques for planning and monitoring multiple complex projects to established deadlines. Excellent knowledge of tools used to design processes and process flows, etc.Proven aptitude in project management and process engineering/re-design Leadership, project management, and highly skilled adaptive verbal and written communication skills in relating to colleagues and associates both inside and outside the organization, across various cultures.Demonstrated accountability, and excellence in interpersonal, communication, negotiation, influencing, and problem-solving capabilities.Demonstrated knowledge of drug development processes, regulatory codes/guidance's, and technologies across ICH regions Demonstrated ability to work with or lead a team in a matrix structure.Experience with XML, Document Management, regulatory milestone reporting tools Ability to synthesize and communicate complex information and analyses to a variety of audiences in both verbal and written format Ability to extract critical information and prepare succinct summaries of regulatory documents, including assessment of the potential impacts to Pfizer.Ability to conduct regulatory metrics analyses, and regulatory trending and impact analyses.Ability to easily navigate information databases and health authority websites to gather necessary information.Understanding the global regulatory environment and its impact on BU strategies.Background in medical or technical writing Highly skilled at identifying the potential provided by innovative thinking, concepts or technologies and translating these into opportunities across the spectrum of labeling processes Comfortable operating and leading in a risk-taking environment, striving for transformational gains while conscious of regulatory risks in different regions. Capable of cutting through complexity to deliver simple solutions with decisiveness and clarity.Anticipating internal/external business and regulatory/ compliance issues that impact PLMDSHave foresight and judgment in complex decisions and troubleshoots in ambiguous situations in PLMDSHave the ability to influence senior management decisions that impact business direction
Education:
Bachelor's Degree or equivalent preferred Advanced academic qualification/degree is desired but not required.
Experience:
Strong experience in global/multi-national pharmaceutical environment, including direct experience either in Labeling, Regulatory Submissions, or Regulatory Affairs role. Experience in ability to function autonomously at senior levels and in a matrix team environment a must.Experience in interpreting and applying global and local regulatory guidance around labelling and associated supportive documentation are desirable but not required.Experience in identifying, driving and implementing innovative solutions
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Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Flexibility
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let's start the conversation!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
DisAbility Confident
We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!
Regulatory Affairs
#LI-Remote #LI-PFE$82k-107k yearly est.2d ago
Trade Marketing Rep. Virtual - Upjohn
$55k-82k yearly est.2d ago
PMO Program Manager
The PMO Program Manager provides comprehensive project management for the execution and delivery of projects from early design or development through lifecycle management (LCM). As a Program Manager, the colleague will manage multiple projects and work activities of significant complexity, using leadership and interpersonal skills to motivate and influence for high team performance.$90.8k-151.3k yearly2d ago
Representante de Salud Cuidado Primario - CDMX
$39k-53k yearly est.2d ago
Director- GPD Enterprise Solution Architecture
This Director of Architecture role manages technology strategy and digital architecture for Pfizer's Global Product Development (GPD) solutions / clinical solutions and applications. This Director influences business stakeholders and Pfizer Digital client partners and creation center resources to plan, design, initiate and execute clinical studies to determine the safety and efficacy of medications, devices, diagnostic products, and treatment regimens intended for human use.$117k-155k yearly est.2d ago
Increase expertise amongst Pfizer statisticians and scientists through dissemination of new RWD analysis and modern analytic methodologies and training on software to implement these approaches.Collaborate with development teams by the development and implementation of techniques based on state-of-the-art research.Take ownership of projects and liaise with team members as appropriate and may oversee the work of contractors. Provide statistical leadership and technical support for Pfizer projects involving real world data (RWD).$96k-133k yearly est.2d ago
Rheum/GI Health & Science Specialist - Boston P1 M1
Present terms of sale of product or existing contract terms where appropriate and with approved language; proactively answer on-label questions; proactively introduce customers to future state Pfizer on-demand portal (Galaxy) with access to appropriate targeted content Colla$40k-57k yearly est.2d ago
Associate Director, Biostatistics
$118k-157k yearly est.2d ago
Ontology and Data Standards Expert
Pfizer Digital ESDE is seeking a talented, results-oriented individual with a passion for knowledge management to contribute to our digital initiative to ensure accuracy and consistency in our data. The Digital ESDE (Enterprise Data Solutions & Engineering) team partners across Pfizer to drive new capabilities for the reuse of cross-domain data and information that enables portfolio decision-making and breakthroughs to change patients' lives. This individual will play a crucial role in the management and oversight of Pfizer's data assets to help provide business users with high-quality data that is easily accessible in a consistent manner by applying FAIR principles.$95k-129k yearly est.2d ago
Oncology Account Specialist - Prostate Cancer - Montgomery, AL
Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure.$51k-69k yearly est.2d ago
