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Pfizer is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative healthcare solutions. They are committed to improving the health and well-being of people around the world. Pfizer's mission is to be a leading force in the fight against diseases and to provide access to safe, effective, and affordable medicines. Their purpose is to make a positive impact on society by advancing medical science, developing breakthrough therapies, and collaborating with healthcare professionals and partners to address unmet medical needs. With a focus on research, development, and the production of pharmaceutical products, Pfizer plays a vital role in shaping the future of healthcare and improving patient outcomes.

Science & Healthcare

Pfizer

Pharmaceuticals

You need a scientific degree, compliance experience, fluency in English, and strong skills in MS Office. You must manage complex projects, collaborate effectively, and possess excellent communication abilities.

You will manage local medical activities, ensure compliance with regulations, support audits and CAPAs, facilitate training, and implement global procedures in collaboration with various teams.

Rome

<div><div>MEDICAL COMPLIANCE ADVISOR - 12 MONTHS CONTRACT WITH RANDSTAD</div><div></div><div>
JOB PURPOSE</div><div>
The Medical Compliance Advisor supports all activities related to Medical Quality, Audit/Inspection Readiness, training, process improvements and Risk Mitigation, across Business Units for Pfizer Country Medical Operations. The Medical Compliance Advisor is expected to interact closely with all in-country Business Unit Medical/Commercial Organizations, the Platform Line organiza</div><div>
tions, other Quality and Compliance representatives</div><div></div><div>
RESPONSIBILITIES</div><ul><li><div>
Management of local medical activities and business support at the market level.</div></li><li><div>
Implementation of continuous Medical inspection readiness efforts in collaboration with applicable headquarters inspections management teams, Business Units, and Platform Line representatives.</div></li><li><div>
Support in management of global audits at Country level including management of audit Corrective &amp; Preventive Actions (CAPAs).</div></li><li><div>
Support in management of Corporate Audit requests as appropriate.</div></li><li><div>
Support in management of Quality Events and Corrective and Preventive Actions (CAPAs)</div></li><li><div>
Facilitate local implementation of global procedures and ensure relevant communication is cascaded accordingly.</div></li><li><div>
Facilitate local training compliance reporting for in-country Medical Affairs, as needed.</div></li><li><div>
Ensure the correct implementation of medical activities in full compliance with local regulation</div></li><li><div>
Ensure the proper support to the activities included in the team responsabilities</div></li></ul><div></div><div>
PROFESSIONAL BACKGROUND EXPERIENCE</div><ul><li><div>
Scientific University degree and past experience in compliance/ procedures management, auditing, quality assurance/control, or related field</div></li><li><div>
Understanding of the local promotional and regulatory compliance environment</div></li><li><div>
Fluent English</div></li><li><div>
High level of competency using Microsoft Office &ndash; Word, Excel, PowerPoint, Business Objects</div></li></ul><div></div><div>
BEHAVIOURAL COMPETENCIES</div><ul><li><div>
Expertise in managing multiple complex projects</div></li><li><div>
Consultancy skills</div></li><li><div>
Ability to work independently and deal with conflict</div></li><li><div>
Verbal, written, and presentation skills</div></li><li><div>
Collaboration, interpersonal and facilitation skills</div></li><li><div>
Continuous Improvement and/ or organizational effectiveness expertise</div></li><li><div>
Display sensitivity to manage relationships and ability to build collaborative working relationships with colleagues and associates both within and external to the organization.</div></li><li><div>
Collaborate efficiently across functional and country boundaries, respecting communication, functional priorities, and cultural differences in interpersonal relationships.</div></li></ul><div></div><div>
LAST DAY TO APPLY: JANUARY 8th 2025</div><div></div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><div>
Purpose</div><div>
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.</div><div></div><div>
Digital Transformation Strategy</div><div>
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.</div><div></div><div>
Flexibility</div><div>
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&rsquo;s start the conversation!</div><div></div><div>
Equal Employment Opportunity</div><div>
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 &ndash; 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.</div><div></div><div>
Disability Inclusion<br>
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!</div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div></div>
Quality Assurance and Control<div></div>
#LI-PFE</div>

MEDICAL COMPLIANCE ADVISOR - 12 MONTHS CONTRACT WITH RANDSTAD
JOB PURPOSE
The Medical Compliance Advisor supports all activities related to Medical Quality, Audit/Inspection Readiness, training, process improvements and Risk Mitigation, across Business Units for Pfizer Country Medical Operations. The Medical Compliance Advisor is expected to interact closely with all in-country Business Unit Medical/Commercial Organizations, the Platform Line organiza
tions, other Quality and Compliance representatives
RESPONSIBILITIES
Management of local medical activities and business support at the market level.
Implementation of continuous Medical inspection readiness efforts in collaboration with applicable headquarters inspections management teams, Business Units, and Platform Line representatives.
Support in management of global audits at Country level including management of audit Corrective & Preventive Actions (CAPAs).
Support in management of Corporate Audit requests as appropriate.
Support in management of Quality Events and Corrective and Preventive Actions (CAPAs)
Facilitate local implementation of global procedures and ensure relevant communication is cascaded accordingly.
Facilitate local training compliance reporting for in-country Medical Affairs, as needed.
Ensure the correct implementation of medical activities in full compliance with local regulation
Ensure the proper support to the activities included in the team responsabilities
PROFESSIONAL BACKGROUND EXPERIENCE
Scientific University degree and past experience in compliance/ procedures management, auditing, quality assurance/control, or related field
Understanding of the local promotional and regulatory compliance environment
Fluent English
High level of competency using Microsoft Office – Word, Excel, PowerPoint, Business Objects
BEHAVIOURAL COMPETENCIES
Expertise in managing multiple complex projects
Consultancy skills
Ability to work independently and deal with conflict
Verbal, written, and presentation skills
Collaboration, interpersonal and facilitation skills
Continuous Improvement and/ or organizational effectiveness expertise
Display sensitivity to manage relationships and ability to build collaborative working relationships with colleagues and associates both within and external to the organization.
Collaborate efficiently across functional and country boundaries, respecting communication, functional priorities, and cultural differences in interpersonal relationships.
LAST DAY TO APPLY: JANUARY 8th 2025
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 Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Quality Assurance and Control
#LI-PFE

Medical Compliance Advisor - Pfizer

Medical Compliance Advisor

You must provide scientific expertise, build relationships with KOLs, ensure ethical practices, support research and education, and deliver accurate medical information to stakeholders.

You will engage KOLs, support clinical research, develop educational content, conduct CME, provide medical insights, and ensure ethical standards in promoting vaccines and medical practices.

Research & Development

Healthcare

Chennai

<div><div>Job Description</div><div>
Job Description</div><ul><li>
Provide scientific expertise, build knowledge and activity based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer&rsquo;s image in the scientific community.</li><li>
To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors.</li><li>
To provide high quality and timely service in the areas of Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, and business support in the areas of New Product Development, Regulatory Affairs, Quality Standards, and Business Technology.</li></ul><div>
The role will act as a critical interface with identified scientific leaders and will build regional, national or international relationships to contribute to understanding of diseases, research and scientific trends, clinical practice guidelines, treatment patterns in areas relevant to our business.</div><div></div><div><br>
Strategic/Policy</div><ul><li>
With support from the mentor or Line manager, provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed</li></ul><div>
Operational</div><ul><li>
Key Opinion Leader / Key Organization Engagement</li><li>
Work in alignment with the concerned medical affairs colleagues to support them in implementing the medical activities relevant to the brand plan strategies for specific products and therapy areas as appropriate.</li><li>
Develop and customize presentations when required and relevant to specific programs/regional requests from KOLs . Ensure approval by concerned Medical Advisor before roll out of the same.</li><li>
Work closely with the concerned medical affairs colleagues to identify and establish relationships with key opinion leaders/organizations in select therapeutic area within the region to support their clinical and research activities by understanding their needs and offering appropriate research projects, continuing medical education programs, clinical/educational grants.</li><li>
Participate/facilitate/conduct customized promotional/educational interactions with Health Care Professionals (HCPs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, etc, by working in close coordination with the concerned medical affairs colleagues.</li><li>
Focus on stage shifting for KOLs (Stage I: Initiate, Stage II: Develop, StageIII: Partner, Stage IV: Impact) numbers as mentioned in the BU specific objectives.</li><li>
Clinical Research</li><li>
Support efforts to identify new investigators and institutions for Clinical Research in order to expand research base.</li><li>
Provide medical support for local studies on request from clinical operations, including need-based visits to study sites</li><li>
Assist in review/interpret data generated; Assist in writing final reports for locally sponsored studies as required</li><li>
Develop and execute publication plan; assist in review/write manuscripts for publication of locally sponsored studies</li><li>
Develop and execute Information Dissemination Plan/Program</li><li>
Medical Initiatives</li><li>
Participate in and provide medical inputs for key opinion leader meetings / advisory boards, Customer Launch Meeting (CLMs).</li><li>
Conduct/facilitate round table meetings/group discussions in coordination with concerned medical advisor for assigned therapy area/product as appropriate.</li><li>
Conduct CMEs as a speaker/moderator for assigned therapy area as per requirement and in coordination with the concerned medical advisor in case of new product.</li><li>
Medical Information</li></ul><div>
Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies</div><div></div><div>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical<div></div>
#LI-PFE</div>

Job Description
Job Description
Provide scientific expertise, build knowledge and activity based relationships with Key Opinion Leaders to advance medical practice and research for the benefit of the society, thus enhancing Pfizer’s image in the scientific community.
To actively contribute to the organization/business by taking responsibility for the scientific, technical and ethical soundness of all policies, statements and endeavors.
To provide high quality and timely service in the areas of Interactions with Healthcare Professionals, Continuing Medical Education, Clinical Research, Sales Force Training, and business support in the areas of New Product Development, Regulatory Affairs, Quality Standards, and Business Technology.
The role will act as a critical interface with identified scientific leaders and will build regional, national or international relationships to contribute to understanding of diseases, research and scientific trends, clinical practice guidelines, treatment patterns in areas relevant to our business.
Strategic/Policy
With support from the mentor or Line manager, provide tactical and strategic inputs, and business/technical expertise, to Product Management towards ethical promotion of assigned products, in the operational areas listed
Operational
Key Opinion Leader / Key Organization Engagement
Work in alignment with the concerned medical affairs colleagues to support them in implementing the medical activities relevant to the brand plan strategies for specific products and therapy areas as appropriate.
Develop and customize presentations when required and relevant to specific programs/regional requests from KOLs . Ensure approval by concerned Medical Advisor before roll out of the same.
Work closely with the concerned medical affairs colleagues to identify and establish relationships with key opinion leaders/organizations in select therapeutic area within the region to support their clinical and research activities by understanding their needs and offering appropriate research projects, continuing medical education programs, clinical/educational grants.
Participate/facilitate/conduct customized promotional/educational interactions with Health Care Professionals (HCPs). These interactions include, but are not limited to, customer launch meetings, advisory boards, CME programs, scientific symposia, institutional presentations, etc, by working in close coordination with the concerned medical affairs colleagues.
Focus on stage shifting for KOLs (Stage I: Initiate, Stage II: Develop, StageIII: Partner, Stage IV: Impact) numbers as mentioned in the BU specific objectives.
Clinical Research
Support efforts to identify new investigators and institutions for Clinical Research in order to expand research base.
Provide medical support for local studies on request from clinical operations, including need-based visits to study sites
Assist in review/interpret data generated; Assist in writing final reports for locally sponsored studies as required
Develop and execute publication plan; assist in review/write manuscripts for publication of locally sponsored studies
Develop and execute Information Dissemination Plan/Program
Medical Initiatives
Participate in and provide medical inputs for key opinion leader meetings / advisory boards, Customer Launch Meeting (CLMs).
Conduct/facilitate round table meetings/group discussions in coordination with concerned medical advisor for assigned therapy area/product as appropriate.
Conduct CMEs as a speaker/moderator for assigned therapy area as per requirement and in coordination with the concerned medical advisor in case of new product.
Medical Information
Provide useful, timely, accurate, and balanced medical information to internal (sales staff) and external (HCPs) customers, in adherence to relevant SOPs/policies
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE

Area Medical Advisor -Vaccines - Pfizer

Area Medical Advisor -Vaccines

You should possess strong leadership skills, extensive healthcare industry experience, strategic thinking, and a proven track record in driving results and managing teams.

You will lead strategic initiatives, manage healthcare partnerships, ensure compliance, and drive operational excellence to improve patient outcomes and organizational performance.

Customer Relations

Sales & Business Development

<div><div>Frontline sales colleague at Trichy HQ in HBU team.</div><div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Sales<div></div>
#LI-PFE</div>

Frontline sales colleague at Trichy HQ in HBU team.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Sales
#LI-PFE

Healthcare Executive - Pfizer

Healthcare Executive

You need a bachelor’s in business, 2+ years in pharma logistics, proficiency in MS tools, strong analytical skills, and shift availability for 24/7 operations. Adaptability and problem-solving are essential.

You will monitor alarms, coordinate with stakeholders, respond to emergencies, document incidents, analyze data, maintain systems, and develop training materials.

Logistics

Madrid

<div><div>ROLE SUMMARY<br>
The Global Command Center (GCC) Operator monitors logistics operations to swiftly respond to changes in temperature, lead time, risk management, and other parameters for network shipments. They ensure timely and accurate information access to support decision making and perform follow-ups to confirm problem resolution.<br>
The GCC Operator initiates the Logistics Incident process for temperature deviations and starts the Claims Management process. This individual contributor role operates within a cross-cultural team providing 24x7 support and reports to the Global Command Center Team Lead.</div><div></div><div>
ROLE RESPONSIBILITIES<br>
<ul><li>Logger Monitoring: Continuously oversee alarm systems, data, and shipments from internal/external plants through to market customs clearance and delivery, expanding scope as capability grows.</li><li>Coordination and Communication: Identify stakeholders and ensure timely, accurate communication for operational continuity.</li><li>Intervention and Emergency Response: Activate response processes, track actions, communicate critical information, and minimize impact of incidents.</li><li>Post-intervention Processes: Document incidents, streamline resolutions, categorize outcomes, and initiate Claims Management.</li><li>Data Analysis: Analyze historical data to identify trends, improve practices, and enhance decision-making.</li><li>System Maintenance: Maintain GCC system functionality, suggest enhancements, and assess automation opportunities.</li><li>Training and Documentation: Develop training materials, standard operating procedures, and update operation rulebooks.</li></ul><br>
BASIC QUALIFICATIONS<br>
<ul><li>Education: Bachelor&rsquo;s degree in business administration, Supply Chain or Logistics.</li><li>Experience: 2+ years in the pharmaceutical industry with expertise in transportation, logistics and supply chain. Experience in Control Tower, Command Center or Call Center roles is preferred.</li><li>Digital Tools: Proficiency in all standard MS applications.</li></ul><br>
OTHER SKILLS<br>
<ul><li>Technical proficiency in transportation, supply chain, cold chain logistics, trade &amp; customs, compliance.</li><li>Collaboration, effective communication, responsibility, and honesty.</li><li>Manage high-pressure situations with tenacity, resiliency, and ownership.</li><li>Critical thinking, problem solving, and attention to detail.</li><li>Time management and organizational skills.</li></ul></div><ul><li>Willingness to learn, adaptability, and flexibility.</li><li>Strong analytical skills for synthesizing data to aid decision-making.</li></ul><br>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS<br>
Availability to work in shifts to support 24x7x365 operational coverage.<div></div><div>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Logistics &amp; Supply Chain Mgmt<div></div>
#LI-PFE</div>

ROLE SUMMARY
The Global Command Center (GCC) Operator monitors logistics operations to swiftly respond to changes in temperature, lead time, risk management, and other parameters for network shipments. They ensure timely and accurate information access to support decision making and perform follow-ups to confirm problem resolution.
The GCC Operator initiates the Logistics Incident process for temperature deviations and starts the Claims Management process. This individual contributor role operates within a cross-cultural team providing 24x7 support and reports to the Global Command Center Team Lead.
ROLE RESPONSIBILITIES
Logger Monitoring: Continuously oversee alarm systems, data, and shipments from internal/external plants through to market customs clearance and delivery, expanding scope as capability grows.Coordination and Communication: Identify stakeholders and ensure timely, accurate communication for operational continuity.Intervention and Emergency Response: Activate response processes, track actions, communicate critical information, and minimize impact of incidents.Post-intervention Processes: Document incidents, streamline resolutions, categorize outcomes, and initiate Claims Management.Data Analysis: Analyze historical data to identify trends, improve practices, and enhance decision-making.System Maintenance: Maintain GCC system functionality, suggest enhancements, and assess automation opportunities.Training and Documentation: Develop training materials, standard operating procedures, and update operation rulebooks.
BASIC QUALIFICATIONS
Education: Bachelor’s degree in business administration, Supply Chain or Logistics.Experience: 2+ years in the pharmaceutical industry with expertise in transportation, logistics and supply chain. Experience in Control Tower, Command Center or Call Center roles is preferred.Digital Tools: Proficiency in all standard MS applications.
OTHER SKILLS
Technical proficiency in transportation, supply chain, cold chain logistics, trade & customs, compliance.Collaboration, effective communication, responsibility, and honesty.Manage high-pressure situations with tenacity, resiliency, and ownership.Critical thinking, problem solving, and attention to detail.Time management and organizational skills.Willingness to learn, adaptability, and flexibility.Strong analytical skills for synthesizing data to aid decision-making.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Availability to work in shifts to support 24x7x365 operational coverage.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Logistics & Supply Chain Mgmt
#LI-PFE

Global Command Center Operator - Pfizer

Global Command Center Operator

You must have a Bachelor's degree, 3+ years in EHS, knowledge of laws/standards, strong communication skills, and advanced Microsoft Office skills.

You will manage EHS compliance, conduct safety programs, investigate incidents, run training, and improve practices while ensuring effective communication and stakeholder engagement.

Dublin

<div>
 <div>
  Why Patients Need You
 </div>
 <div>
  Pfizer believes in holding the highest standards of safety for its patients and its employees. Your role, as a member of the Environmental, Health and Safety team, is important for maintaining these standards and preparing the organization for the necessary compliance activities. Your dedication and hard work will ensure that we provide the best care to our patients and a safe working environment for our colleagues.
 </div>
 <div></div>
 <div>
  What You Will Achieve
 </div>
 <div>
  You will be part of a dynamic team of experts who form Pfizer’s Environmental, Health &amp; Safety division. Due to the importance of this team for Pfizer’s employees and patients, the organization relies heavily on its team members’ timely actions and efficiency. You will be responsible for activities involved in identifying hazardous workplace conditions and take effective steps to ensure that workplace conditions comply with applicable federal and state Occupational Safety and Health standard provisions. You will also participate in Occupational Safety and Health Administration (OSHA) inspections and any procedures that may follow a citation. You will assist in the development and implementation of short and long range plans and continuously improve EHS performance.
 </div>
 <div></div>
 <div>
  As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
 </div>
 <div></div>
 <div>
  It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
 </div>
 <div></div>
 <div>
  How You Will Achieve It
 </div>
 <ul>
  <li>
   <div>
    Contribute to the completion of projects and manage own time to meet agreed targets.
   </div></li>
  <li>
   <div>
    Understand the fundamental business drivers for Pfizer and support the organization's guidelines and policies for Environmental, Health and Safety (EHS).
   </div></li>
  <li>
   <div>
    Review corporate, regional and local EHS requirements and implement applicable standards at the site level to assure full compliance with all applicable requirements.
   </div></li>
  <li>
   <div>
    Manage day-to-day hazardous, biological and special waste activities, interact and communicate with all relevant stakeholders.
   </div></li>
  <li>
   <div>
    Conduct industrial hygiene and toxicology programs in accordance with federal and local regulations.
   </div></li>
  <li>
   <div>
    Support the effective integration of EHS into the day to day management and meeting structures within the functional area.
   </div></li>
  <li>
   <div>
    Become familiar with operational activities, identify opportunities for improvement and coordinate with local safety champions/management to bring forward improvement projects.
   </div></li>
  <li>
   <div>
    Assist in the completion of evaluations for new sites, new projects and equipment, including change management for minor projects.
   </div></li>
  <li>
   <div>
    Investigate incidents and complaints of colleagues regarding safety, health, ergonomics, organizational environment, etc.
   </div></li>
  <li>
   <div>
    Develop and publish Environmental Health and Safety communications, as necessary.
   </div></li>
  <li>
   <div>
    Maintain fire safety precautions and first aid programs, including emergency response, training and simulations.
   </div></li>
  <li>
   <div>
    Manage Audit of the sites’ systems and processes and implement effective EHS cultural improvement and engagement activities.
   </div></li>
  <li>
   <div>
    Review, identify, develop and deliver EHS related training programs.
   </div></li>
 </ul>
 <div></div>
 <div>
  Qualifications
 </div>
 <div>
  Must-Have
 </div>
 <ul>
  <li>
   <div>
    Bachelor's Degree and 3+ years of experience.
   </div></li>
  <li>
   <div>
    Experience in EHS program development, implementation and/or on-going management.
   </div></li>
  <li>
   <div>
    Knowledge of the laws, regulations, standards and best practices governing health and safety.
   </div></li>
  <li>
   <div>
    Good verbal and written communication skills.
   </div></li>
  <li>
   <div>
    Advanced Microsoft Office Suite skills.
   </div></li>
 </ul>
 <div></div>
 <div>
  Nice-to-Have
 </div>
 <ul>
  <li>
   <div>
    Master's degree and relevant pharmaceutical experience.
   </div></li>
  <li>
   <div>
    Knowledge of technical aspects of EHS programs.
   </div></li>
  <li>
   <div>
    Trained in ISO14001 or OHSAS 18001 (Hiring Manger to update trainings as needed).
   </div></li>
  <li>
   <div>
    Demonstrated skill in analysis and problem solving.
   </div></li>
  <li>
   <div>
    Ability to work independently and multi-task effectively.
   </div></li>
 </ul><br> <br> Work Location Assignment: Hybrid
 <div></div>
 <div>
  <div>
   <div>
    <br> Additional Information
   </div>
  </div>
  <div>
   <ul>
    <li>
     <div>
      In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.
     </div></li>
    <li>
     <div>
      Please note there is no relocation support available for this position
     </div></li>
   </ul>
   <div>
    <br>
   </div>
  </div>
  <div>
   <div>
    How to apply
   </div>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you!
     </div></li>
   </ul>
   <div>
    <br>
   </div>
  </div>
 </div>
 <div>
  <div>
   Purpose
  </div>
 </div>
 <div>
  <div>
   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.
  </div>
 </div>
 <div></div>
 <div>
  <div>
   Digital Transformation Strategy
  </div>
  <div>
   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.
  </div>
 </div>
 <div></div>
 <div>
  <div>
   Equal Employment Opportunity
  </div>
  <div>
   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.
  </div>
  <div></div>
  <div>
   Disability Inclusion
  </div>
  <div>
   Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
  </div>
 </div>
 <div></div> Environmental, Health &amp; Safety
 <div></div> #LI-PFE
</div>


 
  Why Patients Need You
 
 
  Pfizer believes in holding the highest standards of safety for its patients and its employees. Your role, as a member of the Environmental, Health and Safety team, is important for maintaining these standards and preparing the organization for the necessary compliance activities. Your dedication and hard work will ensure that we provide the best care to our patients and a safe working environment for our colleagues.
 
 
 
  What You Will Achieve
 
 
  You will be part of a dynamic team of experts who form Pfizer’s Environmental, Health & Safety division. Due to the importance of this team for Pfizer’s employees and patients, the organization relies heavily on its team members’ timely actions and efficiency. You will be responsible for activities involved in identifying hazardous workplace conditions and take effective steps to ensure that workplace conditions comply with applicable federal and state Occupational Safety and Health standard provisions. You will also participate in Occupational Safety and Health Administration (OSHA) inspections and any procedures that may follow a citation. You will assist in the development and implementation of short and long range plans and continuously improve EHS performance.
 
 
 
  As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing important deliverables on time. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams.
 
 
 
  It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
 
 
 
  How You Will Achieve It
 
 
  
   
    Contribute to the completion of projects and manage own time to meet agreed targets.
   
  
   
    Understand the fundamental business drivers for Pfizer and support the organization's guidelines and policies for Environmental, Health and Safety (EHS).
   
  
   
    Review corporate, regional and local EHS requirements and implement applicable standards at the site level to assure full compliance with all applicable requirements.
   
  
   
    Manage day-to-day hazardous, biological and special waste activities, interact and communicate with all relevant stakeholders.
   
  
   
    Conduct industrial hygiene and toxicology programs in accordance with federal and local regulations.
   
  
   
    Support the effective integration of EHS into the day to day management and meeting structures within the functional area.
   
  
   
    Become familiar with operational activities, identify opportunities for improvement and coordinate with local safety champions/management to bring forward improvement projects.
   
  
   
    Assist in the completion of evaluations for new sites, new projects and equipment, including change management for minor projects.
   
  
   
    Investigate incidents and complaints of colleagues regarding safety, health, ergonomics, organizational environment, etc.
   
  
   
    Develop and publish Environmental Health and Safety communications, as necessary.
   
  
   
    Maintain fire safety precautions and first aid programs, including emergency response, training and simulations.
   
  
   
    Manage Audit of the sites’ systems and processes and implement effective EHS cultural improvement and engagement activities.
   
  
   
    Review, identify, develop and deliver EHS related training programs.
   
 
 
 
  Qualifications
 
 
  Must-Have
 
 
  
   
    Bachelor's Degree and 3+ years of experience.
   
  
   
    Experience in EHS program development, implementation and/or on-going management.
   
  
   
    Knowledge of the laws, regulations, standards and best practices governing health and safety.
   
  
   
    Good verbal and written communication skills.
   
  
   
    Advanced Microsoft Office Suite skills.
   
 
 
 
  Nice-to-Have
 
 
  
   
    Master's degree and relevant pharmaceutical experience.
   
  
   
    Knowledge of technical aspects of EHS programs.
   
  
   
    Trained in ISO14001 or OHSAS 18001 (Hiring Manger to update trainings as needed).
   
  
   
    Demonstrated skill in analysis and problem solving.
   
  
   
    Ability to work independently and multi-task effectively.
   
   Work Location Assignment: Hybrid
 
 
  
   
     Additional Information
   
  
  
   
    
     
      In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.
     
    
     
      Please note there is no relocation support available for this position
     
   
   
    
   
  
  
   
    How to apply
   
  
  
   
    
     
      Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you!
     
   
   
    
   
  
 
 
  
   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.
  
 
 
 
  
   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 Inclusion
  
  
   Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
  
 
  Environmental, Health & Safety
  #LI-PFE


Pfizer

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