Work From Home

Large

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 expertise in analytical techniques (HPLC, LC-MS, etc.), method development, validation, project management, and excellent communication skills. A PhD or BSc/MSc in analytical chemistry is preferred.

You will support chemical process development, validate analytical methods, troubleshoot issues, and ensure safe operations while contributing innovative ideas and completing high-quality documentation.

Science

Research & Development

Cork

<div><div><div>Job Summary</div><div><ul><li><div>
Development and implementation of analytics for new API processes and technology in manufacturing sites.</div></li></ul></div><div><ul><li><div>
Provide technical support and leadership for supply assurance projects</div></li></ul></div><div></div><div>
Job Responsibilities</div><div><ul><li><div>
Apply highly specialised analytical skills to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the Development team.</div></li></ul></div><div><ul><li><div>
Develop, evaluate &amp; verify analytical methods across a range of techniques as required to support projects.</div></li></ul></div><div><ul><li><div>
Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team.</div></li></ul></div><div><ul><li><div>
Contribute a range of highly innovative analytical ideas to support global process development projects.</div></li></ul></div><div><ul><li><div>
Demonstrate problem solving delivering process and analytical understanding.</div></li></ul></div><div><ul><li><div>
Provide analytical support in technical transfer of analytical methods to manufacturing sites</div></li></ul></div><div><ul><li><div>
Co-ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands.</div></li></ul></div><div><ul><li><div>
Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups.</div></li></ul></div><div><ul><li><div>
Investigate new technologies and analytical approaches</div></li></ul></div><div><ul><li><div>
Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines.</div></li></ul></div><div><ul><li><div>
Contribute to the analytical team program of continuous improvement.</div></li></ul></div><div><ul><li><div>
Ensure the ongoing safe and efficient operation of facilities.</div></li></ul></div><div></div><div>
Qualifications/Skills</div><div></div><div><div>
Requirements for all Global Job Levels</div></div><div><ul><li><div>
Extensive knowledge and experience of analytical principles and procedures.</div></li></ul></div><div><ul><li><div>
Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC-MS/MS, GC-MS, KF.</div></li></ul></div><div><ul><li><div>
A strong background in impurity isolation and identification using LC-MS to support the development and troubleshooting of chemical processes is desirable.</div></li></ul></div><div><ul><li><div>
Experience in HPLC/UPLC method development. GC method development experience is desirable.</div></li></ul></div><div><ul><li><div>
Experience in pGTI method development and quantification is desirable.</div></li></ul></div><div><ul><li><div>
Experience of method validation and method transfers, including the generation and review of MT and validation protocols and reports is desirable.</div></li></ul></div><div><ul><li><div>
A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project. Project management experience a plus here.</div></li></ul></div><div><ul><li><div>
The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results. Develops advanced ideas and guides their development into a final product.</div></li></ul></div><div><ul><li><div>
Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes.</div></li></ul></div><div><ul><li><div>
Excellent interpersonal skills and the ability to work in a collaborative, team driven environment.</div></li></ul></div><div><ul><li><div>
Excellent written and verbal communication skills.</div></li></ul><ul><li><div>
For Research Analyst (GJL060), a PhD in analytical chemistry ideally combined with 0+ years&rsquo; experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and ideally up to 2+ years&rsquo; experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role.</div></li></ul></div></div><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 &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</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>
Research and Development</div><div></div>

Job Summary
Development and implementation of analytics for new API processes and technology in manufacturing sites.
Provide technical support and leadership for supply assurance projects
Job Responsibilities
Apply highly specialised analytical skills to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the Development team.
Develop, evaluate & verify analytical methods across a range of techniques as required to support projects.
Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team.
Contribute a range of highly innovative analytical ideas to support global process development projects.
Demonstrate problem solving delivering process and analytical understanding.
Provide analytical support in technical transfer of analytical methods to manufacturing sites
Co-ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands.
Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups.
Investigate new technologies and analytical approaches
Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines.
Contribute to the analytical team program of continuous improvement.
Ensure the ongoing safe and efficient operation of facilities.
Qualifications/Skills
Requirements for all Global Job Levels
Extensive knowledge and experience of analytical principles and procedures.
Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC-MS/MS, GC-MS, KF.
A strong background in impurity isolation and identification using LC-MS to support the development and troubleshooting of chemical processes is desirable.
Experience in HPLC/UPLC method development. GC method development experience is desirable.
Experience in pGTI method development and quantification is desirable.
Experience of method validation and method transfers, including the generation and review of MT and validation protocols and reports is desirable.
A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project. Project management experience a plus here.
The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results. Develops advanced ideas and guides their development into a final product.
Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes.
Excellent interpersonal skills and the ability to work in a collaborative, team driven environment.
Excellent written and verbal communication skills.
For Research Analyst (GJL060), a PhD in analytical chemistry ideally combined with 0+ years’ experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and ideally up to 2+ years’ experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role.
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!
Research and Development

Research Analyst - Pfizer

<div>
 <div>
  <div>
   Job Summary
  </div>
  <div>
   <ul>
    <li>
     <div>
      Development and implementation of analytics for new API processes and technology in manufacturing sites.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Provide technical support and leadership for supply assurance projects
     </div></li>
   </ul>
  </div>
  <div></div>
  <div>
   Job Responsibilities
  </div>
  <div>
   <ul>
    <li>
     <div>
      Apply highly specialised analytical skills to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the Development team.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Develop, evaluate &amp; verify analytical methods across a range of techniques as required to support projects.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Provide analytical testing across a range of techniques to support chemical process development, pilot plant demonstrations and full-scale qualification batches as part of the team.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Contribute a range of highly innovative analytical ideas to support global process development projects.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Demonstrate problem solving delivering process and analytical understanding.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Provide analytical support in technical transfer of analytical methods to manufacturing sites
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Co-ordinate and/or contribute to analytical validation and method transfer (MT) activities as required by project demands.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Contribute and/or lead troubleshooting and investigation of analytical issues with existing commercial API processes to support project teams, API sites (internal and external) and global technical groups.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Investigate new technologies and analytical approaches
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Complete reports, memos and lab notebooks experiments to a high standard and meeting required deadlines.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Contribute to the analytical team program of continuous improvement.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Ensure the ongoing safe and efficient operation of facilities.
     </div></li>
   </ul>
  </div>
  <div></div>
  <div>
   Qualifications/Skills
  </div>
  <div></div>
  <div>
   <div>
    Requirements for all Global Job Levels
   </div>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Extensive knowledge and experience of analytical principles and procedures.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Practical experience in a range of analytical techniques including but not limited to HPLC, UPLC, GC, SFC, LC-MS/MS, GC-MS, KF.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      A strong background in impurity isolation and identification using LC-MS to support the development and troubleshooting of chemical processes is desirable.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Experience in HPLC/UPLC method development. GC method development experience is desirable.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Experience in pGTI method development and quantification is desirable.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Experience of method validation and method transfers, including the generation and review of MT and validation protocols and reports is desirable.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      A proven ability to plan and work independently. The candidate must be able to work under consultative direction, toward predetermined long-range goals and objectives for a project. Project management experience a plus here.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      The candidate should have the ability to determine and pursue courses of action necessary to obtain desired results. Develops advanced ideas and guides their development into a final product.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Demonstrated application of 6-sigma tools and practices and a focus on continuous improvement for work processes.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Excellent interpersonal skills and the ability to work in a collaborative, team driven environment.
     </div></li>
   </ul>
  </div>
  <div>
   <ul>
    <li>
     <div>
      Excellent written and verbal communication skills.
     </div></li>
   </ul>
   <ul>
    <li>
     <div>
      For Research Analyst (GJL060), a PhD in analytical chemistry ideally combined with 0+ years’ experience in the pharmaceutical industry, ideally within an analytical development role; or a BSc/MSc in a degree with significant analytical focus and ideally up to 2+ years’ experience in the pharmaceutical industry, ideally within an analytical development role. Experience in project management, complex analytical investigation and method development is desired for this role.
     </div></li>
   </ul>
  </div>
 </div>
 <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> Research and Development
</div>
<div></div>

Research Analyst

You will meet with doctors, generate business in your territory, lead scientific programs, and execute company strategies compliantly from a remote, field-based location.

You will meet with doctors to generate business, conduct scientific programs to update HCPs on advancements, and execute company strategies effectively and compliantly.

Sales & Business Development

Healthcare

Chennai

<div><div>Meeting Doctor's and generating business in assigned territory and conduct scientific programs with HCPs to update the scientific advancement.</div><div>
executing strategies designed by the company in complaint way</div><br>
<br>
Work Location Assignment: Remote - Field Based<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>

Meeting Doctor's and generating business in assigned territory and conduct scientific programs with HCPs to update the scientific advancement.
executing strategies designed by the company in complaint way

Work Location Assignment: Remote - Field Based
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 should possess leadership skills, strategic vision, and a strong background in healthcare to excel in this executive role. A commitment to diversity and equal opportunity is essential.

You will engage with customers daily to drive demand for our product portfolios, focusing on building relationships and promoting sales effectively in the healthcare sector.

Customer Relations

<div><div>Front line Sales colleague to meet customer for creating demand for our portfolios.</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>

Front line Sales colleague to meet customer for creating demand for our portfolios.
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

You need a Bachelor's in a relevant field, 3-5 years in pharma quality, root cause analysis experience, cGMP knowledge, strong communication skills, and the ability to manage multiple projects.

You will conduct investigations, analyze root causes, implement CAPAs, drive continuous improvement, mentor staff, report on metrics, and manage change controls to enhance performance and reduce waste.

Melbourne

<div><div>Why Patients Need You</div><div>
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, production, compliance, your contribution is crucial and will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve.</div><div>
What You Will Achieve</div><div>
In this role, you will be responsible for addressing site deviations by conducting thorough investigations and root cause analyses to identify effective Corrective and Preventative Actions (CAPAs). Your efforts will help reduce the number of repeat deviations at the site. Additionally, you will be responsible for driving improvements through independent proactive CAPAs and Continuous Improvement (CI) ideas from production. Your role includes implementing strategies to enhance performance and reduce waste, driven by proactive CAPAs and CI initiatives, and reporting performance against established standards in line with company objectives.</div><div>
You will be accountable for meeting department, site, and corporate goals and will be expected to report and communicate progress on deviations, status, and closure plans to key stakeholders across the business.</div><div>
How You Will Achieve It</div><ul><li>
Lead complex investigations and create effective project plans to ensure timely closure, engaging site Subject Matter Experts (SMEs), managing meetings, and reporting investigation updates to key personnel across the site.</li><li>
Serve as an Operations technical SME in cross-functional Method 1 (M1) investigations.</li><li>
Utilize Six Sigma investigation tools, including MiniTab, Fishbone, and 5 Whys methodologies, for true root cause identification and effective CAPA implementation.</li><li>
Drive timely closure and quality improvements to reduce repeat deviations, increase performance, and reduce waste and costs.</li><li>
Proactively engage with Operations staff to identify CI initiatives, focusing on safety, quality, compliance, and Materials Usage Variance (MUV)/cost reduction.</li><li>
Provide continued education and mentoring to Operations staff on the importance of proactive data analysis, investigation methods, CI identification, and root cause and CAPA determination, fostering a positive working environment and resilience.</li><li>
Initiate and deliver Change Controls (CC) related to CAPAs and CI initiatives, ensuring timely closures.</li><li>
Present Operations investigation findings during Regulatory inspections and Contract Customer Audits.</li><li>
Monitor and report deviation performance metrics as directed.</li><li>
Perform any other duties as assigned by the Production Compliance Lead.</li></ul><div>
Qualifications</div><div>
Must-Have</div><ul><li>
Bachelor&rsquo;s degree in science, Pharmacy, Engineering, or a related discipline, or equivalent experience in the pharmaceutical or allied industry.</li><li>
3-5 years of experience in pharmaceutical manufacturing/Quality.</li><li>
1-3 years of experience in facilitating investigations using Six Sigma tools, Fishbone, and 5 Whys methodologies for root cause analysis and effective CAPA identification.</li><li>
Knowledge and application of Good Manufacturing Practices (cGMP).</li><li>
Experience with compliance issues resulting from cGMP deviations or product defects.</li><li>
Exceptional communication, negotiation, interpersonal, and leadership skills (both verbal and written).</li><li>
Results-focused with demonstrated Project Management skills, the ability to manage multiple projects, and meet business targets and delivery timelines.</li><li>
Attention to detail, technical knowledge, innovative thinking, and problem-solving abilities, including implementation of resolutions.</li><li>
Ability to work under pressure and meet agreed timelines with high attention to detail.</li><li>
Understanding of quality systems, including the management of deviation investigations, change controls, and quality records.</li><li>
Proficiency with computer packages, including the Microsoft Office suite.</li><li>
Permanent rights to work within Australia.</li><li>
Deviation investigation experience within the pharmaceutical cGMP environment.</li></ul><div>
Nice-to-Have</div><ul><li>
Experience in sterile manufacturing, Process Validation, Engineering, or Quality.</li><li>
Method 1 (M1) &amp; Pfizer Human Performance (PHP) certification.</li><li>
Lean Six Sigma Yellow/Green/Black Belt certification.</li><li>
Experience with MiniTab and TrackWise Quality Management System.</li></ul>
<br>
Work Location Assignment: On Premise<div></div><div><br>
At Pfizer we care about our colleagues&rsquo; wellbeing and offer a range of great benefits for them, including:</div><ul><li><div>
Paid parental leave</div></li><li><div>
Access to Health &amp; Wellness apps</div></li><li><div>
Career Growth Experiences program</div></li><li><div>
Recognition &amp; rewards program</div></li><li><div>
Paid volunteer days</div></li><li><div>
Life Insurance Benefits</div></li><li><div>
Pfizer Learning Academy access to top content providers</div></li><li><div>
Access to flu vaccines &amp; skin checks</div></li><li><div>
Options to purchase additional leave</div></li><li><div>
Salary packaging &amp; novated lease options</div></li></ul><div></div><ul><li>Benefits listed may vary depending on your position and location and may be subject to change.</li></ul><div></div><div>
Pfizer Australia and New Zealand&rsquo;s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity &amp; Inclusion (DE&amp;I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.</div><div></div><div>
If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.</div><br>
<div></div>
Manufacturing<br>
<div></div>
#LI-PFE</div>

Why Patients Need You
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, production, compliance, your contribution is crucial and will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve.
What You Will Achieve
In this role, you will be responsible for addressing site deviations by conducting thorough investigations and root cause analyses to identify effective Corrective and Preventative Actions (CAPAs). Your efforts will help reduce the number of repeat deviations at the site. Additionally, you will be responsible for driving improvements through independent proactive CAPAs and Continuous Improvement (CI) ideas from production. Your role includes implementing strategies to enhance performance and reduce waste, driven by proactive CAPAs and CI initiatives, and reporting performance against established standards in line with company objectives.
You will be accountable for meeting department, site, and corporate goals and will be expected to report and communicate progress on deviations, status, and closure plans to key stakeholders across the business.
How You Will Achieve It
Lead complex investigations and create effective project plans to ensure timely closure, engaging site Subject Matter Experts (SMEs), managing meetings, and reporting investigation updates to key personnel across the site.
Serve as an Operations technical SME in cross-functional Method 1 (M1) investigations.
Utilize Six Sigma investigation tools, including MiniTab, Fishbone, and 5 Whys methodologies, for true root cause identification and effective CAPA implementation.
Drive timely closure and quality improvements to reduce repeat deviations, increase performance, and reduce waste and costs.
Proactively engage with Operations staff to identify CI initiatives, focusing on safety, quality, compliance, and Materials Usage Variance (MUV)/cost reduction.
Provide continued education and mentoring to Operations staff on the importance of proactive data analysis, investigation methods, CI identification, and root cause and CAPA determination, fostering a positive working environment and resilience.
Initiate and deliver Change Controls (CC) related to CAPAs and CI initiatives, ensuring timely closures.
Present Operations investigation findings during Regulatory inspections and Contract Customer Audits.
Monitor and report deviation performance metrics as directed.
Perform any other duties as assigned by the Production Compliance Lead.
Qualifications
Must-Have
Bachelor’s degree in science, Pharmacy, Engineering, or a related discipline, or equivalent experience in the pharmaceutical or allied industry.
3-5 years of experience in pharmaceutical manufacturing/Quality.
1-3 years of experience in facilitating investigations using Six Sigma tools, Fishbone, and 5 Whys methodologies for root cause analysis and effective CAPA identification.
Knowledge and application of Good Manufacturing Practices (cGMP).
Experience with compliance issues resulting from cGMP deviations or product defects.
Exceptional communication, negotiation, interpersonal, and leadership skills (both verbal and written).
Results-focused with demonstrated Project Management skills, the ability to manage multiple projects, and meet business targets and delivery timelines.
Attention to detail, technical knowledge, innovative thinking, and problem-solving abilities, including implementation of resolutions.
Ability to work under pressure and meet agreed timelines with high attention to detail.
Understanding of quality systems, including the management of deviation investigations, change controls, and quality records.
Proficiency with computer packages, including the Microsoft Office suite.
Permanent rights to work within Australia.
Deviation investigation experience within the pharmaceutical cGMP environment.
Nice-to-Have
Experience in sterile manufacturing, Process Validation, Engineering, or Quality.
Method 1 (M1) & Pfizer Human Performance (PHP) certification.
Lean Six Sigma Yellow/Green/Black Belt certification.
Experience with MiniTab and TrackWise Quality Management System.

Work Location Assignment: On Premise
At Pfizer we care about our colleagues’ wellbeing and offer a range of great benefits for them, including:
Paid parental leave
Access to Health & Wellness apps
Career Growth Experiences program
Recognition & rewards program
Paid volunteer days
Life Insurance Benefits
Pfizer Learning Academy access to top content providers
Access to flu vaccines & skin checks
Options to purchase additional leave
Salary packaging & novated lease optionsBenefits listed may vary depending on your position and location and may be subject to change.
Pfizer Australia and New Zealand’s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.
If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.

Manufacturing

#LI-PFE

Investigations Specialist - Pfizer

Investigations Specialist

You need a science or engineering degree, 3-5 years in pharma, GMP knowledge, strong communication skills, project management experience, and attention to detail with a focus on quality systems.

You will manage change requests, update documentation, coordinate with departments, prepare metrics, assess risks, and analyze data to improve compliance and reduce waste.

<div><div>Why Patients Need You</div><div>
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, production, compliance, your contribution is crucial and will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve.</div><div></div><div>
What You Will Achieve</div><div>
As the Production Compliance Specialist, you will be instrumental in supporting the production teams by managing change requests and updating documentation, including but not limited to master supporting documents. You will oversee associated change controls and assist with scheduled periodic reviews to ensure all documentation aligns with company policies, practices, and standards. Your role encompasses implementing strategies to improve performance and reduce waste through proactive CAPAs and Continuous Improvement (CI) initiatives, as well as reporting performance against established standards in line with company objectives. You will be accountable for meeting department, site, and corporate goals and will report and communicate the status of manufacturing compliance activities and closure plans to key stakeholders.</div><div>
How You Will Achieve It</div><ul><li>
Supporting the production teams by managing change requests and updating documentation.</li><li>
Manage associated change controls and assist with the scheduled periodic review of production documentation.</li><li>
Independently coordinate with requesting departments to obtain supporting information, resolve change control issues, and facilitate the review/approval/implementation of changes.</li><li>
Update documentation to align with company policies, practices, and standards.</li><li>
Implement strategies to improve performance and reduce waste through proactive CAPAs and CI initiatives.</li><li>
Preparing monthly and or weekly departmental metrics related to change control and document control processes.</li><li>
Report performance against established standards in line with company objectives.</li><li>
Participate in risk assessment activities.</li><li>
Communicate the strategic plan objectives of the department in daily activities.</li><li>
Foster an environment of open communication and recognition of contribution.</li><li>
Collaborate with business process owners to conduct regulatory requirements gap assessments and implement necessary actions to address any identified gaps.</li><li>
Perform all operations within the Functional Unit according to relevant procedures and standards.</li><li>
Facilitate or complete production compliance activities outside standard working hours as needed.</li><li>
Conduct complex data gathering and analysis using Excel and MiniTab.</li></ul><div>
Qualifications</div><div>
Must-Have</div><ul><li>
Bachelor&rsquo;s degree in science, Engineering, or a related discipline, or equivalent experience in the pharmaceutical or allied industry.</li><li>
3-5 years of experience within the pharmaceutical or allied industry.</li><li>
Knowledge and application of Good Manufacturing Practices (cGMP).</li><li>
Exceptional communication, negotiation, interpersonal, and leadership skills (verbal and written).</li><li>
Results-focused with demonstrated Project Management skills, the ability to manage multiple projects, and meet business targets and delivery timelines.</li><li>
Attention to detail, technical knowledge, innovative thinking, and problem-solving abilities, including implementation of resolutions.</li><li>
Ability to work under pressure and meet agreed timelines with high attention to detail.</li><li>
Understanding of quality systems, including CAPA/CI management, change controls, and quality records.</li><li>
Proficiency with computer packages, including the Microsoft Office suite.</li><li>
Permanent rights to work within Australia.</li></ul><div>
Preferred Qualifications</div><ul><li>
Experience in sterile manufacturing, Process Validation, Engineering, or Quality.</li><li>
Method 1 (M1) and Pfizer Human Performance (PHP) certification.</li><li>
Demonstrated ability and accountability to meet business targets and objectives.</li><li>
Strong awareness of GxP requirements and a proponent of &ldquo;Best-Practice&rdquo; Quality Standards.</li><li>
Demonstrated initiative and ownership in resolving issues or challenges.</li><li>
Participation in the generation and implementation of continuous improvement (CI) ideas.</li><li>
Ability to occasionally work outside standard hours to accommodate all production shifts and business needs.</li></ul>
<br>
Work Location Assignment: On Premise<div></div><div><br>
At Pfizer we care about our colleagues&rsquo; wellbeing and offer a range of great benefits for them, including:</div><ul><li><div>
Paid parental leave</div></li><li><div>
Access to Health &amp; Wellness apps</div></li><li><div>
Career Growth Experiences program</div></li><li><div>
Recognition &amp; rewards program</div></li><li><div>
Paid volunteer days</div></li><li><div>
Life Insurance Benefits</div></li><li><div>
Pfizer Learning Academy access to top content providers</div></li><li><div>
Access to flu vaccines &amp; skin checks</div></li><li><div>
Options to purchase additional leave</div></li><li><div>
Salary packaging &amp; novated lease options</div></li></ul><div></div><ul><li>Benefits listed may vary depending on your position and location and may be subject to change.</li></ul><div></div><div>
Pfizer Australia and New Zealand&rsquo;s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity &amp; Inclusion (DE&amp;I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.</div><div></div><div>
If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.</div><br>
<div></div>
Support Services<br>
<div></div>
#LI-PFE</div>

Why Patients Need You
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, production, compliance, your contribution is crucial and will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the highest standards, making a meaningful difference in the lives of those we serve.
What You Will Achieve
As the Production Compliance Specialist, you will be instrumental in supporting the production teams by managing change requests and updating documentation, including but not limited to master supporting documents. You will oversee associated change controls and assist with scheduled periodic reviews to ensure all documentation aligns with company policies, practices, and standards. Your role encompasses implementing strategies to improve performance and reduce waste through proactive CAPAs and Continuous Improvement (CI) initiatives, as well as reporting performance against established standards in line with company objectives. You will be accountable for meeting department, site, and corporate goals and will report and communicate the status of manufacturing compliance activities and closure plans to key stakeholders.
How You Will Achieve It
Supporting the production teams by managing change requests and updating documentation.
Manage associated change controls and assist with the scheduled periodic review of production documentation.
Independently coordinate with requesting departments to obtain supporting information, resolve change control issues, and facilitate the review/approval/implementation of changes.
Update documentation to align with company policies, practices, and standards.
Implement strategies to improve performance and reduce waste through proactive CAPAs and CI initiatives.
Preparing monthly and or weekly departmental metrics related to change control and document control processes.
Report performance against established standards in line with company objectives.
Participate in risk assessment activities.
Communicate the strategic plan objectives of the department in daily activities.
Foster an environment of open communication and recognition of contribution.
Collaborate with business process owners to conduct regulatory requirements gap assessments and implement necessary actions to address any identified gaps.
Perform all operations within the Functional Unit according to relevant procedures and standards.
Facilitate or complete production compliance activities outside standard working hours as needed.
Conduct complex data gathering and analysis using Excel and MiniTab.
Qualifications
Must-Have
Bachelor’s degree in science, Engineering, or a related discipline, or equivalent experience in the pharmaceutical or allied industry.
3-5 years of experience within the pharmaceutical or allied industry.
Knowledge and application of Good Manufacturing Practices (cGMP).
Exceptional communication, negotiation, interpersonal, and leadership skills (verbal and written).
Results-focused with demonstrated Project Management skills, the ability to manage multiple projects, and meet business targets and delivery timelines.
Attention to detail, technical knowledge, innovative thinking, and problem-solving abilities, including implementation of resolutions.
Ability to work under pressure and meet agreed timelines with high attention to detail.
Understanding of quality systems, including CAPA/CI management, change controls, and quality records.
Proficiency with computer packages, including the Microsoft Office suite.
Permanent rights to work within Australia.
Preferred Qualifications
Experience in sterile manufacturing, Process Validation, Engineering, or Quality.
Method 1 (M1) and Pfizer Human Performance (PHP) certification.
Demonstrated ability and accountability to meet business targets and objectives.
Strong awareness of GxP requirements and a proponent of “Best-Practice” Quality Standards.
Demonstrated initiative and ownership in resolving issues or challenges.
Participation in the generation and implementation of continuous improvement (CI) ideas.
Ability to occasionally work outside standard hours to accommodate all production shifts and business needs.

Work Location Assignment: On Premise
At Pfizer we care about our colleagues’ wellbeing and offer a range of great benefits for them, including:
Paid parental leave
Access to Health & Wellness apps
Career Growth Experiences program
Recognition & rewards program
Paid volunteer days
Life Insurance Benefits
Pfizer Learning Academy access to top content providers
Access to flu vaccines & skin checks
Options to purchase additional leave
Salary packaging & novated lease optionsBenefits listed may vary depending on your position and location and may be subject to change.
Pfizer Australia and New Zealand’s diverse workforce represents the patients we serve and the communities in which we operate. With a focus on Diversity, Equity & Inclusion (DE&I), Pfizer ANZ ensures our people are heard and cared for. We offer engagement opportunities in both Colleagues Resource Groups (CRGs) and workstreams across: Culture and Tradition, Reconciliation @ Pfizer (RAP), Gender Equity (GEN), Disability and through the Out Pfizer Employee Network (OPEN) for our LGBT + colleagues and allies.
If you require reasonable adjustment during your application, please reach out to the Talent Acquisition Manager.

Support Services

#LI-PFE

Pfizer

Mission