At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guides us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe.

#DrugDiscovery #Biotech #Biotechnology #Pharmaceuticals #CRL

Science & Healthcare

Charles River Laboratories

You should have a BTA, Biologielaborant, or BSc in a related field, with expertise in virology and relevant laboratory skills.

You will conduct virology experiments, analyze results, maintain lab equipment, and collaborate with the team to ensure accurate data collection and compliance with safety protocols.

<div>
 <p>For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</p>
 <div>
  <div>
   <div> 
   </div>
   <div>
    <p> </p>
    <p><b>Für die Abteilung Biosafety / Virologie am Standort Köln suchen wir ab sofort unbefristet in Vollzeit eine/n</b></p>
    <p> </p>
    <p><b>Biologisch-Technischen Assistenten (BTA) /</b></p>
    <p> </p>
    <p><b>Biologielaboranten / B.Sc. Biologie-Biotechnologie</b></p>
    <p> </p>
    <p><b>als Technical Officer (m/w/d)</b></p>
    <p> </p>
   </div>
  </div>
  <div></div>
  <div>
   <div>
    <p><b>Zu Deinen Aufgaben zählen:</b><br> </p>
    <ul>
     <li>Laborarbeiten mit Zellkulturen, Mykoplasmen und Viren</li>
     <li> Nachweis von Viren und Mykoplasmen in biologischen Probenmaterialien</li>
     <li> Selbständige Durchführung und Dokumentation bioanalytischer Methoden</li>
     <li> Erstellung von prüfungsbezogenen und übergreifenden Dokumenten</li>
     <li> Allgemeine Laborarbeiten, z.B. Gerätewartung </li>
     <li>Arbeiten und Dokumentation unter GMP-Bedingungen</li>
     <li> Pflege und Aufrechterhaltung des GMP-Systems</li>
     <li> Erstellen von Standardarbeitsanweisungen</li>
    </ul>
    <p> </p>
    <p></p>
    <p><b>Das bringst Du mit:</b><br> </p>
    <ul>
     <li>Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein Studium zum B.Sc. im Bereich Biologie / Biotechnologie / Biochemie etc.</li>
     <li> Wünschenswert sind praktische Kenntnisse im Bereich Zellkultur, Virologie und / oder Mikrobiologie</li>
     <li> Team- und Kommunikationsfähigkeit</li>
     <li> Dienstleistungsorientierung</li>
     <li> Gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie sehr gute Deutsch und gute Englischkenntnisse setzen wir voraus</li>
     <li><b> Bereitschaft ggf. auch am Standort in Erkrath in der gleichen Abteilung zu arbeiten</b></li>
    </ul>
    <p> </p>
    <p></p>
    <p><b>Wir bieten Dir:</b><br> </p>
    <ul>
     <li>eine Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen</li>
     <li> eine intensive Einarbeitung</li>
     <li> flexible Arbeitszeiten</li>
     <li> eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und</li>
     <li> eine angemessene Vergütung</li>
    </ul>
    <p> </p>
    <p></p>
    <p><b>Haben wir Dein Interesse geweckt?</b><br> <br> Wenn ja, bewirb Dich bitte unter der <b>Job-ID</b> <b>222943</b> über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem <b>frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen</b>.<br> Wir freuen uns auf Deine Bewerbung!</p>
    <p> </p>
    <p></p>
    <p><b>Charles River Laboratories Germany GmbH</b><br> Human Resources<br> Max-Planck-Str. 15a<br> 40699 Erkrath<br> Bei Fragen bitte an RecruitBPS@crl.com wenden</p>
    <p> </p>
   </div>
  </div>
 </div>
 <p></p>
 <p><b>About Biologics Testing Solutions</b><br> With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.</p>
 <p> </p>
 <p><b>About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</p>
 <p> </p>
 <p>With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. </p>
 <p></p>
 <p>At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.</p>
 <p> </p>
 <p><b>Equal Employment Opportunity</b><br> Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.</p>
 <p> </p>
 <p>If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.</p>
 <p> </p>
 <p>For more information, please visit www.criver.com.</p>
 <div>
   222943
 </div>
</div>


 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
 
  
    
   
   
     
    Für die Abteilung Biosafety / Virologie am Standort Köln suchen wir ab sofort unbefristet in Vollzeit eine/n
     
    Biologisch-Technischen Assistenten (BTA) /
     
    Biologielaboranten / B.Sc. Biologie-Biotechnologie
     
    als Technical Officer (m/w/d)
     
   
  
  
  
   
    Zu Deinen Aufgaben zählen: 
    
     Laborarbeiten mit Zellkulturen, Mykoplasmen und Viren
      Nachweis von Viren und Mykoplasmen in biologischen Probenmaterialien
      Selbständige Durchführung und Dokumentation bioanalytischer Methoden
      Erstellung von prüfungsbezogenen und übergreifenden Dokumenten
      Allgemeine Laborarbeiten, z.B. Gerätewartung 
     Arbeiten und Dokumentation unter GMP-Bedingungen
      Pflege und Aufrechterhaltung des GMP-Systems
      Erstellen von Standardarbeitsanweisungen
    
     
    
    Das bringst Du mit: 
    
     Ausbildung als Biologisch-technischer Assistent / Biologielaborant (m/w/d) oder ein Studium zum B.Sc. im Bereich Biologie / Biotechnologie / Biochemie etc.
      Wünschenswert sind praktische Kenntnisse im Bereich Zellkultur, Virologie und / oder Mikrobiologie
      Team- und Kommunikationsfähigkeit
      Dienstleistungsorientierung
      Gute Kenntnisse von Microsoft Office (Word, Excel, PowerPoint) sowie sehr gute Deutsch und gute Englischkenntnisse setzen wir voraus
      Bereitschaft ggf. auch am Standort in Erkrath in der gleichen Abteilung zu arbeiten
    
     
    
    Wir bieten Dir: 
    
     eine Stelle mit vielseitigen, anspruchsvollen Tätigkeiten in einem zukunftsorientierten Unternehmen
      eine intensive Einarbeitung
      flexible Arbeitszeiten
      eine aktive Mitgestaltung Deines Tätigkeitsfeldes in einem motivierten Team und
      eine angemessene Vergütung
    
     
    
    Haben wir Dein Interesse geweckt?  Wenn ja, bewirb Dich bitte unter der Job-ID 222943 über unser Karriereportal https://jobs.criver.com/ mit Deinen aussagekräftigen Bewerbungsunterlagen, Deinem frühestmöglichen Eintrittstermin sowie Deinen Gehaltsvorstellungen. Wir freuen uns auf Deine Bewerbung!
     
    
    Charles River Laboratories Germany GmbH Human Resources Max-Planck-Str. 15a 40699 Erkrath Bei Fragen bitte an RecruitBPS@crl.com wenden
     
   
  
 
 
 About Biologics Testing Solutions With more than 50 years of experience and proven regulatory expertise, the Charles River Biologics group can address challenging projects for biotechnology and pharmaceutical companies worldwide. Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks through preclinical and clinical studies to marketed products. Whether clients need stand-alone services, a unique package of testing, or insourced support, our Biologics group can create a custom solution to suit their needs. Each year more than 20,000 biologic testing reports are sent each and over 200 licenses products are supported by our biologics testing solutions team.
  
 About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
  
 With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. 
 
 At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
  
 Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.
  
 If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
  
 For more information, please visit www.criver.com.
 
   222943
 


BTA / Biologielaborant / BSc als Technical Officer (m/w/d) - Virology - Charles River Laboratories

BTA / Biologielaborant / BSc als Technical Officer (m/w/d) - Virology

You should have experience in in vitro assays, strong understanding of DMPK principles, excellent laboratory skills, and a collaborative mindset in a fast-paced environment.

You will conduct in vitro assays, analyze data, support DMPK studies, collaborate with teams, and ensure compliance with protocols in a laboratory environment.

<div>
 <p>For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</p>
 <div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b> Job Summary</b></h2> 
   </div>
   <div>
    <p> </p>
    <p><b>Our Charles River Discovery, Saffron Walden site have an opportunity for an In Vitro Associate Technical Specialist (ADME).</b></p>
    <p> </p>
    <p>This is a lab-based role in our Drug Metabolism and Pharmacokinetic (DMPK) team, with a focus on the performance of in vitro assays to understand the Absorption, Distribution, Metabolism and Excretion properties of potential new therapies.</p>
    <p> </p>
    <p>You will be an integral part of our DMPK team working in a motivated and supportive environment. You will rapidly develop lab skills, as well as working closely with colleagues in multidisciplinary teams to deliver results to your clients.</p>
    <p> </p>
    <p>In addition to developing your practical skills, you will have opportunities to expand your non-lab skills within areas such as communication, scientific writing and operational or continuous improvement initiatives, whilst learning about the drug discovery process in a fast-moving and dynamic contract research organisation.</p>
    <p> </p>
   </div>
  </div>
  <p></p>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>What You'll Be Doing</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>Using robotic liquid handlers, you will perform assays to determine the kinetic solubility, metabolic stability and permeability of novel compounds designed to treat a range of medical conditions. This data is used to select the compounds with the best chance of meeting all the criteria to become a new drug. Attention to detail, accuracy and precision are key.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>You will be using mass spectrometers to detect each compound. Full training will be given in every step of the process, from developing and optimising the detection methods, to sample and data processing.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>As your confidence in using and understanding the instruments grows you will also perform routine instrument validation and maintenance duties.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>You will maintain a safe working environment, and be expected to be an active participant on the general laboratory housekeeping rota’s.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>Skills and Experience</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>BSc in a scientific discipline.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Prior internship / work experience / shadowing.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Previous work experience at similar CROs / pharma / biotech companies is advantageous.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Effective communicator.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Works effectively as part of a team.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Attention to detail.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Strong desire to develop a lab-based career discovering new medicines.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>What We Offer You</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>A very comprehensive benefits package from day one, including a generous pension contribution, private medical for you (and can add family members), private dental care, critical illness cover, bonus and more!</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Access to great discounts via our CREDS discount scheme.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Global opportunities and strong career progression.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>The chance to work on several varied projects and liaise globally and nationally with other business areas.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>To be able make a difference to health and wellbeing of people.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>To continue your own career growth.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Flexible and hybrid working.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Parental leave.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Group Life Assurance and Group Income Protection.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Remote GP access 24/7.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Well-being support and initiatives.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Cycle to work scheme.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Well-being support and initiatives.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Cycle to work scheme.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
 </div>
 <p></p>
 <p><b>About Discovery</b><br> Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.</p>
 <p></p>
 <p><b><br> About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</p>
 <p></p>
 <p><br> With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.</p>
 <p></p>
 <p><br> At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.</p>
 <p></p>
 <p><br> At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.</p>
 <div>
   223867
 </div>
</div>


 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
 
  
   
     Job Summary 
   
   
     
    Our Charles River Discovery, Saffron Walden site have an opportunity for an In Vitro Associate Technical Specialist (ADME).
     
    This is a lab-based role in our Drug Metabolism and Pharmacokinetic (DMPK) team, with a focus on the performance of in vitro assays to understand the Absorption, Distribution, Metabolism and Excretion properties of potential new therapies.
     
    You will be an integral part of our DMPK team working in a motivated and supportive environment. You will rapidly develop lab skills, as well as working closely with colleagues in multidisciplinary teams to deliver results to your clients.
     
    In addition to developing your practical skills, you will have opportunities to expand your non-lab skills within areas such as communication, scientific writing and operational or continuous improvement initiatives, whilst learning about the drug discovery process in a fast-moving and dynamic contract research organisation.
     
   
  
  
  
   
    What You'll Be Doing 
   
   
     
    
     Using robotic liquid handlers, you will perform assays to determine the kinetic solubility, metabolic stability and permeability of novel compounds designed to treat a range of medical conditions. This data is used to select the compounds with the best chance of meeting all the criteria to become a new drug. Attention to detail, accuracy and precision are key.
    
     
    
     You will be using mass spectrometers to detect each compound. Full training will be given in every step of the process, from developing and optimising the detection methods, to sample and data processing.
    
     
    
     As your confidence in using and understanding the instruments grows you will also perform routine instrument validation and maintenance duties.
    
     
    
     You will maintain a safe working environment, and be expected to be an active participant on the general laboratory housekeeping rota’s.
    
     
   
  
  
   
    Skills and Experience 
   
   
     
    
     BSc in a scientific discipline.
    
     
    
     Prior internship / work experience / shadowing.
    
     
    
     Previous work experience at similar CROs / pharma / biotech companies is advantageous.
    
     
    
     Effective communicator.
    
     
    
     Works effectively as part of a team.
    
     
    
     Attention to detail.
    
     
    
     Strong desire to develop a lab-based career discovering new medicines.
    
     
   
  
  
   
    What We Offer You 
   
   
     
    
     A very comprehensive benefits package from day one, including a generous pension contribution, private medical for you (and can add family members), private dental care, critical illness cover, bonus and more!
    
     
    
     Access to great discounts via our CREDS discount scheme.
    
     
    
     Global opportunities and strong career progression.
    
     
    
     The chance to work on several varied projects and liaise globally and nationally with other business areas.
    
     
    
     To be able make a difference to health and wellbeing of people.
    
     
    
     To continue your own career growth.
    
     
    
     Flexible and hybrid working.
    
     
    
     Parental leave.
    
     
    
     Group Life Assurance and Group Income Protection.
    
     
    
     Remote GP access 24/7.
    
     
    
     Well-being support and initiatives.
    
     
    
     Cycle to work scheme.
    
     
    
     Well-being support and initiatives.
    
     
    
     Cycle to work scheme.
    
     
   
  
 
 
 About Discovery Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.
 
  About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
 
  With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
 
  At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
 
  At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
 
   223867
 


In Vitro Associate Technical Specialist - DMPK - Charles River Laboratories

In Vitro Associate Technical Specialist - DMPK

You need a strong background in bioanalytical techniques, knowledge of DMPK, and experience with laboratory protocols to succeed in this role. Attention to detail and problem-solving skills are essential.

You will conduct bioanalytical assays, analyze DMPK data, ensure compliance with protocols, and support project teams in drug development processes.

Cambridge

<div>
 <p>For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</p>
 <div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b> Job Summary</b></h2>
   </div>
   <div>
    <p><br> <b> Our Charles River Discovery, Saffron Walden site have an opportunity for an Associate Technical Specialist (Bioanalysis),</b></p>
    <p> </p>
    <p>This is a lab-based role in our Drug Metabolism and Pharmacokinetic (DMPK) team with a focus on accurately measuring concentrations of potential new therapies in biological samples.</p>
    <p> </p>
    <p>At Charles River, you will be an integral part of our DMPK team working in a motivated and supportive environment. You will rapidly develop lab skills, as well as working closely with colleagues in multidisciplinary teams to deliver results to your clients.</p>
    <p> </p>
    <p>In addition to developing your practical skills, you will have opportunities to expand your non-lab skills within areas such as communication, scientific writing and operational or continuous improvement initiatives, whilst learning about the drug discovery process in a fast-moving and dynamic Contract Research Organisation.</p>
    <p><br> </p>
   </div>
  </div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>What You'll Be Doing</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>You will be processing biological samples to determine the concentration of novel compounds designed to treat a range of medical conditions. This data is used to select the compounds with the best chance of meeting all the criteria to become a new drug. Attention to detail, accuracy and precision are key</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>You will be using mass spectrometers to detect each compound.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Full training will be given in every step of the process, from developing and optimising the detection methods, to sample and data processingAs your confidence in using and understanding the instruments grows you will also perform routine instrument validation and maintenance dutiesYou will maintain a safe working environment, and be expected to be an active participant on the general laboratory housekeeping rota’s.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>The data you generate will be used to determine the pharmacokinetic (PK) profile of compounds and understand the relationship between concentration and effect (pharmacokinetic and pharmacodynamic (PK/PD) relationships), and in support of predicting the dose required in humans to have the desired outcome whilst maintaining safety margin.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>Skills and Experience</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>BSc in a scientific discipline.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Prior internship / work experience / shadowing.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Previous work experience at similar CROs / pharma / biotech companies is advantageous.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Effective communicator.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Works effectively as part of a team.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Attention to detail.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Strong desire to develop a lab-based career discovering new medicines.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
  <div>
   <div>
    <h2 class="jobSectionHeader"><b>What We Offer You</b></h2> 
   </div>
   <div>
    <p> </p>
    <ul>
     <li><p>A very comprehensive benefits package from day one, including a generous pension contribution, private medical for you (and can add family members), private dental care, critical illness cover, bonus and more!</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Access to great discounts via our CREDS discount scheme.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Global opportunities and strong career progression.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>The chance to work on several varied projects and liaise globally and nationally with other business areas.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>To be able make a difference to health and wellbeing of people.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>To continue your own career growth.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Flexible and hybrid working.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Parental leave.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Group Life Assurance and Group Income Protection.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Remote GP access 24/7.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Well-being support and initiatives.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Cycle to work scheme.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Well-being support and initiatives.</p></li>
    </ul>
    <p> </p>
    <ul>
     <li><p>Cycle to work scheme.</p></li>
    </ul>
    <p> </p>
   </div>
  </div>
 </div>
 <p><b>About Discovery</b><br> Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.</p>
 <p></p>
 <p><b><br> About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</p>
 <p></p>
 <p><br> With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.</p>
 <p></p>
 <p><br> At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.</p>
 <p></p>
 <p><br> At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.</p>
 <div>
   223866
 </div>
</div>


 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
 
  
   
     Job Summary
   
   
      Our Charles River Discovery, Saffron Walden site have an opportunity for an Associate Technical Specialist (Bioanalysis),
     
    This is a lab-based role in our Drug Metabolism and Pharmacokinetic (DMPK) team with a focus on accurately measuring concentrations of potential new therapies in biological samples.
     
    At Charles River, you will be an integral part of our DMPK team working in a motivated and supportive environment. You will rapidly develop lab skills, as well as working closely with colleagues in multidisciplinary teams to deliver results to your clients.
     
    In addition to developing your practical skills, you will have opportunities to expand your non-lab skills within areas such as communication, scientific writing and operational or continuous improvement initiatives, whilst learning about the drug discovery process in a fast-moving and dynamic Contract Research Organisation.
     
   
  
  
   
    What You'll Be Doing 
   
   
     
    
     You will be processing biological samples to determine the concentration of novel compounds designed to treat a range of medical conditions. This data is used to select the compounds with the best chance of meeting all the criteria to become a new drug. Attention to detail, accuracy and precision are key
    
     
    
     You will be using mass spectrometers to detect each compound.
    
     
    
     Full training will be given in every step of the process, from developing and optimising the detection methods, to sample and data processingAs your confidence in using and understanding the instruments grows you will also perform routine instrument validation and maintenance dutiesYou will maintain a safe working environment, and be expected to be an active participant on the general laboratory housekeeping rota’s.
    
     
    
     The data you generate will be used to determine the pharmacokinetic (PK) profile of compounds and understand the relationship between concentration and effect (pharmacokinetic and pharmacodynamic (PK/PD) relationships), and in support of predicting the dose required in humans to have the desired outcome whilst maintaining safety margin.
    
     
   
  
  
   
    Skills and Experience 
   
   
     
    
     BSc in a scientific discipline.
    
     
    
     Prior internship / work experience / shadowing.
    
     
    
     Previous work experience at similar CROs / pharma / biotech companies is advantageous.
    
     
    
     Effective communicator.
    
     
    
     Works effectively as part of a team.
    
     
    
     Attention to detail.
    
     
    
     Strong desire to develop a lab-based career discovering new medicines.
    
     
   
  
  
   
    What We Offer You 
   
   
     
    
     A very comprehensive benefits package from day one, including a generous pension contribution, private medical for you (and can add family members), private dental care, critical illness cover, bonus and more!
    
     
    
     Access to great discounts via our CREDS discount scheme.
    
     
    
     Global opportunities and strong career progression.
    
     
    
     The chance to work on several varied projects and liaise globally and nationally with other business areas.
    
     
    
     To be able make a difference to health and wellbeing of people.
    
     
    
     To continue your own career growth.
    
     
    
     Flexible and hybrid working.
    
     
    
     Parental leave.
    
     
    
     Group Life Assurance and Group Income Protection.
    
     
    
     Remote GP access 24/7.
    
     
    
     Well-being support and initiatives.
    
     
    
     Cycle to work scheme.
    
     
    
     Well-being support and initiatives.
    
     
    
     Cycle to work scheme.
    
     
   
  
 
 About Discovery Discovery from Charles River is industry-proven in the successful development of novel therapies, with over 350 patents and 80 preclinical drug candidates delivered to our sponsors in the past 17 years. Backed by more than 650 scientists, our comprehensive, integrated portfolio employs the latest technology and platforms to provide chemistry, biology, and pharmacology services that support clients from the earliest stages of hit identification all the way through to IND. Our client-focused, collaborative approach creates true partnerships that anticipate challenges, overcome obstacles, and move us forward together on the journey of getting new drugs to market.
 
  About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
 
  With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
 
  At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
 
  At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.
 
   223866
 


Bioanalytical Associate Technical Specialist - DMPK - Charles River Laboratories

Bioanalytical Associate Technical Specialist - DMPK

You should possess expertise in microbiology techniques, knowledge of laboratory safety protocols, strong analytical skills, and the ability to work collaboratively in a fast-paced environment.

You will conduct tests, analyze microbial samples, ensure compliance with regulations, document findings, and collaborate with teams to support research and development projects.

Dublin

<ul>
 <div>
  Req ID #: 223112
 </div> 
 <div>
  Dublin, Leinster, IE
 </div>
</ul>
<div></div> 
<br>
<div>
 <p>For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</p> 
 <p><b>IMPORTANT:</b> In order to be considered for this position, <b>a resume/CV must be uploaded and submitted during the application process.</b> Please make sure work history and education are added correctly.</p> 
 <div>
  <div>
   <div>
    <div>
     <b>Job Summary</b>
    </div> 
   </div>
   <div>
    <p>Full-time Lab Technician required to operate under the Technical Services Department for our Microbial Solution Site in Dublin.<br> The successful candidate will be responsible for processing microbial and LAL testing samples in the laboratory utilizing various technology platforms.</p> 
    <p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES:</b></p> 
    <ul>
     <li>Perform LAL testing for different studies as assigned encompassing a full range of LAL techniques, gel-clot, kinetic and PTS.</li> 
     <li>Perform IQ, OQ, PQ of lab equipment such as Biotek, PTS and maintain appropriate documents.</li> 
     <li>Perform contract testing laboratories for Celsis and LAL including method development studies, method validation studies, accessory release, CSE/RSE, LAL water etc as required.</li> 
     <li>Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria.</li> 
     <li>Perform and manage bioburden testing, membrane filtration and, cleaning validations.</li> 
     <li>Ensure adherence to pertinent regulatory requirements (cGMP, FDA, ISO) and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols].</li> 
     <li>Collaborate with inventory check of laboratory consumables and assist with general housekeeping of the laboratory, performing equipment maintenance and scheduling instrument calibrations.</li> 
     <li>Assist management with development and revision of departmental standard operating procedures and qualification documents.</li> 
     <li>Perform all other related duties as assigned.</li> 
    </ul>
    <p><b>QUALIFICATIONS:</b></p> 
    <ul>
     <li><b>Education:</b> Degree in Microbiology, Biology or a related discipline.</li> 
     <li><b>Experience</b><b><i>:</i></b> 2+ years related experience in a microbiology laboratory setting. Experience in cGMP pharmaceutical microbiology environment is preferred.</li> 
     <li><b>Other</b><b><i>:</i></b> Knowledge of windows based programs such as word and excel and a minimum knowledge of algebra.</li> 
    </ul>
    <p><b>PHYSICAL DEMANDS:</b></p> 
    <ul>
     <li>Requires colour vision, close vision and the ability to adjust focus.</li> 
     <li>Regularly works in a stationary position; occasionally moves about the lab/office to access supplies and equipment.</li> 
     <li>Regularly communicates with other employees/customers and must be able to exchange accurate information verbally and in written form.</li> 
     <li>Occasionally operates a computer.</li> 
     <li>Occasionally must perform manual handling.</li> 
     <li>Must be able to wear personal protective equipment (PPE) according to company standards.</li> 
    </ul>
    <p><b>WORK ENVIRONMENT:</b></p> 
    <ul>
     <li>Working in a lab environment. May work with sharp objects, near toxic or caustic chemicals, with biohazards, may be exposed to fumes or airborne particles, unpleasant odors and may be exposed to the risk of radiation.</li> 
     <li>The noise level in the work environment is usually quiet to moderate.</li> 
     <li>While performing the duties of this job, the employee regularly wears protective clothing and equipment (lab coat and safety glasses) when exposed to the laboratory area</li> 
    </ul>
   </div>
  </div>
  <div>
   <div>
    <div>
     <b>Job Qualifications</b>
    </div> 
   </div>
  </div>
 </div>
 <div></div>
 <p><b>IMPORTANT: A resume is required to be considered for this position.</b> If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.</p>
 <br> 
 <p><b>About Microbial Solutions</b><br> Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.</p>
 <br> 
 <p> <br> <b>About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</p>
 <br> 
 <p>With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.</p>
 <br> 
 <p>At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.</p>
 <br> 
 <p><b>Equal Employment Opportunity</b><br> Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.</p> 
 <p>If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.</p>
 <br> 
 <p> <br> For more information, please visit www.criver.com.</p>
</div>


 
  Req ID #: 223112
  
 
  Dublin, Leinster, IE
 

 


 For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. 
 IMPORTANT: In order to be considered for this position, a resume/CV must be uploaded and submitted during the application process. Please make sure work history and education are added correctly. 
 
  
   
    
     Job Summary
     
   
   
    Full-time Lab Technician required to operate under the Technical Services Department for our Microbial Solution Site in Dublin. The successful candidate will be responsible for processing microbial and LAL testing samples in the laboratory utilizing various technology platforms. 
    ESSENTIAL DUTIES AND RESPONSIBILITIES: 
    
     Perform LAL testing for different studies as assigned encompassing a full range of LAL techniques, gel-clot, kinetic and PTS. 
     Perform IQ, OQ, PQ of lab equipment such as Biotek, PTS and maintain appropriate documents. 
     Perform contract testing laboratories for Celsis and LAL including method development studies, method validation studies, accessory release, CSE/RSE, LAL water etc as required. 
     Perform laboratory activities necessary to isolate, grow and maintain cultures of bacteria. 
     Perform and manage bioburden testing, membrane filtration and, cleaning validations. 
     Ensure adherence to pertinent regulatory requirements (cGMP, FDA, ISO) and to departmental policies, practices and procedures [SOPs, safety procedures and biosafety protocols]. 
     Collaborate with inventory check of laboratory consumables and assist with general housekeeping of the laboratory, performing equipment maintenance and scheduling instrument calibrations. 
     Assist management with development and revision of departmental standard operating procedures and qualification documents. 
     Perform all other related duties as assigned. 
    
    QUALIFICATIONS: 
    
     Education: Degree in Microbiology, Biology or a related discipline. 
     Experience: 2+ years related experience in a microbiology laboratory setting. Experience in cGMP pharmaceutical microbiology environment is preferred. 
     Other: Knowledge of windows based programs such as word and excel and a minimum knowledge of algebra. 
    
    PHYSICAL DEMANDS: 
    
     Requires colour vision, close vision and the ability to adjust focus. 
     Regularly works in a stationary position; occasionally moves about the lab/office to access supplies and equipment. 
     Regularly communicates with other employees/customers and must be able to exchange accurate information verbally and in written form. 
     Occasionally operates a computer. 
     Occasionally must perform manual handling. 
     Must be able to wear personal protective equipment (PPE) according to company standards. 
    
    WORK ENVIRONMENT: 
    
     Working in a lab environment. May work with sharp objects, near toxic or caustic chemicals, with biohazards, may be exposed to fumes or airborne particles, unpleasant odors and may be exposed to the risk of radiation. 
     The noise level in the work environment is usually quiet to moderate. 
     While performing the duties of this job, the employee regularly wears protective clothing and equipment (lab coat and safety glasses) when exposed to the laboratory area 
    
   
  
  
   
    
     Job Qualifications
     
   
  
 
 
 IMPORTANT: A resume is required to be considered for this position. If you have not uploaded your resume in your candidate profile, please return to upload field and attach your resume/CV.
  
 About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.
  
   About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
  
 With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
  
 At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
  
 Equal Employment Opportunity Charles River Laboratories is an Equal Opportunity Employer – all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status. 
 If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
  
   For more information, please visit www.criver.com.


Microbiologist - Charles River Laboratories

Microbiologist

You need strong client-facing skills, project management experience, and a background in life sciences or related fields to ensure smooth implementation of services and solutions.

You will manage client onboarding, coordinate project activities, ensure timely implementation, provide support, and facilitate communication between teams and clients for successful project delivery.

<ul>
 <div>
  Req ID #: 223670
 </div> 
 <div>
  Dublin, Leinster, IE;
 </div> 
 <div>
  Cambridge, England, GB 
 </div>
 <div>
  Full time
 </div>
</ul> 
<br>
<div>
 <p>For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.</p> 
 <div>
  <div>
   <div>
    <div>
     <b>Job Summary</b>
    </div> 
   </div>
   <div>
    <p>Responsible for Customer onboarding by managing installation, training, onboarding programs and early-stage support for new customers and for facilitating a smooth transition to the Customer Care Organization. Monitor sales targets quarterly to ensure full and continued utilization of the instrument. in a designated geographical region. In addition, responsible for providing technical guidance in support of the Account Management and Global Account teams</p> 
   </div>
  </div>
  <div>
   <div>
    <div>
     <b>Job Qualifications</b>
    </div> 
   </div>
   <div>
    <p><b>ESSENTIAL DUTIES AND RESPONSIBILITIES:</b></p>
    <br> 
    <ul>
     <li>Drive the onboarding of new customers by installation, training, and on-site validation/application support</li> 
     <li>Build relationship with customer to support their onboarding program, communicate available products and services which contributes to successful product implementation as well as customer satisfaction.</li> 
     <li>Provide technical leadership in training and support in assigned territory reviewing customer data and validation plans.</li> 
     <li>Monitor reagent/consumable consumption on a quarterly bases to insure full and continued utilization of the instrument.</li> 
     <li>Assist in sales program in assigned territory applying technical/scientific skills to develop existing accounts and compete for customers.</li> 
     <li>Assist Account Management with presenting global capabilities, qualifying leads, demonstrating added value, and closing new business opportunities by providing scientific/product support during sponsor teleconference calls, demo, field visits and at scientific trade shows.</li> 
     <li>Assist Global Sales team in providing Customer Data and recommendations (Installed product, product performance as well as consumable consumption) for annual customer care reports</li> 
     <li>Facilitate smooth transition to Customer Care organization after full implementation, confirm service &amp; support tools are available to ensure continued Customer Satisfaction</li> 
     <li>Work closely with Customer Care organization and provide on-site support to troubleshoot customer issues related to instrumentation, application, reagents, and software if required.</li> 
     <li>Establish regular interface and communication with the Account Management and Global Commercial organization to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients.</li> 
     <li>As required, give overview of assigned product line and services to internal and external contacts. Identify new product and service opportunities with customers and share opportunities to appropriate product management.</li> 
     <li>Communicate Business Unit product and services updates to Sales Management team in a timely manner.</li> 
     <li>Share customer feedback/ suggestion for product / workflow improvements</li> 
     <li>Work with Manager to prepare and execute a comprehensive plan for implementation management for new customers, monitor potential opportunities at new accounts and expansion of existing accounts and an analysis of competitor accounts.</li> 
     <li>Utilize CRM to capture customer information.</li> 
     <li>Participate in sales meetings as required.</li> 
     <li>Complete all required sales documentation in a timely manner.</li> 
     <li>Perform all other related duties as assigned.</li> 
    </ul>
    <p><b>QUALIFICATIONS:</b></p> 
    <ul>
     <li>Education: Bachelor’s degree (B.A. /B.S.) or equivalent in related scientific discipline. Experience: Minimum 1-3 years of relevant industry experience using microbiological test methods</li> 
     <li>An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.</li> 
     <li>Certification/Licensure: Valid driver’s license required.</li> 
     <li>Other: Must possess excellent communication and presentation skills. Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail).</li> 
     <li>Proficient in English</li> 
    </ul>
   </div>
  </div>
 </div>
 <p><b>About Microbial Solutions</b><br> Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.</p> 
 <p><b>About Charles River</b><br> Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.</p> 
 <p>With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.</p> 
 <p>At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.</p> 
 <p>At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.</p>
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  Req ID #: 223670
  
 
  Dublin, Leinster, IE;
  
 
  Cambridge, England, GB 
 
 
  Full time
 
 


 For nearly 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about. 
 
  
   
    
     Job Summary
     
   
   
    Responsible for Customer onboarding by managing installation, training, onboarding programs and early-stage support for new customers and for facilitating a smooth transition to the Customer Care Organization. Monitor sales targets quarterly to ensure full and continued utilization of the instrument. in a designated geographical region. In addition, responsible for providing technical guidance in support of the Account Management and Global Account teams 
   
  
  
   
    
     Job Qualifications
     
   
   
    ESSENTIAL DUTIES AND RESPONSIBILITIES:
     
    
     Drive the onboarding of new customers by installation, training, and on-site validation/application support 
     Build relationship with customer to support their onboarding program, communicate available products and services which contributes to successful product implementation as well as customer satisfaction. 
     Provide technical leadership in training and support in assigned territory reviewing customer data and validation plans. 
     Monitor reagent/consumable consumption on a quarterly bases to insure full and continued utilization of the instrument. 
     Assist in sales program in assigned territory applying technical/scientific skills to develop existing accounts and compete for customers. 
     Assist Account Management with presenting global capabilities, qualifying leads, demonstrating added value, and closing new business opportunities by providing scientific/product support during sponsor teleconference calls, demo, field visits and at scientific trade shows. 
     Assist Global Sales team in providing Customer Data and recommendations (Installed product, product performance as well as consumable consumption) for annual customer care reports 
     Facilitate smooth transition to Customer Care organization after full implementation, confirm service & support tools are available to ensure continued Customer Satisfaction 
     Work closely with Customer Care organization and provide on-site support to troubleshoot customer issues related to instrumentation, application, reagents, and software if required. 
     Establish regular interface and communication with the Account Management and Global Commercial organization to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients. 
     As required, give overview of assigned product line and services to internal and external contacts. Identify new product and service opportunities with customers and share opportunities to appropriate product management. 
     Communicate Business Unit product and services updates to Sales Management team in a timely manner. 
     Share customer feedback/ suggestion for product / workflow improvements 
     Work with Manager to prepare and execute a comprehensive plan for implementation management for new customers, monitor potential opportunities at new accounts and expansion of existing accounts and an analysis of competitor accounts. 
     Utilize CRM to capture customer information. 
     Participate in sales meetings as required. 
     Complete all required sales documentation in a timely manner. 
     Perform all other related duties as assigned. 
    
    QUALIFICATIONS: 
    
     Education: Bachelor’s degree (B.A. /B.S.) or equivalent in related scientific discipline. Experience: Minimum 1-3 years of relevant industry experience using microbiological test methods 
     An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. 
     Certification/Licensure: Valid driver’s license required. 
     Other: Must possess excellent communication and presentation skills. Proficient in the use of standard office computer applications (word processing, spreadsheets, presentations, e-mail). 
     Proficient in English 
    
   
  
 
 About Microbial Solutions Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies. 
 About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. 
 With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. 
 At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021. 
 At Charles River Laboratories, we recognize and recruit all talent. We are a company committed to the principle of diversity and inclusion and work daily in this direction.


Charles River Laboratories

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