r&d chemist

UPL Ltd

<div></div><div><div><div><div><div><div><h1 class="jobSectionHeader"><b>Associate Formulation Chemist
</b></h1></div></div></div></div><div></div><div><div><div><div>Job Id: 12924
</div></div></div></div><div><div><div><div>City:
RTP, NC, North Carolina, United States
</div></div></div></div><div><div><div><div>Department: Internal Lab
</div></div></div></div><div><div><div><div>Function: R&amp;D Chemistry
</div></div></div></div><div><div><div><div>Employee Type: Permanent Full Time
</div></div></div></div><div><div><div><div>Seniority Level: Associate
</div></div></div></div><p></p><div><div>
</div></div></div><div></div><div><div><div><div><div>Description:
<div><b>about upl: </b><i>UPL (NSE: UPL &amp; BSE: 512070, LSE: UPLL) is focused on emerging as a premier global provider of total crop solutions designed to secure the world&rsquo;s long-term food supply. Winning farmers hearts across the globe, while leading the way with innovative products and services that make agriculture sustainable, UPL is the fastest growing company in the industry. Our successes in the field add up to powerful financials. UPL delivers results from protecting crops that translate into attractive investor value. Based on the recognition that humankind is one community, UPL&rsquo;s overarching commitment is to improve areas of its presence, workplace and customer engagement</i><b><i>. </i></b>please visit <i>upl-ltd.com</i> and follow us on <i>LinkedIn</i>, <i>Twitter</i>, <i>Instagram</i> and <i>Facebook</i>.</div><br>
<div></div>
<div><b><i>
Our purpose</i></b><i> is</i><b> &lsquo;</b><b>OpenAg&rsquo;. </b><i>An agriculture network that feeds sustainable growth for all. </i><b><i>No limits, no borders</i></b><i>.</i></div><br>
<div></div>
<div><b>
(EOE) Equal opportunity employer statement:</b></div>
<div>
UPL provides equal employment opportunities (EEO) to all employees and applicants irrespective of their race, colour, religion, gender, marital status, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. In addition to federal law requirements, in every location in which the company has facilities, UPL complies with applicable state and local laws governing non-discrimination in employment. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. UPL also reinforces EEO through its Corporate Business Principles and Code of Business Conduct.</div><p><b>
JOB SUMMARY</b><b>:
</b></p><p>The role of the Formulation Chemist will be to develop and test formulations in support of UPL&rsquo;s portfolio and new products, develop, test and compare formulations for new AI additions to portfolio, improve current formulations, find innovative and novel ways to add value, evaluate new AI&rsquo;s and/or raw materials in existing formulations, manufacture samples for product chemistry, efficacy studies and field evaluation as needed and understand and implement federal and global mandated formulations changes.</p>
<p><b>
JOB RESPONSIBILITES:</b></p>
<ul>
<li>Formulation Development (60%) including but not limited to
<ul><li>New formulation development &ndash; Planning and Execution of Experiment</li>
<li>Formulation improvement and evaluation</li>
<li>Reverse engineer competitor products</li>
<li>Act as lead on stability, efficacy and trials associated with formulations</li>
<li>Maintain records as required</li>
<li>Basic Knowledge of Analytical Testing &ndash; GC, HPLC, pH Meter, Densitometer, Rheology meter and etc</li>
<li>Documentation and / or Journal Writing</li>
<li>Basic Knowledge of MSDS</li>
<li>Basic Knowledge of Lab Safety and PPE use</li>
</ul></li><li>Manufacture sample formulations for product chemistry, efficacy studies and sample program as needed (20%).</li>
<li>Schedule and assist with stability studies to support formulations (10%)</li>
<li>Author formula cards including Darwin formulas, particularly formulation processes, product specifications and technology transfers (10%).</li>
</ul>
<p><b>REQUIRED EDUCATION AND EXPERIENCE:</b><b>
</b></p><ul><li>Bachelor&rsquo;s degree in chemistry or science and minimum 2 years&rsquo; formulation lab experience.</li>
<li>Must have a working knowledge of industry manufacturing techniques and capabilities and work with the manufacturing group to optimize the manufacturing process for new formulations.</li>
<li>Good computer skills, proficient in Microsoft office.</li>
</ul>
<p><b>PREFERRED EDUCATION AND EXPERIENCE:</b></p>
<ul>
<li>Master&rsquo;s degree in chemistry or science or PhD</li>
<li>Experience with formulation equipment and general analytical equipment in developing Ag formulations with a knowledge of pesticide formulations and EPA/PMRA/REACH requirements.</li>
<li>Experience working in a fast-paced laboratory environment working in a collaborative team environment with other disciplines and global units.</li></ul><br>
<p></p>
<p><b>We are one team, for maximum impact. One team with shared goals. We all play for the team and no one plays against the team. We have a laser-like focus on what our customers need and want, on anticipating their future needs and on how we can create innovative solutions and experiences for them.</b></p>
<p><b>#UPLJobs</b></p></div></div></div></div></div></div><p></p>

Associate Formulation Chemist

Sika

<div>
 <p>
  Leadership that prioritizes a people-first culture makes a company a great place to work. Employees feel valued, appreciated, and connected, which fosters trust, respect, and open communication. Sika achieve higher employee engagement, attract top talent, and minimize unwanted turnover, contributing to better business success.
  <br/>
  <br/>
  <br/>
  <br/>
 </p>
 <strong>
  Job Description
  <br/>
  <br/>
 </strong>
 <ol>
  <li>
   <strong>
    <u>
     J
    </u>
   </strong>
   <strong>
    <u>
     OB P
    </u>
   </strong>
   <strong>
    <u>
     URPOSE
    </u>
   </strong>
  </li>
 </ol>
 <p>
  Responsible in R&amp;D Department to develop new formulations of epoxy products, cementitious products and PU products.
  <br/>
  <br/>
 </p>
 <p>
  Responsible for defining QC specification for epoxy products, epoxy raw materials, cementitious raw material and cementitious products.
  <br/>
  <br/>
 </p>
 <p>
  Responsible for product modification (based of PMP request) of cementitious, Epoxy and PU products.
  <br/>
  <br/>
 </p>
 <p>
  Responsible for Lab instrument calibration and maintenance.
  <br/>
  <br/>
 </p>
 <ol>
  <li>
   <strong>
    <u>
     E
    </u>
   </strong>
   <strong>
    <u>
     SSENTIAL D
    </u>
   </strong>
   <strong>
    <u>
     UTIES &amp; R
    </u>
   </strong>
   <strong>
    <u>
     ESPONSIBILITIES
    </u>
   </strong>
  </li>
 </ol>
 <p>
  Include the following, while other duties may be assigned thereafter:
  <br/>
  <br/>
 </p>
 <ul>
  <li>
   <ul>
    <li>
     Designing and Carrying out various trails in cementitious, epoxy and PU products
    </li>
    <li>
     Sourcing out new raw materials for cementitious, epoxy and PU products
    </li>
    <li>
     Various cost reduction exercises includes introduction of cheap new raw materials, streamlining the product process co-coordinating with production team
    </li>
    <li>
     Batch correction suggestions
    </li>
    <li>
     Training Lab technicians and Chemists
    </li>
    <li>
     Q.C and R&amp;D records monitoring
    </li>
    <li>
     Adheres to policies regarding confidential information
    </li>
    <li>
     Liaison with production, technical service on day to day basis.
    </li>
   </ul>
  </li>
  <li>
   <ul>
    <li>
     Supporting the lab manager with other tasks that may be delegated.
     <br/>
     <br/>
    </li>
   </ul>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ol>
  <li>
   <ol>
    <li>
     <u>
      <u>
       Educational Credentials
      </u>
     </u>
     <ul>
      <li>
       Major degree in chemistry or related fields.
      </li>
     </ul>
    </li>
   </ol>
  </li>
 </ol>
 <ul>
  <li>
   <ol>
    <li>
     <u>
      <u>
       Work Experience
      </u>
     </u>
    </li>
   </ol>
  </li>
  <li>
   2 years experience in construction chemicals in R&amp;D department.
   <ol>
    <li>
     <u>
      <u>
       Language Skills
      </u>
     </u>
    </li>
   </ol>
  </li>
  <li>
   Fluent in English language (both read, write and speak)
  </li>
  <li>
   Fluent in Arabic if possible.
   <ol>
    <li>
     <u>
      <u>
       Computer Skills
      </u>
     </u>
    </li>
   </ol>
  </li>
  <li>
   Fully conversant with computer operations and having good knowledge on softwares
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Additional Information
  <br/>
  <br/>
 </strong>
 <p>
  Skills:
  <br/>
  <br/>
 </p>
 <ul>
  <li>
   Self-motivated
  </li>
  <li>
   Knowledge in Facade and curtain wall market
  </li>
  <li>
   Problem solving abilities
  </li>
  <li>
   Excellent communication in Arabic and English
  </li>
  <li>
   Teamwork and team building
  </li>
  <li>
   Interpersonal skills
  </li>
  <li>
   Strong negotiations skills
  </li>
  <li>
   Working under pressure
  </li>
 </ul>
 <p>
  We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training.  We are committed to fair and equitable pay practices in accordance with applicable laws and regulations.
  <br/>
  <br/>
 </p>
</div>


Chemist

Sika Corporation

<div><p>About the Role</p>
<div><div><div><b>J</b><b>OB P</b><b>URPOSE</b></div></div><div>
Responsible in R&amp;D Department to develop new formulations of epoxy products, cementitious products and PU products.</div><div>
Responsible for defining QC specification for epoxy products, epoxy raw materials, cementitious raw material and cementitious products.</div><div>
Responsible for product modification (based of PMP request) of cementitious, Epoxy and PU products.</div><div>
Responsible for Lab instrument calibration and maintenance.</div><div><div><b>
E</b><b>SSENTIAL D</b><b>UTIES &amp; R</b><b>ESPONSIBILITIES</b></div></div><div>
Include the following, while other duties may be assigned thereafter:</div><ul><li><ul><li>
Designing and Carrying out various trails in cementitious, epoxy and PU products</li><li>
Sourcing out new raw materials for cementitious, epoxy and PU products</li><li>
Various cost reduction exercises includes introduction of cheap new raw materials, streamlining the product process co-coordinating with production team</li><li>
Batch correction suggestions</li><li>
Training Lab technicians and Chemists</li><li>
Q.C and R&amp;D records monitoring</li><li>
Adheres to policies regarding confidential information</li><li>
Liaison with production, technical service on day to day basis.</li></ul></li><li><ul><li>
Supporting the lab manager with other tasks that may be delegated.</li></ul></li></ul></div>
<p>Your Skills and Experience</p>
<div><div><div><div><div>Educational Credentials<ul><li>
Major degree in chemistry or related fields.</li></ul></div></div></div></div><ul><li><ul><li>
Work Experience</li></ul></li><li>
2 years experience in construction chemicals in R&amp;D department.<ul><li>
Language Skills</li></ul></li><li>
Fluent in English language (both read, write and speak)</li><li>
Fluent in Arabic if possible.<ul><li>
Computer Skills</li></ul></li><li>
Fully conversant with computer operations and having good knowledge on softwares</li></ul></div>
<p>Why Join Us</p>
<div></div><div><div>Skills:</div><ul><li>
Self-motivated</li><li>
Knowledge in Facade and curtain wall market</li><li>
Problem solving abilities</li><li>
Excellent communication in Arabic and English</li><li>
Teamwork and team building</li><li>
Interpersonal skills</li><li>
Strong negotiations skills</li><li>
Working under pressure</li></ul><p></p><div>
We offer competitive salaries, aligned with local market benchmarks and the specific scope and responsibilities of each role. Compensation is determined based skills relevant to the position, education and/or training. We are committed to fair and equitable pay practices in accordance with applicable laws and regulations.</div></div>
<p>About Sika</p>
<div><div>Leadership that prioritizes a people-first culture makes a company a great place to work. Employees feel valued, appreciated, and connected, which fosters trust, respect, and open communication. Sika achieve higher employee engagement, attract top talent, and minimize unwanted turnover, contributing to better business success.</div></div></div>

PepsiCo

<div>
 <strong>
  Overview
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   There is an internal slated candidate being considered for this position. However, all qualified candidates are encouraged to apply.
   <br/>
   <br/>
  </li>
 </ul>
 The role will lead the technical aspects and implementation of medium to high complexity R&amp;D enabled productivity and sustainability projects for the Grains Platform
 <br/>
 <br/>
 <strong>
  Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Leverage expertise inside and outside of the organization to deliver product and process development and innovation.
  </li>
  <li>
   Develop, plan, conduct, and coordinate product development initiatives to use experimental design and data interpretation tools to make technically sound recommendations to business.
  </li>
  <li>
   Engage with Middle East Foods Business Unit Global Procurement &amp; Supply Chain to support and manage technical aspects of productivity agendas of Grains Portfolio
  </li>
  <li>
   Develop product against consumer and business KPIs by leveraging available resources including R&amp;D Laboratory tools, bench top, factory equipment, pilot plants, supplier&rsquo;s technical assets.
  </li>
  <li>
   Coordinate samples requirements with manufacturing plants, global R&amp;D function etc. for NPD, internal screening, bench taste, sensory test, consumer test, shelf life stability, sales samples, scale-up trials, and other needs.
  </li>
  <li>
   Develop &amp; review FC, business P&amp;L and finalize product and ingredient specifications with PQP guardrails.
  </li>
  <li>
   Develop an understanding and demonstrate the application of consumer product testing; sensory and analytical etc. to deliver superior products to the market and establish product intelligence. Actively participate in marketing research programs including focus groups and other consumer research formats.
  </li>
  <li>
   Lead Technical Stage Gate and related work for his/her project and ensure timely completion of all TSG stages and its deliverables.
  </li>
  <li>
   Develop project briefs/Global Innovation Briefs (GIB) and seek R&amp;D and other cross functional alignment (especially Marketing and Supply Chain).
  </li>
  <li>
   Lead exploration of new ingredients, formulation and process technologies and leverage expertise inside and outside the organization to deliver new product and process development.
  </li>
  <li>
   Represent R&amp;D on multi-functional business teams and Influence others through strong communication &amp; interpersonal skills.
  </li>
  <li>
   Develop project briefs/Global Innovation Briefs (GIB) and seek R&amp;D and other cross functional alignment (especially Marketing and Supply Chain).
  </li>
  <li>
   Lead exploration of new ingredients, formulation and process technologies and leverage expertise inside and outside the organization to deliver new product and process development.
  </li>
  <li>
   To plan, organize and run raw material qualification programs.
  </li>
  <li>
   Drive global knowledge growth and thought leadership in emerging process technologies and imbed cross functionally.
  </li>
  <li>
   Drive CAST implementation through leadership of training programs.
  </li>
  <li>
   Work closely with Regulatory to ensure legal compliance
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Graduation degree in Food Science /Engineering (Chemical/industrial) / Food &amp; Nutrition/Pharma
  </li>
  <li>
   Must have FMCG experience of &gt;3 years.
  </li>
  <li>
   Food Science or Engineering related discipline.
  </li>
  <li>
   Good understanding / appreciation of the broader business environment and application of technical and commercial knowledge during project execution.
  </li>
  <li>
   Excellent interpersonal skills with ability to communicate and negotiate effectively across all levels and all functions of the organisation.
  </li>
  <li>
   Good presentation skills (written &amp; verbal).
  </li>
  <li>
   Strong analytical skills &ndash; ability to interpret complex data and distil into useful and actionable information.
  </li>
  <li>
   Ability to explain complex technical issues / solutions to a non-technical audience.
  </li>
  <li>
   Strives for high standards, seeks innovative solutions, drives continuous improvement of products, processes or methods and demonstrates a high degree of intellectual curiosity.
  </li>
  <li>
   Passion for creativity and innovation within a commercially driven environment.
  </li>
  <li>
   Cultural sensitivity / flexibility in responding to diverse teams and environments.
  </li>
  <li>
   Self-starter and motivator.
  </li>
 </ul>
</div>


R&D Associate Scientist

Harvard Medical Faculty Physicians

<div><p><b>Clinical Chemist, Clinical Chemistry
</b></p><p>Department of Pathology</p><p>
Beth Israel Deaconess Medical Center</p><p>
Harvard Medical School, Boston</p><p></p><p>
The Department of Pathology at Beth Israel Deaconess Medical Center (BIDMC) is recruiting a full-time academic clinical chemist/clinical chemistry laboratory director. Recent fellowship graduates and mid-career/senior physicians are strongly encouraged to apply. The candidate will be appointed to the full-time faculty of Harvard Medical School at the appropriate academic rank (Instructor, Assistant Professor, Associate Professor), commensurate with experience.</p><p>
The successful candidate will share responsibility for clinical, academic, and administrative leadership of a comprehensive, high‑complexity clinical chemistry service, with an additional significant leadership role in Point of Care Testing (POCT).</p><p>
Experience in<b> clinical chemistry immunoassays, automated chemistry, and the broad applications of point of care instrumentation </b>is necessary. The successful candidate <b>will contribute to the management of a comprehensive and rapidly growing state-of-the-art laboratory</b> that supports active clinical programs in solid organ and bone marrow transplantation, oncology, cardiology and cardiovascular surgery, immunology, endocrinology, obstetrics and neonatology, and therapeutic drug monitoring and toxicology.</p><p>
This position is ideal for an academic clinical chemist whose primary identity and expertise is in central laboratory chemistry and who is interested in leading and advancing an institution‑wide POCT program as a natural extension of the clinical chemistry mission.</p><p>
Eligible candidates for this position must have an MD (with AP/CP or CP board certification, Clinical Chemistry fellowship training preferred) or PhD (with board certification in Clinical Chemistry).</p><p>
As a teaching hospital of Harvard Medical School, BIDMC and the Department of Pathology, provide a clinically advanced and supportive academic environment for residents, fellows, and faculty. We are also proud and excited to be an integral part of the landmark collaboration among Dana-Farber Cancer Institute (DFCI), Beth Israel Deaconess Medical Center (BIDMC), and Harvard Medical Faculty Physicians (HMFP) to establish New England&rsquo;s only freestanding adult inpatient cancer hospital. The collaboration will provide unparalleled opportunities for Pathology and other physician specialties to be part of DFCI&rsquo;s internationally recognized cancer team.</p><p><b>
Leadership Responsibilities</b></p><ul><li>
Shared oversight of <b>core clinical chemistry operations</b>, including automated chemistry, immunoassays, toxicology, mass spectrometry, and related advanced diagnostics</li><li>
Contribution to test development, validation, quality management, and diagnostic stewardship across the chemistry service line</li><li>
Medical directorship of the <b>Point of Care Testing program</b>, including:<ul><li>
Oversight of POCT test selection, validation, and implementation</li><li>
Regulatory and quality oversight in accordance with <b>CLIA, CAP, Joint Commission</b>, and institutional policies</li><li>
Collaboration with nursing, clinical services, informatics, and operational partners to ensure reliable, safe, and compliant POCT delivery</li></ul></li><li>
Participation in departmental and institutional leadership related to laboratory quality, patient safety, and system integration</li></ul><p></p><p><b>
Beth Israel Deaconess Medical Center</b>, a 743-bed hospital and Level 1 Trauma Center, is a founding member of Beth Israel Lahey Health (BILH). BILH, a health care system with 14 hospitals, brings together academic medical centers and teaching hospitals, community, and specialty hospitals, and more than 4,000 physicians and 39,000 employees in a shared mission to expand access and advance the science and practice of medicine through groundbreaking research and education.</p><p><b>
Harvard Medical Faculty Physicians</b> at Beth Israel Deaconess Medical Center (HMFP) is one of the largest physician organizations in New England, dedicated to excellence and innovation in patient care, education, and research. As a physician-led organization, HMFP partners with more than 2,400 providers to support the delivery of exceptional care, promote professional development, and foster balance at work and home. HMFP physicians have faculty affiliations with Harvard Medical School (HMS) and provide care throughout the BILH system and additional hospitals across Massachusetts.</p><p><b>
For further questions or confidential position inquiries, please contact Dr. Lynne Uhl, Vice Chair of Clinical Pathology at BIDMC: </b><b><i>luhl@bidmc.harvard.edu</i></b></p><p>
Please apply online at <i>www.hmfphysicians.org/careers</i> - Req. #R1593</p></div><p></p>

Clinical Chemist

Syndax Pharmaceuticals

<div><p><b>Syndax Pharmaceuticals is looking for a </b><b>Contractor, </b><b>R&amp;D Operations Associate</b></p>
<p>
At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.</p><br>
<p></p>
<p><b>
The Role:</b></p>
<p>
We are seeking an experienced, proactive, and detail-oriented Operations Associate to provide administrative, operational, and project support. This dynamic position blends high-level executive support with strong administrative coordination, particularly in contract and PO administration, stakeholder management, and cross-functional project execution.</p><br>
<p></p>
<p><b>
Key Responsibilities:</b></p>
<ul>
<li>Provide high-level calendar management, managing internal and external scheduling, prioritizing requests, and troubleshooting conflicts.</li>
<li>Coordinate complex travel arrangements, prepare itineraries, and handle logistics for meetings, conferences, and events.</li>
<li>Handle confidential communications and maintain sensitive records with discretion and accuracy.</li>
<li>Process expense reports and ensure timely submission of reimbursements.</li>
<li>Coordinate the preparation, routing, and execution of contracts, SOWs, consulting agreements, NDAs, and amendments in partnership with legal, finance, and procurement.</li>
<li>Track purchase orders (POs), monitor budget alignment, follow up on vendor invoicing, and ensure proper documentation and reporting.</li>
<li>Serve as a liaison between internal stakeholders and external vendors to facilitate timely execution and compliance with administrative workflows.</li>
<li>Support R&amp;D initiatives by scheduling and organizing meetings, tracking project deliverables, and helping with preparation of agendas, slide decks, and follow-ups.</li>
<li>Partner cross-functionally with departments such as R&amp;D, Regulatory, and Clinical to align timelines and operational dependencies.</li>
<li>Support onboarding of new team members and coordinate candidate interviews.</li>
<li>Seek opportunities to streamline and improve administrative processes, driving consistency and efficiency across R&amp;D operations.</li></ul><br>
<p></p>
<p><b>
Desired Experience/Education and Personal Attributes:</b></p>
<ul>
<li>Bachelor's degree preferred (or equivalent professional experience).</li>
<li>1-2 years of experience in executive support or administrative coordination, ideally in biotech, pharma, or healthcare.</li>
<li>Strong working knowledge of contracting and procurement workflows, including PO systems.</li>
<li>Proven project coordination or planning experience is a plus.</li>
<li>Highly organized with exceptional attention to detail and the ability to manage multiple tasks and deadlines.</li>
<li>Outstanding interpersonal and communication skills&mdash;professional, clear, and collaborative.</li>
<li>Proficient in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint), DocuSign, Concur, Zoom, MS Teams, and project tools like Smartsheet or Microsoft Project.</li>
<li>Able to work independently, exercise sound judgment, and handle confidential information with integrity.</li></ul><br>
<p></p>
<p><b>
Location</b>: Syndax's corporate office is in New York, NY.</p><br>
<p></p>
<p>
The anticipated hourly pay range for this role is $40.00&ndash;$50.00 per hour. Actual pay within this range will be determined based on factors such as relevant experience, skills and qualifications.</p><br>
<p></p>
<p><b>
About Syndax:</b><br>
Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company's pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn.</p><br>
<p></p>
<p><i>
Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.</i></p></div><p></p>

Contractor, R&D Operations Associate

<div><div><div><p><b>Entity:</b> CSL Behring</p>
<p><b>Job Category:</b> Information Technology</p>
<p><b>Job Family:</b> IT Multi Discipline</p>
<p><b>Job Type:</b> Full Time</p>
<p><b>Location</b><b>:</b> King of Prussia, Pennsylvania, United States</p>
<p><b>Employer Reference:</b> R-263434</p>
</div></div><div></div><h2 class="jobSectionHeader"><b>Job Description</b></h2>
<div><div><p>CSL's R&amp;D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we&rsquo;re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.</p><p></p><p>
Could you be our next Associate Director, AI &amp; Advanced Analytics? The job is in our King of Prussia, PA or Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report to the Head of MSPR.</p><p></p><p>
You will support the deployment and scaling of AI/ML models, digital agents, and automation solutions across R&amp;D. Contributes to technical delivery, stakeholder coordination, and responsible governance practices to enable innovation and efficiency.</p><p></p><p>
Responsibilities:<br>
Support development and deployment of AI models, automation scripts, and intelligent agents.<br>
Partner with R&amp;D teams and digital leads to identify and prototype use cases aligned to business needs.<br>
Contribute to MLOps processes, model documentation, and system validation workflows.<br>
Help drive platform integration, compliance tracking, and continuous improvement initiatives.<br>
Collaborate on internal capability building (e.g., hackathons, training) and end-user support.<br>
Track success metrics such as usage, performance, and value delivered.<br>
<br>
Qualifications:</p><p>
Bachelor&rsquo;s or Master&rsquo;s in Data Science, Computer Science, or a related field.<br>
10+ years of experience in AI/ML, analytics, or automation, preferably in R&amp;D or life sciences.<br>
Practical experience building or supporting machine learning pipelines or agent-based tools.<br>
Familiarity with MLOps tools, low-code automation platforms, or scripting languages (e.g., Python, R).<br>
Strong communication and project coordination skills.</p><p></p><p>
#LI-HYBRID</p></div>
</div><h2 class="jobSectionHeader"><b>About CSL Behring</b></h2>
<div><p>CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.</p>
<p>CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.</p>
<p>To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/.</p>
</div>
<h2 class="jobSectionHeader"><b>Our Benefits</b></h2>
<div><p>For more information on CSL benefits visit How CSL Supports Your Well-being | CSL.</p>
</div>
<h2 class="jobSectionHeader"><b>You Belong at CSL</b></h2>
<div><p>At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.</p>
<p>To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging</p>
</div>
<h2 class="jobSectionHeader"><b>Equal Opportunity Employer</b></h2>
<div><p>CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement.</p></div></div><p></p>

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