principal scientist

EPM Scientific

<div>
 
 
 Principal Scientist: Idaho
 
 
 
 
 Position Summary
 
 
 
 
 
 As the Principal Scientist for Skin, Sun &amp; Lip Care, you will serve as the internal subject-matter expert responsible for driving technical execution, advancing new technologies, and elevating product performance. You'll own formulations from concept through commercialization and play a key role in shaping the innovation pipeline.
 
 
 You'll collaborate closely with R&amp;D leadership, product development, regulatory, operations, and marketing teams to deliver high‑performing products that meet consumer expectations, regulatory standards, and business objectives.
 
 
 
 Key Responsibilities
 
 
 
 
 <ul>
 <li>
 Lead innovation by identifying new technologies, ingredients, and formulation opportunities across Skin, Sun, and Lip Care categories
 </li>
 <li>
 Develop and optimize formulations from concept through launch, ensuring efficacy, safety, stability, and sensory performance
 </li>
 <li>
 Design and oversee testing programs, including stability, performance, safety, and clinical evaluation to support claims
 </li>
 <li>
 Conduct competitive benchmarking and technology assessments to inform category strategy and innovation pipelines
 </li>
 <li>
 Partner with Regulatory, Legal, Quality, and Marketing to ensure claims substantiation and global compliance
 </li>
 <li>
 Collaborate cross‑functionally with R&amp;D, Operations, and Marketing to ensure seamless project execution
 </li>
 <li>
 Contribute to intellectual property strategy by supporting patent development and driving scientific excellence
 </li>
 <li>
 Stay up to date on scientific literature, raw material innovations, regulatory changes, and market trends
 </li>
 </ul>
 
 
 Qualifications
 
 
 
 
 <ul>
 <li>
 Bachelor's, Master's, or Ph.D. in Chemistry or related scientific field
 </li>
 <li>
 5+ years of experience in personal care, skincare, sun care, beauty, bath &amp; body, OTC, or similar FMCG categories
 </li>
 <li>
 Strong formulation chemistry expertise with experience in in vitro/in vivo/clinical testing
 </li>
 <li>
 Understanding of global cosmetic regulations, labeling compliance, and GMP/GLP practices
 </li>
 <li>
 Proven ability to develop new formulations, evaluate emerging technologies, and improve existing products
 </li>
 <li>
 Strong analytical skills, including experimental design, data interpretation, and scientific documentation
 </li>
 <li>
 Excellent written and verbal communication, with experience preparing technical reports and supporting IP activities
 </li>
 <li>
 Demonstrated collaboration and leadership capabilities, including mentoring or guiding scientific staff
 </li>
 <li>
 Ability to relocate to the Idaho region and work onsite five days per week
 </li>
 </ul>
</div>

Principal Scientist

<div>Job Description
We have a great opportunity for an Associate Principal Scientist to join our global team.
We aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We use the power of leading-edge science to save and improve lives around the world.
Join us in our mission to shape and facilitate the strategic plan and ongoing transformation of our CMC organization, part of Global Regulatory Affairs and Clinical Safety (GRACS).
What you will do:
Bring energy, knowledge, innovation, and leadership to carry out the following:<ul><li>
Lead, support or project manage the design and implementation of cross-regional or functional business strategies, process improvement initiatives, and operating model projects in collaboration with our strategic partners.</li><li>
Support communication on initiatives progress and implementation, keeping the organization informed and supporting associated change management activities.</li><li>
Coordinate and contribute to the delivery of the Regional CMC strategic plan, operating model transformation initiatives, and key priorities.</li><li>
Support the management of Regional CMC priorities, roadmap, scorecards, and dashboards.</li><li>
Digital transformation, including supporting Digital capabilities build in the Regional CMC team.</li><li>
Strengthen Regional CMC&rsquo;s partnerships with other GRACS and broader enterprise stakeholders across regions, including other GRACS functions, our research &amp; development division functions, and other divisions (HH: Sales, Marketing, our manufacturing division: Supply Chain, Quality).</li><li>
As required, develop CMC regional regulatory strategies for new marketing applications and post-approval changes.</li></ul>
In order to excel in this role, you will more than likely have:<ul><li>
Minimum of 5 years&rsquo; experience in regulatory affairs,</li><li>
2+ years&rsquo; experience in project and change management,</li><li>
Strong collaboration and communication skills.</li><li>
Ability to manage complex projects and initiatives with limited supervision.</li><li>
Strong digital skills and familiarity with digital tools and platforms is required</li><li>
Enterprise mindset with an ability to think strategically across the organization.</li><li>
Experience in managing cross-functional teams and working with strategic partners.</li><li>
Experience with CMC regional regulatory strategies is preferred though not essential</li></ul>
As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.
So, if you are ready to:
Invent solutions to meet unmet healthcare needs, please apply today.
Required Skills:
Accountability, Accountability, Adaptability, Biologics License Application (BLA), Business Strategies, Change Management, Collaborative Communications, Collaborative Development, Cross-Cultural Awareness, Detail-Oriented, Digital Transformation, Electronic Common Technical Document (eCTD), Employee Training Programs, International Regulatory Compliance, Mentorship, Pharmaceutical Process Development, Process Improvement Projects, Process Improvements, Project Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory CMC, Regulatory Strategy Development, Regulatory Submissions, Regulatory Writing {+ 4 more}
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
US and Puerto Rico Residents Only:
Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights
EEOC GINA Supplement
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another&rsquo;s thinking and approach problems collectively.
Learn more about your rights, including under California, Colorado and other US State Acts
U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as &ldquo;remote&rdquo;.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles&rsquo; Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully 
Merck &amp; Co., Inc., Rahway, NJ, USA, also known as Merck Sharp &amp; Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Hybrid
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
03/5/2026<ul><li>A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. 
</li></ul> 
Requisition ID:R385509</div>

Associate Principal Scientist

<div>Site Name: USA - Pennsylvania - Upper Providence 
Posted Date: Feb 23 2026 
Principal Scientist, MMoA Biochemist
At GSK, we are focused on developing breakthrough vaccines and medicines for infectious disease. The Vaccines and Infectious Disease Research Unit is leading the way by pioneering a portfolio of novel modalities to tackle the urgent global threat posed by infectious disease. This position offers an excellent opportunity to join our dedicated team, who have end‑to‑end expertise from early discovery through to commercial launch and to drive discovery and mechanism‑of‑action studies for viral, bacterial and fungal therapeutics.
Find out more: Our approach to R&amp;D
The Principal Scientist will design and execute cutting-edge biochemistry research to define mechanisms of action, collaborate with cross‑functional partners (biology, chemistry, pharmacology, clinical, regulatory, IP), and advance projects from early discovery through preclinical development into filing and launch. The role requires keeping pace with scientific advances and integrating new methods to accelerate discovery and support GSK&rsquo;s mission of improving global health through the development of transformative medicines.
Key Responsibilities:<ul><li>
Lead the strategic design and execution of biochemical experiments, demonstrating thought leadership to define the biochemical mechanism of action of novel therapeutic agents.</li><li>
Execute experimental plans by performing internal experiments and/or managing research studies with external partners to drive scientific progress.</li><li>
Establish and optimize biochemical and biophysical assays to measure biochemical processes, protein binding and kinetics including data collection, statistical analysis, and interpretation of experimental results.</li><li>
Design and generate data packages with structural biology and imaging studies such as cryo-EM in collaboration with cross-functional teams, generate data packages that enable project decisions.</li><li>
Lead communication of scientific findings through written reports, presentations, and publications.</li><li>
Author Regulatory Study Reports and manuscripts in peer-reviewed journals; contribute to IP patent filing and regulatory documents preparation.</li><li>
Maintain expert level knowledge of the latest scientific literature and methodologies, contributing to continual innovation and improvement in research practices.</li><li>
Ensure compliance with regulatory requirements, ethical guidelines, and GSK standards for data integrity, safety, and quality.</li></ul>
Basic Qualifications:<ul><li>
BS with 8 or more years of relevant experience, MS with 6 or more years of relevant experience or a PhD with 3 or more years of relevant experience with the degree in Biochemistry or another relevant major.</li><li>
Three or more years of experience performing a range of biochemical techniques, such as SPR, binding kinetics, DLS, mutagenesis, structural biology and imaging, and other biochemical and biophysical assays.</li><li>
Three or more years performing data analysis and interpretation, utilizing statistical methods and scientific software (e.g., GraphPad Prism, Excel).</li></ul>
Preferred Qualifications:<ul><li>
Ability to demonstrate high attention to detail and ensure accuracy of scientific results and documentation in compliance with GSK data integrity standards.</li><li>
Excellent communication and teamwork skills, with the ability to work both independently and collaboratively in a team environment.</li><li>
Strong problem-solving and analytical skills.</li><li>
Self-motivated and able to resolve technical challenges and deliver consistent results efficiently in a timely manner.</li></ul>
#Li-GSK
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at HR.AmericasSC-CS@gsk.com where you can also request a call.
Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK&rsquo;s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/</div>

Principal Scientist, MMoA Biochemist

<div>Site Name: USA - Pennsylvania - Upper Providence 
Posted Date: Feb 23 2026 
Principal Scientist, MMoA Microbiologist
At GSK, we are focused on developing breakthrough vaccines and medicines for infectious disease. The Vaccines and Infectious Disease Research Unit is leading the way by pioneering a portfolio of novel modalities to tackle the urgent global threat posed by antimicrobial resistance (AMR). This position offers an excellent opportunity to join our dedicated team, who have end‑to‑end expertise from early discovery through to commercial launch and to drive discovery and mechanism‑of‑action studies for viral, bacterial and fungal therapeutics.
Find out more: 
Our approach to R&amp;D
The Principal Scientist will design and execute cutting-edge microbiological research to define mechanisms of action, collaborate with cross‑functional partners (biology, chemistry, pharmacology, clinical, regulatory, IP), and advance projects from early discovery through preclinical development into filing and launch. The role requires keeping pace with scientific advances and integrating new methods to accelerate discovery and support GSK&rsquo;s mission of improving global health through the development of transformative medicines.
Key Responsibilities:
<ul><li>Lead the strategic design and execution of microbiological experiments, demonstrating thought leadership to define the mechanism of action and microbiological inhibitory spectrum of novel therapeutic agents.</li><li>
Execute experimental plans by performing internal experiments and/or managing research studies with external partners to drive scientific progress.</li><li>
Establish and optimize bacterial assays including MIC, MBC, time-kill, resistance studies, and inhibitor characterization.</li><li>
Design and generate data packages in collaboration with cross-functional teams to enable project decisions.</li><li>
Lead communication of scientific findings through written reports, presentations, and publications.</li><li>
Author Regulatory Study Reports and manuscripts in peer-reviewed journals; contribute to IP patent filing and regulatory documents preparation.</li><li>
Maintain expert level knowledge of the latest scientific literature and methodologies, contributing to continual innovation and improvement in research practices.</li><li>
Ensure compliance with regulatory requirements, ethical guidelines, and GSK standards for data integrity, safety, and quality.</li></ul>
Basic Qualifications:
<ul><li>BS with 8 or more years of relevant experience, MS with 6 or more years of relevant experience, or a PhD with 3 or more years of relevant experience with the degree in Molecular Biology or another relevant major.</li><li>
Three or more years of experience performing a range of microbiological techniques, gene expression analysis, mutagenesis, cellular imaging, qPCR, ELISA, and RNA/ DNA transfection.</li><li>
Three or more years of experience in handling infectious bacterial samples and primary human cell samples in compliance with safety and HBSM standards.</li><li>
Three or more years of experience in data analysis and interpretation, utilizing statistical methods and scientific software (e.g., GraphPad Prism, Excel).</li></ul>
Preferred Qualifications:
<ul><li>Ability to demonstrate high attention to detail and ensure accuracy of scientific results and documentation in compliance with GSK data integrity standards.</li><li>
Excellent communication and teamwork skills, with the ability to work both independently and collaboratively in a team environment.</li><li>
Strong problem-solving and analytical skills.</li><li>
Self-motivated and able to resolve technical challenges and deliver consistent results efficiently in a timely manner.</li></ul>
#LI-GSK
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at HR.AmericasSC-CS@gsk.com where you can also request a call.
Please note should your inquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK&rsquo;s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/</div>

Principal Scientist, MMOA Microbiologist

Alignerr

<div>
 
 About The Job
 
 
 
 At Alignerr, we partner with the world&rsquo;s leading AI research teams and labs to build and train cutting-edge AI models.
 
 
 We are seeking a Principal Clinical Scientist to bring senior-level expertise in clinical trial design and regulatory-grade data interpretation into AI-driven research workflows. In this role, you will help ensure that clinical data used to train and evaluate advanced AI systems meets the rigor, structure, and regulatory standards expected in real-world submissions.
 
 
 
 Organization
 
 : Alignerr
 
 Position
 
 : Principal Clinical Scientist
 
 Type
 
 : Hourly Contract
 
 Compensation
 
 : $40&ndash;$80 /hour
 
 Location
 
 : Remote
 
 Commitment
 
 : 10&ndash;40 hours/week
 
 
 
 What You&rsquo;ll Do
 
 
 
 <ul>
 <li>
 Design and review clinical trial protocols used to generate high-quality, regulator-ready datasets.
 </li>
 <li>
 Interpret and audit clinical trial results to ensure accuracy, consistency, and regulatory relevance.
 </li>
 <li>
 Evaluate AI-generated clinical analyses for scientific soundness and alignment with regulatory expectations.
 </li>
 <li>
 Provide expert feedback to improve how AI models reason about clinical trial data and outcomes.
 
 
 </li>
 </ul>
 
 What We&rsquo;re Looking For
 
 
 
 <ul>
 <li>
 Senior-level experience designing clinical trial protocols for regulatory submission.
 </li>
 <li>
 Deep expertise interpreting clinical data for agencies such as FDA, EMA, or equivalent.
 </li>
 <li>
 Strong background in clinical research methodology, biostatistics, or translational science.
 
 
 </li>
 </ul>
 
 Preferred
 
 
 
 <ul>
 <li>
 Prior experience with data annotation, data quality, or evaluation systems
 
 
 </li>
 </ul>
 
 Why Join Us
 
 
 
 <ul>
 <li>
 Competitive pay and flexible remote work.
 </li>
 <li>
 Work directly on frontier AI systems impacting clinical and biomedical research.
 </li>
 <li>
 Influence how AI understands and evaluates real-world clinical evidence.
 </li>
 <li>
 Freelance perks: autonomy, flexibility, and global collaboration.
 </li>
 <li>
 Potential for contract extension.
 
 
 </li>
 </ul>
 
 Application Process (Takes 15&ndash;20 min)
 
 
 
 <ul>
 <li>
 Submit your resume
 </li>
 <li>
 Complete a short screening
 </li>
 <li>
 Project matching and onboarding
 
 
 </li>
 </ul>
 
 PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.
 
</div>

Principal Clinical Scientist

SnapFind

<ul><li>Candidate must have 7+ years of experience in ML, Generative AI, NLP, ASR, and LLMs (preferably healthcare).</li><li>Candidate must have strong Python skills with hands-on experience in PyTorch/TensorFlow and transformer model fine-tuning.</li><li>Candidate must have experience deploying scalable AI solutions on AWS/Azure/GCP with MLOps, Docker, and Kubernetes.</li><li>Candidate must have hands-on experience with LangChain, OpenAI APIs, vector databases, and RAG architectures.</li><li>Candidate must have experience integrating AI with EHR/EMR systems, ensuring HIPAA/HL7/FHIR compliance, and leading AI initiatives.</li></ul>Job DescriptionPrincipal Data Scientist(Healthcare AI | ASR | LLM | NLP | Cloud | Agentic AI)healthcare support services company specializing in:<ul><li>Remote Live Medical Scribing</li><li>AI-Based Medical Scribing</li><li>Medical Coding</li><li>Medical Billing</li><li>Virtual Medical Office Solutions (VMOS)</li></ul>With a strong presence across India through our offices in Bengaluru, Coimbatore, and Mohali, we serve a wide range of healthcare providers in the United States.Job Details<ul><li>Designation: Principal Data Scientist (Healthcare AI, ASR, LLM, NLP, Cloud, Agentic AI)</li><li>Location: Hebbal Ring Road, Bengaluru</li><li>Work Mode: Work from Office</li><li>Shift: Day Shift</li><li>Reporting To: SVP</li><li>Compensation: Best in the industry (for suitable candidates)</li></ul>Educational Qualifications<ul><li>Ph.D. or Master&rsquo;s degree in Computer Science, Artificial Intelligence, Machine Learning, or a related field</li><li>Technical certifications in AI/ML, NLP, or Cloud Computing are an added advantage</li></ul>Experience Required<ul><li>7+ years of experience solving real-world problems using:</li><li>Natural Language Processing (NLP)</li><li>Automatic Speech Recognition (ASR)</li><li>Large Language Models (LLMs)</li><li>Machine Learning (ML)</li><li>Preferably within the healthcare domain</li><li>Experience in Agentic AI, cloud deployments, and fine-tuning transformer-based models is highly desirable</li></ul>Role OverviewWe are building a suite of AI-powered, state-of-the-art web and mobile solutions designed to:<ul><li>Reduce administrative burden in EMR data entry</li><li>Improve provider satisfaction and productivity</li><li>Enhance quality of care and patient outcomes</li></ul>Our solutions combine cutting-edge AI technologies with live scribing services to streamline clinical workflows and strengthen clinical decision-making.The Principal Data Scientist will lead the design, development, and deployment of cognitive AI solutions, including advanced speech and text analytics for healthcare applications. The role demands deep expertise in generative AI, classical ML, deep learning, cloud deployments, and agentic AI frameworks.Key ResponsibilitiesAI Strategy &amp; Solution Development<ul><li>Define and develop AI-driven solutions for speech recognition, text processing, and conversational AI</li><li>Research and implement transformer-based models (Whisper, LLaMA, GPT, T5, BERT, etc.) for speech-to-text, medical summarization, and clinical documentation</li><li>Develop and integrate Agentic AI frameworks enabling multi-agent collaboration</li><li>Design scalable, reusable, and production-ready AI frameworks for speech and text analytics</li></ul>Model Development &amp; Optimization<ul><li>Fine-tune, train, and optimize large-scale NLP and ASR models</li><li>Develop and optimize ML algorithms for speech, text, and structured healthcare data</li><li>Conduct rigorous testing and validation to ensure high clinical accuracy and performance</li><li>Continuously evaluate and enhance model efficiency and reliability</li></ul>Cloud &amp; MLOps Implementation<ul><li>Architect and deploy AI models on AWS, Azure, or GCP</li><li>Deploy and manage models using containerization, Kubernetes, and serverless architectures</li><li>Design and implement robust MLOps strategies for lifecycle management</li></ul>Integration &amp; Compliance<ul><li>Ensure compliance with healthcare standards such as HIPAA, HL7, and FHIR</li><li>Integrate AI systems with EHR/EMR platforms</li><li>Implement ethical AI practices, regulatory compliance, and bias mitigation techniques</li></ul>Collaboration &amp; Leadership<ul><li>Work closely with business analysts, healthcare professionals, software engineers, and ML engineers</li><li>Implement LangChain, OpenAI APIs, vector databases (Pinecone, FAISS, Weaviate), and RAG architectures</li><li>Mentor and lead junior data scientists and engineers</li><li>Contribute to AI research, publications, patents, and long-term AI strategy</li></ul>Required Skills &amp; Competencies<ul><li>Expertise in Machine Learning, Deep Learning, and Generative AI</li><li>Strong Python programming skills</li><li>Hands-on experience with PyTorch and TensorFlow</li><li>Experience fine-tuning transformer-based LLMs (GPT, BERT, T5, LLaMA, etc.)</li><li>Familiarity with ASR models (Whisper, Canary, wav2vec, DeepSpeech)</li><li>Experience with text embeddings and vector databases</li><li>Proficiency in cloud platforms (AWS, Azure, GCP)</li><li>Experience with LangChain, OpenAI APIs, and RAG architectures</li><li>Knowledge of agentic AI frameworks and reinforcement learning</li><li>Familiarity with Docker, Kubernetes, and MLOps best practices</li><li>Understanding of FHIR, HL7, HIPAA, and healthcare system integrations</li><li>Strong communication, collaboration, and mentoring skills</li></ul>Employee Benefits &amp; Perks<ul><li>Medical Insurance: ₹4 Lakhs per annum (Coverage for self, spouse, and 2 children under 25 years of age; non-reimbursable)</li><li>Group Personal Accident Policy: Coverage equivalent to 5 years&rsquo; CTC in case of accidental death</li><li>Complimentary Canteen Facilities for office-based employees</li></ul>Job Types: Full-time, PermanentPay: ₹2,500,000.00 - ₹3,000,000.00 per yearBenefits:<ul><li>Health insurance</li><li>Provident Fund</li></ul>Work Location: In person

Principal Data Scientist

Kraft Heinz

<div><h2 class="jobSectionHeader">Job Description
</h2>Senior Principal Scientist, R&amp;D &ndash; Analytical Sciences
ABOUT
This Senior Principal Scientist position in Analytical Sciences is located at our Glenview, IL Kraft Heinz Innovation Center. This is an ideal opportunity for a scientist passionate about leading the design of experiments, root cause analysis studies, and kinetics studies encompassing, but not limited to, product quality, packaging and shelf-life testing. This position will also serve as the SME for analytical (example: linking chemistry and sensory) data processing, analysis and modelling to elucidate key business insights by leveraging advanced data application software, AI technology and statistical principles for R&amp;D and field-to-shelf business decisions. The position emphasizes cross-functional holistic problem solving with R&amp;D, Product Development, Quality, Operations and Factory personnel to identify needs and develop competitive-edge capabilities advancing KH agenda for a wide range of leading food products.
RELATIONSHIPS (EXTERNAL AND INTERNAL):
<ul><li>Will collaborate with internal clients including R&amp;D, Product Development, Quality, Operations and Factory personnel.
</li></ul><ul><li>Will collaborate and represent KHC well when working with external professionals from accredited consortiums and universities
</li></ul><ul><li>Will interact with instrument and software vendors, ingredient suppliers, co-manufacturing facilities and external lab partners.
</li></ul>QUALIFICATION REQUIREMENTS:
<ul><li>Highly skilled in design of experiment for complex food systems using techniques like Full Factorial, Fractional Factorial and Response Surface Methodologies.
</li></ul><ul><li>Apply statistical models with examples like Minitab, SAS, R, Python and MATLAB to food kinetic data to predict changes in quality and optimize processes
</li></ul><ul><li>Deep knowledge around the fundamentals of kinetics such as substance structure-function, food matrix mechanisms and rates of reactions in the areas of enzymatic browning, lipid oxidation, discoloration, fermentation, packaging interactions and others.
</li></ul><ul><li>Process and interpret data for R&amp;D and cross-functional projects effectively using approaches such as PCA, PLS and regression tree
</li></ul><ul><li>Translate complex data or large data set into effective data visualization and presentation using Tableau or other data visualization tools to deliver business insights to peers, senior leaders and stakeholders.
</li></ul><ul><li>Track record of leading modelling and simulation in other food companies and/or beyond food like the medical field.
</li></ul><ul><li>Set up strategy on predictive modelling and simulation; leading complex, cross-functional R&amp;D projects that will build product categories fundamental know how in an agile way; improving product package superiority within core brands
</li></ul><ul><li>Assume full leadership in the space of Modelling and Simulation. This role will interact with R&amp;D scientists, legal, finance, plant, KHC leadership team as well as external research institutions.
</li></ul><ul><li>Demonstrate advanced analytical skills and hands-on experience using cutting-edge instrumentations such GC-MS and LC-MS. This involves expertise in the entire workflow, from sample preparation and data acquisition to processing, statistical analysis, and compound characterization in complex food systems.
</li></ul><ul><li>Apply analytical science knowledge and experience in both hypothesis validation (targeted) and discovery-driven analysis (untargeted).
</li></ul>&middot; Preferred qualifications include
1) the experience to integrate multidisciplinary data such as microbiology, chemistry, physics, sensory, o-mics (metabolomics, glycomics, proteomics, and lipidomics) to draw big picture conclusions critical to elevate R&amp;D
2) working knowledge of food manufacturing and packaging
<ul><li>Demonstrate critical thinking skills
</li></ul><ul><li>Communicate effectively and openly while working in a cross-functional team
</li></ul><ul><li>Must be a self-starter and resourceful
</li></ul><ul><li>Must be organized, process orientated
</li></ul><ul><li>Independently and collaboratively executing innovation, cost saving, process and product improvements throughout KH portfolio.
</li></ul><ul><li>Identifying opportunities for competitive market advantage, which could include AI technologies, new cost saving solutions or process enhancements.
</li></ul><ul><li>Provide consultation and technical oversight to ensure that an appropriate level of technical knowledge and discipline are being applied and utilized.
</li></ul><ul><li>The successful candidate will directly or indirectly supervise technical professionals in assigned areas, while maintaining responsibility for own projects.
</li></ul><ul><li>The candidate will have significant impact on direction and quality of work done by other senior technical people.
</li></ul>Education and Experience:
<ul><li>M.S in Food Science, Chemistry, Biology, Engineering, or related fields with minimum of 10 years of relevant experience or PhD in the above fields with minimum 8 years of relevant experience
</li></ul><ul><li>Preferred: License or Certificate or Additional Degree in the area of Statistics, Data Modelling and Analytical Science. Track record of leading modelling and simulation in other food companies and/or beyond food like the medical field.
</li></ul><ul><li>Excellent organizational, interpersonal &amp; project management skills.
</li></ul><ul><li>Excellent written and verbal communication skills.
</li></ul><ul><li>TRAVEL: 0-20%
</li></ul>Our Total Rewards philosophy is to provide a meaningful and flexible spectrum of programs that equitably support our diverse workforce and their families and complement Kraft Heinz&rsquo; strategy and values.
New Hire Base Salary Range:
$118,400.00 - $148,000.00
Bonus: This position is eligible for a performance-based bonus as provided by the plan terms and governing documents.
The compensation offered will take into account internal equity and may vary depending on the candidate's geographic region, job-related knowledge, skills, and experience among other factors
Benefits: Coverage for employees (and their eligible dependents) through affordable access to healthcare, protection, and saving for the future, we offer plans tailored to meet you and your family&rsquo;s needs. Coverage for benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.
Wellbeing: We offer events, resources, and learning opportunities that inspire a physical, social, emotional, and financial well-being lifestyle for our employees and their families.
You&rsquo;ll be able to participate in a variety of benefits and wellbeing programs that may vary by role, country, region, union status, and other employment status factors, for example:
<ul><li>Physical - Medical, Prescription Drug, Dental, Vision, Screenings/Assessments
</li><li>Social - Paid Time Off, Company Holidays, Leave of Absence, Flexible Work Arrangements, Recognition, Training
</li><li>Emotional &ndash; Employee Assistance Program , Wellbeing Programs, Family Support Programs
</li><li>Financial &ndash; 401k, Life, Accidental Death &amp; Dismemberment, Disability
</li></ul>Location(s)
Glenview R&amp;D Center 
 
Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes. In order to ensure reasonable accommodation for protected individuals, applicants that require accommodation in the job application process may contact NAZTAOps@kraftheinz.com for assistance.</div>

Senior Principal Scientist, R&D – Analytical Data Scientist

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