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<h3>Job Description</h3>
Job DescriptionDescription:
*Note: This is an on-site, temporary position with the possibility of conversion to full-time employment after 9 months*
 
Company Overview: 
 
Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space.
 
We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression.
 
Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune in 2022, 2023, and 2024.
 
Job Summary: 
 
The successful candidate will have hands-on experience designing and executing in vitro experiments to support the pre-clinical advancement of drug discovery projects.
Requirements:
Essential Duties and Responsibilities:
<ul>
<li>Independently perform in vitro experiments with primary cells and/or cell lines, analyze data, and interpret and communicate results. </li>
<li>Perform a variety of immunological and molecular biology techniques to support target discovery and drug development, including flow cytometry, ELISA, western blot, Luminex, CRISPR, and qPCR. </li>
<li>Work collaboratively within the Immunology group to develop target validation assays.</li>
</ul>
Experience and education requirements: 
<ul>
<li>BS with 4+ years or MS with 2+ years of industry experience (Prior experience in immunology-based projects strongly preferred).</li>
<li>Proficiency in hands-on experience with flow cytometry assays, data acquisition, and analysis. Experience with multicolor panel design and cell sorting is highly desirable. </li>
<li>High competency executing in vitro immunology assays, including cellular-based assays and functional assays with PBMCs and whole blood from human and animal samples.</li>
<li>Experience maintaining and working with cell lines and/or primary-derived cells. </li>
<li>Competency performing techniques such as ELISA, Luminex, Western blot, RNA extraction and qPCR</li>
<li>Competency performing ex vivo experiments using rodent cells and tissues (spleen, Lymph nodes, skin, etc.)</li>
<li>Outstanding problem-solving, organization, and communication skills.</li>
</ul>
Required Key Attributes: 
<ul>
<li>Effective troubleshooting and problem-solving skills.</li>
<li>Excellent oral and written communication skills.</li>
<li>Be an effective team player and strong individual contributor, flexible, and able to handle multiple tasks and deliver high-quality results under tight timelines.</li>
</ul>
Pay &amp; Benefits: 
 
The hourly pay for this position ranges from $36.00 to $44.00 depending on relevant skills, experience, and education. 
 
EEO &amp; Employment Eligibility:
 
Vividion Therapeutics, Inc. is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
 
Privacy Policy:
 
The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit <a href="https://vividion.com/publication/privacy-noticeforcalifornia-candidates/" target="_blank">https://vividion.com/publication/privacy-noticeforcalifornia-candidates/</a>.

Senior Research Associate, Immunology (Temp)

<h3>Job Description</h3>
Job Description
Adecco is hiring immediately for a Night Shift Clean Room Technician with a local client in Santa Clara, CA. Pay is $30.00/hr - $40.00/hr. 
Duties:
· Night Shift 11pm - 7:30am (8 hrs x 5 day) Mon – Fri
· Clean room worker for operating 300mm glass wafer substrate process and inspection tools
· Follow SOP and MES operation procedure instruction and process the wafers
· Collect the inspection data and provide data to engineering review
· Follow engineering instruction and assist experimental wafer processing
· Comply all safety requirements and IP protection protocols.
Requirements:
· Requires wearing clean room full garments
· Prior semiconductor clean room experience preferred. 
Click on apply now for immediate consideration for this Night Shift Clean Room Technician in Santa Clara, CA. We look forward to hearing from you!
Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria.
 
 Pay Details: $30.00 to $40.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.adecco.com/en-us/candidate-privacy" target="_blank">https://www.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>

Night Shift Clean Room Technician

<h3>Job Description</h3>
Job DescriptionDescription:
SUMMARY 
Responsible for all aspects of purification process development from process definition to process characterization for support of pipeline projects. Designs a series of experiments that contribute to project objectives. Develops new processes and technologies to achieve improved product quality and reduce production cost. Interacts with management on advanced technical matters.
 
JOB RESPONSIBILITIES
ESSENTIAL FUNCTIONS
<ul>
<li>Applies engineering and scientific principles in the process definition, process optimization, scale-up, technology transfer, process characterization, and process validation activities associated with the purification of biopharmaceuticals.</li>
<li>Designs, implements, and conducts a series of scientific experiments which contribute to project objectives. Leads troubleshooting processes, instrumentation, and equipment.</li>
<li>Serves as a technical resource in technology transfer from process development to clinical cGMP manufacturing including definition of bill of materials, batch record drafting/review, and discrepancy resolution. Serves as a process development representative during purification operations. Provides technical troubleshooting and recommends process equipment improvements.</li>
<li>Designs and perform a series of bench scale experiments such as sterile membrane filtration, depth filtration, tangential flow filtration, viral clearance filtration, as well as chromatography.</li>
<li>Develop and recommend new processes and technologies to achieve cost effectiveness and improved product quality. Proactively identifies purification issues and suggests solutions.</li>
<li>Consistently demonstrates scientific leadership in the laboratory.</li>
</ul>
Supplementary Responsibilities
<ul>
<li>Collaborates with cell culture, formulation, analytical, MSAT, Quality, and Validation for achievement of project objectives. May manage external collaborators.</li>
<li>Effective communicator of ideas, project goals and results across functions.</li>
<li>Interacts with management on advanced technical matters.</li>
<li>Authors and reviews regulatory filing documentation as well as process validation and characterization reports. Authors internal reports at appropriate milestones.</li>
</ul>
 
JOB REQUIREMENTS
Education and Experience
<ul>
<li>BS with 9 years’ experience, MS with 6 years’ experience, or PhD with 0 years’ experience in purification within a pharmaceutical process development group with a degree in chemical/biochemical engineering, biochemistry, or related scientific discipline.</li>
</ul>
Knowledge, skills and abilities
<ul>
<li>Proficient in programming, operating, and troubleshooting the following chromatography systems: AKTA pure, AKTA ready, and AKTA pilot.</li>
<li>Proficient in designing and conducting chromatography development studies.</li>
<li>Proficient in designing and conducting filtration studies using Scilog FilterTec and labscale TFF systems.</li>
<li>Understands purification process design limits for implementation in a clinical manufacturing environment.</li>
<li>Initiates, designs, and executes experiments independently. Capable of independent data interpretation. May apply advanced modeling or statistical analysis tools where appropriate.</li>
<li>Highly skilled communicator of ideas, project goals, and results.</li>
<li>Capable of working effectively in teams.</li>
<li>Knowledge of cGMP and familiarity with large scale manufacturing support.</li>
</ul>
Requirements:

Scientist, Purification Development

<h3>Job Description</h3>
Job DescriptionDescription:
About GondolaBio
GondolaBio is a collection of biopharmaceutical companies focused on developing next-generation therapeutics for genetic diseases. Originally carved out of BridgeBio, GondolaBio secured $300M in private financing from external investors in 2024 and became an independent company within the BridgeBio ecosystem. GondolaBio aims to leverage cutting-edge biological research to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases.
Neurofibromatosis Type 1 (NF1), a genetic condition where tumors grow on the nerves and skin, is the focus of a pre-clinical stage program in GondolaBio’s portfolio. NF1 affects multiple organ systems, with a wide range of manifestations ranging from neurofibromas (benign nerve sheath tumors) that carry the risk of malignant transformation, to learning difficulties and bone abnormalities. Despite having two FDA-approved MEK inhibitors for NF1 patients, there is still a huge unmet need in providing safer and more efficacious treatment options to the NF1 patients, and GondolaBio strives to address this gap.
Who You Are
The primary responsibilities of this position are to serve as a DMPK representative on multi-disciplinary drug discovery teams, provide guidance and support to project teams for candidate selection, and further characterize the pharmacokinetic and drug metabolism properties of molecules through early development to IND. This individual will have the opportunity to be exposed to a broad spectrum of therapeutic areas across the portfolio.
Requirements:
Responsibilities
<ul>
<li>Work closely with cross-functional project team members. Participate as a functional representative on the NF1 project team</li>
<li>Provide guidance on discovery project teams for candidate selection, develop and drive DMPK strategies for lead optimization, and solve ADME-related issues</li>
<li>Design, coordinate, and interpret in vitro and in vivo DMPK studies</li>
<li>Determine PK parameters for nonclinical studies using Phoenix WinNonlin and assist with the application of modeling approaches (PK, PKPD) to support human PK and dose predictions</li>
<li>Support GLP toxicology studies, review toxicokinetic reports, and monitor regulated bioanalysis</li>
<li>Monitor bioanalytical method development, validation, sample analysis, and review/approve reports</li>
<li>Generate, analyze and present data, both orally and as written reports</li>
<li>Potential to work across multiple discovery programs</li>
</ul>
No matter your role at GondolaBio, successful team members are:
<ul>
<li>Patient Champions, who put patients first and uphold strict ethical standards</li>
<li>Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset</li>
<li>Truth Seekers, who are detailed, rational, and humble problem solvers</li>
<li>Individuals Who Inspire Excellence in themselves and those around them</li>
<li>High-quality executors, who execute against goals and milestones with quality, precision, and speed</li>
</ul>
Education, Experience &amp; Skills Requirements
<ul>
<li>PhD or Pharm D. in Pharmacokinetics, Pharmaceutical Sciences, or related field with a specific focus on small molecule pharmacokinetics and metabolism with at least 3-6 years of relevant industry experience</li>
<li>Strong understanding of DMPK principles and drug development processes</li>
<li>Expertise in drug metabolism is desirable</li>
<li>Hands-on experience using pharmacokinetic data analysis software such as Phoenix WinNonlin</li>
<li>Able to work independently and possess excellent interpersonal skills</li>
<li>Possess effective problem-solving, oral, and written communication skills</li>
</ul>
What We Offer
<ul>
<li>Patient Days, where we are fortunate enough to learn more about the lives we are looking to impact and a real exchange of ideas as to how we can improve our efforts</li>
<li>A culture inspired by our values: put patients first; think independently; be radically transparent; every minute counts; and let the science speak</li>
<li>Collaborative business environment</li>
<li>A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science</li>
<li>A place where you own the vision – both for your program and your own career path</li>
<li>A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game</li>
<li>Robust and market-competitive compensation &amp; benefits package (Base, Performance Bonus, Equity)</li>
<li>Flexible PTO</li>
<li>Rapid career advancement for strong performers</li>
<li>Work with the most productive groups of R&amp;D operators in the industry</li>
<li>A platform for meaningful scientific contributions to shine</li>
</ul>
At GondolaBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. GondolaBio is a multi-state employer, and this salary range may not reflect positions based in other states. 
 
Compensation Range: $220-260K

Principal Scientist/Director, DMPK

<h3>Job Description</h3>
Job Title: In Vivo Research Associate
Location: Foster City, CA
Duration: 12+ Months
 
Job Description:
We are seeking a highly motivated In Vivo Research Associate to join our Oncology in vivo pharmacology team. The selected candidate will provide in vivo study support for evaluating novel oncology therapeutics in pre-clinical models and will be responsible for daily in vivo study execution, data analysis and organization, as well as project team responsibilities. A minor amount of scheduling flexibility, including off-shift and weekend, may be required.
 
The successful candidate will be proficient in murine handling techniques including various dosing routes (IV, IP, PO, RO, subcutaneous), in-life and terminal blood collection, and handling of tissues during necropsy and processing for ex vivo analysis. The day-to-day responsibilities will include daily dosing, daily tumor measurements, tissue collections, and assisting with various aspects of study and facility maintenance.
 
In addition to daily hands-on lab responsibilities, the position will have project team responsibilities including attending meetings to determine appropriate study design, organization of data, and presentation of results.
 
Required Years of Experience: Minimum of 2-3 years of post-graduate hands on experience or demonstrate equivalent work experience with murine models of cancer, inflammation, and/or immunology. Strong biology background
 
Top 3 Required Skill Sets: Animal handling (mouse). Understanding of basic pharmacology. Demonstrated ability to design, execute, and analyze experiments
 
Top 3 Nice to Have Skill Sets: In Vitro and wet-lab experience. Proficiency with MS suite including PowerPoint, Excel, and word.
 
Required Degree or Certification: MS or BS

Research Associate

<h3>Job Description</h3>
AI Research Scientist
 
&amp;#x1F9E0; Design and evaluate novel AI/ML models across foundational and applied domains
&amp;#x1F4CA; Drive innovation in LLMs, deep learning, and reinforcement learning techniques
&amp;#x1F4DA; Collaborate with cross-functional teams to bring research into production
&amp;#x1F680; Publish, present, and patent high-impact findings in AI and machine learning
 
&amp;#x1F6E0; Key Responsibilities
<ul>
<li>Conduct cutting-edge research in artificial intelligence, including areas such as natural language processing, computer vision, generative models, and reinforcement learning</li>
<li>Design and implement novel algorithms and model architectures for experimentation and deployment</li>
<li>Analyze large-scale datasets to extract insights, train models, and validate hypotheses</li>
<li>Collaborate with engineering teams to translate research into scalable solutions and production-ready systems</li>
<li>Stay current with the latest literature and contribute to the AI research community through papers, presentations, or patents</li>
<li>Build and evaluate proof-of-concept systems and prototypes for real-world application</li>
<li>Mentor junior researchers and data scientists in scientific rigor, model development, and experimentation</li>
<li>Support internal IP development and contribute to strategic technical roadmaps</li>
</ul>
 
✅ Qualifications
<ul>
<li>Advanced degree (Ph.D. or Master’s) in Computer Science, Machine Learning, Mathematics, or a related field</li>
<li>Strong publication record in top-tier conferences (e.g., NeurIPS, ICML, ACL, CVPR, ICLR) is highly preferred</li>
<li>Expertise in machine learning, deep learning, or statistical modeling</li>
<li>Experience with model development using TensorFlow, PyTorch, JAX, or similar frameworks</li>
<li>Proficiency in Python and familiarity with large-scale data processing</li>
<li>Solid understanding of model evaluation, optimization techniques, and deployment workflows</li>
<li>Ability to independently design and drive research agendas with business impact</li>
</ul>
 
&amp;#x1F91D; Why Join Us
Join a world-class team of scientists and engineers pushing the boundaries of what’s possible with AI. Your research will not only advance the field—it will shape real-world applications across industries.
 
&amp;#x1F9EC; About Us
We are an innovation-first organization bridging advanced research and product development. Our work combines rigorous experimentation with practical application, bringing novel AI solutions to life in scalable, meaningful ways.

AI Research Scientist

<h3>Job Description</h3>
Job DescriptionHybrid Remote - Established Structural and Geotechnical Engineering Firm in SF - Excellent Benefits + Upward Mobility This Jobot Job is hosted by: Caitlyn Hardy Are you a fit? Easy Apply now by clicking the "Apply Now" buttonand sending us your resume. Salary: $80,000 - $110,000 per year 
A bit about us:
 Our new building portfolio includes significant collaborations with internationally acclaimed architects on a variety of building types. We pride ourselves in our ability to provide creative and practical solutions that support great architectural visions. Our services also include seismic evaluations and retrofits of existing buildings. We have many new and exciting projects in the institutional and commercial sectors, both in the U.S. and abroad. 
Why join us?
 
<ul>
<li>Multiple medical plan options including PPO and HSA</li>
<li>Dental and vision insurance</li>
<li>Pre-tax flex spending and transit plans</li>
<li>Paid personal time off</li>
<li>Retirement plans including 401(k) plan</li>
<li>Continuing education allowance</li>
<li>Hybrid workplace</li>
</ul>
 
Job Details
 Skilled in seismic hazard analysis, liquefaction evaluation and mitigation, shallow and deep foundation design, slope stability analysis, and report writing. 
<ul>
<li> Experience with healthcare (HCAI, formerly OSHPD), educational (DSA), and public agency clients is</li>
</ul>
 desirable. 
<ul>
<li> Proficiency with geotechnical software:</li>
</ul>
 – Required: gINT, ALLPILE, CLIQ, LPILE, AutoCAD and Microsoft Office suite of programs. – Preferred: PLAXIS, Settle3, LiqSVs. 
<ul>
<li> Excellent communication and organizational skills with strong attention to detail.</li>
<li> Excellent analytical, multitasking, and judgment capabilities and an ability to work both independently</li>
</ul>
 and in a team environment. Interested in hearing more? Easy Apply now by clicking the "Apply Now" button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.Company DescriptionJobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values. Founded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA). Ready to find a good job? Create your profile today at Jobot.com. 
<h3>Company Description</h3>
Jobot is on a mission to connect good people with good jobs. By combining AI-powered technology with the expertise of Jobot Pros, our experienced recruiters, we help you find career opportunities that align with your goals and values.\r\n\r\nFounded in 2018 and employee-owned since 2024, Jobot is committed to fostering a culture of kindness, respect, innovation, and connection. As an industry leader, we’ve been recognized as a top workplace by Forbes, Fortune, USA Today, and Staffing Industry Analysts (SIA).\r\n\r\nReady to find a good job? Create your profile today at Jobot.com.

Geotechnical Design Engineer

<h3>Job Description</h3>
Job Description
Job Title:
Science Director – Biophysics
Location: Princeton NJ or Los Angeles CA&nbsp; - must be local to either of these offices or willing to relocate
Vaccination against COVID-19 is a prerequisite for employment at CHDI Management
Salary range: $120,000-220,000.&nbsp; Exact compensation will vary based on experience
Job Description:
CHDI Management seeks an experienced, innovative, and passionate drug discovery scientist to join the preclinical team as Science Director, Biophysics, to support the Foundation’s mission to accelerate meaningful therapies for Huntington’s disease (HD). Partnering with the internal Computational Drug Discovery and Structural Biology Science Director the successful candidate will be a biophysics domain knowledge expert and participate on interdisciplinary teams to advance the understanding of HD biology, to identify and characterize potential HD drug targets and to support the discovery of novel agents for pharmacologic proof-of-concept. The position involves collaborating with internal CHDI scientists, Contract Research Organization (CRO) collaborators, industrial partners and external academic experts.
The position reports to the Vice President, Chemistry
Job Responsibilities:
<ul>
<li>Manage external biophysics resources at CRO partners by providing strategic and technical oversight of biophysical assay deployment across the CHDI project portfolio.</li>
<li>Collaborate with partners including HD biology-focused thematic areas, structural biologists, medicinal chemists and informaticians. Participate as a biophysics domain knowledge expert to interdisciplinary project teams.</li>
<li>Co-develop project workplans as a member of interdisciplinary project teams with strategic line-of-sight to achieve program objectives.</li>
<li>Generate and deliver impactful biophysical data and insight to characterize biomolecular interactions and provide discovery teams with detailed interaction analyses (e.,&nbsp;protein-compound, nucleic acid-compound, protein-protein, and protein-nucleic acid) in cell-free and cellular systems.</li>
<li>Develop and deploy ligand-protein interaction experiments using biophysical methods (e.g. SPR, ITC, NMR, thermal shift, native MS) to measure binding of small molecule hits and leads to potential drug targets.</li>
<li>Design and conduct experiments to deconvolute biophysical mechanisms of active agents to understand residence time, predict efficacy and pharmacology, and select the best molecules for pharmacologic proof-of-concept.</li>
<li>Collaborate with the Research Informatics and Computational Drug Discovery team to prepare, organize, combine and integrate biophysics data and accelerate the development of tool compounds</li>
<li>Identify and partner with external collaborators (CRO, academic) to develop impactful, cutting-edge biophysical methods for their strategic application to projects in support of Foundation objectives.</li>
</ul>
Qualifications:
<ul>
<li>PhD. in Biophysics, Biophysical Chemistry, Chemistry and Chemical Biology or a related discipline.</li>
<li>6 plus years of industry experience in target validation and/or integrated drug discovery projects.</li>
<li>Demonstrated expertise in the use of biophysical methods (SPR, GCII, HTRF, MST, AS-MS, SwitchSense and thermal stability assays such as DSF) for characterization of biomolecular interactions (protein-compound, nucleic acid-compound, protein-protein, and/or protein-nucleic acid).</li>
<li>Experience in designing and building mechanistic assays to support elucidation of novel disease-relevant biology and target validation.</li>
<li>Experience in the application of emerging biophysical methods (e.g., single-molecule fluorescence microscopy, single-molecule force microscopy, magnetic force microscopy to interrogate macromolecular assemblies within their native environment highly preferred.</li>
<li>Experience working in a multidisciplinary team-oriented environment.</li>
<li>Excellent written and oral communication skills.</li>
<li>Experience in oversight of CRO collaborators.</li>
</ul>
About CHDI Foundation, Inc.
CHDI Foundation, Inc. is a privately-funded, not-for-profit, biomedical research organization that is exclusively dedicated to rapidly discovering, accelerating and developing therapies that slow the progression of Huntington’s disease (HD). Our scientists work closely with a network of more than 600 researchers in academic and industrial laboratories around the world in the pursuit of these innovative therapies, providing strategic scientific direction to ensure that our common goals remain in focus. This helps bridge the translational gap that often exists between academic and industrial research pursuits and that adds costly delays to therapy development. In its role as a collaborative enabler, CHDI seeks to bring the right partners together to identify and address critical scientific issues and move drug candidates to clinical evaluation as rapidly as possible. Our activities extend from exploratory biology to the identification and validation of therapeutic targets, and from drug discovery and development to clinical studies and trials. More information about CHDI can be found at&nbsp;<a href="http://www.chdifoundation.org" target="_blank">www.chdifoundation.org</a>
About CHDI Management, Inc.
CHDI Management, Inc. was established in 2002 to provide administrative, management and grant making services to CHDI Foundation, Inc.
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Director, Biophysics (Los Angeles CA or Princeton NJ)

<h3>Job Description</h3>
Job DescriptionJob Title: Chemist – Personal Care &amp; Cosmetics Pay: $100-125k/year DOE + great benefits! Location: Gardena, CA Reports To: R&amp;D Manager -Job Summary: We are seeking a detail-oriented and innovative R&amp;D Chemist to join our R&amp;D team. The ideal candidate will be responsible for formulating and testing personal care and cosmetic products such as skincare, haircare, body care, and color cosmetics. This role plays a key part in developing high-performance, safe, and compliant formulations in line with marketing briefs and regulatory standards. -Qualifications: • Bachelor’s degree in Chemistry, Cosmetic Science, Chemical Engineering, or related field (Master’s preferred). • 5+ years of hands-on lab experience in cosmetic or personal care product formulation. • Strong understanding of regulatory guidelines. • Excellent organizational, documentation, and communication skills. • Ability to work independently and collaboratively in a fast-paced environment. Please send resume to Veronica Vasquez. Thank you! AppleOne Ventura Equal Opportunity Employer / Disabled / Protected Veterans The Know Your Rights poster is available here: <a href="https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf" target="_blank">https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRi…</a> The pay transparency policy is available here: <a href="https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf" target="_blank">https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_…</a> For temporary assignments lasting 13 weeks or longer, the Company is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team. AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program. <a href="https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf" target="_blank">https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Partici…</a> We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. #1111 Company DescriptionThis company offers growth and a great group of people to work with. 
<h3>Company Description</h3>
This company offers growth and a great group of people to work with.

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