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<h3>Job Description</h3>
Job DescriptionEngineering Geologist Engineering Geologist Position Overview We are seeking a skilled Engineering Geologist to join our team. The ideal candidate will play a crucial role in assessing geological conditions at various sites, conducting geotechnical investigations, and providing expert recommendations for engineering projects. The Engineering Geologist will work closely with project managers and engineers to ensure the safety and viability of construction projects by analyzing soil and rock properties. Key Responsibilities
<ul>
<li>Conduct geotechnical investigations and site assessments to evaluate geological conditions.</li>
<li>Analyze soil and rock samples to determine their properties and suitability for construction projects.</li>
<li>Prepare detailed reports outlining findings, recommendations, and compliance with regulatory standards.</li>
<li>Collaborate with engineers and other professionals to develop solutions for geological challenges in projects.</li>
<li>Conduct field sampling and testing to gather data for analysis.</li>
<li>Utilize geospatial analysis and modeling software to visualize geological data.</li>
<li>Ensure adherence to environmental assessments and regulations during site investigations.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Geology, Geotechnical Engineering, or a related field.</li>
<li>Proven experience in geotechnical engineering and site investigation.</li>
<li>Strong knowledge of soil analysis and hydrogeology principles is preferred.</li>
<li>Familiarity with environmental assessment practices and regulatory compliance requirements.</li>
<li>Experience in rock mechanics and groundwater modeling is a plus.</li>
<li>Proficiency in data analysis and report writing.</li>
<li>Possess strong communication skills to effectively convey technical information.</li>
</ul>
 - For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa. CyberCoders will consider for Employment in the City of Los Angeles qualified Applicants with Criminal Histories in a manner consistent with the requirements of the Los Angeles Fair Chance Initiative for Hiring (Ban the Box) Ordinance.This job was first posted by CyberCoders on 09/05/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.CyberCoders is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. &nbsp;CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please contact a member of our Human Resources team to make arrangements.

Engineering Geologist

<h3>Job Description</h3>
Job DescriptionDescription:
About GondolaBio
GondolaBio is a clinical-stage biopharmaceutical company focused on developing next-generation therapeutics for genetic diseases. Originally launched as BridgeBioX, a subsidiary of BridgeBio, GondolaBio secured $300M in private financing from external investors in 2024 and became an independent company within the BridgeBio ecosystem. The company aims to leverage cutting-edge biological research to create breakthrough medicines addressing high unmet needs across multiple therapeutic areas, including neurology, pulmonology, cardiology, nephrology, and endocrinology. Located on the Stanford Life Sciences campus, GondolaBio fosters a unique hybrid environment where top scientists from around the world collaborate with senior leadership and advisors, blending industry expertise with academic innovation. 
 
Who you are
We're seeking an entrepreneurial scientific leader who combines intellectual rigor with practical execution skills to advance our antisense oligonucleotide (ASO) pipeline at GondolaBio. You will serve as a scientific lead for multiple preclinical ASO programs which will involve collaboration with the n-Lorem foundation. You will play a pivotal role in designing, executing, and interpreting experiments. This position offers the opportunity to shape research strategy while mentoring junior scientists and contributing to a growing, interdisciplinary team. 
 
Requirements
Key Responsibilities
<ul>
<li>Serve as a subject matter expert for ASO discovery, design, and preclinical evaluation across multiple programs </li>
<li>Lead the design and execution of in vitro studies across multiple preclinical programs using the ASO modality </li>
<li>Develop and optimize functional assays and disease models (e.g., iPSC-derived and patient primary cell-derived) to support target engagement and efficacy assessments </li>
<li>Perform and interpret molecular, protein, and functional analyses (e.g., qPCR, Western blot), integrating findings with in vivo and translational data </li>
<li>Design and interpret in vivo efficacy, safety, and target engagement experiments for ASOs in multiple indications </li>
<li>Supervise and mentor junior scientists, fostering a high-performing and collaborative research environment </li>
<li>Oversee external research activities, including CRO and academic collaborations, ensuring high-quality and timely data delivery </li>
<li>Stay abreast of emerging science, engage with external experts, and represent the company at scientific meetings </li>
<li>Communicate results and strategic insights to senior leadership; contribute to publications and IP </li>
<li>Partner with leadership to shape and execute a cohesive research strategy that advances program objectives across discovery and translational stages </li>
</ul>
Education, Experience, &amp; Skills Requirements
<ul>
<li>PhD in chemistry, biology, or a related field with 4+ years of industry experience; strong publication record is a plus </li>
<li>Modality expertise in ASOs and experience with preclinical discovery, design, and testing of ASO efficacy and safety </li>
<li>Experience with in vitro and in vivo disease models across multiple therapeutic areas (neuroscience and renal experience is a plus) </li>
<li>Proficiency in preclinical ASO experiments, including qPCR, Western blot, iPSC and patient primary cell culture </li>
<li>Sound knowledge of disciplines involved in drug discovery (cell-based disease models, target engagement and target modulation assays, cell viability assays, biomarker discovery, PD/PK, and efficacy studies) and experience with plate-based cellular and biochemical assays </li>
<li>Demonstrated ability to manage projects and lead junior team members </li>
<li>Strong problem-solving, communication, and cross-functional collaboration skills </li>
<li>Experience in biotech or pharmaceutical R&amp;D preferred </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>
What We Offer 
<ul>
<li>Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn 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>An unyielding commitment to always putting patients first. </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>Access to learning and development resources to help you get in the best professional shape of your life </li>
<li>Robust and market-competitive compensation &amp; benefits package (Base, Performance Bonus, Equity, health, welfare &amp; retirement programs) </li>
<li>Flexible PTO </li>
<li>Rapid career advancement for strong performers </li>
<li>Potential ability to work on multiple GondolaBio Pharma programs across multiple therapeutic areas over time </li>
<li>Partnerships with leading institutions </li>
<li>Commitment to Diversity, Equity &amp; Inclusion </li>
</ul>
The base pay range for this position is $190,000 to $205,000 per year. The actual compensation offered will be determined based on a number of job-related factors, including experience, skills, qualifications, and location. A bonus plan and equity will also be offered.
 
Requirements:

Principal Scientist, ASO Biologist

<h3>Job Description</h3>
Job Description
Palo Alto Veterans Institute for Research (PAVIR) supports the nation's second largest research program conducted among the VA Hospitals and is looking for a part-time Clinical Research Assistant. The Research Assistant will support the study of psychedelic medications treatments for severe depression and PTSD, led by the Principal Investigator - Dr. Trisha Suppes - as part of the Stanford/VA Exploratory Therapeutics Laboratory. 
The Research Assistant will play an important role in implementation of clinical research studies with an understanding of the underlying rationale, and follow best practices in working with research participants with serious mental illness.
This a part-time, 10-20 hours/week, position, located in Palo Alto, CA.
BENEFITS
PAVIR is delighted to offer a robust and comprehensive employee benefits package with exceptional offerings such as sick pay policies, a 401(k) with a fully vested 6% company match and 3% profit share, commuter benefits, wellness program, employee assistance program, and professional development training.
JOB RESPONSIBILITIES 
<ul>
<li>Assist with identification, screening, and enrollment of study subjects;</li>
<li>Communicate with subjects about study procedures and obtain informed consent;</li>
<li>Coordinate with study team and subjects to schedule visits and conduct follow-ups;</li>
<li>Administer questionnaires and assessment instruments to subjects;</li>
<li>Collaborate with study team to ensure that protocols are followed completely, labs are ordered and reviewed as required, and that all elements of patient safety and protection are present;</li>
<li>Oversee data collection and data reconciliation; check data for completeness and verify as needed;</li>
<li>Prepare treatment room for participants, including setting up video and audio recordings of sessions</li>
<li>Travel to Stanford research space and VA Community-Based Outpatient Clinics (CBOC) occasionally for recruitment;</li>
<li>Attend weekly lab meetings with study team.</li>
<li>Provide information as needed to other clinic staff regarding clinical issues with specific patients, adherence to study protocols, administration of research instruments, and general procedures in clinical research;</li>
<li>Assist with administrative duties.</li>
<li>Perform simple lab procedures per study requirements (blood pressure, calculation of body mass index);</li>
<li>Assist Principal Investigator in compiling summary data from trials;</li>
<li>Perform literature searches and retrieve needed information from retrieved articles;</li>
<li>Help prepare supplemental materials and text for manuscripts, publications, and grants.</li>
<li>Assist with other study-related duties as needed.</li>
</ul>
QUALIFICATIONS
<ul>
<li>Required: A bachelor's degree or equivalent experience;</li>
<li>at least 1 year of relevant clinical research experience, including subject recruitment and screening; </li>
<li>Valid Driver's License.</li>
<li>Preferred: Master's degree;</li>
<li>2 years or more of relevant clinical research experience; Prior experience in a mental health setting;</li>
<li>Organized, detail-oriented, self-directed, and dependable;</li>
<li>Strong time management skills and ability to prioritize workload;</li>
<li>Ability to work as part of a team;</li>
<li>Ability to communicate effectively with study participants and the research staff; </li>
<li>Working knowledge of MS Word and Excel; Familiarity with REDCap, Qualtrics, and R is highly desired. </li>
<li>Able to learn VA regulations and procedures regarding research;</li>
<li>Effective interpersonal skills, excellent verbal communication and written skills;</li>
<li>General knowledge of research procedures gained through education or experience.</li>
</ul>
ABOUT PALO ALTO VETERANS INSTITUTE FOR RESEARCH (PAVIR)
PAVIR facilitates research and education activities conducted at the VA Palo Alto Health Care System. At PAVIR we work with more than 160 uniquely talented medical scientists. We recruit and retain talented employees who believe in making a difference in the lives of others through innovative health research.
READY TO JOIN OUR RESEARCH TEAM?
If you feel that you would be right for this job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
PAVIR is a nonprofit foundation affiliated with the Veterans Affairs Palo Alto Health Care System (VAPAHCS). As a condition of employment, all PAVIR employees are required to have an approved appointment with VAPAHCS and complete a background check before they can commence work.
PAVIR is pleased to be an Equal Opportunity Employer. Minorities, Women, Veterans, and Individuals with a Disability are encouraged to apply. We welcome and encourage diversity in the workplace regardless of race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you need special assistance or an accommodation to apply for a posted position, please contact <a href="mailto:jobs@pavir.org" target="_blank">jobs@pavir.org</a> - Human Resources department.
 Job Posted by ApplicantPro

CR Research Assistant - Psychedelic Medications Treatments

<h3>Job Description</h3>
Job Description
Palo Alto Veterans Institute for Research (PAVIR) supports the nation's second largest research program conducted among the VA Hospitals and is looking for a part-time Clinical Research Assistant. The Research Assistant will support the study of psychedelic medications treatments for severe depression and PTSD, led by the Principal Investigator - Dr. Trisha Suppes - as part of the Stanford/VA Exploratory Therapeutics Laboratory. 
The Research Assistant will play an important role in implementation of clinical research studies with an understanding of the underlying rationale, and follow best practices in working with research participants with serious mental illness.
This a full-time, 30 hours/week, position, located in Palo Alto, CA.
BENEFITS
PAVIR is delighted to offer a robust and comprehensive employee benefits package with exceptional offerings such as health, dental and vision insurance, 14 paid holidays, generous vacation and sick pay policies, a 401(k) with a fully vested 6% company match and 3% profit share, a wellness program, commuter benefits, and professional development training. Plus, we pay for life, short-term disability, and long-term disability insurance.
JOB RESPONSIBILITIES 
<ul>
<li>Assist with identification, screening, and enrollment of study subjects;</li>
<li>Communicate with subjects about study procedures and obtain informed consent;</li>
<li>Coordinate with study team and subjects to schedule visits and conduct follow-ups;</li>
<li>Administer questionnaires and assessment instruments to subjects;</li>
<li>Collaborate with study team to ensure that protocols are followed completely, labs are ordered and reviewed as required, and that all elements of patient safety and protection are present;</li>
<li>Oversee data collection and data reconciliation; check data for completeness and verify as needed;</li>
<li>Prepare treatment room for participants, including setting up video and audio recordings of sessions</li>
<li>Travel to Stanford research space and VA Community-Based Outpatient Clinics (CBOC) occasionally for recruitment;</li>
<li>Attend weekly lab meetings with study team.</li>
<li>Provide information as needed to other clinic staff regarding clinical issues with specific patients, adherence to study protocols, administration of research instruments, and general procedures in clinical research;</li>
<li>Assist with administrative duties.</li>
<li>Perform simple lab procedures per study requirements (blood pressure, calculation of body mass index);</li>
<li>Assist Principal Investigator in compiling summary data from trials;</li>
<li>Perform literature searches and retrieve needed information from retrieved articles;</li>
<li>Help prepare supplemental materials and text for manuscripts, publications, and grants.</li>
<li>Assist with other study-related duties as needed.</li>
</ul>
QUALIFICATIONS
<ul>
<li>Required: A bachelor's degree or equivalent experience;</li>
<li>at least 1 year of relevant clinical research experience, including subject recruitment and screening; </li>
<li>Valid Driver's License.</li>
<li>Preferred: Master's degree;</li>
<li>2 years or more of relevant clinical research experience; Prior experience in a mental health setting;</li>
<li>Organized, detail-oriented, self-directed, and dependable;</li>
<li>Strong time management skills and ability to prioritize workload;</li>
<li>Ability to work as part of a team;</li>
<li>Ability to communicate effectively with study participants and the research staff; </li>
<li>Working knowledge of MS Word and Excel; Familiarity with REDCap, Qualtrics, and R is highly desired. </li>
<li>Able to learn VA regulations and procedures regarding research;</li>
<li>Effective interpersonal skills, excellent verbal communication and written skills;</li>
<li>General knowledge of research procedures gained through education or experience.</li>
</ul>
ABOUT PALO ALTO VETERANS INSTITUTE FOR RESEARCH (PAVIR)
PAVIR facilitates research and education activities conducted at the VA Palo Alto Health Care System. At PAVIR we work with more than 160 uniquely talented medical scientists. We recruit and retain talented employees who believe in making a difference in the lives of others through innovative health research.
READY TO JOIN OUR RESEARCH TEAM?
If you feel that you would be right for this job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
PAVIR is a nonprofit foundation affiliated with the Veterans Affairs Palo Alto Health Care System (VAPAHCS). As a condition of employment, all PAVIR employees are required to have an approved appointment with VAPAHCS and complete a background check before they can commence work.
PAVIR is pleased to be an Equal Opportunity Employer. Minorities, Women, Veterans, and Individuals with a Disability are encouraged to apply. We welcome and encourage diversity in the workplace regardless of race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you need special assistance or an accommodation to apply for a posted position, please contact <a href="mailto:jobs@pavir.org" target="_blank">jobs@pavir.org</a> - Human Resources department.
 Job Posted by ApplicantPro

<h3>Job Description</h3>
Job Description Mammoth BioSciences OPPORTUNITYMammoth Biosciences is seeking a highly motivated Scientist II or Senior Scientist I to join our CMC team in a hands-on, cross-functional role that blends scientific ingenuity with operational excellence. This position is critical for developing, optimizing, scaling, and characterizing LNP-based delivery production processes for Mammoth's cutting-edge gene editing platforms. The ideal candidate will thrive at the interface of process development, analytics, and manufacturing—someone who can transition smoothly between the bench and discussions with external partners. This is a great opportunity to play a key role in advancing transformative gene editing therapies into the clinic and beyond.KEY RESPONSIBILITIES
<ul>
<li>Design and optimize LNP manufacturing processes by applying Quality by Design (QbD) principles and execute Design of Experiments (DoEs) to identify and control critical process parameters (CPPs)</li>
<li>Optimize analytical methods such as DLS, Ribogreen, HPLC-CAD, IP-RP-HPLC, and endotoxin to identify and access critical quality attributes (CQAs) </li>
<li>Interpret analytical data to assess process robustness and guide iterative development efforts</li>
<li>Collaborate with internal teams to support process improvements and drive innovation</li>
<li>Clearly present scientific findings and project updates in internal meetings and to external collaborators</li>
<li>Drive technology transfer activities with external CDMO partners by preparing comprehensive technical documentation such as development reports, process summaries, and tech transfer packages to ensure successful external manufacturing</li>
<li>Stay current with emerging trends in LNP technologies and contribute to strategic process improvements</li>
<li>Track inventory, plan experiments, and contribute to an organized, quality-focused lab environment</li>
</ul>
REQUIRED QUALIFICATIONS
<ul>
<li>Ph.D. in Chemical Engineering, Bioengineering, Pharmaceutical Sciences, Chemistry, or a related field with minimum of 3 years relevant industry experience; or M.S. with 6 years; or B.S. with 8 years </li>
<li>Demonstrated expertise in LNP formulation and process development, including hands-on experience with microfluidic and high-shear mixing technologies, tangential flow filtration and dead-end filtration</li>
<li>Proficiency in analytical characterization techniques for LNPs, including DLS, fluorescence-based assays and HPLC/UPLC methods (CAD, UV, IP-RP, SEC, IEX), including method development, troubleshooting, and data interpretation</li>
<li>Experience with in-process and drug product stability studies </li>
<li>Proven success in applying DoEs and statistical analysis tools for process optimization</li>
<li>Experience supporting technology transfer of processes to external manufacturing environments, with a strong understanding of tech transfer best practices</li>
<li>Demonstrated strong organizational skills </li>
<li>A self-starter with demonstrated strong troubleshooting skills, capable of driving projects independently while contributing effectively in a collaborative, multidisciplinary environment</li>
</ul>
PREFERRED QUALIFICATIONS
<ul>
<li>Knowledge of regulatory expectations for CMC development</li>
<li>Familiarity with high-throughput screening methods</li>
<li>Exposure to cell-based assays for LNP functional characterization</li>
<li>Familiarity with data analysis tools and statistical methods such as JMP</li>
<li>Experience with AAV vector process development or a strong interest and adaptability to learn viral delivery systems</li>
</ul>
BENEFITS
<ul>
<li>Company-paid health/vision/dental benefits</li>
<li>Unlimited vacation and generous sick time</li>
<li>Company-sponsored meals and snacks</li>
<li>Wellness, caregiver and ergonomics benefits</li>
<li>401(k) with company matching</li>
</ul>
Base Salary Range: $138,000 - $178,000 per year Actual base salary will be determined by relevant professional experience, applicable skills, and internal equity. COMPANYMammoth Biosciences is a biotechnology company focused on leveraging its proprietary ultracompact CRISPR systems to develop long-term curative therapies, as well as other applications such as decentralized precision diagnostics. Founded by CRISPR pioneer and Nobel laureate Jennifer Doudna and Trevor Martin, Janice Chen, and Lucas Harrington, the company’s ultracompact proteins are designed to enable in vivo gene editing in difficult to reach tissues utilizing both nuclease applications and new editing modalities beyond double stranded breaks, including base editing, gene writing, and epigenetic editing. The company is building out its pipeline of potential in vivo gene editing therapeutics and capabilities and has partnerships with leading pharmaceutical and biotechnology companies to broaden the reach of its innovative and proprietary technology. Mammoth’s deep science and industry experience, along with a robust and differentiated intellectual property portfolio, have enabled the company to further its mission to transform the lives of patients and deliver on the full promise of CRISPR technologies. It is our policy and intent to provide equal opportunity to all persons without regard to race, color, religion, political affiliation, sex/gender (including gender expression/identity, pregnancy, childbirth and related medical conditions), marital status, registered domestic partner status, sexual orientation, age, ancestry, national origin, veteran status, disability, medical condition, genetic characteristics, and/or any other basis protected by law. This policy covers all facets of employment including, but not limited to: recruitment, selection, placement, promotions, transfers, demotions, terminations, training, and compensation. Mammoth Biosciences requires that all employees be vaccinated against COVID as a condition of at-will employment, with exceptions for medical or religious reasons in compliance with local, state, and federal law. 
PIf51ed5d7391b-25405-37791932

Scientist II/Senior Scientist I, LNP Process Development

<h3>Job Description</h3>
Immediate need for a talented Research Associate - I. This is a 03+ Months Contract opportunity with long-term potential and is located in Foster City, CA (Onsite). Please review the job description below and contact me ASAP if you are interested.
 
Job ID:25-84014
 
Pay Range: $41 - $41.99/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:
 
<ul>
<li>Transfer samples into pre-labeled barcode-compliant matrix tubes using the appropriate liquid handling platform.</li>
<li>Verify and update sample volume and concentration in the inventory spreadsheet.</li>
<li>Submit transferred samples to CRO for Sanger sequencing and verify sequence identity using the Geneious Prime sequence alignment tool.</li>
<li>Archive and register confirmed physical DNA stock in the inventory spreadsheet.</li>
<li>Consolidate sample tubes into matrix tube racks, barcode scan all samples, and record barcode information in the spreadsheet.</li>
</ul>
 
Key Requirements and Technology Experience:
 
<ul>
<li>Required Years of Experience: 0.5-3</li>
<li>Top 3 Required Skill Sets: Nucleic acid handling, Microsoft excel , DNA sequence alignment and analysis skill</li>
<li>Top 3 Nice to Have Skill Sets: Liquid handler operation eg Biomek etc,</li>
<li>Unique Selling Point of this role:</li>
<li>Required Degree or Certification Bachelor’s degree in related science discipline.</li>
</ul>
 
Our client is a leading Pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type 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.
 
By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

Research Associate - I.

<h3>Job Description</h3>
Job DescriptionPOSITION SUMMARY - Temp position (6 months) - On site in San Carlos, CANatera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. Schedule is Mon-Fri, from 830am-5pm. PRIMARY RESPONSIBILITIES
<ul>
<li>Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors</li>
<li>Responsible for maintaining updated understanding and knowledge of methods performed in the lab</li>
<li>Follows GLP (good laboratory practice): maintain cleans and organized work space</li>
<li>Completes training and other deadlines on time.</li>
<li>Recognizes and escalates equipment malfunctions; troubleshoots common errors on the lab floor</li>
<li>Recognizes, documents, and escalates protocol deviations in lab to lead/supervisor</li>
<li>Communicates with team and other departments (including via e-mail)</li>
<li>Provides feedback on day-to-day schedule and tasks to lead/supervisor</li>
<li>Assists teammates in completing daily tasks</li>
<li>Conducts himself/herself in a professional manner</li>
<li>Adheres to departmental expectations</li>
<li>This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job</li>
<li>Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.</li>
<li>Must maintain a current status on Natera training requirements.</li>
<li>Performs other duties as assigned.</li>
</ul>
QUALIFICATIONS
<ul>
<li>BS/BA in a biological science or similar field of study</li>
<li>0-2 years of industry-related experience</li>
</ul>
KNOWLEDGE, SKILLS AND ABILITIES
<ul>
<li>Excellent interpersonal, communication, computer, and pipetting skills</li>
<li>Excellent oral and written communication skills</li>
<li>Word processing and data management</li>
<li>Duties may require working various shifts, weekends, and/or overtime</li>
</ul>
The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years &amp; depth of experience, certifications and specific office location. This may differ in other locations due to cost of labor considerations.San Carlos, CA $1—$1 USD
OUR OPPORTUNITY
Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women's health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.
The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other. When you join Natera, you'll work hard and grow quickly. Working alongside the elite of the industry, you'll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.
WHAT WE OFFER
Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!
For more information, visit <a href="http://www.natera.com" target="_blank">www.natera.com</a>.
Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.
If you are based in California, we encourage you to read this important information for California residents. 
Link: <a href="https://www.natera.com/notice-of-data-collection-california-residents/" target="_blank">https://www.natera.com/notice-of-data-collection-california-residents/</a>
Please be advised that Natera will reach out to candidates with a @natera.com email domain ONLY. Email communications from all other domain names are not from Natera or its employees and are fraudulent. Natera does not request interviews via text messages and does not ask for personal information until a candidate has engaged with the company and has spoken to a recruiter and the hiring team. Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
For more information: - BBB announcement on job scams - FBI Cyber Crime resource page

Clinical Lab Associate I

<h3>Job Description</h3>
Job Description NOW HIRING ENTRY LEVEL CANDIDATES FOR A MEDICAL DEVICE COMPANY
Job Description
We are seeking a diligent and detail-oriented Clean Room Assembler to join our dynamic team. This role involves assembling components on a manufacturing line, working collaboratively with a team to complete assemblies, and ensuring all processes are conducted smoothly and accurately.
Responsibilities
<ul>
<li>Assemble components as part of a manufacturing line team.</li>
<li>Monitor and operate semi-automated manufacturing processes.</li>
<li>Work across four different lines including inspections, running automated machines, sub-assembly/welding, and testing.</li>
<li>Review batch records and ensure documentation accuracy.</li>
<li>Maintain a clean and safe work environment.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency with hand tools and following work instructions.</li>
<li>Experience with assembly in a cleanroom environment.</li>
<li>Ability to operate machinery in a fast-paced production setting.</li>
<li>Understanding of mechanical assembly and medical device protocols.</li>
<li>Knowledge of GMP standards and inspection processes.</li>
</ul>
Pay and Benefits
The pay range for this position is $17.40 - $17.40/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in San Diego,CA.
Application Deadline
This position is anticipated to close on Sep 19, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Clean Room Assembler

<h3>Job Description</h3>
Job DescriptionDescription:
Company Background
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.
GalactaBio is a preclinical stage biotechnology company developing a novel potential best-in-class AAV gene therapy for classic galactosemia, a severe genetic metabolism disorder.
 
Who You Are
We are seeking an experienced Principal Scientist/Associate Director in Bioanalytical Sciences to lead bioanalytical strategy and execution for our AAV-based gene therapy asset for the treatment of classic galactosemia. This individual will play a key leadership role in overseeing bioanalytical and biomarker method development, qualification, and validation through effective CRO management and cross-functional collaboration. The ideal candidate brings deep expertise in bioanalytical sciences for gene therapy, strong vendor management skills, and experience contributing to regulatory filings.
Requirements:
Responsibilities
<ul>
<li>Lead the design and execution of bioanalytical strategies for AAV gene therapy programs, spanning preclinical through clinical development.</li>
<li>Oversee and manage CROs/contract labs performing bioanalytical assays (qPCR/ddPCR, ELISA, ECL, LC-MS/MS, NGS, etc.) for biodistribution, pharmacokinetics, pharmacodynamics, immunogenicity, and biomarker assessments.</li>
<li>Provide scientific and technical oversight of assay development, validation, and sample analysis at CROs to ensure regulatory compliance (GLP/GCP).</li>
<li>Serve as the primary point of contact between internal teams and CRO partners to ensure quality, timelines, and deliverables.</li>
<li>Partner with preclinical, clinical, and regulatory colleagues to integrate bioanalytical data into study design, data interpretation, and regulatory submissions (e.g., IND, CTA, BLA).</li>
<li>Author/review bioanalytical sections of protocols, validation reports, study reports, and regulatory filings.</li>
<li>Monitor emerging regulatory guidance in gene therapy bioanalytics and ensure alignment of internal and CRO practices.</li>
<li>Travel: up to 20% of time</li>
</ul>
 
Education, Experience &amp; Skills Requirements
<ul>
<li>Ph.D. in Molecular Biology, Biochemistry, Pharmacology, or related discipline with 8+ years of industry experience in bioanalytical sciences; or M.S. with 10+ years.</li>
<li>Demonstrated expertise in nucleic acid and protein bioanalytical methods (qPCR/ddPCR, ELISA, ECLIA, immunoassays, LC-MS/MS, etc.).</li>
<li>Extensive experience managing CROs, including method development, qualification/validation, and sample analysis.</li>
<li>Strong knowledge of GLP/GCP and regulatory expectations for bioanalytical assays supporting gene therapy programs (FDA/EMA/ICH).</li>
<li>Experience authoring bioanalytical strategy in regulatory submissions.</li>
<li>Excellent leadership, communication, and vendor management skills; ability to drive execution through external partners.</li>
<li>Previous experience with AAV or other gene therapy platforms strongly preferred.</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>Excellent compensation package (Base, Performance Bonus, Equity)</li>
<li>Excellent benefits package</li>
<li>Flexible PTO</li>
<li>A fast-paced, data-driven, work environment with world-class R&amp;D minds and capabilities</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. 
 
The base pay range for this position is $190,000 to $ 250,000 per year. The actual compensation offered will be determined based on a number of job-related factors, including experience, skills, qualifications, and location. A bonus plan and equity will also be offered.

Principal Scientist/Associate Director, Bioanalytical Sciences

<h3>Job Description</h3>
Job Description
🚗 Why us? Your car and your home are the two most expensive things you’ll ever own — and the hardest to manage. At Jerry.ai, we’re building the first super app to help everyday Americans take control of both. From insurance and financing to repairs and real estate, we’re reimagining what it means to own and maintain your car and home. This is a $5 trillion+ problem — and we’re the only company tackling it end to end.
2024 was a milestone year for Jerry.ai. We delivered nearly 50% year-over-year revenue growth while reaching profitability for the first time in our history.
And we're just getting started! Our growth is driven by forward-thinking technology; Harvard Business Review covered the success of our chatbot less than a year after its launch and Jerry.ai is getting mentioned in many conversations about our use of GenAI, such as this Forbes article.
&amp;#x1F4BB; About the opportunity
We are looking for a Staff Applied Data Scientist (PhD) who is energized by working with a high caliber team and making a material difference in the lives of millions to join us! Reporting directly to our cofounder/CTO, you will architect and deploy advanced ML models with massive real-world applications (e.g. model &amp; predict user behavior, leverage LLMs and custom-built components to optimize our chatbot &amp; voicebot, etc). Come play a key role in helping us grow from 5M to 50M customers and become a $10B company in the next 4 years!
We have a fast-paced startup culture that empowers you to move quickly, test, iterate, and own projects end-to-end in an environment where your ideas matter and your impact is felt from day one. You’ll work with extremely talented and passionate engineers, data scientists, and analysts from companies like NVIDIA, Meta, Amazon, ByteDance, Square, Robinhood and more.
🫵 How you will make an impact
<ul>
<li>
Develop and architect complex machine learning models to address critical business challenges and drive company-wide strategic initiatives
</li>
<li>
Take ownership of the end-to-end modeling process, from initial ideation to model deployment and maintenance
</li>
<li>
Conduct thorough data preparation and analysis to ensure the quality and relevance of input data for modeling tasks
</li>
<li>
Collaborate closely with cross-functional teams, including Product and Data Engineering to productize and deploy models into production systems
</li>
<li>
Contribute to large-scale company initiatives aimed at solving problems that haven’t yet been touched by anyone at Jerry.ai
</li>
</ul>
🚀 Requirements
<ul>
<li>
PhD in Physics or related field
</li>
<li>
5+ years of experience building and deploying models from scratch.
</li>
<li>
Deep understanding of machine learning algorithms and techniques, with experience in building and deploying models from scratch.
</li>
<li>
Strong analytical and problem-solving skills, with the ability to translate complex business requirements into practical modeling solutions.
</li>
<li>
Passion for real-world application of machine learning, with a desire to make a significant impact on large-scale business initiatives.
</li>
</ul>
While we appreciate your interest and application, only applicants under consideration will be contacted.
Jerry.ai is proud to be an Equal Employment Opportunity employer. We prohibit discrimination based on race, religion, color, national origin, sex, pregnancy, reproductive health decisions or related medical conditions, sexual orientation, gender identity, gender expression, age, veteran status, disability, genetic information, or other characteristics protected by applicable local, state or federal laws. 
Jerry.ai is committed to providing reasonable accommodations for individuals with disabilities in our job application process. If you need assistance or an accommodation due to a disability, please contact us at <a href="mailto:recruiting@jerry.ai" target="_blank">recruiting@jerry.ai</a>
About Jerry.ai:
Jerry.ai is America’s first and only super app to radically simplify car ownership. We are redefining how people manage owning a car, one of their most expensive and time-consuming assets.&nbsp;
Backed by artificial intelligence and machine learning, Jerry.ai simplifies and automates owning and maintaining a car while providing personalized services for all car owners' needs. We spend every day innovating and improving our AI-powered app to provide the best possible experience for our customers. From car insurance and financing to maintenance and safety, Jerry.ai does it all.
We are the #1 rated and most downloaded app in our category with a 4.7 star rating in the App Store. We have more than 5 million customers — and we’re just getting started.&nbsp;
Jerry.ai was founded in 2017 by serial entrepreneurs and has raised more than $240 million in financing.
Join our team and work with passionate, curious and egoless people who love solving real-world problems. Help us build a revolutionary product that’s disrupting a massive market.

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