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<h3>Job Description</h3>
Job Description 
Position Summary:
The Electroless Cuposit Operator plays a key role in the application and maintenance of the Electroless Cuposit process, a specialized chemical plating method used to deposit a uniform, conductive copper layer on non-conductive surfaces in printed circuit board (PCB) manufacturing. This process is essential for forming interconnects through vias and drilled holes prior to electrolytic copper plating.
This position is responsible for preparing panels, managing the chemical bath parameters, analyzing process performance, and ensuring the Electroless Cuposit process meets production, quality, and reliability standards. 
Qualifications: To perform this job successfully, an individual must have a minimum of four (4) years’ in the printed circuit board industry and must be able to perform each essential duty satisfactory. The requirements listed below are representative of the knowledge, skill and/or ability required.
 
Responsibilities:
<ul>
<li>Operate and monitor the electroless copper plating line according to process specifications and safety protocols.</li>
<li>Prepare and load PCB panels into cuposit racks.</li>
<li>Handle and prepare chemical solutions safely and accurately.</li>
<li>Inspect boards for defects or process issues before and after electroless plating.</li>
<li>Clean and maintain equipment, tanks, and work areas in accordance with safety and quality standards.</li>
<li>Coordinate with Quality Assurance to ensure product conformance to specification.</li>
<li>Report equipment malfunctions or process deviations to maintenance or supervision.</li>
<li>Follow all environmental, health, and safety regulations including proper handling and disposal of hazardous materials.</li>
</ul>
Required Skills: 
<ul>
<li>Basic understanding of chemistry and plating processes preferred.</li>
<li>Strong attention to detail and commitment to quality.</li>
<li>Ability to read and interpret work instructions and production travelers.</li>
<li>Ability to work in a fast-paced manufacturing environment.</li>
<li>Good communication and teamwork skills.</li>
</ul>
Education/Experience:
<ul>
<li>High School Diploma or equivalent</li>
<li>Minimum four (4) years experience in the printed circuit industry, and three (3) years in copper plating.</li>
</ul>
Physical Requirements:
<ul>
<li>Ability to lift up to 50 lbs.</li>
<li>Standing, walking, and reaching for extended periods.</li>
<li>Use of PPE including gloves and goggles.</li>
</ul>
 
ITAR Compliance Notice
This position requires compliance with the International Traffic in Arms Regulations (ITAR). Under ITAR, candidates must be a U.S. citizen, U.S. lawful permanent resident (e.g., "Green Card" holder), asylee, or refugee as defined by 8 U.S.C. 1324b(a)(3). Applicants who do not meet this requirement may not be eligible for employment in this position.
Summit Interconnect is an Equal Opportunity Employer We are committed to fostering an inclusive and diverse workplace where everyone is valued and respected. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic.

Electroless Cuposit Operator (Grave Shift)

<h3>Job Description</h3>
Job Description
K2 Space is building large, high-powered spacecraft for the next generation of space development. Backed by Lightspeed Venture Partners, Altimeter Capital, and many others ($200M raised to date), we intend to mass produce the highest-powered satellite platforms ever built for missions across LEO to Deep Space. 
The rise of launch vehicles like Falcon 9 and Starship enables the move from an era of mass constraint to one of mass abundance. We believe this new era requires spacecraft with a fundamentally different design in order to fully utilize the massive rockets coming to market. 
We're a team that believes the future lies in building large, high-powered satellites that can handle multiple orbits. This is a necessity if we ever want to develop the solar system, and become a Kardashev Type II (K2) civilization. 
If you are a motivated individual who thrives in a fast-paced environment and you're excited about contributing to the success of a groundbreaking Series B space startup, we'd love for you to apply. 
The Role
You will be responsible for the day-to-day management of our CAD system and its integration with our Product Lifecycle Management (PLM) system. You will work directly with the engineering end users, our software vendors, and our internal IT Systems team. You will be the lead SME and owner for the technical communication with external software vendors and integrators, and you will be responsible for the success of implementing upgrades, customizations, and addressing any issues with the implementation. 
Responsibilities
<ul>
<li>Drive and contribute to improvements in PLM processes and the resulting changes in NX and supported CAD systems </li>
<li>Work with users to develop/update tool customizations to improve efficiency </li>
<li>Lead the development and maintenance of common parts and features </li>
<li>Create and manage templates and best practices to maintain consistency and high quality across all of the design teams </li>
<li>Provide a robust CAD operating environment through promptly responding to user requests for support </li>
<li>Administer and support user access, permissions, and licensing to provide secure access to NX and supported CAD systems </li>
<li>Work with our IT team to manage and maintain CAD tool servers &amp; databases </li>
<li>Support and provide training to new and existing staff </li>
<li>Create and maintain documentation for user support processes </li>
<li>Develop and deploy proprietary and 3rd party NX and Teamcenter Tools </li>
</ul>
Qualifications
<ul>
<li>3+ years of experience supporting CAD/PLM for a hardware engineering team </li>
<li>Experience with implementation of CAD integration on Siemens NX and Teamcenter PLM </li>
<li>Experience with developing tools, automations, and custom configurations in NX and Teamcenter </li>
<li>Experience with creating and maintaining templates, libraries, and user best practices </li>
<li>Demonstrated strong knowledge of CAD modeling, drawing creation, and drafting processes </li>
</ul>
Nice to Have
<ul>
<li>Bachelor of Science degree in a technical field with experience in developing, documenting, and training to CAD standards, including formal drafting standards and modeling standards. </li>
<li>Experience with Altium products, ECAD/MCAD collaboration, and associated integrations </li>
<li>Experience with the drafting, the practical application of GD&amp;T, and hardware inspections </li>
<li>Experience with design for metallic machined, composite, and tooling structures </li>
<li>Experience with MES, MRP, and other production systems </li>
<li>Experience with NX Open </li>
<li>Experience with Oracle or SQL Server databases </li>
<li>Independent and self-motivated mindset, with strong organizational, written, and oral communication skills </li>
</ul>
Compensation and Benefits:
<ul>
<li>Base salary range for this role is $90,000 - $150,000 + equity in the company </li>
<li>Salary will be based on several factors including, but not limited to: knowledge and skills, education, and experience level </li>
<li>Comprehensive benefits package including unlimited paid time off, medical/dental/vision coverage, life insurance, paid parental leave, and many other perks </li>
</ul>
If you don't meet 100% of the preferred skills and experience, we encourage you to still apply! Building a spacecraft unlike any other requires a team unlike any other and non-traditional career twists and turns are encouraged!
If you need a reasonable accommodation as part of your application for employment or interviews with us, please let us know.
Export Compliance
As defined in the ITAR, "U.S. Persons" include U.S. citizens, lawful permanent residents (i.e., Green Card holders), and certain protected individuals (e.g., refugees/asylees, American Samoans). Please consult with a knowledgeable advisor if you are unsure whether you are a "U.S. Person."
The person hired for this role will have access to information and items controlled by U.S. export control regulations, including the export control regulations outlined in the International Traffic in Arms Regulation (ITAR). The person hired for this role must therefore either be a "U.S. person" as defined by 22 C.F.R. § 120.15 or otherwise eligible for a federally issued export control license.
Equal Opportunity
K2 Space is an Equal Opportunity Employer; employment with K2 Space is governed on the basis of merit, competence and qualifications and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability or any other legally protected status.

Teamcenter / NX Administrator

<h3>Job Description</h3>
Job Description
Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.
Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.
Summary: 
This leadership role within Medical and Clinical Affairs is responsible for strategic management of Scientific Affairs activities including scientific communications, publication and podium planning, KOL engagement and pre-clinical evidence generation. The role requires cross-functional collaboration with Clinical Operations, Marketing, R&amp;D, Sales, and Regulatory to drive impactful outcomes. The ideal candidate will have a deep understanding of scientific research and clinical development and will oversee medical writing, as well as biostatistical support for all scientific affairs research engagements. This position requires strong communication skills and the ability to lead and support a fast-paced, dynamic team 
In This Role, You Will:
<ul>
<li>Scientific Communication </li>
</ul>
<ul>
<li>Develop project management tools that clearly demonstrate scientific communication plans (i.e., publication and podium plans) </li>
</ul>
<ul>
<li>Manage the development and submission of high-quality peer-reviewed publications, abstracts and presentations by overseeing medical writing. Directly write, edit, and analyze data as needed </li>
</ul>
<ul>
<li>Manage biostatistics and programming requests required for all scientific communication deliverables </li>
</ul>
<ul>
<li>Own relationships with investigators / authors of publications, abstracts and presentations. This includes administrative oversight of HCP engagements, contracts and payments </li>
</ul>
<ul>
<li>In-person support of KOL presentations at meetings as requested </li>
</ul>
<ul>
<li>Pre-clinical and Clinical Research </li>
</ul>
<ul>
<li>Support trial design, protocol development and statistical analysis plans by deploying available resources </li>
</ul>
<ul>
<li>Organize and/or lead meetings with clinical operations, clinical development engineering and R&amp;D ensuring evidence generation is aligned with major urology meetings. Elevate risks as they emerge </li>
</ul>
<ul>
<li>Assist with and eventually lead strategic evaluation of pre-clinical investigator-initiated studies </li>
</ul>
<ul>
<li>Marketing Initiatives </li>
</ul>
<ul>
<li>Translate scientific data for the commercial team and ensure marketing messages are fair and balanced </li>
</ul>
<ul>
<li>Distill scientific evidence that will be presented at urology meetings focusing on SURE/CVAC and relevant competitors. Assist with organizing meeting coverage </li>
</ul>
<ul>
<li>Support medical communications review, train medical writers on content review </li>
</ul>
<ul>
<li>Regulatory and Reimbursement Initiatives </li>
</ul>
<ul>
<li>Oversee medical writing and literature reviews for all FDA submissions and Clinical Evaluation Reports (CERs) as requested by deploying available resources </li>
</ul>
<ul>
<li>Manage healthcare claims analysis including benchmark research and vendor identification </li>
</ul>
<ul>
<li>Organize meetings or liaise with the market access team to ensure evidence generation and publication plans meet foreseeable needs </li>
</ul>
<ul>
<li>Other requirements </li>
</ul>
<ul>
<li>Attend in-person team building events and contribute meaningfully </li>
</ul>
<ul>
<li>Attend society meetings as requested to ensure a successful podium plan and seek out immersive research presentations </li>
</ul>
<ul>
<li>Contribute to a culture of innovation, collaboration and scientific excellence </li>
</ul>
<ul>
<li>Perform additional activities as assigned by supervisor </li>
</ul>
Who You Will Report To:
<ul>
<li> Director, Scientific Affairs</li>
</ul>
Requirements:
<ul>
<li>PhD preferred with proven biostatistical training and application in a relevant scientific discipline (e.g., Life Sciences, Pharmaceutical Sciences, Clinical Research, or similar fields) </li>
</ul>
<ul>
<li>Minimum of 3 years of experience in scientific affairs or clinical research within the biotech industry. Direct experience in urology or nephrology required </li>
</ul>
<ul>
<li>Strong publication record required with at least 2 first author publications and multiple first author research abstracts submitted to society meetings. Please include publication record as part of your resume or CV </li>
</ul>
<ul>
<li>Demonstrated ability and past experience interacting with urologists and/or endourologists </li>
</ul>
<ul>
<li>Experience having direct reports, teaching or overseeing graduate or undergraduate students required </li>
</ul>
<ul>
<li>Management of various research related projects including but not limited to clinical pipeline deliverables, regulatory submissions, pre-clinical experimentation, competitive intelligence gathering and databased analyses </li>
</ul>
<ul>
<li>Strong strategic thinking and interpersonal skills with the ability to work in a fast-paced, dynamic start-up environment </li>
</ul>
<ul>
<li>Exceptional written and verbal communication skills, with the ability to translate complex scientific data into clear, concise messaging for diverse audiences </li>
</ul>
<ul>
<li>Ability to work independently with sound autonomous decision making </li>
</ul>
<ul>
<li>Work location: Pleasanton, CA. </li>
</ul>
<ul>
<li>Travel: Up to 25% </li>
</ul>
<ul>
<li>Full-time employment </li>
</ul>
<ul>
<li>Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, and all other international regulatory requirements with which the company complies </li>
</ul>
<ul>
<li>Compliance with relevant county, state, and Federal rules regarding vaccinations. </li>
</ul>
What We Offer:
At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself. 
We also offer an attractive compensation package, which includes: 
<ul>
<li>A competitive base salary range of $140,000 - $155,000 and variable incentive plan </li>
</ul>
<ul>
<li>Stock options – ownership and a stake in growing a mission-driven company </li>
</ul>
<ul>
<li>Employee benefits package that includes 401(k), healthcare insurance and paid vacation </li>
</ul>
Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued, but prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities which strengthen our focus and fuel our growth.
Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth. Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics
Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. 
Disclaimer:
At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:
<ul>
<li>Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.</li>
<li>Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.</li>
<li>Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of <a href="mailto:firstname.lastname@calyxoinc.com" target="_blank">firstname.lastname@calyxoinc.com</a>. If you receive a request for information from any other domain, please contact us directly at <a href="mailto:info@calyxoinc.comto" target="_blank">info@calyxoinc.comto</a> verify the legitimacy of the communication.</li>
</ul>
We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.

Manager Scientific Affairs- Pleasanton, CA

<h3>Job Description</h3>
Job DescriptionAI Research Scientist/Engineer
Menlo Park, CA | On-Site | Full-Time/Direct Hire 
Seeking top-tier PhDs (Bay Area preferred) with ICML/ICLR publications in LLM training and inference optimization—no vision/audio, just pure language; diffusion model experience a plus.
 Client Opportunity | Through Phizenix (WBENC &amp; Minority-Certified Recruiting Partner)
Join a trailblazing AI startup that's reinventing how large language models are built—with diffusion-powered LLMs that generate faster, adapt smarter, and handle multimodal data like no other.
We're looking for a Research Scientist / Engineer who's ready to move beyond traditional autoregressive methods and help shape the next wave of generative AI. You'll collaborate with pioneers in AI research, design novel model architectures, and scale your ideas from paper to production.
What You'll Be Doing
<ul>
<li>
Design and refine LLM architectures built on a diffusion-first paradigm
</li>
<li>
Develop cutting-edge training strategies and custom loss functions
</li>
<li>
Translate research into real-world systems for enterprise-scale deployments
</li>
<li>
Explore constraint-aware generation and controlled outputs
</li>
<li>
Push the limits of model efficiency, scalability, and multi-modal capabilities
</li>
</ul>
Must-Haves
<ul>
<li>
Must have a PhD in Computer Science, Machine Learning, or a related field
</li>
<li>
Hands-on experience with PyTorch and LLM fundamentals (transformers, KV caching, etc.)
</li>
<li>Should have recent/or any ICLR/ICML publications in LLM inference optimization would be ideal. </li>
<li>
Familiarity with diffusion models and distributed model training
</li>
<li>
Solid research-to-production mindset with 2+ years in an ML/AI role
</li>
</ul>
Bonus Points For
<ul>
<li>
Training LLMs from scratch and optimizing large-scale runs
</li>
<li>
Advanced training tactics (e.g., mixed precision, gradient accumulation)
</li>
<li>
Experience with cross-modal modeling and inference frameworks like vLLM, TensorRT
</li>
<li>
A background in model efficiency, optimization theory, or infrastructure-aware research
</li>
</ul>
At Phizenix, we're proud to partner with diverse and inclusive teams building AI that matters. If you're ready to build, innovate, and publish with one of the boldest teams in AI—this is your moment.
California Pay Range$180,000—$200,000 USD

AI Research Scientist/Engineer

<h3>Job Description</h3>
Job Description
About Cleerly
We're Cleerly – a healthcare company that's revolutionizing how heart disease is diagnosed, treated, and tracked. We were founded in 2017 by one of the world's leading cardiologists and are a growing team of world-class engineering, operations, medical affairs, marketing, and sales leaders. We raised $223M in Series C funding in 2022 which has enabled rapid growth and continued support of our mission. In December 2024 we received an additional $106M in a Series C extension funding. Most of our teams work remotely and have access to our offices in Denver, Colorado, New, York, New York, Dallas, Texas, and Lisbon, Portugal with some roles requiring you to be on-site in a location. 
Cleerly has created a new standard of care for heart disease through value-based, AI-driven precision diagnostic solutions with the goal of helping prevent heart attacks. Our technology goes beyond traditional measures of heart disease by enabling comprehensive quantification and characterization of atherosclerosis, or plaque buildup, in each of the heart arteries. Cleerly's solutions are supported by more than a decade of performing some of the world's largest clinical trials to identify important findings beyond symptoms that increase a person's risk of heart attacks. 
At Cleerly, we collaborate digitally and use a wide variety of systems. Our people use Google Workspace (GMail, Drive, Docs, Sheets, Slides), Slack, Confluence/Jira, and Zoom Video, prior experience in these areas is a plus. Role or department specific technology needs may vary and will be listed as requirements in the job description. 
About the Opportunity
Cleerly's Core Lab has a great opportunity to join our team of imaging professionals as an Analyst in the US Imaging Services. An analyst reviews CT exams after AI algorithm processing has been completed. This is a mostly remote role with some travel required, including in-person training. Required travel is approximately 4 weeks per year, but may vary based on departmental needs. No experience in coronary analysis is required. The ideal candidate should enjoy working in a process oriented environment with a highly motivated team helping Cleerly reach our mission of creating a world without heart attacks. West coast time-zone a plus, but will accept qualified candidates in other time zones which will require evening shifts for coverage needs. Weekend shifts in the future are possible, but not yet implemented. The candidate will have to travel to the Washington, DC area for an extensive 2 week in-person training session during onboarding and a follow-up one-week session approximately 2 months later. Potential to travel abroad in the future, so the candidate must have a passport or apply for one upon hiring. 
We are looking for someone based in the West Coast. This role does require working on holidays,weekend shifts and having flexible schedules to help the business. 
About the Team
The Core Lab is a team of imaging professionals in the United States and Portugal, focused on helping Cleerly reach its mission of creating a world without heart attacks. These professionals review AI outputs of Coronary CTA exams prior to report approval. 
Responsibilities
<ul>
<li>Analyze outputs generated by artificial intelligence from Coronary CTA exams.</li>
<li>Evaluate Coronary CTA exams for image quality.</li>
<li>Perform administrative duties as required.</li>
<li>Support to the Applications Team liaising with sites, if necessary</li>
<li>Participation in continuous improvement projects</li>
<li>Comply with process and quality standards.</li>
</ul>
Requirements
<ul>
<li>Associates Degree in Radiography</li>
<li>ARRT certification</li>
<li>Experience in CT a plus, but not required</li>
<li>Coronary CTA or 3D post-processing experience is a plus, but not required</li>
<li>High attention to detail</li>
<li>Great interpersonal skills - must be able to work well in a team environment</li>
<li>Desire and ability to learn new technologies - willing to learn</li>
<li>Mostly remote work from home, so must have high speed internet.</li>
<li>Shift work, including evenings and weekends possible in the future.</li>
<li>Some travel (2-4 weeks per year expected, but may vary)</li>
<li>Reside in New York (tri-state area included) or Denver, CO</li>
<li>Able to work pacific time and/or evening shifts from other time zones to provide required time zone coverage.</li>
<li>Valid US passport</li>
</ul>
TTC*: $82,500 - $93,500
*Total Target Compensation (TTC): Total Cash Compensation (including base pay, variable pay, commission, bonuses, etc.). We hire employees anywhere within the United States and account for geography when determining base salary.
Working at Cleerly takes HEART. Discover our Core Values:
<ul>
<li>H: Humility- be a servant leader</li>
<li>E: Excellence- deliver world-changing results</li>
<li>A: Accountability- do what you say; expect the same from others</li>
<li>R: Remarkable- inspire &amp; innovate with impact</li>
<li>T: Teamwork- together we win</li>
</ul>
Don't meet 100 percent of the qualifications? Apply anyway and help us diversify our candidate pool and workforce. We value experience, whether gained formally or informally on the job or through other experiences. Job duties, activities and responsibilities are subject to change by our company.
OUR COMPANY IS AN EQUAL OPPORTUNITY EMPLOYER. We do not discriminate on the basis of race, color, national origin, ancestry, citizenship status, protected veteran status, religion, physical or mental disability, marital status, sex, sexual orientation, gender identity or expression, age, or any other basis protected by law, ordinance, or regulation.
By submitting your application, you agree to receive SMS messages from Cleerly recruiters throughout the interview process. Message frequency may vary. Message and data rates may apply. You can STOP messaging by sending STOP and get more help by sending HELP. For more information see our Privacy Policy (<a href="https://cleerlyhealth.com/privacy-policy" target="_blank">https://cleerlyhealth.com/privacy-policy</a>). All official emails will come from @cleerlyhealth.com email accounts. 
#Cleerly

Analyst, Core Lab-Imaging Services (PT hours)

<h3>Job Description</h3>
Job Description
Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing.
Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates.
Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI &amp; San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. 
The Position
Arrowhead is seeking a highly motivated Research Technician I to join our growing in Vivo Pharmacology teamwithin the Research Department at our San Diego site. The successful candidate will be joining a team dedicated to discovering, developing, and translating novel drug targets.
Responsibilities 
<ul>
<li>Performs animal health checks which may include performing post dose observations and documents study related health changes</li>
<li>Performs sanitation of vivarium</li>
<li>Performs routine cage changes</li>
<li>Performs routine animal colony health surveillance</li>
<li>Performs general husbandry duties</li>
<li>Performs animal receiving
<ul>
<li>Housing</li>
<li>Ear tagging</li>
<li>Create cage cards</li>
<li>Update study in Benchling In Vivo</li>
</ul>
</li>
<li>May assist with In Vivo activities such as labeling tubes, shaving animals prior to surgery, or euthanizing animals</li>
<li>Assists with Operations / Administrative Activities
<ul>
<li>Updates inventory of commonly used supplies</li>
<li>Maintains and updates study paperwork</li>
</ul>
</li>
<li>May work with the mouse breeding colony</li>
<li>Weekend and holiday health checks, as needed</li>
<li>Other duties as assigned</li>
</ul>
Qualifications
<ul>
<li>High school diploma with a minimum of at least 2 years demonstrated experience working with rodents in a research laboratory setting is preferred
<ul>
<li>Alternatively, a Bachelor's degree in Biology or related field</li>
</ul>
</li>
<li>Background in animal husbandry, restraint and handling preferred</li>
<li>Must demonstrate a commitment to quality care of laboratory animals </li>
<li>Must possess a strong attention to detail </li>
<li>Ability to read, record and communicate information </li>
</ul>
California pay range $48,000—$52,000 USD
Arrowhead provides competitive salaries and an excellent benefit package. 
All applicants must have authorization to work in the US for a company. 
California Applicant Privacy Policy

Research Technician I, In Vivo Husbandry

<h3>Job Description</h3>
Job Description
About the Company:
Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market. For over a decade, we've remained steadfast in our commitment to core values of excellence, integrity, and respect for people. Our team of professionals collaborates tirelessly to pioneer advancements in manufacturing, distribution, and quality control, ensuring a holistic approach to healthcare. Through vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. We prioritize our employees' well-being by offering competitive pay, comprehensive benefits, and robust training and development opportunities. By investing in our workforce and fostering a culture of growth and support, we empower our team to drive innovation and make a positive impact in the healthcare industry. At Nivagen, our mission is clear: to make a meaningful difference in people's lives by delivering high-quality, affordable medications while upholding the highest standards of integrity and excellence.
Job Location:
Nivagen Pharmaceuticals Inc., Sacramento, CA
3900 Duckhorn Dr, Sacramento, CA 95834
About the Job: 
Title of the Position: QC Chemist
As a QC chemist at Nivagen you will be responsible for conducting analytical tests on pharmaceutical products, ensuring that they meet regulatory standards such as those set by the FDA and ICH. This role involves performing tests on raw materials, intermediates, and finished dosage forms to guarantee product safety, efficacy, and quality in compliance with Good Manufacturing Practices (GMP) and other regulatory standards.
Responsibilities:
<ul>
<li>Operate and maintain analytical instruments such as GC, GC-MS, LC-MS, UPLC, and HPLC, which are equipped with UV-Vis, PDA, and CAD detectors. </li>
<li>Ensure proper calibration and regular maintenance of laboratory equipment to guarantee accuracy and precision in results.</li>
<li>Assist in developing and validating analytical methods for new products, ensuring compliance with regulatory guidelines, including those from ICH and FDA.</li>
<li>Perform qualitative and quantitative analyses on raw materials, in-process materials, and finished products using validated methods to ensure compliance with required specifications.</li>
<li>Conduct stability studies on products following ICH guidelines, adhering to stability protocols, and documenting results for regulatory submissions.</li>
<li>Investigate deviations and out-of-specification (OOS) results, conduct root cause analysis, and implement corrective and preventive actions (CAPA) to address and prevent recurrence.</li>
<li>Ensure all testing adheres strictly to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant regulatory standards.</li>
<li>Implement ICH Q2 (R1) guidelines for method validation and participate in internal and external audits to maintain laboratory compliance.</li>
<li>Collaborate with R&amp;D, production, and quality assurance teams to support product development and commercialization efforts, and provide assistance during regulatory inspections.</li>
<li>Perform any additional tasks as assigned by the Chief Scientific Officer (CSO).</li>
</ul>
Qualifications:
Education/Experience:
<ul>
<li>Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related field.</li>
<li>1-5 years of experience in a pharmaceutical quality control laboratory.</li>
</ul>
Knowledge, Skills, and Abilities:
<ul>
<li>Proficiency in analytical techniques (HPLC, GC, FTIR, UV-Vis, Dissolution Testing, etc.).</li>
<li>Strong understanding of pharmaceutical regulations (FDA and ICH).</li>
<li>Experience with GMP, GLP, and GDP requirements.</li>
<li>Ability to troubleshoot analytical issues and conduct root cause analysis.</li>
<li>Strong communication and documentation skills.</li>
<li>Excellent attention to detail and organizational skills.</li>
<li>Familiarity with FDA, ICH guidelines, including ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients) and ICH Q10 (Pharmaceutical Quality System).</li>
<li>Knowledge of stability testing guidelines, including ICH Q1A.</li>
<li>Ability to stand and work for extended periods in a laboratory environment.</li>
<li>Comfortable handling chemicals and pharmaceutical substances.</li>
</ul>
Requirements:
<ul>
<li>Must live or willing to move to Sacramento Metropolitan Region (Approx. 40 miles' radius)</li>
</ul>
Benefits:
<ul>
<li>Pay range $70,000 - 75,000 per Year</li>
<li>Yearly bonus eligibility</li>
<li>Benefits: Nivagen offers a wide variety of benefits and programs to support health and well-being</li>
<li>Medical, dental and vision coverage</li>
<li>Paid time off plan</li>
<li>401k savings plan</li>
</ul>
Additional Information:
Nivagen to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.

QC chemist

<h3>Job Description</h3>
Job Description
Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date.
We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team.
We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment.
For more information see: <a href="http://www.septerna.com" target="_blank">www.septerna.com</a>.
The Role:
We are seeking an accomplished and motivated DMPK scientist to join our team as a Staff Scientist/Senior Staff Scientist, DMPK. This individual will play a pivotal role in driving our drug discovery efforts while also providing strategic support to our development-stage programs as needed. The role offers a unique opportunity to work across the R&amp;D continuum – from lead optimization through candidate nomination and IND-enabling studies – collaborating with innovative, cross-functional teams committed to developing safe and efficacious medicines for patients. 
The successful candidate will serve as a scientific leader within the DMPK function, providing subject matter expertise and program-facing support across small molecule discovery programs. They will play a key role in ensuring continuity of DMPK strategies as programs advance into development and will contribute to functional strategy and capacity-building within the DMPK function.
Key responsibilities:
<ul>
<li>Provide strategic and hands-on leadership of DMPK activities for multiple discovery-stage programs, including ADME/PK optimization, candidate nomination, and early development support</li>
<li>Represent DMPK in cross-functional project teams and provide integrated ADME/PK guidance aligned with project objectives, timelines, and regulatory expectations</li>
<li>Design, interpret, and report in vitro and in vivo studies (internal and CRO-based), including PK profiling, in vitro to in vivo correlations, and drug-drug interaction risk assessment</li>
<li>Elucidate predictive ADME relationships, assess in vitro to in vivo correlations, PK/PD relationships, and perform human efficacious dose predictions using different approaches</li>
<li>Guide development candidate selection through integration of ADME, PK/PD, physicochemical, and translational PK/PD modeling</li>
<li>Author and review high-quality regulatory documents (e.g., INDs, IBs, and other regulatory filings) and contribute to regulatory strategy in collaboration with project and regulatory teams</li>
<li>Collaborate closely with research and development colleagues and contribute to the growth of DMPK capabilities across the organization</li>
<li>Provide scientific input to portfolio-level discussions and help align DMPK strategies with overall project and organizational goals</li>
</ul>
Qualifications:
<ul>
<li>Doctorate degree in Pharmaceutical Sciences, Drug Metabolism, Pharmacokinetics, Biochemistry, or related discipline with 6+ years of relevant industry experience; or MS/BS degree with 10+ years of hands-on experience in DMPK within the pharmaceutical/biotech industry</li>
<li>Proven track record of impactful scientific contributions to discovery and development programs (such as regulatory submissions and/or literature publications) demonstrating technical proficiency, independent thinking, and scientific creativity</li>
<li>Deep understanding of DMPK science and its application to drug discovery and development, including a working knowledge of PK/PD modeling and human PK projection approaches</li>
<li>Demonstrated technical proficiency, scientific creativity, strategic thinking, problem solving ability, and capable of independently designing and executing impactful hypothesis-driven experiments</li>
<li>Experience supporting IND-enabling studies, including DDI risk assessments, human dose projection, and authoring of regulatory documents</li>
<li>Up to date knowledge of technological and regulatory advances in the DMPK functional area</li>
<li>Outstanding communication skills with demonstrated ability to make effective presentations in a broad range of settings, with strong collaboration and organizational skills</li>
<li>The successful candidate will be motivated to discover new disease-modifying therapeutics for patients and enjoy working in a fast-paced dynamic team environment</li>
</ul>
The anticipated salary range for candidates who will work in South San Francisco, CA is $140,000 - $175,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions.
We are 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.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited.
Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are 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. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Staff Scientist/Senior Staff Scientist, DMPK (industry experience required)

<h3>Job Description</h3>
Job Description
Location: San Francisco (Hybrid in SF highly preferred, US only)
What is Verse? 
Organizations today are under growing pressure to navigate the transition to clean energy — not just to meet sustainability goals, but to manage risk, control costs, and build long-term resilience. Yet the complexity of energy markets and a lack of accessible tools have made it difficult for most companies to take meaningful action. Verse was created to change that.
Our mission is to make the case for clean energy irrefutable. Through our AI-powered platform, Aria, we help organizations plan, procure, and operate clean energy to achieve their financial and sustainability goals. Verse transforms clean energy ambition into action — giving businesses the clarity and confidence to lead in a rapidly evolving energy landscape.
The Role
Verse is seeking an experienced Quantitative Analyst to join our Data Science Team. In this position, you will play a key role in advancing cutting-edge algorithms to solve problems in electricity markets, renewable procurement, and risk management. Your research will help our customers deploy and operate renewable energy and battery storage resources, and will contribute to the transition toward a low-carbon economy. As a member of the Verse team, you will work in an interdisciplinary and collaborative environment where your expertise in energy systems, machine learning, optimization, and statistical methods will be key to delivering impactful solutions.
Key Responsibilities
<ul>
<li>Conduct Advanced Research: Lead and contribute to high-impact research focused on energy systems, including renewable energy (solar, wind, etc.), energy storage, and novel technologies (e.g. green hydrogen). Independently develop data-driven solutions to problems our customers in this sector are facing.</li>
<li>Machine Learning &amp; Optimization: Apply machine learning algorithms, optimization techniques, and statistical methods to analyze energy data, advance our software offerings, and improve support for decision-making in the energy sector.</li>
<li>Data Analysis and Modeling: Use advanced data analysis techniques, simulations, and energy modeling tools to forecast and provide insights relative to the performance of renewable energy resources, battery storage, and novel technologies.</li>
<li>Collaboration and Teamwork: Work closely across business units and with our customers to share findings and ensure research outcomes are applied to real-world problems.</li>
<li>Stay Current with Industry Trends: Stay up-to-date with developments in electricity markets and in advancements in quantitative research methods.</li>
</ul>
What We're Looking For (Minimum Qualifications)
<ul>
<li>Masters Degree (or higher) in Engineering, Economics, Computer Science, Operations Research, or a related field. A bachelor's degree in a quantitative discipline with 3 years of experience in the energy industry may be considered in place of a graduate degree.</li>
<li>Expertise in machine learning, optimization techniques, and statistical methods applied to energy systems.</li>
<li>Understanding of energy technologies, including solar, wind, battery storage, and grid integration.</li>
<li>Strong analytical, problem-solving, and critical thinking skills, particularly in the application of machine learning and optimization methods to energy challenges.</li>
<li>Proficiency in Python programming and data analysis tools.</li>
<li>Strong experience in applying statistical methods to real-world energy data.</li>
<li>Excellent written and verbal communication skills, with the ability to present complex findings clearly to both technical and non-technical audiences.</li>
<li>Ability to collaborate effectively in multidisciplinary teams.</li>
</ul>
What Will Make You Standout (Preferred Qualifications)
<ul>
<li>PhD in Engineering, Operations Research, Economics or related field.</li>
<li>Familiarity with electricity markets (US and global), grid-scale and/or BTM battery storage, energy project development and operation is highly desirable.</li>
<li>Previous experience in a consulting role is a plus, particularly related to energy systems or technology development.</li>
<li>Deep knowledge of electricity markets and financial risk.</li>
<li>Previous experience working in industry or with government agencies on energy-related projects.</li>
</ul>
What Makes Verse a Great Place to Work? 
<ul>
<li>Lead with Empathy: We lift each other up with humility and kindness, always putting colleagues and customers first</li>
<li>Be Honest &amp; Transparent: We prioritize effective communication to build trust with our team, customers, and stakeholders</li>
<li>Move with Balance &amp; Precision: We believe speed and perseverance must be accompanied by thoughtfulness and reflection</li>
<li>Leave the World a Better Place: We are passionate about our mission, and we strive to create a sustainable world for future generations</li>
</ul>
Base Pay Range
$120,000 - $155,000
This is the estimated base salary range for this position, which does not include the value of benefits or a potential equity grant. A wide range of factors are considered in making compensation decisions, including but not limited to skill sets, market conditions, experience and training, licensure and certifications, and business and organizational needs.
Benefits and Employee Perks 
<ul>
<li>Competitive compensation and equity grant at a high-growth start up </li>
<li>Comprehensive benefits package including medical, dental and vision insurance, and 401k </li>
<li>Flexible hours and unlimited PTO </li>
<li>Diverse and inclusive working environment </li>
</ul>
Verse is an equal opportunity employer. All applicants and employees are considered for hire, promotion, and compensation without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, marital or familial status.

Quantitative Analyst

<h3>Job Description</h3>
Job Description
Xometry (NASDAQ: XMTR) powers the industries of today and tomorrow by connecting the people with big ideas to the manufacturers who can bring them to life. Xometry's digital marketplace gives manufacturers the critical resources they need to grow their business while also making it easy for buyers at Fortune 1000 companies to tap into global manufacturing capacity.
Xometry is seeking a Principal Data &amp; ML Scientist to join our Generative AI team. The ideal candidate will have a passion for advancing machine learning and generative AI capabilities, particularly for fine-tuning generative and language models, multimodal document understanding, and structured data extraction. This person will leverage their expertise in generative models and data science to develop and optimize innovative AI-driven solutions that enhance Xometry's service offerings.
Responsibilities:
<ul>
<li>Provide technical leadership to the Generative AI team, setting technical direction, defining best practices, and ensuring the team follows industry standards in AI and ML development.</li>
<li>Lead strategic planning and roadmap development for generative AI initiatives, identifying high-impact projects and aligning them with Xometry's business objectives.</li>
<li>Develop and deploy generative AI models and large language models (LLMs) for multimodal document processing, focusing on extracting structured data from technical drawings, purchasing orders, and other complex documents.</li>
<li>Lead the exploration and development of innovative text and image-based data processing solutions, including training and fine-tuning generative and language models.</li>
<li>Design and implement efficient workflows for data preparation, cleaning, and augmentation to support the training of generative AI models.</li>
<li>Utilize cloud platforms (e.g., Amazon Web Services) for large-scale data processing, model training, and deployment.</li>
<li>Collaborate with cross-functional teams, including engineering and business teams, to align generative AI solutions with business needs and drive impactful applications.</li>
<li>Mentor and guide team members on advanced machine learning techniques, model architecture design, and problem-solving strategies to elevate the team's technical capabilities.</li>
<li>Continuously experiment and iterate on model performance, tuning architectures and parameters to improve accuracy and efficiency in a fast-paced, agile environment.</li>
<li>Stay updated with the latest research in generative AI, deep learning, and multimodal data processing, incorporating best practices and advancements into model development.</li>
</ul>
Qualifications:
<ul>
<li>A bachelor's degree is required, but an advanced degree (M.S. or PhD) in computer science, machine learning, AI, or a related field is highly preferred.</li>
<li>7+ years of experience in data science and machine learning, focusing on generative models, LLMs, or computer vision.</li>
<li>Expertise in large-scale language and vision models (e.g., Transformers, GPT, VLMs).</li>
<li>Experience with multimodal data processing (e.g., combining text, image, and 3D data).</li>
<li>Proficient in Python, including key libraries such as PyTorch, TensorFlow, pandas, and numpy.</li>
<li>Strong background in probability, statistics, and optimization techniques relevant to generative modeling.</li>
<li>Familiarity with cloud computing resources and tools for model training and deployment (e.g., AWS SageMaker).</li>
<li>Familiar with software engineering principles, including version control, reproducibility, and continuous integration.</li>
<li>Experience in the manufacturing, supply chain, or similar industries is a plus.</li>
</ul>
#LI-Hybrid
Xometry is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.
For US based roles: Xometry participates in E-Verify and after a job offer is accepted, will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

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