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<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: Microbiologist (Full Time)
At Nivagen as a Microbiologist you will be responsible for ensuring that pharmaceutical products meet quality standards during the manufacturing process. This role involves real-time monitoring, sampling, testing, and documentation to identify and address any quality issues as they arise, ensuring that all production activities comply with Good Manufacturing Practices (GMP) and regulatory requirements.
Position Summary
As a Microbiologist you will play a critical role in the success of our operations. This position is integral to our commitment to excellence, as it involves developing and validating microbiological test methods, maintaining detailed records, and preparing reports, protocols, and standard operating procedures (SOPs). Your expertise will directly contribute to Quality and affordable medication.
Collaboration is key in this role. You will work closely with cross-functional teams to meet project objectives and timelines and identify opportunities for process improvements. Your proactive approach and innovative mindset will help us enhance efficiency and effectiveness within our microbiology laboratory and reinforce our dedication to quality and compliance.
Additionally, in this influential role you will be a mentor, providing training and guidance to microbiology staff, fostering an environment of continuous learning and professional growth.
Joining Nivagen as a Microbiologist means being part of a visionary team dedicated to expanding access to quality, affordable medication. If you are passionate about quality, service, and innovation, and are eager to make a difference in people's lives, we invite you to bring your expertise and enthusiasm to our dynamic team.
Duties and Responsibilities
<ul>
<li>Conducts microbiological testing of primary packaging materials, raw materials, in process sample, finished products, and environmental samples using various techniques, including microbial enumeration, identification, and antimicrobial effectiveness testing.</li>
<li>Develops and validates microbiological test methods in accordance with compendial and regulatory requirements.</li>
<li>Maintains accurate and detailed records of all microbiological testing and analysis performed. Prepares and reviews reports, protocols, and SOPs related to microbiological activities.</li>
<li>Ensures compliance with regulatory standards, current Good Manufacturing Practices (cGMP) requirements, and company policies and procedures. Participate in internal and external audits as needed.</li>
<li>Microbiology-related projects, including method transfers, validations, and investigations.</li>
<li>Collaborates with cross-functional teams to achieve project objectives and timelines.</li>
<li>Provides training and mentorship to microbiology staff.</li>
<li>Shares knowledge and expertise to promote continuous learning and development within the microbiology team.</li>
<li>Identifies opportunities for process improvements and optimization within the microbiology laboratory.</li>
<li>Implements best practices and innovative solutions to enhance efficiency and effectiveness.</li>
<li>Performs a variety of Microbiology testing to assess the strength, identity, and purity of test samples and/or materials.</li>
<li>Performs other duties as assigned.</li>
</ul>
While performing the responsibilities of the job, the employee is required to talk and hear. Must be able to bend at the waist and knees as well as twist at the trunk. Must be able to lift up to 25 lbs. Must be able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. Personal protective equipment and Respirators are essential for the health and safety of employees. Position requires working in the laboratory as well as sitting Microbiological method development and method validation procedures like BET, Sterility, MLT, Bio Assay and Disinfectant qualification and microbiological hold time validation, Container closure integrity validation.
Knowledge and Skills
<ul>
<li>Strong knowledge of microbiological testing techniques, methods, and equipment.</li>
</ul>
Key Competencies
<ul>
<li>Customer Focus: Ability to build strong customer relationships and deliver customer centric solutions.</li>
<li>Optimizes Work Processes: Know the most effective and efficient processes to get things done, with a focus on continuous improvement.</li>
<li>Collaborates: Builds partnerships and works collaboratively with others to meet shared objectives.</li>
<li>Resourcefulness: Secures and deploys resources effectively and efficiently.</li>
<li>Manages Complexity: Makes sense of complex, high quality, and sometimes contradictory information to effectively solve problems.</li>
<li>Ensures Accountability: Holds self and others accountable to meet commitments and objectives.</li>
<li>Situational Adaptability: Adapts approach and demeanor in real time to match shifting demands of different situations.</li>
<li>Communicates Effectively: Develops and delivers multi-mode communications that convey a clear understanding of the unique needs of different audiences.</li>
</ul>
Values
People: Our people define who we are as a company. We believe that understanding and addressing the needs of our team, clients, and community is fundamental to fostering a culture of support and growth. By prioritizing the well-being and development of our employees, we create an environment where everyone can thrive and contribute their best.
Quality: Quality stands at the core of our mission. It reflects our commitment to excellence in every medication we produce. We adhere to the highest standards of quality control and continuously strive to improve our processes to ensure that our products meet the needs of those we serve. Our dedication to quality is unwavering and is evident in every aspect of our work.
Service: We are here to serve others. Every interaction with our patients, providers, employees, and other stakeholders comes from a place of service. We are committed to delivering exceptional service and ensuring that every experience with our company is positive and impactful. Our service-oriented approach helps us build strong, lasting relationships and fulfill our mission of improving healthcare outcomes.
Innovation: By continuously exploring new methodologies and embracing technology, we ensure that every solution we offer is at the forefront of pharmaceutical care. Innovation drives us to find better ways to serve our patients, improve our products, and streamline our operations. We are committed to staying ahead of industry trends and leveraging cutting-edge technology to enhance the value we provide.
In summary, our core values—People, Quality, Service, and Innovation—are integral to everything we do. They guide our actions, shape our culture, and inspire us to achieve excellence in all our endeavors. By staying true to these values, we ensure that we fulfill our mission and make a positive impact on the lives of those we serve.
Experience and Qualifications
<ul>
<li>Bachelor's degree in microbiology, Biology, or related field required; Master's degree preferred.</li>
<li>Minimum of 3 years of experience in a microbiology laboratory required.</li>
<li>Previous experience in a pharmaceutical or compounding environment preferred.</li>
<li>Experience with compendia testing: United States Pharmacopeia, and regulatory requirements (Food and Drug Administration and cGMP) preferred.</li>
<li>Experience with microbiological method development and method validation procedures like Sterility Testing, Endotoxin Testing, Disinfectant Efficacy Study, Water Testing, Method Validation, Environment Monitoring, Microbial Limit Testing, PET, and microbiological hold time validation, container closure integrity.</li>
</ul>
Benefits:
<ul>
<li>Pay range $70,000 - 85,000 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.
We are focused on building a diverse and inclusive workforce. If you're excited about this role, but do not meet 100% of the qualifications listed above, we encourage you to apply.

Microbiologist

<h3>Job Description</h3>
Job Description
The Company
Tupos Therapeutics is led by a seasoned team of drug hunters and developers with a proven track record of advancing transformative therapies. Our collective experience includes the discovery and development of first-in-class medicines such as vemurafenib and pexidartinib, along with multiple clinical-stage programs across diverse indications.
Our founding team helped pioneer a paradigm-shifting approach to small molecule drug discovery—anchoring structure-based drug design in the discovery and validation of novel chemical scaffolds, an innovation widely recognized as a major contribution to the field. At Tupos, we extend this legacy by integrating cutting-edge computational chemistry, machine learning and advanced chemical toolkits. This multifaceted approach allows us to tackle some of the most challenging problems in drug discovery and accelerate the path from program initiation to clinical entry. Headquartered near the geographic center of the San Francisco Bay Area—with an easy commute from the Peninsula, East Bay, and South Bay—Tupos is advancing a pipeline of novel therapies that target key immunological pathways—driven by a robust discovery platform and deep domain expertise.
The Opportunity
We are seeking a highly motivated Senior Immunologist with industry experience to join our growing R&amp;D team. This is a unique opportunity to shape scientific strategy and help lay the foundation for future clinical success in a dynamic startup environment. The ideal candidate will bring a deep understanding of immunology, strong experimental and analytical skills, and a hands-on approach to scientific problem-solving. You will play a central role in characterizing immune mechanisms, demonstrating biological differentiation, addressing key translational questions, and advancing breakthrough therapies to patients in need.
Responsibilities
<ul>
<li>Provide strategic and scientific leadership in immunology to guide the discovery and early development of novel therapeutics targeting immune-related pathways.</li>
<li>Design, execute, and interpret complex in vitro, in vivo, and ex vivo studies to elucidate mechanisms of action and assess pharmacodynamic responses, and support candidate selection.</li>
<li>Formulate and refine mechanistic hypotheses related to immune modulation, driving the development of differentiated therapeutic strategies.</li>
<li>Evaluate and select disease-relevant models and biomarker approaches to support translational planning and clinical readiness.</li>
<li>Lead cross-functional discovery efforts in close collaboration with medicinal chemistry, molecular biology, pharmacology, and clinical development to advance programs through key milestones.</li>
<li>Represent the immunology function in internal governance forums and external partnerships, contributing to program prioritization and portfolio strategy.</li>
<li>Author and deliver high-quality scientific communications, including internal reports, regulatory submissions, conference presentations, and peer-reviewed publications.</li>
</ul>
Qualifications
<ul>
<li>Ph.D. in Immunology or a related field, with 8+ years of relevant experience in a biopharma or biotechnology setting; experience in early drug discovery is strongly preferred.</li>
<li>Deep expertise in immunology, with a strong understanding of immune signaling pathways, disease mechanisms, and immune modulation strategies.</li>
<li>Demonstrated success in designing and interpreting in vitro, in vivo, and ex vivo studies to support target validation, mechanism-of-action, and biomarker development.</li>
<li>Experience with a range of immunological assays (e.g., flow cytometry, cytokine profiling, cell co-culture systems) and disease-relevant models.</li>
<li>Proven track record of advancing immunology-focused programs through early discovery to development candidate nomination.</li>
<li>Strong leadership skills, with experience managing or guiding scientific teams and external collaborators.</li>
<li>Effective cross-functional collaborator with the ability to influence decision-making across disciplines including chemistry, translational science, and clinical development.</li>
<li>Excellent scientific communication skills, with experience presenting at internal governance meetings, external conferences, and contributing to peer-reviewed publications.</li>
</ul>
Benefits and Pay
The expected salary range for this position is $200,000 - $280,000. We encourage candidates of all levels to apply as there is sometimes flexibility on job level and responsibilities. Compensation and title will be based on a variety of factors, including experience, qualifications, and other job-related factors permitted by law. This position is also eligible for an annual bonus, equity, paid time off, and a benefits package. Benefits include company-subsidized medical, dental, and vision plans, and 401(K) matching. Employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Tupos Therapeutics is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
To all recruitment agencies: Tupos Therapeutics does not accept agency resumes. Please do not forward resumes to our jobs alias or to Tupos Therapeutics employees. Tupos is not responsible for any fees related to unsolicited resumes.

Senior Immunologist/Head of Immunology

<h3>Job Description</h3>
Job Description
POSITION SUMMARY: 
The Senior Clinical Scientist, Oncology will leverage their scientific and medical expertise in oncology to lead and execute clinical development activities for one or more assigned studies in molecular residual disease monitoring. Acting as a key leader on study teams and departmental initiatives, they will drive the development of clinical strategy, incorporating insights from the competitive landscape and aligning with the broader company vision to advance innovative solutions in oncology.
PRIMARY RESPONSIBILITIES: 
<ul>
<li>Develop study concepts, including overall study design, schedule of assessments, objectives / endpoints, and eligibility criteria. Integrate feedback from internal and external stakeholders including senior leadership, key investigators, internal stakeholders, and regulatory agencies</li>
<li>Contribute to authoring of the study protocol and provide critical feedback and review of supporting documents; help to respond to health authority feedback</li>
<li>Provide protocol trainings to internal and CRO teams</li>
<li>Work with the Clinical Operations team to contribute to the design of study-specific case report form (CRF), ensure CRFs are aligned with study requirements during user acceptance testing, and author study-specific sections of the CRF completion guidelines</li>
<li>Ensure study manuals, etc. are aligned with the study protocol</li>
<li>Seek input from key investigators on study design and methodology to ensure alignment with research objectives, and actively participate in pre-site selection discussions, site initiation visits, and investigator meetings to support successful study execution</li>
<li>Serve as clinical science representative on internal and external meetings</li>
<li>Contribute to and oversee real-time clinical data reviews (including oversight of CROs when applicable)</li>
<li>Support advisory boards, steering committee meetings, consultant meetings and investigator meetings, including preparation and delivery of presentations</li>
<li>Engage Natera medical directors, medical science liaisons for clinical projects, abstract writing and content creation</li>
<li>Deliver presentations/posters at scientific meetings and company promotional events as needed; represent company at trade shows and medical conferences (&lt;10% travel)</li>
<li>This role works with PHI on a regular basis both in paper and electronic form and has 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>Ph.D./RN/MS </li>
<li>At least 5-8 years experience as a Clinical Scientist preferred with preference given to oncology clinical strategy and execution</li>
<li>Experience with randomized controlled trials preferred</li>
<li>Experience with project management, clinical research and scientific writing</li>
<li>Periodic travel (~15-20; includes overnight domestic and international travel to study sites, conferences, and meetings)</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES: 
<ul>
<li>Demonstrated ability to identify problems and develop right-sized solutions </li>
<li>Fast learner who can develop in-depth technical understanding of Natera's products </li>
<li>Exceptional communication skills (oral and written) and attention to detail </li>
<li>Demonstrated ability to work independently AND collaborate with team members</li>
<li>Analytical thinker</li>
<li>Motivated to be creative and brainstorm innovative solutions </li>
<li>Familiarity with Google and Microsoft suite of work products </li>
<li>A desire to work for a dynamic molecular diagnostic laboratory and manage growth for optimal success </li>
</ul>
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

Senior Clinical Scientist

<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 Type:
Full Time
Job Location:
Nivagen Pharmaceuticals Inc., Sacramento, CA
About the Job: 
Title of the Position: Senior Scientist - Formulation Development
We are seeking a highly skilled and experienced Senior Scientist to join our Formulation Development team. The successful candidate will play a critical role in the development and optimization of drug formulations from early-stage research through commercialization. This position requires a deep understanding of formulation principles, a strong scientific background, and a proven track record of success in the pharmaceutical industry.
Responsibilities:
<ul>
<li>Lead the design, development, and optimization of complex injectable and sterile dosage forms.</li>
<li>Develop and implement robust formulation development strategies aligned with regulatory guidelines (e.g., Quality by Design, FDA).</li>
<li>Apply scientific fundamentals and creative problem-solving skills to solve complex technical issues</li>
<li>Conduct rigorous experimental design studies (e.g., factorial design) to achieve project objectives.</li>
<li>Collaborate closely with cross-functional teams, including Technical Services, Operations, and Regulatory Affairs.</li>
<li>Define scope, timeline, and resource needs of functional activities and keep team on schedule</li>
<li>Participate in evaluation of new product opportunities.</li>
<li>Ensure timely and high-quality documentation for regulatory submissions.</li>
<li>Stay updated with all FDA and regulatory requirements/guidelines.</li>
<li>Provide mentorship and leadership to team members.</li>
<li>Stay up to date with the latest scientific advancements in formulation development and applying new technologies to improve product performance.</li>
<li>Author and review technical reports, protocols, and regulatory documents.</li>
<li>Additional duties and assignments as needed.</li>
</ul>
Qualifications:
Education/Experience:
<ul>
<li>Ph.D. or Postgraduate degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.</li>
<li>3+ years of hands-on experience in sterile/Injectable pharmaceutical formulation development. (Strong candidates with combinations of education and experience will be considered.)</li>
<li>Strong understanding of formulation principles, excipients, and drug delivery systems.</li>
<li>Hands-on experience with various formulation techniques and equipment.</li>
<li>Proven track record of successful formulation development and commercialization.</li>
<li>Experience with statistical design of experiments (DOE) and data analysis.</li>
</ul>
Knowledge, Skills, and Abilities:
<ul>
<li>Proven track record of successful formulation development for various sterile dosage forms.</li>
<li>Strong leadership, project management, and organizational skills.</li>
<li>Expertise in complex injectable and sterile dosage form development.</li>
<li>Demonstrated ability to conduct independent research and problem-solving.</li>
</ul>
Requirements:
<ul>
<li>Must live in or be willing to move to the Sacramento Metropolitan Region (approximately 40 miles in radius).</li>
</ul>
Benefits:
<ul>
<li>Pay range $70,000-$90,000 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.

Senior Scientist - Formulation Development

<h3>Job Description</h3>
Job Description
The Associate Scientist initiates and executes laboratory experiments to aid in product development. This position requires investigating the feasibility of applying a wide variety of scientific principles and concepts to potential inventions, products and problem solving. We are seeking an individual who maintains broad knowledge of state-of-the-art principles and theories and can work well in an exciting fast paced environment.
PRIMARY RESPONSIBILITIES:
<ul>
<li>
Autonomously and accurately design experimental plans and execute complex laboratory experiments such as analyte extractions, next-generation library preparation, hybrid capture and sequencing.
</li>
<li>
Evaluate and integrate new emerging technologies in genomics.
</li>
<li>
Write protocols and document results and scientific interpretations.
</li>
<li>
Contribute insight toward experimental findings and trouble-shoot laboratory processes and protocols.
</li>
<li>
Communicate and discuss results with a multidisciplinary team including biologists, bioinformaticians, statisticians, software engineers and managers.
</li>
<li>
Perform basic data analysis.
</li>
<li>
This role will have occasional access to PHI both in paper and electronic form and have occasional 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>
Performs other duties as assigned.
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
Bachelor's in molecular biology, biochemistry or closely related field with a minimum of 6 years of industry experience. Master's in molecular biology, biochemistry or closely related field, with 2 years of industry experience.
</li>
</ul>
KNOWLEDGE, SKILLS, AND ABILITIES:
<ul>
<li>
Must have hands-on experience with basic molecular biology techniques, including PCR, QRT-PCR, digital PCR, nucleic acids extractions or sequencing.
</li>
<li>
Must be able to handle manual work/pipetting involving high throughput sample testing.
</li>
<li>
Must have experience in data analysis using Excel or other data analysis tools.
</li>
<li>
Demonstrated success in applying independent scientific judgment in experimental design and analysis.
</li>
<li>
Experience with next generation sequencing (NGS) methods and techniques.
</li>
<li>
Experience in optimizing laboratory methodologies and troubleshooting complex problems.
</li>
<li>
Experience in writing clear plans, reports and SOPs.
</li>
<li>
Experience in epigenetic/methylation, target enrichment, working with cfDNA/RNA/FFPE tissues and NGS data analysis is a plus.
</li>
<li>
Experience in programming and operating liquid handlers is a plus.
</li>
<li>
Experience in programming languages such as python is a plus.
</li>
<li>
Must have excellent communication, organizational, record-keeping, planning, attention to detail and time management skills.
</li>
</ul>
#LI-TH1 #LI-OnsiteThe 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 $96,400—$120,500 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

Assoc Scientist R&D

<h3>Job Description</h3>
Job Description
$200,000-220,000 base salary (5 days/Onsite)
About The Role
We are seeking a highly effective, motivated scientist to join our team. You will experience all facets of building a startup at a cutting edge biotech company in San Carlos! You will work with an experienced team of founders, scientists and RAs designing, executing, and interpreting experiments. You are a good fit for this role if you resonate with our values, namely if you work hard, are ambitious, creative, and honest, write python scripts to solve your problems, and will do whatever it takes to win.
Application Requirements:
<ul>
<li>Your cover letter should be one page and give clear examples of the following:
<ul>
<li>An instance in which you designed an experiment including tradeoffs considered and iterative improvements</li>
<li>An instance in which you demonstrated high executive planning ability</li>
<li>Highlight two (or more) orthogonal skills in which you've demonstrated excellence</li>
</ul>
</li>
</ul>
<ul>
<li>This job is not 9-5
<ul>
<li>This is an opportunity to work very hard, learn a lot, and develop skills that will serve you well throughout your career</li>
<li>This is not an opportunity to focus on work life balance</li>
</ul>
</li>
</ul>
Key Responsibilities:
<ul>
<li>Design studies, experiments, and assays pertaining to therapeutic biologics and QC of therapeutic products</li>
<li>Review literature (research papers, textbooks, financial reports, regulatory documents)</li>
<li>Evaluate scientific results and present readouts and conclusions</li>
<li>Assign tasks to RAs</li>
<li>Design templates and record experimental results in Benchling</li>
<li>Whatever else is needed for the company to succeed</li>
</ul>
Who You Are:
<ul>
<li>PhD in natural science such as biology, biochemistry, biophysics, bioengineering, etc.</li>
<li>&lt;=2 years since completion of PhD</li>
<li>Extremely strong work ethic</li>
<li>Python scripting ability</li>
<li>Highly motivated and ambitious</li>
<li>Proficiency with Google Sheets and Google Slides</li>
<li>Live within a 30 minute commute of San Carlos</li>
</ul>
Nice to Haves:
<ul>
<li>Experience working with C2C12 cells or human primary myoblasts</li>
<li>Experience using a confocal microscope</li>
<li>Experience in high throughput biologic expression and characterization</li>
<li>Experience using an Agilent Seahorse or other respirometer</li>
</ul>
Why Join Us?
<ul>
<li>Contribute to groundbreaking therapies in a dynamic, AI-driven environment.</li>
<li>Collaborate with cross-functional teams of scientists, AI specialists, and drug developers.</li>
<li>Opportunities for professional growth in a mission-driven startup.</li>
</ul>
Details:
<ul>
<li>This is an in-person role in San Carlos, CA</li>
<li>The compensation range for this role is $200,000-220,000 along with equity options in the company and benefits</li>
</ul>
Life at Bioworks
<ul>
<li>Comprehensive Health Coverage – Medical, dental, and vision insurance to keep you at your best</li>
<li>Financial Security – 401(k) with company matching and fully covered life insurance</li>
<li>Time to Recharge – Unlimited PTO, generous company holidays, and flexibility to take the time you need</li>
<li>Connection &amp; Community – Team lunches, office hangouts, and offsite meetups to build meaningful relationships</li>
<li>High-Impact Work – Shape the future of healthcare at a pivotal moment in our growth</li>
<li>Competitive Compensation – Top-tier salary and a generous equity package</li>
<li>Fast-Paced &amp; Exciting – Join a hypergrowth team that moves fast and builds with purpose</li>
<li>World-Class Team – Work alongside top researchers, scientists, and engineers in a high-performance environment</li>
</ul>
Prime Location – Enjoy a sunny workspace in San Carlos
Equal Opportunity Employer
We are proud to be an equal opportunity workplace who prohibits discrimination and harassment of any kind. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. We provide a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual qualifications without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, disability status, protected veteran status, or any other protected characteristic as outlined by federal, state, or local laws.
We welcome all with a drive to work, and a curiosity to learn. We are here to build and be a part of science encompassing the full power and possibility for breakthrough innovation! 
To view our current job openings and apply, please visit our job portal. If you think you have what it takes but don't see a job fitting your skillset email us at <a href="mailto:recruiting@aequitabioworks.com" target="_blank">recruiting@aequitabioworks.com</a>.

Research Scientist

<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
3050 Fite Circle, Suite 100, Sacramento, CA 95827
About the Job: 
Title of the Position: Senior Chemist (Full Time)
At Nivagen as a Senior Chemist you will be responsible to leads projects, ensuring accurate results, innovative solutions, and optimized processes. This role involves collaborating with engineering, production, and quality assurance teams to support product development, testing, and compliance.
Responsibilities:
<ul>
<li>Communicate with CMO regarding analytical activities.</li>
<li>Handle product deficiencies.</li>
<li>Ensure adherence to FDA guidelines and regulations.</li>
<li>Responsible for maintaining cleanliness of lab areas.</li>
<li>Guide team regarding analytical method development on instruments like HPLC and GC.</li>
<li>Ensure compliance with quality system.</li>
<li>Train new personnel.</li>
<li>Prepare analytical budget for the lab.</li>
<li>Plan analyses in accordance with production schedule.</li>
<li>Develop analytical methods.</li>
<li>Perform PDR-related activities and documentation</li>
<li>Investigate OOT and OOS results.</li>
<li>Prepare and review SOPs.</li>
<li>Prepare and review COAs.</li>
<li>Prepare other documents related to analytical activities, including protocols, templates, reports, specifications, and STPs.</li>
<li>Review validation protocols, reports, and datasheets.</li>
<li>Perform patent work under the guidance of the CSO.</li>
</ul>
Qualifications:
Education/Experience:
<ul>
<li>Bachelor's degree in Chemistry, Biochemistry, or a related field (Master's or Ph.D. preferred).</li>
<li>Minimum of 5–7 years of hands-on experience in a laboratory or industrial setting.</li>
</ul>
Knowledge, Skills, and Abilities:
<ul>
<li>Proficiency in advanced analytical techniques such as spectroscopy, chromatography (HPLC, GC), and other instrumentation.</li>
<li>In-depth understanding of chemical properties, reaction mechanisms, and regulatory guidelines (e.g., FDA, EPA, OSHA).</li>
<li>Knowledge of chemical handling procedures, including safety precautions and documentation such as Safety Data Sheets (SDS).</li>
<li>Strong problem-solving, communication, and project management skills.</li>
<li>Proficiency in Microsoft Office is required.</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 $75,000-$85,000 per Year</li>
<li>Yearly bonus and stock options 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.

Senior Chemist

<h3>Job Description</h3>
Job Description
The Company
Tupos Therapeutics is led by a seasoned team of drug hunters and developers with a proven track record of advancing transformative therapies. Our collective experience includes the discovery and development of first-in-class medicines such as vemurafenib and pexidartinib, along with multiple clinical-stage programs across diverse indications.
Our founding team helped pioneer a paradigm-shifting approach to small molecule drug discovery—anchoring structure-based drug design in the identification and validation of novel chemical scaffolds, an innovation widely recognized as a major contribution to the field. At Tupos, we extend this legacy by integrating cutting-edge computational chemistry, machine learning, and a growing arsenal of advanced chemistry toolkits. This multifaceted approach enables us to tackle some of the most persistent challenges in drug discovery and accelerate the path from program initiation to clinical entry. Headquartered near the geographic center of the San Francisco Bay Area—with an easy commute from the Peninsula, East Bay, and South Bay—Tupos is advancing a pipeline of novel therapies that target key immunological pathways—powered by a robust discovery platform and deep domain expertise.
The Opportunity
We are seeking an accomplished and highly motivated Computational Chemist to join our discovery team and lead the design of novel small molecules across multiple therapeutic programs. The ideal candidate will bring deep expertise in computational chemistry and structure-based drug design, a creative and mission-driven mindset, and a strong track record of advancing programs from early discovery through development candidate nomination. This is a high-impact role with the opportunity to shape discovery strategy, collaborate closely with cross-functional teams, and contribute significantly to the development of transformative therapies in a fast-paced environment.
Responsibilities
<ul>
<li>Design novel small molecules with exceptional potency, selectivity, and drug-like properties by applying cutting-edge computational and machine learning techniques, modern structure-based drug design methods, and deep SAR insights to drive innovation and differentiation.</li>
<li>Collaborate closely with cross-functional teams, including medicinal and synthetic chemistry, biology, DMPK, and translation medicine, to shape and execute discovery strategy, troubleshoot complex problems, and accelerate the progression of programs through key discovery milestones.</li>
<li>Integrate and interpret diverse data streams, including biophysical/chemical, cellular, ADME, pharmacological, and structural biology data, to refine compound design hypotheses and enable rapid, data-driven decision-making in a fast-paced environment.</li>
<li>Advance chemical series through iterative design cycles, proactively identifying and addressing liabilities related to efficacy, selectivity, pharmacokinetics, and developability, while contributing to intellectual property strategy and creation.</li>
<li>Maintain fluency with emerging tools, technologies, and scientific literature in computational chemistry, machine learning, and drug discovery to bring forward novel approaches and continuously improve internal capabilities.</li>
<li>Clearly and effectively communicate scientific insights, strategic recommendations, and project progress through written reports, team discussions, and internal or external presentations.</li>
</ul>
Qualifications
<ul>
<li>Ph.D. in Computational Chemistry, Structural Biology, Medicinal Chemistry, Theoretical Chemistry, or a related discipline, with 5+ years of industry experience in small molecule drug discovery.</li>
<li>Proven expertise in modern computer-aided drug discovery, including structure-based drug design, SAR analysis, and optimization of pharmacokinetic and physicochemical properties.</li>
<li>Demonstrated success in advancing small molecule programs from hit identification through lead optimization and development candidate nomination.</li>
<li>Experience collaborating in multidisciplinary teams and deep understanding of drug discovery principles, including ADME, pharmacology, and safety profiling, with the ability to synthesize complex datasets into clear, actionable design strategies.</li>
<li>Proficient in using industry-standard computational tools and capable of scripting to automate workflows and analyze large datasets.</li>
<li>Strong record of scientific communication, including authorship of publications, patent filings, and internal reports or presentations.</li>
<li>Strategic thinker with excellent problem-solving skills, scientific curiosity, and the ability to thrive in a fast-paced, collaborative environment.</li>
<li>Prior experience in immune-related indications or emerging therapeutic modalities such as targeted protein degradation or molecular glues is highly desirable.</li>
<li>Familiarity with AI/ML approaches that can meaningfully accelerate small molecule discovery, such as generative modeling, property prediction, structure-focused learning, and integration of multi-modal datasets, is a strong plus.</li>
</ul>
Qualifications
<ul>
<li>Ph.D. in Immunology or a related field, with 8+ years of relevant experience in a biopharma or biotechnology setting; experience in early drug discovery is strongly preferred.</li>
<li>Deep expertise in immunology, with a strong understanding of immune signaling pathways, disease mechanisms, and immune modulation strategies.</li>
<li>Demonstrated success in designing and interpreting in vitro, in vivo, and ex vivo studies to support target validation, mechanism-of-action, and biomarker development.</li>
<li>Experience with a range of immunological assays (e.g., flow cytometry, cytokine profiling, cell co-culture systems) and disease-relevant models.</li>
<li>Proven track record of advancing immunology-focused programs through early discovery to development candidate nomination.</li>
<li>Strong leadership skills, with experience managing or guiding scientific teams and external collaborators.</li>
<li>Effective cross-functional collaborator with the ability to influence decision-making across disciplines including chemistry, translational science, and clinical development.</li>
<li>Excellent scientific communication skills, with experience presenting at internal governance meetings, external conferences, and contributing to peer-reviewed publications.</li>
</ul>
Benefits and Pay
The expected salary range for this position is $160,000 - $200,000. We encourage candidates of all levels to apply as there is sometimes flexibility on job level and responsibilities. Compensation and title will be based on a variety of factors, including experience, qualifications, and other job-related factors permitted by law. This position is also eligible for an annual bonus, equity, paid time off, and a benefits package. Benefits include company-subsidized medical, dental, and vision plans, and 401(K) matching. Employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Tupos Therapeutics is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
To all recruitment agencies: Tupos Therapeutics does not accept agency resumes. Please do not forward resumes to our jobs alias or to Tupos Therapeutics employees. Tupos is not responsible for any fees related to unsolicited resumes.

Senior Computational Chemist

<h3>Job Description</h3>
Job Description
Job Title: Math Teacher + Business Operation Specialist - H1b Sponsored
Location: San Jose, CA 
Job Type: Full-Time, Contract
Intended Start Date: As soon as possible
About Think Academy:
Think Academy US (<a href="http://www.TheThinkAcademy.com" target="_blank">www.TheThinkAcademy.com</a>), a 100% owned subsidiary of TAL Education Group (NYSE: TAL), is recently established education technology (Ed-Tech) company to provide PreK-12 extra-curricular learning services through science and technology. At Think Academy, we provide full cycle service to foster local children's ability to think critically, to strengthen their logic skills, and to help them fulfill their goals through innovative teaching techniques. We believe Love and Technology can make education better. Each week, more than 6 million students are enrolled in TAL's online and offline education platform.
About This Role:
This is a full-time position designed for recent graduates and junior level professionals who are passionate in education and have the drive to grow into a future leader in education industry. The successful candidate will work alongside our Silicon Valley teaching team while also focusing on the operational aspects of our business.
You will have the resources to become a great math educator and provide world-class teaching services to PreK-9th graders of all levels. In order to foster a well-rounded leader in the education industry, this role will also give you the chance to participate in Think Academy's business functions including operations and marketing. This role is ideal for those wanting to become branch directors, department managers, and even a part of Think Academy's global expansion in emerging markets. 
We welcome applicants from all different backgrounds as no prior teaching-related experience is required. With the right mindset, this position will strengthen your teaching abilities and leadership competency and be a stepping stone to your goals in the education industry. 
Job Responsibilities: 
<ul>
<li>Plan and execute teaching related activities which including
<ul>
<li>Teaching short-term and long-term group classes in classroom setting</li>
<li>Hold office hours and provide 1-on-1 help</li>
<li>Grade students' homework and assignments</li>
</ul>
</li>
<li>Develop tailored mathematical learning plans for students based on their current abilities and goals, facilitating their enrollment in short-term or long-term courses</li>
</ul>
Requirements &amp; Qualifications:
<ul>
<li>Open to all major - we provide training and professional growth program</li>
<li>Previous experience teaching or tutoring students.</li>
<li>Passionate about the education industry, and has the strong will to motivate and inspire students; must be patient and empathetic with working with students.</li>
<li>Excellent organizational skills and has a strong sense of responsibility.</li>
<li>A team player that is able to collaborate effectively with other teachers and staff.</li>
</ul>
Compensation &amp; Benefits:
<ul>
<li>H1B and OPT sponsorship available!</li>
<li>Start at $40/teaching hour + $20/non-teaching hour -- Opportunity to earn up to $90,000 yearly in teaching hours!</li>
<li>Enjoy benefits such has medical insurance and 401k</li>
<li>Gain hands on experience in an education driven environment</li>
<li>Potential for future employment opportunities based on performance</li>
</ul>
Think Academy is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Business Operation Specialist + Math Content Teacher - H1b Sponsored

<h3>Job Description</h3>
Job Description
We are global private markets specialists delivering tailored investment solutions, advisory services, and impactful, data driven insights to the world's investors. Leveraging the power of our platform and our peerless intelligence across sectors, strategies, and geographies, we help identify the advantages and the answers our clients need to succeed.
Position Overview:
As a Portfolio Management Senior Associate, AI &amp; Quantitative Solutions at StepStone, you will play a pivotal role at the intersection of quantitative finance and cutting-edge artificial intelligence. This position is central to researching, developing, and implementing AI/Machine Learning solutions across the firm, particularly focusing on Private Equity secondaries use cases and the development of advanced quantitative models. You will transform how we manage portfolios, conduct research, and generate insights. Leveraging diverse data, including complex unstructured formats from private market reporting, to build predictive models and streamline analytical processes that benefit both internal teams and our global client base. This role entails leading initiatives in model testing, validation, and deployment within our liquidity management and portfolio construction frameworks, aligning bespoke solutions with diverse client needs and complex risk/return profiles. You will be a key collaborator with our Data Science, Research, and SPAR teams, driving the acquisition, robust cleaning, and deep understanding of critical data fields to enable advanced AI applications. 
Essential Job Functions:
<ul>
<li>AI/ML Model Development &amp; Research: Design, develop, train, and validate advanced AI and Machine Learning models (including Natural Language Processing applications) to solve complex problems in portfolio construction, liquidity management, risk modeling, and performance attribution. </li>
<li>Data Engineering for AI Pipelines: Utilize Python, SQL (MySQL), and R for advanced data retrieval, cleaning, transformation, and feature engineering, optimizing data for AI consumption across various sources, including unstructured private market reports (e.g., PDF parsing). </li>
<li>Model Deployment &amp; MLOps: Collaborate closely with the web development group to integrate and deploy AI/ML solutions into production environments. </li>
<li>Quantitative Research &amp; Backtesting: Conduct rigorous quantitative research, model backtesting, and scenario analysis to assess model performance, robustness, and limitations against varied financial problem statements. </li>
<li>Communication &amp; Collaboration: Effectively communicate complex AI model outputs, assumptions, limitations, and strategic implications to both technical and non-technical stakeholders, including senior management and external clients. This involves fostering strong relationships with key internal teams, by actively listening to their needs, and proactively identifying how technology can enhance their workflows and adoption. Engage in thought leadership regarding the merits of new AI applications and analytical approaches. </li>
<li>Innovation &amp; Strategic Impact: Demonstrate an independent and efficient working style, consistently translating high-level strategic ideas and business challenges into actionable, AI-driven solutions and model outputs that deliver tangible impact across the firm. </li>
<li>Continuous Learning: Stay abreast of the latest advancements in AI, machine learning, and quantitative finance, proactively identifying opportunities for their application within private markets. </li>
</ul>
Qualifications:
<ul>
<li>Bachelors, Master's degree or Ph.D. in a highly quantitative field such as Computer Science, Artificial Intelligence, Machine Learning, Mathematics, Statistics, Econometrics, or a related discipline. </li>
<li>6-8 years of experience in quantitative research, AI/Machine Learning model development, risk modeling, portfolio construction, or performance attribution at a financial institution. </li>
<li>Excellent written communication and presentation skills, with the ability to articulate complex technical concepts to a diverse audience. </li>
<li>Willingness to work a flexible schedule.</li>
<li>High level of confidentiality.</li>
</ul>
Required Knowledge, Skills, and Abilities:
<ul>
<li>Deep proficiency in Private Market investments and advanced financial modeling, including quantitative model development and application. </li>
<li>Expertise in machine learning and deep learning algorithms, statistical modeling, Natural Language Processing (NLP), and numerical algorithms. </li>
<li>Advanced proficiency in Python (including libraries like Pandas, NumPy, Scikit-learn, TensorFlow/PyTorch) and SQL. Experience with AI/ML lifecycle platforms (e.g., Kubeflow, AWS SageMaker, Azure ML) and MLOps best practices for model versioning, testing, and deployment. </li>
</ul>
Salary Range: $125,000 - $145,000
The salary range is an estimate of pay for this position. Actual pay may vary depending on job-related factors that can include location, education, skill, and experience. The salary range does not include any benefits or other forms of possible compensation that may be available to employees.
At StepStone, we believe that our people are our most important asset and crucial to our success. We are an Equal Opportunity Employer that strives to create an environment that empowers our employees and allows them to be heard, regardless of title or tenure. Our organizational community features multiple Employment Resource Groups as well as mentorship programs to enhance the employee experience for all. 
As an Equal Opportunity Employer, StepStone does not discriminate on the basis of race, creed, color, religion, sex, national origin, citizenship status, age, disability, marital status, sexual orientation, gender identity, gender expression, genetic information or any other characteristic protected by law.
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