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BioAge Labs

Clinical-stage biotech developing aging-targeted therapeutics

Knowledge Graph Engineer

Full-TimeUpdated on 10/22/2026
$140k - $175k
Mid
Bachelor's
Remote in USA
RemoteRemote within the United States.
Data & AnalyticsData Engineering

About the job

Requirements
  • A bachelor's degree or higher in computer science, data engineering, AI, or a related field, and at least 3 years of industry experience in data engineering.
  • Experience working with biological or biomedical data, such as genomics, proteomics, clinical, or phenotype data, and familiarity with standard biomedical ontologies and identifiers such as UniProt, Gene Ontology, EFO, and MONDO.
  • Hands-on experience with graph databases such as Neo4j, Stardog, or GraphDB, including writing and optimizing queries in Cypher or SPARQL.
  • Working knowledge of semantic modelling concepts and standards such as RDF and OWL, and the ability to turn an ontology into a working schema.
  • Experience designing and building APIs, such as REST or GraphQL using frameworks such as FastAPI, to provide applications and users access to graph data.
  • Experience building data-quality or validation frameworks.
  • Familiarity with Google Cloud and BigQuery.
  • Strong Python skills and working knowledge of JavaScript for building data pipelines, graph integrations, and production applications.
  • Strong software engineering practices, including data modeling, system design, testing, documentation, and version control.
  • Clear written and verbal communication, including the ability to explain architecture decisions and technical trade-offs to clients and stakeholders.
  • Ability to work effectively across data engineering, biology, and AI teams.
Responsibilities
  • Maintain and extend the knowledge graph, including its schema, ingestion pipelines, and query layer using Neo4j, Cypher, Apache Jena Fuseki, and BigQuery on Google Cloud.
  • Build and run validation and data-governance pipelines to maintain data quality, consistency, and performance, including schema and constraint checks, identifier reconciliation, provenance, and versioning.
  • Maintain ontologies and semantic models with biology and data science teams, and develop the mapping tool scientists use to annotate new terms and analyses, including validation that keeps mappings consistent with the graph.
  • Integrate knowledge graph solutions with cloud platforms and enterprise data ecosystems, including Google Cloud and BigQuery.
  • Collaborate with data engineering, data science, AI, and biology teams to make graph data accessible and useful for downstream applications.
  • Write clean, testable, production-grade code and apply engineering best practices throughout development and delivery.
  • Own solutions from architecture and technology selection through implementation, testing, and performance optimization, working with data engineers, AI teams, and stakeholders to turn business requirements into reliable systems.
Desired Qualifications
  • Experience with large language model or agent systems.
  • Experience with Open Targets and other drug-discovery knowledge bases.

About the company

BioAge Labs develops therapies for age-related diseases by using a human-first discovery platform that maps human aging and translates those insights into a portfolio of drugs. Its approach starts from human aging profiles to identify drug targets and then creates medicines that prevent or treat diseases of aging, with the aim of extending healthy lifespan. The company operates in the clinical stage, developing longevity-focused therapeutics that can be sold to healthcare providers and patients as they progress through trials and gain approvals. What sets BioAge Labs apart is its focus on human aging biology as the starting point for drug development and its goal to address aging itself, not just individual diseases, providing a path to broader healthspan extension compared to traditional disease-focused approaches. The overarching goal is to deliver longevity medicine that delays or prevents age-related decline and improves healthspan for patients.

Company Size

51-200

Company Stage

Series D

Total Funding

$293.9M

Headquarters

Emeryville, California

Founded

2015

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Simplify's Take

What believers are saying

  • BioAge dosed QUELL-CV on June 16, 2026, targeting obesity-linked cardiovascular inflammation.
  • BioAge dosed QUELL-DME on September 8, 2026, expanding BGE-102 into diabetic macular edema.
  • BioAge held $381.3 million cash at June 30, 2026, funding execution through 2029.

What critics are saying

  • BGE-102 remains unproven in Phase 2; negative Q4 2026 readouts would crush the pipeline.
  • The March 2026 securities case dismissed with prejudice remains on appeal at the Ninth Circuit.
  • BioAge lost azelaprag in January 2025; another clinical failure leaves it a cash-burning shell.

What makes BioAge Labs unique

  • BioAge's human-first omics platform mines aging biology, not mouse models, for drug targets.
  • BGE-102 is an oral, brain-penetrant NLRP3 inhibitor built for cardiometabolic and ocular disease.
  • The company pairs machine-learning discovery with biomarker-rich trials and broad aging-pathway focus.

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Benefits

  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • 401(k) Company Match
  • Remote Work Options
  • Paid Holidays
  • Fertility Treatment Support
  • Family Planning Benefits
  • Professional Development Budget
  • Wellness Program
  • Childcare Support

Growth & Insights and Company News

Headcount

6 month growth

0%

1 year growth

0%

2 year growth

2%
GlobeNewswire
Oct 14th, 2026
Deep Origin announces multi-target ai-driven drug discovery collaboration with BioAge Labs; validated hits confirmed against first target.

Deep Origin announces multi-target ai-driven drug discovery collaboration with BioAge Labs; validated hits confirmed against first target. Partnership applies Deep Origin's virtual screening architecture to BioAge's targets, identified from human data, to accelerate discovery of novel cardiometabolic therapies. October 14, 2026 08:00 ET | Source: Deep Origin SOUTH SAN FRANCISCO, Calif., Oct. 14, 2026 (GLOBE NEWSWIRE) - Deep Origin today announced a multi-target AI-driven drug discovery collaboration with BioAge Labs, Inc. (Nasdaq: BIOA), a clinical-stage biopharmaceutical company developing therapeutic product candidates for cardiometabolic diseases by targeting the biology of human aging. The collaboration has reached its first milestone: novel small-molecule hits identified computationally by Deep Origin against a novel BioAge target have been validated in BioAge's wet lab. The collaboration aims to speed drug development against novel targets by utilizing hybrid AI and physics-based models for computational drug discovery. Under the agreement, Deep Origin applies its computational drug discovery platform to BioAge's selected targets to find novel hits against them. BioAge then verifies the functional activity of those hits in its own laboratory and leads hit-to-lead optimization, selection of development candidates, and clinical development. Deep Origin is eligible to receive success-based milestone payments. Before any compound reaches the bench, Deep Origin filters its candidate hits against BioAge's medicinal chemistry criteria so that any confirmed wet-lab hits will be suitable starting points for optimization. Deep Origin's virtual screening architecture is built on DODock and DOScore, proprietary engines that predict the orientation and affinity of small molecule binding to functionally active sites in proteins. The company described its virtual screening methods in an August 2026 preprint on bioRxiv, which reported prospective wet-lab hits against four targets of increasing difficulty, including a 30.6% hit rate on CD73, about 100 times the rate of a previously published machine-learning screen of the same target. As part of the collaboration with BioAge, Deep Origin's platform delivered multiple structurally distinct hits against the first target in less than three months. With validated hits in hand, BioAge is advancing its first target into hit-to-lead optimization. Work is ongoing to validate additional hits against defined targets. "BioAge finds its targets in human data, from people followed for decades, and many are novel targets with little known chemistry," said Michael Antonov, co-founder and chief executive officer of Deep Origin. "This is exactly the problem our virtual screening was built to solve. BioAge set a high bar for what its chemists would take forward, and the molecules that we delivered give BioAge's chemists strong starting points for optimization and position BioAge to move quickly through preclinical stages into the clinic." "We believe AI can help shorten the path from human biology to new medicines, and this collaboration demonstrated its potential to accelerate early small molecule drug discovery," said Kristen Fortney, Ph.D., co-founder and chief executive officer of BioAge. "Deep Origin's platform delivered high-quality chemical matter against a novel target in just months. We're thrilled with what we've accomplished together so far and look forward to extending the work to additional targets." In addition to virtual screening assessments, the agreement enables BioAge to draw on Deep Origin's later-stage computational tools, including free energy perturbation calculations and virtual human avatars of toxicology: interconnected organ models simulating the physical and chemical events inside a body to predict drug safety. About BioAge Labs, Inc. BioAge is a clinical-stage biopharmaceutical company developing therapeutic product candidates for cardiometabolic diseases by targeting the biology of human aging. The Company's lead product candidate, BGE-102, is a potent, orally bioavailable, brain-penetrant small-molecule NLRP3 inhibitor being developed for diseases driven by inflammation, including diabetic macular edema and cardiovascular risk. BGE-102 has completed a Phase 1 SAD/MAD trial demonstrating a well-tolerated profile and potential best-in-class reductions in hsCRP and other inflammatory biomarkers. Phase 2 cardiovascular proof-of-concept data from QUELL-CV are anticipated in the second half of 2026, and Phase 2 diabetic macular edema data from QUELL-DME are anticipated in the second half of 2027. The Company is also developing long-acting injectable and oral small molecule APJ agonists for obesity. BioAge[[ʼ]]s additional preclinical programs, which leverage insights from the Company[[ʼ]]s proprietary discovery platform built on human longevity data, address key pathways involved in metabolic aging. About Deep Origin Deep Origin is building computational discovery systems that model life, to close the gap between preclinical predictions and clinical outcomes. Co-founded by Michael Antonov, co-founder of Oculus, and Garegin Papoian, Ph.D., former Monroe Martin Professor of biochemistry at the University of Maryland, Deep Origin runs drug discovery programs - its own and its partners' - through hybrid AI-mechanistic models that span biological scales from quantum to cellular to human body scale. The company engages through discovery partnerships and SaaS platform access. Deep Origin is backed by more than $50 million in capital and more than $32 million in non-dilutive funding, including an ARPA-H CATALYST award to build in silico models that can reduce reliance on animal testing in preclinical drug development. For more information, visit deeporigin.com. BioAge Forward-Looking Statements This press release contains "forward-looking statements" within the meaning of, and made pursuant to the safe harbor provisions of, the Private Securities Litigation Reform Act of 1995. In some cases, you can identify forward-looking statements by terms such as "aim," "may," "will," "should," "expect," "forecast," "plan," "anticipate," "could," "intend," "target," "project," "contemplate," "believe," "estimate," "predict," "potential" or "continue" or the negative of these terms or other similar expressions, although not all forward-looking statements contain these words. All statements other than statements of historical fact contained in this press release, including without limitation statements regarding its plans to develop and commercialize its product candidates, including BGE-102 and its APJ programs, the potential for BGE-102 as a treatment for diabetic macular edema, the expected timeline for data readouts from its ongoing Phase 2 clinical trials, the expected timing and results of its ongoing or planned preclinical studies and clinical trials, risks associated with clinical trials, including its ability to adequately manage clinical activities for BGE-102 and its APJ programs, unexpected concerns that may arise from additional data or analysis obtained during clinical trials, the timing of and its ability to obtain and maintain regulatory approvals, the clinical utility of its future product candidates, its commercialization, marketing and manufacturing capabilities and strategy, its expectations about the willingness of healthcare professionals to use its product candidates, the sufficiency of its cash, cash equivalents and marketable securities, general economic conditions, the impact of industry and market conditions on its operations, including fluctuating interest rates and inflation, increased volatility in the debt and equity markets, legislative or regulatory healthcare reforms in the United States, significant political, trade or regulatory developments, including tariffs, federal government shutdowns, or shifting priorities within the U.S. Food and Drug Administration, cybersecurity incidents, and global regional conflicts, and the plans and objectives of management for future operations and capital expenditures are forward-looking statements. The forward-looking statements in this press release are only predictions and are based largely on its current expectations and projections about future events and financial trends that GovCloud Network believe may affect its business, financial condition and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of known and unknown risks, uncertainties and assumptions, including those described under the headings "Risk Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" included in BioAge's Quarterly Report on Form 10-Q filed with the U.S. Securities and Exchange Commission (SEC) on August 5, 2026, and BioAge's other filings with the SEC filed from time to time. Because forward-looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified and some of which are beyond its control, you should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in its forward-looking statements may not be achieved or occur and actual results could differ materially from those projected in the forward-looking statements. Moreover, GovCloud Network operate in an evolving environment. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties. BioAge undertakes no obligation to publicly update any forward-looking statement, whether written or oral, that may be made from time to time, whether as a result of new information, future developments or otherwise. Deep Origin Media Contact: Steve Cooper, Orangefiery [email protected] BioAge Media Contact: Chris Patil [email protected]

MarketBeat
Sep 5th, 2026
BioAge Labs (NASDAQ:BIOA) lowered to strong sell rating by Wall Street Zen.

BioAge Labs (NASDAQ:BIOA) lowered to strong sell rating by Wall Street Zen. September 5, 2026 Key points. * Wall Street Zen downgraded BioAge Labs to "strong sell" from "sell," although broader analyst sentiment remains "Moderate Buy," with six buy ratings and one sell rating. * Analysts' consensus price target is $36.57, but individual targets vary widely from $21 to $50; the stock opened at $9.59 and has traded between $4.58 and $25.95 over the past year. * BioAge reported a quarterly loss of $0.58 per share, better than the expected $0.65 loss, on $2.45 million in revenue. The company remains deeply unprofitable, with a negative net margin of 912.26%. * Five stocks to consider instead of BioAge Labs. BioAge Labs (NASDAQ:BIOA - Get Free Report) was downgraded by Wall Street Zen from a "sell" rating to a "strong sell" rating in a research note issued to investors on Saturday, Wall Street Zen reports. A number of other equities research analysts also recently weighed in on the stock. Jefferies Financial Group set a $21.00 price target on shares of BioAge Labs in a research report on Friday, July 31st. Weiss Ratings reissued a "sell (d-)" rating on shares of BioAge Labs in a research report on Tuesday, July 21st. BTIG Research restated a "buy" rating and set a $40.00 price objective on shares of BioAge Labs in a research note on Monday, August 3rd. Roth Capital reaffirmed a "buy" rating and issued a $25.00 price objective on shares of BioAge Labs in a report on Friday, July 31st. Finally, Needham & Company LLC cut their target price on BioAge Labs from $50.00 to $35.00 and set a "buy" rating for the company in a research report on Friday, July 31st. Six research analysts have rated the stock with a Buy rating and one has given a Sell rating to the company's stock. According to MarketBeat.com, BioAge Labs currently has an average rating of "Moderate Buy" and a consensus price target of $36.57. BioAge Labs stock performance. BIOA stock opened at $9.59 on Friday. The company's 50-day simple moving average is $16.50 and its 200 day simple moving average is $17.82. BioAge Labs has a 52 week low of $4.58 and a 52 week high of $25.95. The company has a market capitalization of $440.18 million, a PE ratio of -4.03 and a beta of 0.94. BioAge Labs (NASDAQ:BIOA - Get Free Report) last released its quarterly earnings results on Wednesday, August 5th. The company reported ($0.58) EPS for the quarter, topping analysts' consensus estimates of ($0.65) by $0.07. The business had revenue of $2.45 million for the quarter. BioAge Labs had a negative net margin of 912.26% and a negative return on equity of 28.99%. On average, analysts forecast that BioAge Labs will post -2.45 EPS for the current year. Institutional investors weigh in on BioAge Labs. Institutional investors and hedge funds have recently added to or reduced their stakes in the business. BlackRock Inc. acquired a new stake in shares of BioAge Labs in the 2nd quarter valued at $69,831,000. Jupiter Topco LLC acquired a new position in shares of BioAge Labs during the 2nd quarter worth $52,597,000. Janus Henderson Group PLC lifted its position in shares of BioAge Labs by 411.8% during the 1st quarter. Janus Henderson Group PLC now owns 2,094,270 shares of the company's stock worth $36,597,000 after buying an additional 1,685,063 shares during the last quarter. Octagon Capital Advisors LP boosted its stake in BioAge Labs by 9.4% in the first quarter. Octagon Capital Advisors LP now owns 1,748,000 shares of the company's stock valued at $30,573,000 after buying an additional 150,000 shares in the last quarter. Finally, Vanguard Group Inc. boosted its stake in BioAge Labs by 6.0% in the third quarter. Vanguard Group Inc. now owns 1,651,247 shares of the company's stock valued at $9,709,000 after buying an additional 93,694 shares in the last quarter. About BioAge Labs. BioAge Labs NASDAQ: BIOA is a clinical-stage biotechnology company focused on discovering and developing therapies that address age-associated diseases. The company leverages its proprietary analytics platform to mine large-scale human biological data for insights into the molecular mechanisms of aging. By targeting fundamental aging pathways, BioAge aims to create interventions that extend healthspan and treat conditions that disproportionately affect older populations. Discover more Stock split calculator Financial News Stock profit calculator At the core of BioAge's operations is its integrated drug discovery platform, which combines human omics datasets, machine learning algorithms and experimental validation to identify novel drug targets. This instant news alert was generated by narrative science technology and financial data from MarketBeat in order to provide readers with the fastest reporting and unbiased coverage. Please send any questions or comments about this story to [email protected]. Continue following MarketBeat Before you consider BioAge Labs, you'll want to hear this. MarketBeat keeps track of Wall Street's top-rated and best performing research analysts and the stocks they recommend to their clients on a daily basis. MarketBeat has identified the five stocks that top analysts are quietly whispering to their clients to buy now before the broader market catches on... and BioAge Labs wasn't on the list. While BioAge Labs currently has a Moderate Buy rating among analysts, top-rated analysts believe these five stocks are better buys. Robotics and automation are rapidly becoming essential infrastructure across healthcare, manufacturing, logistics, and many other industries. "Physical AI" is coming. Learn which seven companies are most positioned to benefit as intelligent robots enter the workforce.

PharmaVoice
Aug 10th, 2026
Did Novo's phase 3 flop kill the inflammation hypothesis in heart disease?

Did Novo's phase 3 flop kill the inflammation hypothesis in heart disease? While a disappointing late-stage readout sent biotech stocks tumbling, all hope may not be lost for the emerging approach to treating cardiovascular events. Published Aug. 10, 2026 By Kelly Bilodeau When Novo Nordisk recently reported that its experimental heart drug ziltivekimab failed to reduce the risk of heart attacks and strokes in a late-stage trial, the market reaction was swift. Novo's stock fell as much as 10%, while shares of several other companies also tumbled amid fears the results cast doubt on whether targeting inflammation could reduce the risk of serious cardiovascular events. The phase 3 Zeus trial enrolled over 6,300 people with atherosclerotic cardiovascular disease, chronic kidney disease and inflammation, following participants for up to four years. Although ziltivekimab produced the expected biological effect, lowering interleukin-6 and high-sensitivity C-reactive protein (hsCRP), it failed to reduce major adverse cardiovascular events (MACE) - cardiovascular death, nonfatal heart attack or stroke - compared with placebo. While investors may have been spooked by the failure, it didn't necessarily mark a death knell for the inflammation hypothesis, according to William Blair analyst Andy Hsieh. Instead, he said, the result may say more about IL-6 inhibition (and hsCRP as a surrogate marker) than it does about inflammation itself. "In our view, the bearish read-through is more limited to hsCRP's surrogacy for cardio protection in the context of IL-6 inhibition," he said in an email. The better approach to reducing cardiovascular events might involve targeting a different protein, interleukin-1beta (IL-1β). In Novartis' Cantos trial, for instance, a 150-mg dose of the drugmaker's IL-1β inhibitor Ilaris significantly reduced recurrent cardiovascular events compared with placebo. "We have validation that IL-1beta inhibition leads to MACE reduction," Hsieh said. "This effect was dependent on hsCRP reduction magnitude (2 mg/L cutoff). So I wouldn't say the data invalidates the inflammatory hypothesis in its entirety." The Novo readout's ripple effect. While the inflammation hypothesis may not be dead, Novo's phase 3 results could dampen enthusiasm for NLRP3 inhibitors, a broader anti-inflammatory approach that can also affect IL-6 expression. For instance, BioAge Labs' shares fell roughly 60% in premarket trading after Novo's Zeus readout, according to the William Blair note. BioAge is testing BGE-102 in the phase 2 Quell-Cv trial in patients at elevated cardiovascular risk and plans a phase 1b/2a study in diabetic macular edema. "Despite plans to examine BGE-102 in ophthalmology indications, we believe the approach remains high-risk and difficult to build an investment thesis around," Hsieh and William Blair colleagues wrote in a biotech note. Neumora, which is developing the preclinical NLRP3 inhibitor NMRA-215 for obesity and cardiometabolic disease, saw a 5% premarket drop after the ziltivekimab failure. William Blair sees less read-through to the program, however, because NLRP3 inhibition acts more broadly than IL-6 blockade and NMRA-215's lead indication is obesity. Ziltivekimab's story may not be over. Novo acquired the drug in its 2020 acquisition of Corvidia Therapeutics, and it remains in two additional phase 3 trials: Hermes in heart failure and Artemis in patients following an acute heart attack. Readouts for those trials are expected in the first half of 2027. "While ziltivekimab did not achieve the MACE benefit we had hoped for, this does not change our strategic commitment to cardiovascular disease," said Martin Holst Lange, Novo's executive vice president, chief scientific officer and head of research and development, in a press release. "The study provides important scientific evidence that will inform its ongoing cardiovascular research and the development of treatments for patients who continue to face substantial unmet need.

Associated Press
Aug 5th, 2026
BioAge doses first patient in Phase 2 trial of NLRP3 inhibitor BGE-102

BioAge Labs has dosed the first participant in QUELL-CV, a Phase 2 trial testing BGE-102, its oral NLRP3 inhibitor, in patients with obesity and elevated cardiovascular risk. The randomised, placebo-controlled trial will evaluate three dose levels in approximately 160 adults, with topline data expected in the second half of 2026. The company plans to initiate QUELL-DME, a Phase 1b/2a trial of BGE-102 in diabetic macular edema, in mid-2026, with results anticipated in mid-2027. Phase 1 data showed BGE-102 achieved up to 98% suppression of IL-1β and median hsCRP reductions of 86% at certain doses. For Q2 2026, research and development expenses were $24.4 million, up from $19.8 million year-over-year. Net loss was $26.1 million. BioAge held approximately $381.3 million in cash and marketable securities as of 30 June 2026.

Yahoo Finance
Jun 30th, 2026
BioAge Labs initiates Phase 2 cardiovascular study for BGE-102 with $384.9M cash reserves

BioAge Labs has dosed the first participant in QUELL-CV, a Phase 2 proof-of-concept study evaluating BGE-102, an orally available NLRP3 inhibitor designed for once-daily administration targeting cardiovascular risk reduction. The clinical-stage biopharmaceutical company previously reported Phase 1 data showing BGE-102 achieved median reductions of 86% in hsCRP levels from baseline with no serious adverse events. The company plans to begin a Phase 2 dose-ranging study in participants with elevated cardiovascular risk in mid-2026. In its first quarter 2026 results, BioAge Labs reported collaboration revenue of $2.8 million and research and development expenses of $20.4 million. The company held approximately $384.9 million in cash, cash equivalents and marketable securities as of 31 March 2026.