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Her practice focuses on representing clients in the consumer products, pharmaceutical and medical device industries in nationwide product liability and personal injury litigation. With over ten years of litigation experience in federal and state courts, Rebeca combines deep trial experience with strategic leadership, guiding trial teams through complex, high-exposure cases to achieve successful outcomes. [[--readmore--]]\u003c/p\u003e\n\u003cp\u003eMost recently, Rebeca served as a federal prosecutor and Deputy Chief in the Narcotics and Dangerous Drugs Section of the U.S. Attorney\u0026rsquo;s Office for the Northern District of Georgia. In that role, she investigated and prosecuted various federal offenses, including large-scale, multi-state narcotics trafficking, firearms trafficking, and money laundering. 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Her practice focuses on representing clients in the consumer products, pharmaceutical and medical device industries in nationwide product liability and personal injury litigation. With over ten years of litigation experience in federal and state courts, Rebeca combines deep trial experience with strategic leadership, guiding trial teams through complex, high-exposure cases to achieve successful outcomes. [[--readmore--]]\u003c/p\u003e\n\u003cp\u003eMost recently, Rebeca served as a federal prosecutor and Deputy Chief in the Narcotics and Dangerous Drugs Section of the U.S. Attorney\u0026rsquo;s Office for the Northern District of Georgia. In that role, she investigated and prosecuted various federal offenses, including large-scale, multi-state narcotics trafficking, firearms trafficking, and money laundering. She was previously an associate in King \u0026amp; Spalding\u0026rsquo;s Product Liability and Mass Torts practice group from 2014 to 2020, supporting multiple teams in pharmaceutical, consumer product and pro bono cases, both at trial and in the coordination of mass tort litigation. She also served on teams conducting risk assessments for pharmaceutical industry clients regarding the marketing of new pharmaceutical products.\u003c/p\u003e\n\u003cp\u003eRebeca has experience leading trial teams, drafting complex evidentiary motions and appellate briefs. She has managed discovery strategy and fact development in cases involving allegations of breach of warranty, strict liability, and negligence. Through her work at the U.S. Attorney\u0026rsquo;s office, she has led high-impact investigations in partnership with the DEA, ATF, HSI, FBI, and state agencies, including strategic decision-making on highly sensitive enforcement matters\u003c/p\u003e\n\u003cp\u003eRebeca received her J.D. from The University of Texas School of Law, where she served as Editor-in-Chief of the American Journal of Criminal Law and as a William Wayne Justice Center Pro Bono Scholar.\u003c/p\u003e","recognitions":[{"title":"Leadership Award","detail":"Georgia Hispanic Bar Association, 2025"},{"title":"LEAD Atlanta","detail":"Leadership Atlanta Program, 2025"},{"title":"Superior Performance by a Litigative Team Award","detail":"U.S. Attorney’s Office, 2024"},{"title":"Top 50 Most Influential Latinos in Georgia","detail":"Georgia Hispanic Chamber of Commerce, 2023"},{"title":"Rising Star Award","detail":"Georgia Hispanic Bar Association, 2019"}]},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":13290}]},"capability_group_id":3},"created_at":"2026-01-30T21:53:34.000Z","updated_at":"2026-01-30T21:53:34.000Z","searchable_text":"Ojeda{{ FIELD }}{:title=\u0026gt;\"Leadership Award\", :detail=\u0026gt;\"Georgia Hispanic Bar Association, 2025\"}{{ FIELD }}{:title=\u0026gt;\"LEAD Atlanta\", :detail=\u0026gt;\"Leadership Atlanta Program, 2025\"}{{ FIELD }}{:title=\u0026gt;\"Superior Performance by a Litigative Team Award\", :detail=\u0026gt;\"U.S. Attorney’s Office, 2024\"}{{ FIELD }}{:title=\u0026gt;\"Top 50 Most Influential Latinos in Georgia\", :detail=\u0026gt;\"Georgia Hispanic Chamber of Commerce, 2023\"}{{ FIELD }}{:title=\u0026gt;\"Rising Star Award\", :detail=\u0026gt;\"Georgia Hispanic Bar Association, 2019\"}{{ FIELD }}Rebeca Ojeda is a partner in King \u0026amp; Spalding’s Product Liability \u0026amp; Mass Torts practice group, based in the Atlanta office. Her practice focuses on representing clients in the consumer products, pharmaceutical and medical device industries in nationwide product liability and personal injury litigation. With over ten years of litigation experience in federal and state courts, Rebeca combines deep trial experience with strategic leadership, guiding trial teams through complex, high-exposure cases to achieve successful outcomes. \nMost recently, Rebeca served as a federal prosecutor and Deputy Chief in the Narcotics and Dangerous Drugs Section of the U.S. Attorney’s Office for the Northern District of Georgia. In that role, she investigated and prosecuted various federal offenses, including large-scale, multi-state narcotics trafficking, firearms trafficking, and money laundering. She was previously an associate in King \u0026amp; Spalding’s Product Liability and Mass Torts practice group from 2014 to 2020, supporting multiple teams in pharmaceutical, consumer product and pro bono cases, both at trial and in the coordination of mass tort litigation. She also served on teams conducting risk assessments for pharmaceutical industry clients regarding the marketing of new pharmaceutical products.\nRebeca has experience leading trial teams, drafting complex evidentiary motions and appellate briefs. She has managed discovery strategy and fact development in cases involving allegations of breach of warranty, strict liability, and negligence. Through her work at the U.S. Attorney’s office, she has led high-impact investigations in partnership with the DEA, ATF, HSI, FBI, and state agencies, including strategic decision-making on highly sensitive enforcement matters\nRebeca received her J.D. from The University of Texas School of Law, where she served as Editor-in-Chief of the American Journal of Criminal Law and as a William Wayne Justice Center Pro Bono Scholar. Partner Leadership Award Georgia Hispanic Bar Association, 2025 LEAD Atlanta Leadership Atlanta Program, 2025 Superior Performance by a Litigative Team Award U.S. Attorney’s Office, 2024 Top 50 Most Influential Latinos in Georgia Georgia Hispanic Chamber of Commerce, 2023 Rising Star Award Georgia Hispanic Bar Association, 2019 Vanderbilt University Vanderbilt University School of Law The University of Texas at Austin The University of Texas School of Law Seton Hall University Seton Hall University School of Law U.S. Court of Appeals for the Eleventh Circuit U.S. District Court for the Northern District of Georgia Florida Georgia Georgia Hispanic Bar Association: Board Member (2025-Present), Co-President (2024), Vice President (2017-2018) Hispanic National Bar Association (HNBA): Regional President, Region VII - Alabama, Georgia, Mississippi, (2021-2023), Young Lawyers Division Representative, Region VII (2019-2021) Northern District of Georgia Civics Education Committee: Program Co-Chair (2023), Member (2021-2024) Leadership Council on Legal Diversity: Co-City Lead, Atlanta (2020-2021), Pathfinder (2018)","searchable_name":"Rebeca M. Ojeda","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":437153,"version":1,"owner_type":"Person","owner_id":7200,"payload":{"bio":"\u003cp\u003eJohn O\u0026rsquo;Brien leverages nearly two decades of experience in legal practice and senior in-house counsel roles to advise clients on legal, regulatory, compliance and enforcement matters across FDA-regulated industries, including tobacco.\u0026nbsp;\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003ePrior to joining King \u0026amp; Spalding, John served as Vice President and Assistant General Counsel at Reynolds, where he counseled Reynolds\u0026rsquo; operating companies on various high-profile regulatory, marketing, and litigation matters. John focuses on advising tobacco manufacturers, wholesalers, distributors, retailers, and suppliers in all aspects of their businesses, including tobacco taxation matters, compliance with the Family Smoking Prevention and Tobacco Control Act and related FDA rules and guidance, administrative disputes involving federal and state governmental entities, and commercial agreements. He works with clients in all segments of the tobacco industry, including electronic nicotine delivery systems and other novel products and traditional tobacco products such as cigarettes, cigars, snus, and moist snuff. John also assists clients with FDA premarket and postmarket requirements, including substantial equivalence (SE), premarket tobacco applications (PMTA), modified risk tobacco product applications (MRTPA), and has helped companies obtain numerous FDA marketing orders for new tobacco products, including FDA\u0026rsquo;s first marketing granted order for an e-cigarette.\u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eJohn frequently presents on tobacco regulatory matters at conferences, including the Food and Drug Law Institute, Next Generation Nicotine Delivery USA, American Tobacco and Nicotine Forum, and CStore Connections conferences.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eIn addition to his extensive tobacco regulatory experience, John spent over a decade in private practice, counseling food, supplement, and other consumer packaged goods companies on FDA, USDA, and FTC regulatory matters, including enforcement actions, civil litigation, investigations, inspections, product recalls, claims substantiation, labeling, and compliance.\u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cem\u003eAdmitted\u0026nbsp;only\u0026nbsp;in\u0026nbsp;IL\u0026nbsp;and\u0026nbsp;GA.\u0026nbsp;Supervised\u0026nbsp;by\u0026nbsp;D.C.\u0026nbsp;Bar\u0026nbsp;Members\u003c/em\u003e\u003c/p\u003e","slug":"john-o-brien","email":"jobrien@kslaw.com","phone":null,"matters":null,"taggings":{"tags":[],"meta_tags":[{"id":3933}]},"expertise":[{"id":21,"guid":"21.capabilities","index":0,"source":"capabilities"},{"id":74,"guid":"74.capabilities","index":1,"source":"capabilities"},{"id":23,"guid":"23.capabilities","index":2,"source":"capabilities"},{"id":81,"guid":"81.capabilities","index":3,"source":"capabilities"},{"id":17,"guid":"17.capabilities","index":4,"source":"capabilities"},{"id":127,"guid":"127.capabilities","index":5,"source":"capabilities"},{"id":105,"guid":"105.capabilities","index":6,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":7,"source":"capabilities"}],"is_active":true,"last_name":"O'Brien","nick_name":"John","clerkships":[],"first_name":"John","title_rank":9999,"updated_by":202,"law_schools":[{"id":2204,"meta":{"degree":"J.D.","honors":"","is_law_school":"1","graduation_date":null},"order":1,"pin_order":null,"pin_expiration":null}],"middle_name":"F.","name_suffix":"","recognitions":null,"linked_in_url":null,"seodescription":"John F. O'Brien is a counsel of our Product Liability \u0026 Mass Torts Practice Group. Read more.","primary_title_id":14,"translated_fields":{"en":{"bio":"\u003cp\u003eJohn O\u0026rsquo;Brien leverages nearly two decades of experience in legal practice and senior in-house counsel roles to advise clients on legal, regulatory, compliance and enforcement matters across FDA-regulated industries, including tobacco.\u0026nbsp;\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003ePrior to joining King \u0026amp; Spalding, John served as Vice President and Assistant General Counsel at Reynolds, where he counseled Reynolds\u0026rsquo; operating companies on various high-profile regulatory, marketing, and litigation matters. John focuses on advising tobacco manufacturers, wholesalers, distributors, retailers, and suppliers in all aspects of their businesses, including tobacco taxation matters, compliance with the Family Smoking Prevention and Tobacco Control Act and related FDA rules and guidance, administrative disputes involving federal and state governmental entities, and commercial agreements. He works with clients in all segments of the tobacco industry, including electronic nicotine delivery systems and other novel products and traditional tobacco products such as cigarettes, cigars, snus, and moist snuff. John also assists clients with FDA premarket and postmarket requirements, including substantial equivalence (SE), premarket tobacco applications (PMTA), modified risk tobacco product applications (MRTPA), and has helped companies obtain numerous FDA marketing orders for new tobacco products, including FDA\u0026rsquo;s first marketing granted order for an e-cigarette.\u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eJohn frequently presents on tobacco regulatory matters at conferences, including the Food and Drug Law Institute, Next Generation Nicotine Delivery USA, American Tobacco and Nicotine Forum, and CStore Connections conferences.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003eIn addition to his extensive tobacco regulatory experience, John spent over a decade in private practice, counseling food, supplement, and other consumer packaged goods companies on FDA, USDA, and FTC regulatory matters, including enforcement actions, civil litigation, investigations, inspections, product recalls, claims substantiation, labeling, and compliance.\u0026nbsp;\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cem\u003eAdmitted\u0026nbsp;only\u0026nbsp;in\u0026nbsp;IL\u0026nbsp;and\u0026nbsp;GA.\u0026nbsp;Supervised\u0026nbsp;by\u0026nbsp;D.C.\u0026nbsp;Bar\u0026nbsp;Members\u003c/em\u003e\u003c/p\u003e"},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":12885}]},"capability_group_id":2},"created_at":"2025-09-11T20:12:29.000Z","updated_at":"2025-09-11T20:12:29.000Z","searchable_text":"O'Brien{{ FIELD }}John O’Brien leverages nearly two decades of experience in legal practice and senior in-house counsel roles to advise clients on legal, regulatory, compliance and enforcement matters across FDA-regulated industries, including tobacco.  \nPrior to joining King \u0026amp; Spalding, John served as Vice President and Assistant General Counsel at Reynolds, where he counseled Reynolds’ operating companies on various high-profile regulatory, marketing, and litigation matters. John focuses on advising tobacco manufacturers, wholesalers, distributors, retailers, and suppliers in all aspects of their businesses, including tobacco taxation matters, compliance with the Family Smoking Prevention and Tobacco Control Act and related FDA rules and guidance, administrative disputes involving federal and state governmental entities, and commercial agreements. He works with clients in all segments of the tobacco industry, including electronic nicotine delivery systems and other novel products and traditional tobacco products such as cigarettes, cigars, snus, and moist snuff. John also assists clients with FDA premarket and postmarket requirements, including substantial equivalence (SE), premarket tobacco applications (PMTA), modified risk tobacco product applications (MRTPA), and has helped companies obtain numerous FDA marketing orders for new tobacco products, including FDA’s first marketing granted order for an e-cigarette.  \nJohn frequently presents on tobacco regulatory matters at conferences, including the Food and Drug Law Institute, Next Generation Nicotine Delivery USA, American Tobacco and Nicotine Forum, and CStore Connections conferences. \nIn addition to his extensive tobacco regulatory experience, John spent over a decade in private practice, counseling food, supplement, and other consumer packaged goods companies on FDA, USDA, and FTC regulatory matters, including enforcement actions, civil litigation, investigations, inspections, product recalls, claims substantiation, labeling, and compliance.  \nAdmitted only in IL and GA. Supervised by D.C. Bar Members John F. O'Brien lawyer Counsel Northwestern University Northwestern Pritzker School of Law University of Illinois at Urbana-Champaign University of Illinois College of Law University of Illinois at Urbana-Champaign University of Illinois College of Law Georgia Illinois","searchable_name":"John F. O'Brien","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null},{"id":447114,"version":1,"owner_type":"Person","owner_id":7319,"payload":{"bio":"\u003cp\u003eDanielle O'Neal is a senior associate in King \u0026amp; Spalding\u0026rsquo;s Houston office and a member of the firm\u0026rsquo;s Products Liability and Mass Torts practice. Drawing on her scientific background\u0026nbsp;and meaningful trial experience, she represents clients in the chemical, life sciences, pharmaceutical, and energy industries. Danielle is known for translating technical subject matter into clear, compelling advocacy and for partnering closely with clients to craft practical, business-focused solutions tailored to each client\u0026rsquo;s objectives.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDanielle brings a unique combination of scientific training, litigation insight, and practical problem-solving to her work on high-stakes product liability and mass tort matters. Her experience spans single-plaintiff actions, consolidated proceedings, and multidistrict litigation, where she has played key roles in developing case strategy, managing discovery, preparing expert witnesses, and supporting trial teams in jurisdictions across the country. Danielle\u0026rsquo;s ability to understand and distill complex technical concepts\u0026mdash;ranging from biological processes to pharmaceutical product design\u0026mdash;allows her to collaborate effectively with experts and present sophisticated issues in a clear and compelling manner.\u003c/p\u003e\n\u003cp\u003eDanielle also draws on her nearly year-long secondment with a Fortune 100 pharmaceutical company, where she worked closely with in-house counsel and business stakeholders on a wide range of litigation and regulatory matters. This experience deepened her understanding of the operational, strategic, and commercial considerations that shape corporate decision-making, and it informs her ability to deliver advice that is both legally sound and aligned with broader business priorities. Her time in-house strengthened her appreciation for efficient communication, cross-functional coordination, and proactive risk management skills she brings to every client engagement.\u003c/p\u003e","slug":"danielle-o-neal","email":"doneal@kslaw.com","phone":null,"matters":null,"taggings":{"tags":[],"meta_tags":[]},"expertise":[{"id":17,"guid":"17.capabilities","index":0,"source":"capabilities"},{"id":16,"guid":"16.capabilities","index":1,"source":"capabilities"},{"id":5,"guid":"5.capabilities","index":2,"source":"capabilities"},{"id":103,"guid":"103.capabilities","index":3,"source":"capabilities"},{"id":74,"guid":"74.capabilities","index":4,"source":"capabilities"},{"id":1193,"guid":"1193.smart_tags","index":5,"source":"smartTags"}],"is_active":true,"last_name":"O'Neal","nick_name":"Danielle","clerkships":[],"first_name":"Danielle","title_rank":9999,"updated_by":202,"law_schools":[{"id":565,"meta":{"degree":"J.D.","honors":"Magna Cum Laude","is_law_school":"1","graduation_date":null},"order":1,"pin_order":null,"pin_expiration":null}],"middle_name":" ","name_suffix":"","recognitions":null,"linked_in_url":null,"seodescription":null,"primary_title_id":75,"translated_fields":{"en":{"bio":"\u003cp\u003eDanielle O'Neal is a senior associate in King \u0026amp; Spalding\u0026rsquo;s Houston office and a member of the firm\u0026rsquo;s Products Liability and Mass Torts practice. Drawing on her scientific background\u0026nbsp;and meaningful trial experience, she represents clients in the chemical, life sciences, pharmaceutical, and energy industries. Danielle is known for translating technical subject matter into clear, compelling advocacy and for partnering closely with clients to craft practical, business-focused solutions tailored to each client\u0026rsquo;s objectives.\u0026nbsp;[[--readmore--]]\u003c/p\u003e\n\u003cp\u003eDanielle brings a unique combination of scientific training, litigation insight, and practical problem-solving to her work on high-stakes product liability and mass tort matters. Her experience spans single-plaintiff actions, consolidated proceedings, and multidistrict litigation, where she has played key roles in developing case strategy, managing discovery, preparing expert witnesses, and supporting trial teams in jurisdictions across the country. Danielle\u0026rsquo;s ability to understand and distill complex technical concepts\u0026mdash;ranging from biological processes to pharmaceutical product design\u0026mdash;allows her to collaborate effectively with experts and present sophisticated issues in a clear and compelling manner.\u003c/p\u003e\n\u003cp\u003eDanielle also draws on her nearly year-long secondment with a Fortune 100 pharmaceutical company, where she worked closely with in-house counsel and business stakeholders on a wide range of litigation and regulatory matters. This experience deepened her understanding of the operational, strategic, and commercial considerations that shape corporate decision-making, and it informs her ability to deliver advice that is both legally sound and aligned with broader business priorities. Her time in-house strengthened her appreciation for efficient communication, cross-functional coordination, and proactive risk management skills she brings to every client engagement.\u003c/p\u003e"},"locales":["en"]},"secondary_title_id":null,"upload_assignments":{"headshot":[{"id":13433}]},"capability_group_id":3},"created_at":"2026-03-27T22:04:25.000Z","updated_at":"2026-03-27T22:04:25.000Z","searchable_text":"O'Neal{{ FIELD }}Danielle O'Neal is a senior associate in King \u0026amp; Spalding’s Houston office and a member of the firm’s Products Liability and Mass Torts practice. Drawing on her scientific background and meaningful trial experience, she represents clients in the chemical, life sciences, pharmaceutical, and energy industries. Danielle is known for translating technical subject matter into clear, compelling advocacy and for partnering closely with clients to craft practical, business-focused solutions tailored to each client’s objectives. \nDanielle brings a unique combination of scientific training, litigation insight, and practical problem-solving to her work on high-stakes product liability and mass tort matters. Her experience spans single-plaintiff actions, consolidated proceedings, and multidistrict litigation, where she has played key roles in developing case strategy, managing discovery, preparing expert witnesses, and supporting trial teams in jurisdictions across the country. Danielle’s ability to understand and distill complex technical concepts—ranging from biological processes to pharmaceutical product design—allows her to collaborate effectively with experts and present sophisticated issues in a clear and compelling manner.\nDanielle also draws on her nearly year-long secondment with a Fortune 100 pharmaceutical company, where she worked closely with in-house counsel and business stakeholders on a wide range of litigation and regulatory matters. This experience deepened her understanding of the operational, strategic, and commercial considerations that shape corporate decision-making, and it informs her ability to deliver advice that is both legally sound and aligned with broader business priorities. Her time in-house strengthened her appreciation for efficient communication, cross-functional coordination, and proactive risk management skills she brings to every client engagement. Senior Associate Spelman College  DePaul University DePaul University College of Law DePaul University DePaul University College of Law Illinois Texas","searchable_name":"Danielle O'Neal","is_active":true,"featured":null,"publish_date":null,"expiration_date":null,"blog_featured":null,"published_by":202,"capability_group_featured":null,"home_page_featured":null}]}}