Title: California-Based Associate - Litigation and/or Merger Control - Antitrust Job Responsibilities: As a California-Based Associate specializing in Litigation and/or Merger Control within the Antitrust & Competition Practice Group, the candidate will be expected to engage in high-stakes disputes representing companies,...
Title: Litigation Associate Job Responsibilities: - Engaging in briefing complex issues of first impression, which involves crafting arguments and presenting legal theories that may not have been extensively litigated or decided in past cases. - Conducting advanced legal research to support case development,...
large international New York law firm founded in 1934 has established a full-service presence. Clients include large corporations and individuals as well as small and medium-sized businesses. The firm represents a wide range of industrial, financial and commercial enterprises, both...
Title: Litigation Associate, Consumer Products, Mid-Level to Senior Job Responsibilities: The law firm is seeking a mid-to-senior level associate to join its Consumer Products practice. The primary responsibilities include representing consumer product companies in responding to private plaintiff demand letters and government...
The following jobs are no longer active but were real openings previously posted by employers. These listings provide valuable insight into employer hiring trends and frequently lead to job offers. In many cases, employers are still hiring or open to strong candidates even if no new job is posted. Applying to these listings often makes you the only applicant, increasing your chances of being hired.
Junior Medical Devices, FDA Regulatory Associate The candidate... will work on medical device regulatory matters. Duties and responsibilities include: researching FDA medical device regulatory issues,... providing advice on regulatory pathways; drafting regulatory submissions such as 510(k) Notices, Investigational Device Exemptions (IDEs), De Novo Requests and Premarket Approval Applications (PMAs); as well as preparing responses to FDA premarket review and post... market compliance... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory Associate The candidate... must have experience researching FDA medical device regulatory issues;... providing advice on regulatory pathways; drafting regulatory submissions such as 510(k) Notices, Investigational Device Exemptions (IDEs), De Novo Requests and Premarket Approval Applications (PMAs); preparing responses to FDA premarket review; and posting... market compliance questions and deficiencies. Scientific, health or biotech background is preferred. Experience... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory Associate The candidate... should have . Bar membership in good standing. Must have 2-5 years of experience or demonstrated interest in handling FDA medical device matters (scientific,... health or biotech background preferred). Experience researching FDA medical device regulatory issues;... providing advice on regulatory pathways; drafting regulatory submissions such as 510(k) Notices, Investigational Device Exemptions (IDEs), De Novo Requests and Premarket Approva... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory & Compliance Associate... The candidate will join fast-growing FDA regulatory and compliance practice.... Would not work in silos but would advise on all product areas and will advise on issues throughout a product’s life cycle, including product development strategy, clinical trial compliance, product submissions, labeling, advertising and promotion, adverse event reporting, product recalls, good manufacturing practices (GMPs), agency inspections and remediation of... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
Mid-level FDA Associate The candidate must... have 3-5 years of experience. Should preferably have exposure to a range of FDA regulatory issues including pharmaceutical... products, medical devices, digital health, and regulated consumer packaged goods. Must be admitted to and be a member in good standing of the CA State Bar.... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
Gibson Dunn is a premier international law firm with more than 1,300 lawyers in 20 offices located in major cities throughout the United States, Europe, the Middle East, Asia and South America. The firm provides a full range of legal services to clients worldwide. # Lateral Associate - FDA & Health Care Gibson Dunn's... San Francisco office is looking to hire a Lateral Associate - FDA & Health Care with... 3 or more years of experience in regulatory or enforcement matters involvi... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory and Risk Management... Associate The candidate should be a senior-level associate to handle complex regulatory issues. Must have 7+ years of experience representing pharmaceutical and medical device companies in connection with a wide variety of regulatory issues governed by the Food and Drug Administration and be able to parse complex regulatory schemes. Should also have stellar academic credentials, and excellent written and verbal communication skills.... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory Attorney The candidate... should be a mid- to senior-level attorney with strong academic credentials and excellent research skills to assist clients with complex FDA regulatory issues. Must have... 6+ years of experience in FDA regulatory matters related to... drug, biologicals, medical devices (including in vitro diagnostics), and/or combination products, such as premarket review issues, product jurisdiction questions, post-market CGMP compliance, advertising and prom... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
Junior to Mid-level FDA / Medical Devices Associate... The candidate will work on medical device regulatory matters. Duties and responsibilities include: researching FDA medical device regulatory issues,... providing expert advice on regulatory pathways; drafting regulatory submissions such as 510(k) Notices, Investigational Device Exemptions (IDEs), De Novo Requests and Premarket Approval Applications (PMAs); as well as preparing responses to FDA premarket review and post... market... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here
FDA Regulatory Manager or Senior... Manager The candidate should have relevant expertise to work on medical device regulatory matters. Should have a deep understanding of the . Food and Drug Administration’s (FDA’s) medical device regulatory issues as well as demonstrated ability to successfully navigate the FDA’s complex submission and review process, and experience guiding clients through the FDA approval process. Experience with... FDA policies and requirements, product... deve... read more
Note: This job is no longer active. It was originally posted on [Date] and is part of LawCrossing’s historical archive of legal jobs. While the position may have been filled, employers often remain open to exceptional candidates for similar roles. LawCrossing has tracked this employer's hiring activity for over 25 years. This listing is provided for informational and outreach purposes and may still lead to employment. Learn more about archive jobs and how powerful they are for your search, click here