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,...
Impact Litigation Attorney (3-6 years of practice; SF & NY)* Law firm **Members Only** is seeking an experienced and passionate attorney to join its Impact Litigation group. The ideal candidate for this position should have 3+ years of...
Title California-Based Associate - Litigation and/or Merger Control - Antitrust Job Responsibilities The associate will be a part of the law firm's Global Antitrust and Competition Practice. The primary responsibilities include: - Representing companies, financial institutions, private equity firms, and...
The following jobs are no longer active but were real openings previously posted by employers.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 to Mid-level Pharmaceuticals and Biotechnology Associate The candidate will work with other attorneys at the firm who specialize in the regulation of pharmaceutical and biotechnology products by the US Food and Drug Administration (FDA)... and the Drug Enforcement Administration (DEA), including... assisting the firm's clients in obtaining FDA approval of new drugs and biotechnology products, advising on exclusivity and product life cycle issues and understanding the regula... 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Note: This job is no longer active.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
Junior to Mid-level Pharmaceuticals and Biotechnology Associate The candidate will work with other attorneys at the firm who specialize in the regulation of pharmaceutical and biotechnology products by the US Food and Drug Administration (FDA)... and the Drug Enforcement Administration (DEA), including... assisting the firm's clients in obtaining FDA approval of new drugs and biotechnology products, advising on exclusivity and product life cycle issues and understanding the regula... 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
Food and Beverage Regulatory Attorney... The candidate must have 5+ years food and beverage regulatory 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
Medical Device and Technology Associate The candidate will join Food Drug, Medical Device and... Agriculture practice. Prefer experience with FDA medical device pre-market clearance and approval matters as well as post-market compliance and quality systems requirements. Experience at FDA would be a plus as would be relevant work experience in the medical device, pharmaceutical or biotechnology industries. Academic background in science or engineering would be helpful. Must have... 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
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
to Senior Corporate Associate – M&A and Private Equity/Venture Finance The candidate must have managed a significant number of middle-market M&A transactions and private equity and venture capital financings, and be experienced in overseeing diligence processes, drafting and negotiating transaction and ancillary documents and managing deal teams to and through closing, and should as well have solid general corporate practice experience. Experience in healthcare, fo... 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
Medical Devices, Postmarket Compliance Associate The candidate will join the FDA Medical Devices group to 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 FD... 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
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