VP, Legal & General Counsel

Sorry, this job was removed at 03:38 p.m. (CST) on Monday, Jul 08, 2024
Hiring Remotely in South San Francisco, CA
Remote
250K-380K Annually
7+ Years Experience
Biotech
The Role

Position Summary 


We are seeking a VP of Legal & General Counsel who will play a key role in overseeing the legal department and managing all worldwide legal resources, structuring complex commercial transactions, as well as drafting and negotiating commercial agreements. This person will be responsible for advising on legal aspects of the Company's financing activities and corporate structure considerations, including assessing and advising on current and future business structures and legal entities; as well as managing intellectual property matters like strategic filing decisions. 


Candidates should be creative problem solvers who take pride in personal excellence, with a proven ability to thrive in an environment with frequently shifting priorities. Candidates should demonstrate qualifications consistent with our shareholders’ long-term objectives of maximizing shareholder value. Proven experience of overseeing a process to prepare a company to be a public company and functioning as General Counsel of a public company are highly desirable.


Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grow.


Responsibilities

  • Lead the Company in structuring, negotiating, drafting, and closing complex commercial contracts, strategic partnership deals, technology arrangements, and financing deals to ensure both business and legal objectives are met
  • Manage the Company's general corporate legal activities; including, employment and other HR matters, corporate governance, regulatory, employee equity plans, and other corporate and financial matters
  • Partner with all areas of the business, including Finance, Sales, Business Development, and Human Resources, to advise on legal risks, business strategies, and other issues related to corporate transactions
  • Partner with and advise internal business clients on legal issues and risks, company policies and procedures, etc.
  • Educate the company, clients, and partners about how to manage privacy issues given current and upcoming regulations
  • Advise executives on the status, legal risks, and business terms of high-value, strategic deals
  • Provide general legal and business advice to the Company's senior management and Board of Directors
  • Manage the Legal Department budget and maintain ultimate responsibility for the department’s performance
  • Advise the Company on IP piracy issues
  • Support HR to maintain and update Employee’s Handbook and general HR policies and provide legal support in all HR related matters (labor contracts, disciplinary proceedings, litigation)
  • Monitor new legislation and supervise the lobbying activities on any relevant new legislation
  • Lead the company’s litigation strategies
  • Advise and counsel on general securities law, NYSE/NASDAQ matters, and general corporate governance matters
  • Collaborate with internal stakeholders on SEC filings, such as 10-Ks, 10-Qs, 8-Ks, and proxy statements
  • Advise and support organizational growth with a global mindset while balancing business risk
  • Coordinate Board of Director meetings and act as the corporate secretary preparing meeting minutes and maintaining appropriate corporate records
  • Consult with outside law firms as necessary to assist in legal functions

Requirements

  • J.D. from a highly regarded university 
  • 15+ years of relevant experience in a law firm and as in-house legal counsel within one or more fast growing companies within the Company’s sector
  • Must be a member of a state bar
  • Previous experience working within the life sciences industry is required. Experience working within a start-up is highly desired
  • Previous track record of excellence in corporate law, including drafting commercial contracts of high value, structuring international agreements/partnerships etc.
  • Exceptional analytical and problem-solving skills with the ability to think strategically and provide sound business advice
  • Experience with either an initial public offering or managing legal work for a public company (such as proxies and ’34 Act filings)
  • Strong interpersonal skills and ability to partner with employees of all levels throughout the organization
  • Hire, lead, and develop high functioning legal professionals to build a world class legal department
  • Ability to prepare clear, concise, and complete legal documents, reports, correspondence and other communications on complex legal issues
  • Highly responsible, self-motivated, and able to thrive in an energetic, fast pace, high growth, entrepreneurial environment
  • Excellent communication skills - written, verbal, and interpersonal
  • Must be able to maintain a high degree of confidentiality
  • Strong business fluency in English required
  • Must be a highly ethical and proactive leader who can maximize the resources of a growth company
  • Be able to work independently in a fast-paced environment
  • Willingness to travel up to 50% of the time

Annual Salary Range: $250,000-400,000


Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.


This is Cellares


Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.

The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.


Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.


The Company
HQ: South San Francisco, CA
109 Employees
On-site Workplace
Year Founded: 2019

What We Do

Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patients who can benefit.

The clinical impact of cell therapy in treating cancer has been proven, but this therapeutic approach has several limitations, especially in manufacturing, leaving extremely sick patients waiting for treatment and desperate for hope.
Since cell therapy is currently produced for a single patient at a time, it is expensive to manufacture, requiring significant time and resources, and is difficult to scale.

Preclinical and clinical scientists, as well as commercial cell therapy manufacturers also lack the options to fully automate their manufacturing process quickly, safely, cost-effectively and at the scale they need.

The Cell Shuttle is an automated and closed end-to-end manufacturing solution that is flexible and scalable, enabling customers to run exact processes specified for their cell therapy. Compared with the current manual manufacturing processes for cell therapy, the Cell Shuttle’s next-generation automated manufacturing solution has 10 times the scalability (meaning 10 times more patient doses can be produced simultaneously), enables a three-fold reduction in process failure rates and will reduce the per-patient manufacturing cost by up to 70 percent for most processes.

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