At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.

Job Description
 

We are looking for an attorney with experience in manufacturing and supply contracts to support Gilead’s  operations.  While this role primarily supports the Pharmaceutical Development & Manufacturing organizations, this attorney may support other general contract matters.

Specific Responsibilities and Skills

 

This individual will be responsible for, among other things:

• Drafting and negotiating a full range of development and supply agreements for various types of  manufacturing transactions, involving clinical supply, commercial supply, collaborations, drug products and medical devices.
• Preparing manufacturing and supply agreements, license agreements, consulting agreements, confidential disclosure agreements, material transfer agreements, and other commercial agreements in support of our Pharmaceutical Development & Manufacturing organizations.
• Partnering with senior management throughout Pharmaceutical Development & Manufacturing and the broader company to ensure smooth, efficient, practical and quality coordination between the business and legal teams.
• Develop materials for internal practices; implement and meet with Pharmaceutical Development & Manufacturing stakeholders to implement new processes and procedures.
• Advising on and resolving transactional negotiation escalations and potential contract disputes.
• Maintaining and improving productive and efficient ways of working with a wide range of cross-functional colleagues and subject-matter experts.

 

Basic Qualifications

• A J.D. from an accredited law school

• 6+ years of experience at a nationally recognized law firm and/or in-house legal department drafting, reviewing, negotiating and advising on commercial transactions.

• Admission to the California Bar, registration as California in-house counsel, or ability to obtain admission or registration within 90 days of hire.

Preferred Qualifications:

 

In light of these responsibilities, the ideal candidate will have:

• Prior industry or law firm experience providing legal counsel on manufacturing operations matters;
• Expertise in drafting, negotiating and interpreting a wide range of manufacturing contracts as well as commercial and vendor agreements, such as master services agreements, consulting agreements, license agreements, and confidentiality agreements;
• Expertise with manufacturing transactions, and familiarity with medical devices, small molecule and biologic drug products;
• Experience developing and implementing contract processes and knowledge resources, such as contract templates, playbooks, back-up provisions, client guidance, and team and client training materials;
• Excellent analytical, problem-solving, written and presentation skills;
• A high degree of client service orientation and ability to recognize and respond quickly and pragmatically to urgent, complex situations and demanding clients;
• Must be able to work both independently and collaboratively in a dynamic fast-paced environment;
• Prior supervisory experience or significant leadership experience though leading cross-functional teams;
• Willingness and ability to coordinate activities of many stakeholders across various departments, not only within the company’s headquarters in Foster City, but also throughout the company’s international organization;
• Experience using a contract lifecycle management software;
• Knowledge of Gilead’s business and the pharmaceutical industry in general, including knowledge of regulations governing the pharmaceutical industry;

 

The salary range for this position is: $226,185.00 - $292,710.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

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YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.
 

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.