Skip to main content

This job has expired

You will need to login before you can apply for a job.

Sr. Associate, Outsourced Manufacturing - API/Drug Substance

Employer
Gilead Sciences, Inc.
Location
Foster City, CA
Start date
Apr 1, 2023

Job Details

Sr. Associate, Outsourced Manufacturing - API/Drug Substance
United States - California - Foster City

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead’s therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the company’s five core values. That’s because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible

For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.

At Gilead we believe every employee deserves a great leader. As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth and retention of talent, and empower teams to align and achieve goals.
Job Description



Sr. Associate, Outsourced Manufacturing - Foster City, CA

Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases. The Clinical Supply Manager is a leader that inspires teams while providing expertise for Gilead's global clinical trials. They work collaboratively with Clinical Supply Chain Management (CSCM) team, Pharmaceutical Development and Manufacturing teams to execute strategies, meet project deliverables, and solve business problems. The position includes all elements of the clinical supply chain from the protocol design through manufacturing to distribution and inventory management of clinical supplies at clinical sites globally.

The Sr. Associate of Outsourced Manufacturing will play an important role within the Chemical Development and Manufacturing (CDM) organization to drive projects to progress as planned, at both clinical development and commercial manufacturing stages and ensure delivery of clinical and/or commercial materials (API drug substance, intermediates and raw materials) on time, in acceptable quality and in full compliance. They will also be responsible for financial planning/tracking, contract establishment, work order/purchase order generation, timeline/deliverable monitoring and project management. The Senior Associate will have the opportunity to work with and learn from colleagues across Gilead (Process Chemistry, Regulatory, Formulations, Analytical, Quality, Supply Chain, etc.), as well as multiple CRO and CMO organizations.

Specific Responsibilities:
  • In collaboration with key stakeholders, manages execution and completion of project deliverables within established timelines and in compliance with legal contracts and agreements
  • Ensures all related manufacturing conforms to the appropriate regulations (GMP, ICH, QA, Regulatory, etc.)
  • Manages technical transfer activities to new supplier sites
  • Negotiates manufacturing schedules and prices with external suppliers
  • Reviews contractor documentation including master batch records, specifications, deviations and change controls for GMP compliance and alignment with Gilead standards
  • Closely monitors and manages supply and demand of commercial and/or clinical materials using advanced planning tools
  • Identifies and purchases custom raw materials, reagents, and other services necessary for the supply of drug substances
  • Manages logistics activities for outsourced materials such as warehousing, transportation, customs clearance and invoicing
  • Frequently interacts with other functional peer group managers within Gilead and CMOs to support process development or manufacturing activities
  • Organizes and participates in teleconferences and face-to-face meetings with CXOs; works closely with Gilead teams to establish agenda and keep track of key decisions and action items
  • Proactively communicates issues, project changes to key stakeholders, and facilitates timely discussion and resolution
  • Maintains and updates documentation and timelines to accurately reflect the status of the outsourced activities
  • Works on special and non-routine projects focused on continuous improvement, teamwork/teambuilding, and operational excellence


Skills and Experience:
  • Basic understanding of synthetic chemistry and/or pharmaceutical process development
  • Ability to effectively manage multiple priorities
  • Working knowledge of GMPs and associated regulations
  • Sound organizational and time management skills
  • Exceptional presentation, oral and written communication skills, and the ability to interact effectively with senior management
  • Ability to collaborate with cross functional teams
  • Ability to work under uncertainty and to resolve conflict in a constructive manner
  • Experience working with contract manufacturing/research organizations
  • This position may require domestic and international travel time up to 10%


Minimum Education/Experience:
  • 5+ years of experience in Chemistry or Engineering fields of progressively responsible experience in a related field, including process development, manufacturing, or outsourcing in the pharmaceutical industry OR 3+ years of relevant experience and a MA/MS degree OR 0+ years of experience with a PhD


About Gilead:

Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

If this is not the right move for you now but remain interested in a career at Gilead Sciences please connect with us via our talent community: https://gilead.avature.net/Gilead

The salary range for this position is: $112,030.00 - $144,980.00. 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:


As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 careers@gilead.com for assistance.

Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Gilead has made the decision to require all U.S., Canada, Australia, Singapore, and Hong Kong employees and contractors to receive the COVID-19 vaccines as a condition of employment. “Full vaccination” is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation.​

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

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

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 log onto your Internal Career Site to apply for this job.






jeid-ff8213dd331f6e408e71adbea65fdf5d

Company

Gilead Sciences is a biopharmaceutical company that discovers, develops, and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide. Headquartered in Foster City, California, Gilead has operations in North America, Europe and Australia.
 

Company info
Website
Location
333 Lakeside Drive
Foster City
California
94404
United States

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert