Senior Manager Of Supply Chain - Contract Development And Manufacturing Operations (Cdmo)

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.

Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Would you like to join us in this mission?

We are seeking a highly motivated individual to join us as a Senior Manager to support Kite’s goals in securing external supply from contract development and manufacturing organizations (CMOs/CDMOs). This opportunity will closely collaborate with both external manufacturing partners and internal teams as well as report to the Associate Director – External Supply Partnerships at Kite.

The Senior Manager will play a critical role within our external manufacturing team and will be passionate about managing external manufacturing partners and supporting internal, cross-functional collaboration. As such, the Incumbent will be responsible for supporting day to day activities, planning, direction, and oversight of end-to-end programmatic requirements as it relates to CMO/CDMO activities, as well as recommending and implementing process optimizations.

Key responsibilities include close collaboration with external manufacturing partners to develop and maintain relationship alongside the current external manufacturing team, and leading internal focus factory teams to ensure external supply targets are met and operational activities are completed. The Senior Manager will have opportunities to work with and share knowledge with leaders and partners across Kite’s Technical Operations organization (e.g. Process Development and MSAT, Regulatory, Quality, Finance, Manufacturing, and Supply Chain), and collaborate cross functionally to identify, escalate, and propose mitigation plans for project related risks and develop project related dashboards and regular status updates. The Senior Manager will also be responsible for day-to-day activities including but not limited to contractual review and support, document review and approval, batch documentation review, planning and oversight of supply related activities, implementation of metric planning, ongoing evaluation of existing and potential CDMOs and development of value propositions, and creation of ad hoc reports and presentations as necessary.

The ideal candidate will have excellent communication skills and problem-solving abilities and will have technical background while being committed to collaboration and continuous improvement. Experience with data analysis is also preferred.

To create a deep partnership with stakeholders and leaders across the corporation, as well as to foster continued professional growth, we would like the Senior Manager to be based onsite 3 days a week at Kite's Global HQ in Santa Monica, CA (and will provide a comprehensive relocation package as needed). Additionally, the Incumbent should expect domestic and international business travel 30% to 40% of the time.

Responsibilities of the Senior Manager of Supply Chain - Contract Development and Manufacturing Operations (CDMO):

• Supports the current CDMO team in routine communications with CDMOs and internal stakeholders
• Assists on development of risk mitigation planning and implementation
• Owns Change Controls and deviation investigations as needed for clinical and commercial materials
• Evaluates current and potential CDMOs and associated make versus buy evaluation
• Collaborates with Operations Teams and Regulatory to ensure program timelines are met and regulatory preparation has been aligned with the CDMO
• Supports Sourcing and Procurement in sourcing events, RFPs, and contract development
• Leads and participates in continuous improvement initiatives at the CDMOs and within the internal Kite network
• Maintains updated CDMO data
• Supports contract review and negotiation and development Scope of Work proposals
• Provides strong understanding of GMP operations and Quality systems required to maintain a GMP environment
• Material planning and ordering to ensure no disruption to patient supply
• Collaborates with External Quality Operations and Product Quality Leads on disposition planning
• Collaborates with key business stake holders to ensure URSs, Specifications, Part Numbers and other business enabling documents are created to support work with CMOs
• Supports development and maintenance of CDMO performance metrics and reporting

Basic Qualifications:

PhD

OR

MA / MS with 6+ years of Supply Chain and/or Operations and/or External Manufacturing experience

OR

BA / BS Degree with 8+ years of Supply Chain and/or Operations and/or External Manufacturing Experience

OR

Associate Degree with 10+ years of Supply Chain and/or Operations and/or External Manufacturing Experience

OR

High School Diploma / GED and 12+ years of Supply Chain and/or Operations and/or External Manufacturing experience

Preferred Qualifications:

• Ability to establish credibility and influence diverse audiences so as to be perceived as a lead
• Ability to analyze, summarize, and present insights based on the needs of the audience
• Strong project management and organizational skills
• Ability to conduct benchmarking to address cost, quality, risk and innovation considerations
• Familiar with smartsheet and data analytics platforms
• Ability to develop business cases and champion opportunities with quantifiable financial benefits
• Experience with optimization and statistical data analysis resources
• Knowledge of sourcing, contract negotiations, and supplier oversight
• Demonstrated experience in identifying and utilizing full set of levers to drive value for customers
• Exceptional understanding and application of Procurement principles, concepts, practices, and standards (i.e. effective negotiation, supplier relationship management, business partnering, supplier diversity etc.) along with an in-depth knowledge of industry practices
• 2+ years working in cell therapy manufacturing
• 5+ years of experience working in External Manufacturing
• 5+ years of experience working in the biotechnology and/or pharmaceutical industry
• Demonstrated experience with internal stakeholder management, data/information management, category management, process redesign and continuous improvement expertise, project management and performance measurement skills

Does this sound like you? If so, please apply today!

#IND123

#LI-ML1

The salary range for this position is: $136,000.00 - $176,000.00. 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 [email protected] for assistance.

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 jobs in France:

Conformément à la Loi « Informatique et Libertés » (06/01/78), nous vous informons du fait que les données personnelles renseignées pourront faire l'objet d'un traitement informatique par Gilead et pourront être transmises aux Organismes Sociaux. Par ailleurs, vous disposez d'un droit d'accès, de rectification et de suppression des données vous concernant. Vous pouvez exercer ce droit en contactant: [email protected]