Associate Director, Manufacturing

Associate Director, Manufacturing

Netherlands - Hoofddorp

Manufacturing Operations & Supply Chain

Regular Job Description

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

As Associate Director (AD) Manufacturing you will be responsible for managing a team of Manufacturing Team Leads (TL) and Operational (Ops) Managers in a commercial cell therapy cGMP environment. They lead the Cell Therapy Specialists (CTS) who are responsible for Cell Therapy production. The total team of CTS working in a shift is approximately 120/130 colleagues. You will be coordinating the day-to-day operations of the team in collaboration with the other ADs/Sr. Managers Manufacturing in Kite's state-of-the-art manufacturing facility and building relationships in the Global Kite organization as well as be part of building the strategy and culture of the organization. About Kite Pharma, A GILEAD Company Today, Kite Pharma is the leader in cell therapy. We are advancing a pipeline of oncology therapies centered on what we believe is the power of cell therapy to fundamentally change the way cancer is treated. As we extend our global reach with a new, state-of-the-art facility in Hoofddorp, we need colleagues interested in change, in challenge, and in building a new future together. Join us and discover your sense of purpose. We are seeking an enthusiastic Associate Director Manufacturing to join the Manufacturing organization (460+ pp) in which people of all backgrounds and experiences are respected, and where working together focused on saving lives, by finding the cure for cancer, is a daily activity. Your will report to the Senior Director Manufacturing. Key responsibilities of this job: Execute production and resource schedule against the operational plan linked to the company goals. Supervise and ensure right first-time operations of commercial cell therapy manufacturing following the cGMP guidelines. Build a high performing team, provide necessary training and ongoing mentoring and recognition of direct staff, including performance reviews according to Kite standards. Support technology transfers and continued expansion of the facilities. Support in crisis management and business continuity events. Process monitoring, including management of data to support business reporting requirements. Support regulatory inspections and quality audits, both internal and external. Encourages and drives a team culture to continuously improve safety, compliance, efficiency and cost reductions within operations. Encourages and drives a culture of ownership and integrity where people feel safe to speak up, give feedback to each other according to the Kite Culture standards. Build relationships and harmonize on a global level. Initiate, lead and/or participate in multi-functional (global) project teams, applying Lean Manufacturing principles. Develop and maintain collaborative work relationships with internal and external stakeholders Participates in strategic initiatives by leading them and reporting results back to Site Head Has a flexible mindset and is willing to perform varying duties depending on the shifting needs of the Site Head Experience & Qualifications: The ideal candidate for this position of Sr. Manager Manufacturing is a true people leader with strong people management and influencing skills and a proven track record in cGMP manufacturing. Bachelor’s or Master's degree (for instance: Biochemistry, Life Science & Technology, Biology). A minimum of 10 years of cGMP production experience, including at least 8 years in a leadership role. Strong leadership and influencing skills. Demonstrated ability to build, develop, and coach a high performing team of people leaders focusing on behaviors. Experience in manufacturing and/or lab management is required. Ability to work together with other ADs/Sr. Managers in Manufacturing aligning operations, driving efficiency and structure and able to adjust workload based upon changing priorities to meet set goals and timelines. Knowledgeable of Current Good Manufacturing Practices (cGMPs) Strong analytical and problem-solving skills Demonstrated capability of guiding operational excellence (Lean methodology) and other improvement trajectories. Excellent interpersonal, verbal, written communication skills and stakeholder management. Enterprise thinking and able to deal with ambiguity. If you have the ability to thrive in a dynamic and fast-paced environment and are willing to transform this environment in a proactive and stable one, the moment has come for you to be part of such an exciting journey towards eliminating the burden of chronic cancer care, don’t miss out on this opportunity Apply now! Only candidates in possession of a valid EU work permit will be considered for this job. Recruitment agencies: We seldom make use of agencies, and when we do, we have a PSL in place. We would appreciate if you did not contact hiring managers or the Talent Acquisition team directly, since we will not be able to respond to you.

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

poster. 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:

Share: Job Requisition ID

R0041223 Full Time/Part Time

Full-Time Job Level

Associate Director Click below to return to the Gilead Careers site Click below to see a list of upcoming events Click below to return to the Kite, a Gilead company Careers site

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