Director, Site Supply Chain
About The Position
We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. 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 Kite and help create more tomorrows.
Requirements
- Demonstrates in-depth understanding and application of GMP principles, concepts, practices, and standards in the US and internationally.
- Demonstrates strong knowledge of aseptic processing, solid dose, and general pharmaceutical manufacturing.
- Demonstrates substantial knowledge of industry best practices and trends.
- Is comfortable interacting with regulatory agencies as needed and possesses the ability to represent Gilead in public forums.
- Is an experienced auditor and has demonstrated acumen in resolving challenging audit situations.
- Demonstrates excellent verbal, written, and interpersonal communication skills.
- 12+ years of relevant experience, and BS or related fields.
- Prior experience and deep knowledge of a cGMP-related industry is required, within Biopharmaceutical or Pharmaceutical industry preferred.
Nice To Haves
- MS, MD, PharmD, PhD or an advanced business degree such as an MBA is desirable.
- Broad experience across areas such as manufacturing and understanding of Parenteral, Aseptic, and API operations is a plus.
- Prior people management experience, including supervision of other managers, strongly preferred.
Responsibilities
- Directs activities within the Manufacturing Department to meet company goals including production schedules, environmental concerns, and safety issues.
- Responsible for delegating and ensuring completion of personnel management activities, including hiring, training, evaluating, and performance review.
- Coordinates maintenance of production equipment; interfaces with contract filling sites.
- Coordinates production flow from Process Development to Manufacturing.
- Ensures all regulatory requirements are met in the Manufacturing Department.
- Responsible for manufacturing of products, which directly impact budget line of the department.
- Supervises and monitors performance of Manufacturing Managers & Senior Managers.
- Coordinates with supply chain on the creation and revision of production schedules, based on sales and/or clinical requirements.
- Schedules product filling at off-site contracts.
- Ensures availability of required components at contractor sites.
- Ensures cGMP training of all Manufacturing employees.
- Ensures manufacturing areas and equipment meet all current GMP and all other regulatory specifications.
- Assists in transfer of new technology from Process Development to Manufacturing.
- Recommends and assists in development of practices and policies in manufacturing area.
- Creates cost reduction opportunities as related to materials, labor, or overhead.
- Determines organizational objectives and interprets company policies.
- Responsible for continuous improvement in all operation processes.
Benefits
- company-sponsored medical, dental, vision, and life insurance plans.
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What This Job Offers
Job Type
Full-time
Career Level
Director
