Kite Pharma, Inc. Oceanside , CA 92049
Posted 4 days ago
For Current Kite Pharma Employees and Contractors:
Please log onto your Internal Career Site to apply for this job.
At Kite, we empower our leaders to step up, share ideas, listen, learn, and lead. We're welcoming bright, diverse, and imaginative minds; we're nurturing them to foster an environment of inclusion and growth where innovation is encouraged. We expect our people leaders to model that environment, and to focus on creating inclusion, developing talent, and enabling teams.
Job Description
Everyone at Kite is grounded by one common goal - curing cancer. Every single day, we seek to establish a line between that purpose and our day-to-day work. Join us in our mission!
We are seeking a highly effective Maintenance Specialist to be responsible for supporting the design, engineering, and implementation of capital projects at Oceanside viral vector manufacturing site as well as the delivery of ongoing improvements to facilities, utilities, installations, and equipment.
Responsibilities (include but are not limited to):
Provides daily oversight, training and guidance regarding the activities of Maintenance and Instrumentation Technicians in the maintenance, repair, calibration of equipment and/or mechanical, electrical systems in respective area of responsibility, ensuring that Standard Operating Procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements are followed.
Ensure all single-use, commercial manufacturing equipment is operational and ready for viral vector production
Provides work direction to Maintenance and Instrumentation Technicians, including organizing and prioritizing daily tasks, performing training, and writing performance reviews.
Authors SOP documents.
Works with MRO and Facility Specialist to procure spare parts, labor, special tools, contracts, and equipment availability for work execution.
Manages and implements investigation, assessment, and delivery of ongoing improvements to facilities, utilities, installations, and equipment.
Serves as a mentor to Jr. technicians
Author and assess quality records such as deviations and CAPAs
Ensures that Standard Operating Procedures (SOPs), current Good Manufacturing Practices (GMPs) and all other regulatory requirements are followed
Provides refresher training to departmental size groups
Will participate in regulatory audits to include internal, vendors or contract manufacturers.
Estimates jobs showing sequence of steps, the number of mechanics and required man-hours for each step
Ensures the safety needs are given a top priority in work planning and scheduling.
Receives all work orders from the requesting departments of the areas to which he/she is assigned, except for emergency work that is requested of the appropriate maintenance supervisor for immediate attention
These duties can be delegated to designated deputies of a satisfactory qualification level as needed.
Additional duties as assigned.
Knowledge and Skills
In-depth understanding and application of cleanroom design, facilities, and utilities such as WFI, compressed gases, electrical infrastructure,
In-depth knowledge of current Good Manufacturing Practices (cGMPs).
Extensive working knowledge of facilities, utilities, and commercial manufacturing
Extensive knowledge of industry & Good Engineering practices.
Excellent verbal, written, and interpersonal communication skills are required.
Ability to guide and train members of a team.
Demonstrated investigation and report writing skills.
Proficient in Microsoft Office applications.
Basic Qualifications:
M.S. degree in mechanical, electrical, or chemical engineering with 3+ years of experience in facilities, utilities engineering in the biotech/pharma industry
B.S. degree in mechanical, electrical, or chemical engineering with 5+ years of experience in facilities, utilities engineering in the biotech/pharma industry Or
High School diploma with 9+ years of experience in facilities, utilities engineering in the biotech/ pharma industry
Preferred Qualifications:
Excellent leadership capabilities - Able to provide guidance, work direction and training.
8+ years of previous experience in biotech or pharmaceuticals industry working in a cGMP environment. Experience with commercial manufacturing is preferred
Has previous experience in facilities, utilities, or process engineering in highly regulated manufacturing environments, ideally commercial, biopharma cGMP facilities
Experience providing maintenance support for Single Use Systems/Technologies/Equipment
Regulatory Agency Experience is greatly preferred
Excellent verbal and written communication skills
Ability to work cross-functionally in a matrix environment.
Able to work well under pressure in a fast-paced environment.
Excellent collaboration skills and the ability to work well with teams.
Able to demonstrate the company's core values of Excellence, Integrity, Teamwork, Inclusion and Accountability in work and actions.
The salary range for this position is: $104,805.00 - $135,630.00. Kite 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
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.
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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 ApplicantAccommodations@gilead.com for assistance.
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For Current Kite Pharma Employees and Contractors:
Please log onto your Internal Career Site to apply for this job.
Kite Pharma, Inc.