QC Microbiology Tech I

Kite Pharma•Frederick, MD

2d•$55,930 - $72,380•Onsite

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

Entry-level knowledge of current Good Manufacturing Practices (cGMPs).
Basic understanding of aseptic operations.
Foundational knowledge of microbiology techniques, including gram staining, aseptic technique, and plate streaking.
Basic knowledge of USP and regulatory requirements.
Ability to work effectively in a team-oriented environment.
Strong verbal, written, and interpersonal communication skills.
Entry-level proficiency in Microsoft Office applications.
High School diploma with 1+ year of relevant experience in a laboratory, manufacturing, or regulated environment.

Responsibilities

Maintain laboratory areas in a clean, organized, and sanitized condition in accordance with GMP standards.
Perform environmental monitoring and utility sampling as a primary responsibility, ensuring accurate data collection and compliance with procedures.
Receive, quarantine, and properly store microbiological media pending laboratory release.
Monitor and manage biohazardous waste, coordinating safe removal with qualified safety personnel.
Prepare and wrap equipment for sterilization processes.
Support validation activities and commercial and/or developmental manufacturing operations, as required.
Follow all SOPs, safety guidelines, and regulatory requirements to maintain compliance and data integrity.