Associate Manager, Flow Cytometry

IQVIA•Santa Clarita, CA

1d•Onsite

About The Position

We are seeking an Associate Manager, Flow Cytometry to join IQVIA Laboratories at Valencia. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Associate Manager, Flow Cytometry, you will lead daily laboratory operations, supervise a team of scientists, and ensure high‑quality, compliant delivery of flow cytometry testing.

Requirements

Bachelor’s degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or related field.
Minimum 4 years of experience in a regulated laboratory environment, including at least 2 years in flow cytometry.
Demonstrated experience supervising, training, or mentoring laboratory staff.
Strong technical background in laboratory operations, including hands‑on skills such as pipetting and assay execution.
Other equivalent combinations of education, training, and experience may be accepted in lieu of degree
In‑depth knowledge of flow cytometry, clinical testing procedures, quality control, and laboratory regulations (CAP/CLIA).
Strong leadership, communication, and problem‑solving skills with the ability to manage multiple priorities.
Working knowledge of quality assurance, safety standards, root‑cause analysis, and CAPA processes.
Ability to collaborate across teams, drive process improvements, and maintain a high‑performance laboratory environment.

Responsibilities

Lead and supervise a team of laboratory staff to ensure accurate and timely operational delivery.
Oversee daily workflow, assign tasks, and resolve technical or workload challenges.
Hire, train, mentor, and evaluate staff performance under the guidance of senior management.
Monitor reagent and supply inventory, ensuring availability and adherence to budget.
Ensure compliance with safety, quality, CAP/CLIA, and regulatory requirements.
Review laboratory metrics to identify process improvement opportunities and drive efficiency initiatives.
Partner with cross‑functional stakeholders to implement new tests, equipment, and procedures.
Serve as a backup for daily laboratory operations as needed.