Find & Apply For Clinical Laboratory Manager Jobs in Costa Mesa, California

Laboratory Manager LCMS Operator Gold Standard Toxicoligy Costa Mesa, CA Job Details Part-time | Full-time $50 - $78 an hour 10 hours ago Qualifications Project team coordination Biology Instrumentation troubleshooting Staff supervision Biology research Teamwork Histological laboratory techniques Microsoft Excel Team supervision Equipment troubleshooting Molecular biology techniques Bachelor's degree Data management Attention to detail Managing clinical research teams Leading team collaboration initiatives Mass spectrometers (MS) Biomedical regulatory compliance Managing projects Research regulatory compliance Technical troubleshooting support Productivity software Laboratory information systems (LIS) GMP for research safety and compliance Research and development project management Technical Proficiency Liquid chromatography machines Cross-functional communication FDA regulations Data analysis software Full Job Description Overview We are seeking a dynamic and detail-oriented Laboratory Manager and LCMS (Liquid Chromatography-Mass Spectrometry) Operator to lead our analytical laboratory operations. In this pivotal role, you will oversee the day-to-day management of laboratory activities, ensuring compliance with regulatory standards such as GLP (Good Laboratory Practice), FDA regulations, and CGMP (Current Good Manufacturing Practice). Your expertise in LCMS techniques, microbiology, histology, molecular biology, and research laboratory procedures will drive high-quality data collection and support our research and development initiatives. This position offers an exciting opportunity to manage a talented team, coordinate complex projects, and uphold the highest standards of laboratory excellence in a fast-paced research environment. Duties Lead and supervise laboratory teams engaged in LCMS analysis, microbiology, histology, molecular biology, and other research techniques to ensure accurate and reliable results. Manage laboratory operations in compliance with

GLP, FDA

regulations, CGMP standards, and other regulatory requirements to maintain audit readiness. Oversee the maintenance, calibration, and troubleshooting of laboratory instruments including LCMS systems and other analytical equipment. Develop, review, and optimize laboratory procedures to enhance efficiency and data integrity while ensuring adherence to regulatory guidelines. Coordinate with cross-functional teams on clinical trials and research projects, providing technical guidance and project management oversight. Utilize Laboratory Information Management Systems (LIMS) and Microsoft Office tools for data collection, documentation, reporting, and record keeping. Ensure safety protocols are followed diligently; conduct regular training sessions on laboratory techniques, safety procedures, and regulatory compliance. Manage inventory of reagents, supplies, and equipment; oversee procurement processes to support ongoing laboratory activities. Supervise technical staff by providing mentorship, conducting performance evaluations, and fostering a collaborative team environment focused on continuous improvement. Requirements Bachelor's or higher degree in Chemistry, Biology, Microbiology or related scientific discipline; advanced degrees preferred. Proven experience managing laboratories within regulated environments such as GLP or GMP settings; familiarity with FDA regulations essential. Extensive hands-on experience with LCMS instrumentation including method development, validation, troubleshooting, and data analysis. Strong background in microbiology, histology techniques, molecular biology methods, and clinical laboratory procedures. Demonstrated leadership skills with previous supervisory or management experience overseeing technical teams in a research or clinical setting. Proficiency with Laboratory Information Management Systems (LIMS), Microsoft Office Suite (Word, Excel), and data analysis tools. Knowledge of regulatory compliance standards including GLP, GxP (Good Practice), CGMPs; understanding of clinical trials processes highly desirable. Excellent communication skills for cross-functional collaboration; ability to manage multiple projects simultaneously while maintaining attention to detail. Strong analysis skills combined with technical proficiency in laboratory instruments and techniques necessary for high-quality research output. Join us to lead innovative research efforts while fostering a collaborative environment that values precision, compliance, and scientific excellence!

Pay:

$50.00 - $78.00 per hour

Work Location:

In person