cGMP Manufacturing Specialized Laboratory Technician
cGMP Manufacturing Specialized Laboratory Technician
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
$ 26 - 29
1 Vacancy
Job Description
The University of Southern California (USC) founded in 1880 is located in the heart of downtown L.A. and is the largest private employer in the City of Los Angeles. As an employee of USC you will be a part of a worldclass research university and a member of the Trojan Family which comprises the faculty students and staff that make the university what it is.
USCs Keck School of Medicine current Good Manufacturing Practices (cGMP) facility is seeking a dynamic individual to work on the process development and manufacturing of cell and gene therapies and other biological products for internal/external users. The cGMP Manufacturing Specialized Lab Technician at the USC/CHLA cGMP Facility is responsible for supporting the aseptic manufacturing of cell therapy products in a fully gowned cleanroom environment. This role involves performing cell culture media preparation cryopreservation and cell expansion following strict cGMP protocols. The Manufacturing Specialized Lab Tech ensures proper operation maintenance and calibration of equipment assists in the of process transfer activities and participates in process optimization efforts by collecting and analyzing data. Additionally the technician monitors inventory of supplies supports process scaleup and contributes to a clean safe working environment in compliance with cGMP regulations and safety standards.
Job Accountabilities:
- Performs moderate to complex laboratory procedures related to cell therapy development. Utilizes specialized techniques and technology to achieve results (e.g. media preparation cell expansion harvesting cryopreservation and cell culture) and conducts quality control testing to ensure product safety purity and compliance utilizing methods such as sterility testing endotoxin assessment mycoplasma detection and flow cytometry. Supports cGMP manufacturing activities by performing aseptic techniques in a fully gowned cleanroom environment. Assists in executing laboratory experiments related to process development (e.g. preparing operating cleaning equipment).
- Performs routine quality control tests and assays on materials products and processes to ensure compliance with standards. Conducts environmental monitoring in cGMP cleanrooms (e.g. viable and nonviable particulate monitoring and surface sampling). Follows established SOPs and adheres to regulatory guidelines ensuring compliance with cGMP and safety protocols. Maintains awareness of emerging laws regulations industry best practices and advancements in cell therapy and cGMP manufacturing.
- Prepares calibrates and maintains laboratory equipment for use. Participates in routine lab maintenance and ensures a clean safe and organized working environment across all departments. Monitors inventory of lab supplies and materials ensuring sufficient stock for ongoing operations and timely ordering.
- Collects documents and records data accurately maintaining detailed and organized electronic records. Assists with technology transfer activities ensuring smooth transition of processes between development and manufacturing. Supports process optimization efforts by gathering and analyzing data from experiments and production runs.
- Stays up to date with the latest advancements regulations and best practices in cell therapy and cGMP manufacturing. Engages in professional development and training to enhance skills and ensure compliance with evolving industry standards.
- Promotes an environment that fosters inclusive relationships and creates unbiased opportunities for contributions through ideas words and actions that uphold principles of the USC Code of Ethics.
- Performs other related duties as assigned or requested. The university reserves the right to add or change duties at any time.
Successful Candidates Must Demonstrate:
Degree in a directly related specialized scientific field. Demonstrated knowledge of all aspects of biotechnology and cell therapy. Demonstrated passion for solving complex scientific issues. Experience with Food and Drug Administration regulations and clinical trials. Strong communication and writing skills with demonstrated ability to work as an individual contributor and in a dynamic team environment.
Salary Range:
The hourly rate range for this position is $26.50 $29.81. When extending an offer of employment the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position the candidates work experience education/training key skills internal peer equity federal state and local laws contractual stipulations grant funding as well as external market and organizational considerations.
*This is a 3 year fixedterm position.
USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying.
Minimum Education: Bachelors degree in Biological Science And/Or BiotechnologyMinimum Experience: 2 years in cell therapy development
Preferred Education: Masters degree
Preferred Experience: 3 years in cell therapy development
Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention to detail and ability to follow standard operating procedures (SOPs) and quality assurance principles meticulously. Excellent communication and teamwork skills to collaborate effectively with crossfunctional teams. Ability to troubleshoot and resolve technical issues in a timely manner. Knowledge of regulatory requirements and guidelines (e.g. FDA EMA) related to cGMP.
USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance and with due consideration for patient and student safety. Please refer to theBackground Screening Policy Appendix Dfor specific employment screen implications for the position for which you are applying.
We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone ator by email at. Inquiries will be treated as confidential to the extent permitted by law.
- Notice of Nondiscrimination
- Employment Equity
- Read USCs Clery Act Annual Security Report
- USC is a smokefree environment
- Digital Accessibility
If you are a current USC employee please apply to thisUSC job posting in Workday by copying and pasting this link into your browser:
Experience:Director
Employment Type
Full-Time
Key Skills
Similar Jobs
Dr. Job is an online platform that connects employers with skilled job seekers, facilitating the search for job opportunities and top talent. Established in 2015. Dr. Job Pro has emerged as the world premier job portal, attracting thousands of job seekers every day from all over the world.
Follow Dr.Job
Dr Job FZ LLC. 2025 © All Rights Reserved