- Join a company on the cusp of rapid growth
- Opportunity to grow cross functionally
- Robust internal culture
- GMP and cleanroom experience
- Assay experience: flow cytometry, mammalian cell culture, ddPCR, cytotoxicity
- Ability to work 4x10 - Sunday-Wednesday, 1st shift
- Execution of complex biological assays with high technology instrumentation per SOPs
- Perform hands-on laboratory testing utilizing various analytical techniques including ddPCR, flow cytometry, cell counting, and cytotoxicity assays in support of MP clinical manufacturing.
- Perform cell culture work to support cGMP clinical manufacturing.
- Perform statistical and analytical analysis of experiments as appropriate to ensure analytical assay trending and control; contribute to data packages for regulatory agencies, presentations, and publications.
- Write and revise SOPs and technical / summary reports with some supervision.
- Execution of QC assay studies or qualifications to meet laboratory GMP requirements under supervision
- Support analytical technology transfer from Research and Process Development to Quality Control.
- Perform and document quality investigations to support out-of-specification results and data summaries.
- General QC laboratory maintenance and EH&S
- Operate, qualify, and maintain equipment within the Quality Control laboratory.
- Follow all Quality standards and environmental health and safety guidelines.
- Support setup and implementation of a Quality Control Laboratory.
- Continuous improvement of Assay procedures
- Author continuous improvement of Assay procedures under supervision
- Work cross-functionally with Preclinical Discovery, Translational Sciences, Clinical Development, Clinical Operations, Biometrics, Regulatory and Safety to execute on corporate goals.
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
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Quality Control Associate - Agoura Hills, United States - Actalent
Description
Growing cell therapy company in Agoura is looking for a Quality Control Associate to join their analytical team GMP experience with analytical assay experience is REQUIRED for this position.
Our mission is to extend the reach of cell therapy to tackle the next frontier in cancer treatment: solid tumors. Our team is dedicated to pushing the boundaries of science to transform medicine and turn the tide on serious illness. Central to achieving this mission is our focus on recruiting the best talent and building an environment that enables our team to do the best work of their careers and make an impact on patients and society at large.
What's in it for you:
Requirements:
Job Description:
We are seeking a highly motivated Quality Control Associate to join our team. In this role, you will perform and evaluate the analytical quality control testing studies to support assay characterization and qualification and Phase 1 manufacturing for cell therapy – collaborating with internal partners and external CMOs / CROs.
Responsibilities:
Skills:
Mammalian cell culture, qPCR, Report writing, cGMP, ddPCR, SOP revision, flow cytometry, method development, assay development
Experience Level:
Intermediate Level
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
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The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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