Actalent
QC Manager
Job Description
We are seeking a proactive and detail-driven Quality Control (QC) Manager to oversee day-to-day QC operations and ensure consistent execution of GMP-compliant testing for our iPSC-derived neuronal cell therapy programs. This role is ideal for someone with strong technical acumen and people management skills who thrives in a fast-paced, early-stage biotech environment and is eager to grow with the organization.
Responsibilities
Maintain a comprehensive inventory of completed activities across manufacturing and quality functions at both sites, with a strong emphasis on accurate tracking.
Lead problem-solving efforts for any issues or deviations that arise during operations.
Conduct root cause analyses and recommend strategic solutions to address underlying problems.
Review protocols provided by the San Diego site and oversee sample running in accordance with those protocols (ddPCR, ELISA, flow cytometry).
Prepare and document CAPA reports.
Apply knowledge of regulatory standards, with a preference for familiarity with GMP (Good Manufacturing Practices).
Collaborate on projects involving stem cells.
Essential Skills
Bachelor's Degree in Cell Biology, Molecular Biology, Biotechnology, or a related discipline.
Cell therapy experience is very ideal, but not required.
Minimum of 3+ years of experience in a QC GMP (ideally cGMP) environment in QC Leadership.
Must have minimum of 1 year experience, ideally 2 years in flow cytometry, ddPCR, and ELISA.
Familiarity with phase-appropriate QC systems and regulatory expectations (FDA/EMA, ICH guidelines).
Experience with CAPAs and writing CAPA reports.
Experience troubleshooting.
Previous leadership and management skills.
Work Environment
The company is a growing biotechnology organization that provides high-purity, iPSC-derived human neurons, astrocytes, and microglia for translational research and drug discovery. Utilizing proprietary technology, they generate a variety of assay-ready, subtype-specific cells of the CNS, relevant to a range of neurological disorders. Each cell subtype can be produced from unique iPSC lines into custom batches ranging from 50 million to 10 billion viable cells. The work environment is vibrant and collaborative, fostering a space where talented individuals can thrive and make a meaningful impact. The team currently consists of 5-6 individuals, with plans for expansion once the QC Manager is hired. The manager will have the opportunity to influence the hiring and building of this team. The company is in the process of building a whole GMP lab, offering the new manager control and the chance to be part of something great in the future.
Pay and Benefits
The pay range for this position is $100000.00 - $125000.00/yr.
Medical, dental, vision, bonus
Workplace Type
This is a fully onsite position in Madison,WI.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
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.
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.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
We are seeking a proactive and detail-driven Quality Control (QC) Manager to oversee day-to-day QC operations and ensure consistent execution of GMP-compliant testing for our iPSC-derived neuronal cell therapy programs. This role is ideal for someone with strong technical acumen and people management skills who thrives in a fast-paced, early-stage biotech environment and is eager to grow with the organization.
Responsibilities
Maintain a comprehensive inventory of completed activities across manufacturing and quality functions at both sites, with a strong emphasis on accurate tracking.
Lead problem-solving efforts for any issues or deviations that arise during operations.
Conduct root cause analyses and recommend strategic solutions to address underlying problems.
Review protocols provided by the San Diego site and oversee sample running in accordance with those protocols (ddPCR, ELISA, flow cytometry).
Prepare and document CAPA reports.
Apply knowledge of regulatory standards, with a preference for familiarity with GMP (Good Manufacturing Practices).
Collaborate on projects involving stem cells.
Essential Skills
Bachelor's Degree in Cell Biology, Molecular Biology, Biotechnology, or a related discipline.
Cell therapy experience is very ideal, but not required.
Minimum of 3+ years of experience in a QC GMP (ideally cGMP) environment in QC Leadership.
Must have minimum of 1 year experience, ideally 2 years in flow cytometry, ddPCR, and ELISA.
Familiarity with phase-appropriate QC systems and regulatory expectations (FDA/EMA, ICH guidelines).
Experience with CAPAs and writing CAPA reports.
Experience troubleshooting.
Previous leadership and management skills.
Work Environment
The company is a growing biotechnology organization that provides high-purity, iPSC-derived human neurons, astrocytes, and microglia for translational research and drug discovery. Utilizing proprietary technology, they generate a variety of assay-ready, subtype-specific cells of the CNS, relevant to a range of neurological disorders. Each cell subtype can be produced from unique iPSC lines into custom batches ranging from 50 million to 10 billion viable cells. The work environment is vibrant and collaborative, fostering a space where talented individuals can thrive and make a meaningful impact. The team currently consists of 5-6 individuals, with plans for expansion once the QC Manager is hired. The manager will have the opportunity to influence the hiring and building of this team. The company is in the process of building a whole GMP lab, offering the new manager control and the chance to be part of something great in the future.
Pay and Benefits
The pay range for this position is $100000.00 - $125000.00/yr.
Medical, dental, vision, bonus
Workplace Type
This is a fully onsite position in Madison,WI.
Application Deadline
This position is anticipated to close on Oct 10, 2025.
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.
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.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.