Jobs · OTHR · California

cGMP MSAT Manager

UC Irvine · Irvine, CA · Yesterday
On-siteOTHRFull-time

About the role

The MSAT Manager will oversee process development for novel gene and cell therapy products within the newly constructed GMP Good Manufacturing Practice (GMP) Facility at the University of California, Irvine (UCI).

Responsibilities

  • Maintain the viability of the GMP facility for the development, scale-up, and production of cellular therapeutics.
  • Support clinical trials of cell therapeutics, including stem cell populations and bone marrow transplantation, as well as Chimeric Antigen Receptor (CAR) T-cells.
  • Manage a seven-room GMP cellular therapy and viral vector facility, including a quality control laboratory.
  • Collaborate with UCI Health and external organizations to ensure the successful implementation of cell processing and therapeutic development.

Requirements

  • Adhere to excellent customer service principles.
  • Prioritize duties in an ever-changing environment.
  • Possess technical vocabulary and knowledge of medical terminology, basic human anatomy, chemistry, biology, and molecular biology.
  • Communicate effectively, both verbally and in writing.
  • Utilize effective listening and questioning techniques.
  • Write clear technical reports in the scientific format.
  • Maintain logs and documentation appropriately.
  • Maintain appropriate interdepartmental communication.
  • Show tact and diplomacy in a highly interactive position.
  • Work well under pressure, manage multiple projects, and prioritize assignments.
  • Work as a member of a team and assist colleagues as needed.
  • Function and work in a diverse work environment.
  • Have in-depth knowledge of GMP laboratory policies and procedures.
  • Teach and communicate effectively with students and postdoctoral fellows.

Preferred

  • Some graduate level coursework preferred.
  • Experience working in a GMP facility, focusing on process development and manufacturing of cellular therapy products.
  • Previous experience managing in vivo studies to support the development of novel cell therapies.

Special Conditions

  • Experience in or knowledge of GMP production procedures and facilities is preferred.
  • Alternatively, willingness to be trained for a period of at least 3-6 months in a GMP facility with extensive experience in cell manufacturing.

Total Rewards

We offer a comprehensive benefits package including medical insurance, sick and vacation time, retirement savings plans, and access to various discounts and perks. For more details, please visit this page.

Conditions of Employment

  • Background Check and Live Scan
  • Employment Misconduct*
  • Legal Right to work in the United States
  • Vaccination Policies
  • Smoking and Tobacco Policy
  • Drug Free Environment
  • Misconduct Disclosure Requirement

Closing Statement

The University of California 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, disability, age, protected veteran status, or other protected categories covered by the UC Anti-Discrimination Policy. We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.

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