Job Title: Project Manager
Location: Los Angeles, CA (On-site with potential for hybrid work based on project needs)

Contract Duration: 12 months (long-term contract with expected support beyond 2025)

Proposed Start Date: ASAP

Job Description:
We are seeking a highly skilled Project Manager to lead and oversee multiple GMP-focused projects for a Cell Therapy-based client in the Life Sciences industry. The Project Manager will handle projects valued up to $1MM, including those involving QC operations, making exposure in this area a strong advantage. This role requires a deep understanding of GMP regulations and regulatory compliance within Life Sciences.
The ideal candidate will have a passion for Oncology, as well as a keen interest in innovative treatments for Alzheimer’s and Diabetes. You will manage a small team comprised of both full-time employees (FTEs) and contract resources, ensuring successful project delivery within scope, time, and budget.
This is an on-site position in Los Angeles, CA, with flexibility for hybrid work depending on project requirements.

Key Responsibilities:

• Manage and deliver multiple projects up to $1MM with a strong focus on GMP requirements.

• Lead projects related to Cell Therapy with an emphasis on regulatory compliance and quality control (QC) operations.

• Direct and mentor a team of FTEs and contract resources to ensure successful project execution.

• Collaborate with cross-functional stakeholders to identify project objectives, scope, and deliverables.

• Oversee project timelines, budgets, and resource allocation to drive projects to completion.

• Ensure all projects comply with GMP standards and regulatory requirements in Life Sciences.

• Develop and maintain detailed project plans, risk assessments, and progress reports.

• Support continuous improvement initiatives across QC and GMP operations.

• Foster a strong interest and engagement in oncology and related therapeutic advancements, including Alzheimer’s and Diabetes treatments.

Qualifications:

• PMI Certification or equivalent project management qualification preferred.

• Proven experience managing GMP-focused projects within the Life Sciences industry.

• Exposure to QC operations and regulatory compliance is a significant advantage.

• Strong understanding of regulatory requirements and industry standards (e.g., FDA, EMA).

• Experience leading small teams, including managing contract resources.

• Ability to manage project budgets, timelines, and deliverables effectively.

• Excellent leadership, organizational, and communication skills.

• Demonstrated interest in Oncology, Alzheimer’s, and Diabetes treatments is a bonus.

If you are a motivated Project Manager looking to make a meaningful impact in a fast-paced, GMP-regulated environment within Cell Therapy, we encourage you to apply.