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Full-time
postgraduate degree
Posted 10d ago
~40 hrs/week
Responsibilities
The Director of Cellular Therapies leads GMP and GTP laboratory operations to ensure the safe and compliant manufacture of cell therapy products. This role oversees regulatory readiness, quality systems, and cross-functional collaboration to support clinical trials and patient care.
Requirements
Candidates must hold a Ph.D. in a biological or scientific field and possess at least five years of experience in GMP/clinical grade cell therapy manufacturing. A minimum of three years in a management or supervisory role is required, along with expertise in FDA compliance and CMC documentation.
Full job description
Note: If you are CURRENTLY employed at Children's and/or have an active badge or network access, STOP here. Submit your application via Workday using the Career App (Find Jobs).
Work Shift
Day
Work Day(s)
Monday-Friday
Shift Start Time
Variable
Shift End Time
Variable
Worker Sub-Type
Regular
Children’s is one of the nation’s leading children’s hospitals. No matter the role, every member of our team is an essential part of our mission to make kids better today and healthier tomorrow. We’re committed to putting you first, and that commitment is at the heart of our company culture: People first. Children always. Find your next career opportunity and make a difference doing what you love at Children’s.
Job Description
This position is responsible for leading the Good Manufacturing Practice (GMP) and Good Tissue Practice (GTP) Laboratory operations teams to support the manufacture and processing of cell therapy products across all protocols at Children’s Healthcare of Atlanta. The role ensures full compliance with the Foundation for the Accreditation of Cellular Therapy (FACT), current GMP and GTP requirements, and all applicable Food and Drug Administration (FDA) and State regulations, with a primary focus on ensuring the safety, quality, and integrity of products administered to patients. This leader oversees day-to-day laboratory operations, quality systems, regulatory readiness, and continuous process improvement across both GMP and GTP environments. A strong scientific background and hands-on experience managing operations within an academic or commercial cell therapy facility are required.
Experience
Minimum of five years in manufacturing GMP/clinical grade cell therapy products
Minimum of three years of management or supervisory experience
Advanced leadership and management skills
Strong written and verbal communications skills, including expertise in Chemistry, Manufacturing and Controls (CMC) writing
Experience managing validation programs supporting GMP manufacturing and clinical laboratory testing and writing and maintaining records in compliance with FDA requirements
Experience providing oversight or governance of cellular therapy clinical laboratories and/or translational research laboratories
Demonstrated project management skills in regulated laboratory environments
Preferred Qualifications
Six Sigma Green or Black belt
GMP Laboratory Control Professionals Certification or GMPCP Certified Professional
Experience working in a FACT accredited facility
Experience leading multi‑disciplinary laboratory teams (e.g., GMP manufacturing, cellular therapy clinical lab, and/or translational research labs) and coordinating activities across these functions to support clinical trials and patient care.
Education
Ph.D. in a biologic or scientific field
Certification Summary
No professional certifications required
Knowledge, Skills, and Abilities
Relevant experience in manufacturing GMP/Clinical grade MCB and WCB of various cells, MSCs, TIL, CAR-T cells, T-Reg cells, and Gamma-Delta T cells
Experience in Vector plasmid, Adenovirus, Retrovirus, Gamma-Retrovirus and Lentivirus for cell and gene therapies
Experience overseeing translational assay development, validation, and technology transfer into clinical or GMP laboratories
Expertise in CMC writing and maintaining records in compliance with FDA requirements
Record of successfully managing validation programs in support of GMP operations
Knowledge and experience in the operation of an academic or commercial cell processing facility, including demonstrated education and experience in areas of hematopoietic progenitor cell transplantation principles and practices, MSCs, T-Regs, Gamma-Delta T cells, MCB and WCB of various cell types, TIL and CAR T expansion
Knowledge and expertise of functional testing and assay development for quality control testing of the various cell therapies including, flow cytometry, gram staining, BacT/Alert, Endotoxin testing, Mycoplasma testing, ELISA, qPCR, VCN and RCR testing.
Experience in the use of bioreactors and in process automation
Experience in research interactions with cell therapies-based companies
Strong leadership track record especially in the areas of leading in a global and matrixed environment, working cross functionally and developing strong technical talent
Strong written and verbal communication skills
Ability to organize, prioritize and complete multiple assignments independently
Highly motivated self-starter who can motivate others
Advanced leader with ability to create strong culture for continuous improvement
Sound and responsive decision-making and problem-solving skills
Excellent oral and written communication skills to convey complex information clearly to all levels
Ability to act with diplomacy and patience while interacting with colleagues, including
Job Responsibilities
Partners with the Director of Operations, Medical Director, Marcus Center for Pediatric Cellular Therapy Scientific Director, and Research & Academic Administration, to build a team providing GMP grade clinical products for experimental use. Actively participates in workforce management for GMP facility staffing, study capacity management to ensure the appropriate flow of products required to meet study enrollment and timelines, and training and quality assurance.
Leads laboratory managers and senior scientific staff across manufacturing, clinical, and translation laboratories
Collaborates with translational laboratory activities, including assay development and technology transfer
Maintains compliance with FACT regulations, current Good Manufacturing Practice (cGMP) requirements and FDA and State regulations, including the production of sterile drug products to ensure the safety of patients receiving those products.
Ensures consistent, rigorous, and compliant manufacturing approaches are implemented for all gene and cell therapy products manufactured in the facility.
Writes and maintains all policies, standard operating procedures, and batch process records for the GMP Facility.
Review, approve, and where appropriate align standard operating procedures and work instructions across GMP, Cellular Therapy Lab, and Translational research activities.
Manages the set-up and completion of complex manufacturing processes, including master cell bank (MCB) production, working cell bank (WCB) production, Mesenchymal Stromal Cells (MSCs), Gamma-Delta T cells, CAR-T cells, Tumor infiltrating Lymphocytes (TIL), DC vaccines and T-Regs.
Responsible for filing and maintaining the Facility’s Drug Master File (DMF) with the FDA.
Participates and plays an active role in all meetings with the FDA, including Initial Targeted Engagement for Regulatory Advice on CBER products (INTERACT) meetings, pre-IND meetings, and Type-A and Type-B meetings.
Performs FDA regulated manufacturing processes, including completion of documents and data required for reporting purposes.
Oversee the budgeting, staff management and general operations of the laboratory facilities.
Create quality tracking metrics and dashboards. Extends quality and performance metrics, where appropriate, to include key indicators from the Cellular Therapy Clinical Lab and Translational Lab (e.g., turnaround times, error rates, assay performance, and study milestones).
Create staff performance metrics and dashboards.
Create a culture of continuous improvement for laboratory Facility processes.
Provides leadership, coaching, and mentoring to laboratory leaders and staff across the GMP Facility, Cellular Therapy Clinical Lab, and Translational Lab (as applicable), fostering collaboration, shared best practices, and professional development.
Help advance the science of the Marcus Center for Pediatric Cell Therapy through leadership, strategic direction, guidance, coordination, and oversight of projects.
Facilitates translation of discoveries from the Translational Lab into GMP‑compliant manufacturing processes and clinical laboratory assays, supporting the full bench‑to‑bedside continuum of cell and gene therapy development.
Children’s Healthcare of Atlanta is an equal opportunity employer committed to providing equal employment opportunities to all qualified applicants and employees without regard to race, color, sex, religion, national origin, citizenship, age, veteran status, disability or any other characteristic covered by applicable law.
For the bumps, bruises and every curveball in between, go to Children's for that.
Industry
Hospitals and Health Care
Company size
10,001+ employees
Headquarters
Atlanta, Georgia
LinkedIn followers
143,798
Total funding
$6M
For more than 100 years, Children’s Healthcare of Atlanta has depended on clinical and nonclinical employees to help make kids better today and healthier tomorrow. Consistently ranked as one of the leading pediatric healthcare systems in the country by U.S. News & World Report, Children’s is the only freestanding pediatric healthcare system in Georgia and one of the largest pediatric clinical care providers in the country. We’re also one of Atlanta’s leading employers and have been recognized as one of the nation’s top places to work.
Our System includes:
• 789 licensed beds
• Three hospitals
• Urgent Care Centers
• Marcus Autism Center
• Center for Advanced Pediatrics
• Support Center for nonclinical staff
• Nearly 15,000 employees, including more than 4,500 nurses and 1,200 pediatric physicians representing more than 60 pediatric specialties and programs
Why Children’s?
Here are some of the reasons new graduates and experienced clinicians alike choose Children’s.
• We manage more than 1.2 million patient visits and 46,000 surgical procedures annually.
• We are home to the only Level 1 and one of the only Level 2 pediatric trauma centers in Georgia.
• We take a team approach to care. Our clinicians collaborate with social workers, chaplains, music therapists, therapy dogs and many others to help ensure kids receive comprehensive care.
Offices: 1575 Northeast Expy NE, Atlanta, Georgia 30329, US
Based on 1577 listings with disclosed salaries, most healthcare jobs in Georgia pay between $72k–$163k per year. Individual offers vary with seniority, company size, and specialization.
How many Healthcare jobs are open in Georgia right now?
There are currently 17,442 open healthcare positions in Georgia listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Georgia?
Companies currently hiring include PruittHealth, Northside Hospital, Piedmont HealthCare, Emory Healthcare, Wellstar Health System, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Georgia?
Yes — 1498 of the 17442 open healthcare positions offer remote or hybrid work (573 remote, 925 hybrid).
How do I apply for Healthcare jobs in Georgia?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.