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Gene Therapy Manufacturing Supervisor Jobs (NOW HIRING)

Actalent

Manufacturing Associate

Bothell, WA

Manufacturing Associate II - cGMP Cell & Gene Therapy The Manufacturing Associate II supports day-to-day operations at a cGMP clinical manufacturing site producing plasmids, viral vectors, and ...

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Gene Therapy Manufacturing Supervisor information

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$34.5K

$71.4K

$108K

How much do gene therapy manufacturing supervisor jobs pay per year?

As of Sep 12, 2026, the average yearly pay for gene therapy manufacturing supervisor in the United States is $71,398.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,500.00 and $82,500.00 per year, depending on experience, location, and employer.

What does a gene therapy manufacturing supervisor do?

A Gene Therapy Manufacturing Supervisor oversees the production of gene therapy products in a biomanufacturing environment. This role involves managing daily operations in the manufacturing facility, ensuring compliance with regulatory standards, maintaining product quality, and supervising a team of technicians and operators. They are responsible for coordinating schedules, troubleshooting production issues, and implementing process improvements. The supervisor also ensures all documentation is accurate and that safety protocols are strictly followed.

What are the key skills and qualifications needed to thrive as a gene therapy manufacturing supervisor, and why are they important?

To thrive as a Gene Therapy Manufacturing Supervisor, you need a strong background in biology or biotechnology, experience with GMP (Good Manufacturing Practice) environments, and a relevant degree such as a B.S. or M.S. in a life science field. Familiarity with manufacturing execution systems (MES), process control software, and quality management systems, as well as certifications like Six Sigma or Lean Manufacturing, are typically used in this role. Leadership, problem-solving, and effective communication are vital soft skills for guiding teams and ensuring compliance with rigorous standards. These skills ensure the safe, efficient, and consistent production of gene therapies, which is critical for patient safety and regulatory approval.

What are common challenges faced by gene therapy manufacturing supervisors, and how can they be addressed?

Gene Therapy Manufacturing Supervisors often encounter challenges such as ensuring strict compliance with Good Manufacturing Practices (GMP), managing complex production schedules, and maintaining product quality in a rapidly evolving field. Addressing these challenges requires strong communication skills to coordinate with cross-functional teams, adaptability to implement new technologies and protocols, and a proactive approach to troubleshooting issues on the manufacturing floor. Continuous training and close collaboration with quality assurance and regulatory departments are essential to keep processes efficient and compliant.

What is the difference between Gene Therapy Manufacturing Supervisor vs Manufacturing Technician?

AspectGene Therapy Manufacturing SupervisorManufacturing Technician
CredentialsBachelor's degree in life sciences or related field, GMP training, leadership experienceAssociate's or bachelor's degree, GMP training, technical skills
Work EnvironmentSupervises manufacturing teams in cleanroom settings, oversees processesPerforms hands-on manufacturing tasks in cleanroom or production areas
Employer & IndustryBiotech and pharmaceutical companies specializing in gene therapyBiotech, pharmaceutical, or contract manufacturing organizations

The Gene Therapy Manufacturing Supervisor oversees manufacturing teams and ensures compliance with GMP standards, focusing on process management and team leadership. In contrast, Manufacturing Technicians perform the hands-on tasks required to produce gene therapy products. Both roles are essential in the production process, but the supervisor has a broader responsibility for oversight and coordination.

What are popular job titles related to Gene Therapy Manufacturing Supervisor jobs?

For Gene Therapy Manufacturing Supervisor jobs, the most frequently searched job titles are:

Infographic showing various Gene Therapy Manufacturing Supervisor job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $71,398 per year, or $34.3 per hour.

Cell and Gene Therapy Business Supervisor

Charleston, SC • On-site

MUSC Health & Medical University of SC
Hospitality Services • 10K+ employees
Learn more about MUSC Health & Medical University of SCexternal

Full-time

Medical

Posted 17 days ago

MUSC Health rating

6.9

Company rating: 6.9 out of 10

Based on 203 frontline employees who took The Breakroom Quiz

Job description

Job Description Summary
The Cell and Gene Therapy Business Coordinator Supervisor provide day-to-day operational leadership and supervisory oversight for the Cell and Gene Therapy Business Coordinator team.
The Supervisor leads a team responsible for insurance verification, prior authorization, payer communications, financial clearance, authorization tracking, contract coordination, and billing documentation to ensure timely patient access to care, regulatory compliance, and accurate reimbursement. This role develops and standardizes workflows that minimize financial risk to both patients and the organization while supporting a seamless patient experience across the continuum of care.
Entity
Medical University Hospital Authority (MUHA)
Worker Type
Employee
Worker Sub-Type
Regular
Cost Center
CC000283 CHS - Cell and Gene Therapy Program
Pay Rate Type
Salary
Pay Grade
Health-28
Scheduled Weekly Hours
40
Work Shift
Day (United States of America)
Job Description
The Cell and Gene Therapy Business Coordinator Supervisor provide day-to-day operational leadership and supervisory oversight for the Cell and Gene Therapy Business Coordinator team.
The Supervisor leads a team responsible for insurance verification, prior authorization, payer communications, financial clearance, authorization tracking, contract coordination, and billing documentation to ensure timely patient access to care, regulatory compliance, and accurate reimbursement. This role develops and standardizes workflows that minimize financial risk to both patients and the organization while supporting a seamless patient experience across the continuum of care.
Working collaboratively with program director, program manager, physicians, advanced practice providers, nursing, apheresis, pharmacy, social work, revenue cycle, finance, contracting, compliance, and other interdisciplinary stakeholders, this position advances operational excellence, financial stewardship, and program growth within a rapidly evolving cell and gene therapy landscape.
Primary responsibilities include authorizations processes for inpatient and outpatient cellular and gene therapy services; and pricing changes for cellular therapy products; overseeing purchase orders and financial reconciliation; providing guidance on wholesale acquisition cost (WAC) and 340B pricing strategies; evaluating reimbursement considerations for clinical trials and commercial therapies; and serving as the primary financial liaison with pharmaceutical manufacturers, payers, and institutional stakeholders. Through leadership of the Business Coordinator team, this position supports financial sustainability, regulatory compliance, and continued growth of the Cell and Gene Therapy Program.
Additional Job Description
Minimum Qualifications
  • Associate degree in a work-related field/discipline from an accredited college or university.
  • 3+ years of directly related work experience in healthcare operations, insurance authorization, patient access, managed care, revenue cycle, financial counseling, or a related field.
  • 1+ year of experience as a prior lead, supervisory, or team coordination experience.
  • Knowledge of healthcare insurance, payer requirements, prior authorization, benefits verification, and reimbursement processes.
  • Demonstrated leadership, communication, and interpersonal skills with the ability to effectively supervise staff and collaborate across multidisciplinary teams.
  • Strong analytical, organizational, and problem-solving skills with the ability to prioritize competing demands and resolve complex operational and financial issues.
  • Ability to identify and implement process improvement initiatives that enhance patient access, operational efficiency, and financial performance.

Preferred Qualifications
  • Bachelor's degree in a work-related field/discipline from an accredited college or university.
  • 3+ years of prior lead, supervisory, or team coordination experience.
  • Knowledge of financial clearance, reimbursement, and authorization processes specific to oncology, hematopoietic cell transplantation, cellular therapy, or gene therapy.
  • Experience leading high-performing teams in a complex healthcare or academic medical center environment.
  • Knowledge of healthcare regulatory, accreditation, and compliance standards affecting specialty care programs (e.g., FACT, CMS, FDA).
  • Demonstrated experience using data analytics and performance metrics to improve operational outcomes, revenue cycle performance, and patient access.

If you like working with energetic enthusiastic individuals, you will enjoy your career with us!
The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need.
Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees

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About MUSC Health

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MUSC is located in Charleston, SC, frequently named one of the best places in America to live. If charming, historic, vibrant, cultural, and coastal are adjectives that you find appealing, it's all here. In Charleston, you might find yourself dining at a world class restaurant tonight and relaxing on a boat as you explore our many waterways tomorrow. You might stroll along cobblestone streets, amidst centuries old homes by day and attend a jazz concert by night. Charleston is a place where you can live your life to its fullest.

Industry

Hospitality services

Company size

10,000+ Employees

Headquarters location

Charleston, SC, US

Year founded

1824

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