Supervisor, Aseptic Manufacturing

iovancebiotherapeutics; Philadelphia (Philadelphia County); On-site; USD 90,000 - 130,000; Full time

Job summary

Iovance Biotherapeutics, Inc. is seeking a Supervisor for Aseptic Manufacturing to oversee production processes and ensure safety and compliance. The role emphasizes timely document review, staff development, and implementing a First-time right program to meet growing demand.

The successful candidate will lead autologous cell therapy manufacturing operations in ISO class 5 cleanrooms, with strong background in cell culture and regulatory requirements. Travel ~10% is expected.

Qualifications

• Minimum BS in biology, biochemistry, bioengineering or related field.
• 5+ years GMP biopharma manufacturing with cell culture experience.
• 2+ years in a Lead/Leadership/Supervisory role desired.
• Strong knowledge of aseptic processing in cleanroom environments.

Responsibilities

• Supervision and development of direct reports (operators), mentoring to foster continuous improvement.
• Schedule and coordinate day-to-day activities according to the production plan.
• Develop deep understanding of current production processes as SME in a specific area.
• Oversee manufacturing to ensure cGMP compliance and proper aseptic techniques.
• Review batch documentation and logbooks for completeness and accuracy.
• Lead on deviations, CAPAs, and training program effectiveness.

Skills

GMP manufacturing

Cell culture

Leadership

Training

Aseptic processing

Education

Bachelor's degree in biology/biochemistry/biotech

Tools

cGMP knowledge

Job description

About Iovance Biotherapeutics, Inc. Iovance Biotherapeutics , Inc. is the global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) cell therapies for patients with solid tumors. Amtagvi® (lifileucel) is the first FDA-approved, one-time treatment for previously treated advanced melanoma, now approved in three global markets and available at more than 95 authorized treatment centers. The Iovance TIL platform spans registrational trials and next-generation programs in additional solid tumors, including gene‑edited and IL‑12 tethered TIL therapies, next‑generation IL‑2, and precision immuno‑oncology approaches. As the first and only company to take TIL therapy from concept to a broadly accessible commercial treatment, Iovance operates as an end‑to‑end cell therapy company, anchored by fully owned, centralized U.S.-based manufacturing that is scaled to serve thousands of cancer patients worldwide each year. For more information, please visit www.iovance.com .

Amtagvi® and its accompanying design marks, Proleukin ® , Iovance ® , and IovanceCares™ are trademarks and registered trademarks of Iovance Biotherapeutics, Inc. or its subsidiaries. All other trademarks and registered trademarks are the property of their respective owners.

Information on Iovance's broad, industry‑leading patent portfolio is available on the Intellectual Property page on www.iovance.com .

Overview

The Supervisor for Aseptic Manufacturing oversees the production process to ensure that all materials are produced safely and follow the company's standards. This position requires timely document review and ensuring all targets are met. In addition, the supervisor will be responsible for developing staff and implementing an effective "First‑time right" program to meet Iovance's growing demands. The successful candidate will also help onboard new team members and manage deviations and CAPAs for the training and learning team. It is crucial that the supervisor has innovative technical knowledge and contributes significantly to the overall manufacturing operation. As a leadership team member for autologous cell therapy manufacturing operations, a background in cell culture and manufacturing in ISO class 5 cleanrooms is necessary.

Rotation Schedule

• Week 1: Shift A: Sunday to Wednesday from 0700 to 1830
• Week 2 Shift A: Sunday to Tuesday from 0700 to 1930

Essential Functions and Responsibilities

• Supervision and Development direct reports (operators), mentoring/coaching to motivate and mentor peers/ staff to foster a culture of continuous improvement and operational excellence.
• Schedule and coordinate day‑to‑day activities, ensuring conformance to the daily schedule.
• Develop a comprehensive understanding of the current production process, as this role is viewed as a subject matter expert within a specific area. Significant experience in aseptic processing techniques and a thorough understanding of regulatory requirements for a cGMP manufacturing facility are required.
• Provide oversight of the manufacturing process, ensuring technicians follow cGMP practices and utilize proper aseptic techniques.
• Review batch documentation and logbooks for completeness and accuracy.
• Ability to work under limited supervision and handle problems of a more complex nature.
• Continuously seek and support new approaches, practices, and processes to improve the efficiency and efficacy of the operation.
• Establish objectives and conduct performance reviews, monitor progress toward goals, and provide timely feedback to Management.
• Author and revise documentation, including drafting and approval of SOPs, Batch Records, Deviations, CAPAs, etc.
• Ensure the department understands and complies with quality standards and requirements as documented.
• Ensure efficient operations and compliance with cGMPs and safety regulations.
• Work in a cleanroom with biohazards, human blood components, and chemicals
• Must adhere to Iovance Biotherapeutics' core values, policies, procedures, and business ethics.
• Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
• Perform miscellaneous duties as assigned.
• Travel - 10%

Required Education, Skills, and Knowledge

• Minimum B.S. in biology, biochemistry, bioengineering, related technical field, or equivalent industry and technical experience.
• Minimum of 5 years of experience in biopharmaceutical‑based GMP manufacturing operations, including experience in cell culture and associated downstream processing. A minimum of 2 years in a Lead/Leadership/Supervisory Role is desired.
• Demonstrated technical knowledge of aseptic processing in cleanroom environments is a must.
• Strong knowledge and experience of the end‑to‑end learning process, i.e., learning needs assessment, program design and delivery, and learning evaluation and training effectiveness assessment.
• Demonstrates strong oral and written communication skills and actively contributes to training,