Cell Therapy Experts – Full Time & Per Diem

This is a remote position.

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues.

We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology.

Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety.

Visit us at www.pharmavise.com Responsibilities: Lead and contribute to cell therapy research and development projects aimed at advancing novel cellular therapies for various diseases and conditions.

Design and optimize cell therapy manufacturing processes, including cell isolation, expansion, differentiation, and characterization.

Develop innovative strategies to enhance the efficacy, safety, and scalability of cell therapy products.

Collaborate cross-functionally with research, translational, clinical, and regulatory teams to advance cell therapy programs from preclinical development through to clinical trials and commercialization.

Stay abreast of emerging technologies, scientific advancements, and regulatory requirements in the field of cell therapy.

Contribute to the preparation and review of regulatory submissions, including INDs, BLAs, and marketing authorization applications.

Mentor and provide guidance to junior staff members and collaborators working on cell therapy projects.

Qualifications: PhD or equivalent degree in cell biology, immunology, regenerative medicine, or related field.

Minimum of 5 years of experience in cell therapy research and development within the biotechnology or pharmaceutical industry.

Strong expertise in cell culture techniques, cell engineering, and cell-based assays.