ZipRecruiter

Log In

1

Cell Therapy Process Development Scientist Jobs in Florida

Open Scientific

Sr. Engineer of Process Development

Sunrise, FL · On-site

$99K - $128K/yr

... and Life Sciences worldwide. This is a great step for someone who is looking to take a seat in a ... Design, evaluate, implement and monitor processes and operating systems for the manufacture aortic ...

Open Scientific

Sr. Engineer of Process Development

Sunrise, FL · On-site

$99K - $128K/yr

... and Life Sciences worldwide. This is a great step for someone who is looking to take a seat in a ... Design, evaluate, implement and monitor processes and operating systems for the manufacture aortic ...

next page

Showing results 1-20

All JobsCell Therapy Process Development Scientist JobsCell Therapy Process Development Scientist Jobs in Florida

Cell Therapy Process Development Scientist information

What is the difference between Cell Therapy Process Development Scientist vs Cell Manufacturing Associate?

AspectCell Therapy Process Development ScientistCell Manufacturing Associate
CredentialsTypically requires a Master's or PhD in biology, biochemistry, or related fieldsUsually holds a Bachelor's degree in life sciences or related areas
Work EnvironmentResearch labs, process development facilities, R&D settingsManufacturing floors, production facilities, GMP environments
Industry UsageDesigning and optimizing cell therapy processes, early-stage developmentExecuting manufacturing protocols, batch production, quality control

The Cell Therapy Process Development Scientist focuses on developing and refining cell therapy processes in research and development settings, often requiring advanced degrees. In contrast, the Cell Manufacturing Associate works primarily on executing manufacturing procedures in GMP environments, typically with a bachelor's degree. Both roles are essential in the cell therapy industry but differ in responsibilities, work environment, and required qualifications.

What are popular job titles related to Cell Therapy Process Development Scientist jobs in Florida? For Cell Therapy Process Development Scientist jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Cell Therapy Process Development Scientist jobs in Florida look for? The top searched job categories for Cell Therapy Process Development Scientist jobs in Florida are:
What cities in Florida are hiring for Cell Therapy Process Development Scientist jobs? Cities in Florida with the most Cell Therapy Process Development Scientist job openings:
Cell Therapy Process Development Scientist jobs near you
Grant Writer for Cell and Gene Therapy Lab

Grant Writer for Cell and Gene Therapy Lab

Gift of Life Marrow Registry

Boca Raton, FL • On-site

$70K - $80K/yr

Full-time

Re-posted 9 days ago

Job description

Education

Bachelor’s degree with Biology or recognized equivalent. Minimum of (4) years’ experience in NIH grant writing. Minimum (3) years’ experience in cell & gene therapy or regenerative medicine.

Summary Statement

The Cell Therapy Grant Writer is an experienced professional with extensive expertise in cell and gene therapy. This role involves leading the development, writing, and submission of competitive grant applications, primarily focusing on NIH funding opportunities. The ideal candidate will collaborate closely with scientific leadership and researchers to translate complex translational and preclinical research into fundable proposals. Previous experience with NIH grants is required. The Cell Therapy Grant Writer will report directly to the Chief Scientific Officer (CSO).

Responsibilities

  • Identify grant opportunities in cell therapy.
  • Interpret NIH funding opportunity announcements and align proposals accordingly.
  • Lead the preparation of NIH grant applications, including sections such as Specific Aims, Research Strategy, Significance, Innovation, Approach, and Impact.
  • Collaborate with the CSO and R&D scientists to gain a deep understanding of the underlying science that will support the grants.
  • Develop clear and persuasive scientific narratives from complex scientific data.
  • Manage grant timelines, submission logistics, and ensure compliance with NIH and institutional requirements.
  • Coordinate the preparation of biosketches, facilities/resources sections, budget justifications, and other supporting documents.
  • Review and edit drafts for clarity, consistency, and alignment with reviewer expectations.
  • Track funding outcomes and maintain internal documentation related to grants.
  • Stay informed about grant opportunities, review criteria, and trends in cell and gene therapy funding.
  • Maintain organized records of submissions, outcomes, and reporting requirement.
  • Assist the team with writing SOPs as needed.
  • Support the R&D team by writing scientific papers and preparing PowerPoint presentations as needed.
  • Perform other duties and follow procedures as assigned.

Knowledge, Skills, and Experience

  • Experience working in academic research, healthcare, biotechnology, or life sciences.
  • Familiarity with federal compliance requirements and research administration.
  • Extensive experience with NIH grants (minimum 4-year experience).
  • Experience with scientific publications.
  • Understanding of human subjects, animal research, and regulatory documentation.
  • Demonstrated track record of successful NIH grant submissions.
  • In-depth knowledge of NIH structure, review criteria, and submission systems (e.g., ASSIST, eRA Commons, Grants.gov).
  • Exceptional writing, editing, and organizational skills.
  • Ability to manage multiple deadlines and projects simultaneously
  • Strong collaboration and communication skills across interdisciplinary teams
  • Demonstrate ability to prioritize required duties and responsibilities
  • Excellent oral and written communication skills.
  • Strong organizational skills with attention to detail.
  • Ability to work both independently and within teams
  • Flexibility to adjust to changes in schedules, working hours, and procedures. Position may require extended hours at intervals.
  • Ability to work in highly stressful situations.
  • Travel as needed to attend relevant industry conferences to meet continuing education requirements.