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Cell Therapy Process Development Jobs in Haverhill, FL

Pursuit Aerospace

CNC Programmer - 2nd Shift

Stuart, FL · On-site

$77K - $102K/yr

Participates in process development, including creation of detailed router instructions, operation ... Incorporates lean manufacturing in cell environment and quick-change set-up, etc. * Performs other ...

Pursuit Aerospace

CNC Programmer - 2nd Shift

Stuart, FL · On-site

$22.25 - $30.50/hr

Participates in process development, including creation of detailed router instructions, operation ... Incorporates lean manufacturing in cell environment and quick-change set-up, etc. * Performs other ...

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All JobsCell Therapy Process Development JobsCell Therapy Process Development Jobs in Haverhill, FL

Cell Therapy Process Development information

See Haverhill, FL salary details

$18

$33

$48

How much do cell therapy process development jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for cell therapy process development in Haverhill, FL is $33.18, according to ZipRecruiter salary data. Most workers in this role earn between $27.21 and $40.72 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a cell therapy process development professional?

To thrive in Cell Therapy Process Development, you need a solid background in cell biology, biotechnology, or a related field, often supported by a relevant degree and experience with cell culture techniques. Familiarity with bioprocessing equipment, Good Manufacturing Practice (GMP) regulations, and analytical tools such as flow cytometry and PCR is typically required. Strong problem-solving skills, attention to detail, and effective teamwork enhance performance in this collaborative and innovative environment. These competencies ensure the safe and efficient development of cell therapies, meeting rigorous quality standards and advancing clinical applications.

What are some typical challenges faced by professionals in cell therapy process development, and how are they addressed?

Professionals in Cell Therapy Process Development often encounter challenges such as scaling up production processes from laboratory to clinical or commercial scale while maintaining product quality and consistency. Additional hurdles include adhering to strict regulatory requirements and managing complex collaborations across cross-functional teams, like quality assurance, regulatory affairs, and manufacturing. These challenges are typically addressed through rigorous process optimization, thorough documentation, and ongoing communication with stakeholders to ensure that all aspects of the process meet industry standards and regulatory expectations.

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

AspectCell Therapy Process DevelopmentCell Therapy Manufacturing Specialist
CredentialsTypically requires a degree in biology, biochemistry, or biomedical engineering; certifications in GMP or cell therapy are commonSimilar credentials; often holds degrees in related fields and GMP certifications
Work EnvironmentResearch labs, development facilities, early-stage process optimizationManufacturing plants, production floors, quality control labs
Industry UsageFocuses on developing and optimizing cell therapy processesInvolved in large-scale production and process execution

Cell Therapy Process Development professionals focus on designing and refining cell therapy procedures, while Cell Therapy Manufacturing Specialists handle the production and quality assurance in manufacturing settings. Both roles require similar educational backgrounds and certifications but differ mainly in their work environment and specific responsibilities.

What is cell therapy process development?

Cell Therapy Process Development refers to the design, optimization, and scaling up of manufacturing processes for cell-based therapies, such as CAR-T cells or stem cell products. Professionals in this field work on translating laboratory research into reproducible, efficient, and safe production methods that meet regulatory standards. This involves working with cell culture techniques, bioreactors, quality control, and process validation to ensure that therapies can be produced consistently for clinical and commercial use. The goal is to develop robust processes that deliver safe and effective cell therapies to patients.
What cities near Haverhill, FL are hiring for Cell Therapy Process Development jobs? Cities near Haverhill, FL with the most Cell Therapy Process Development job openings:
Cell Therapy Process Development jobs near you
Infographic showing various Cell Therapy Process Development job openings in Haverhill, FL as of August 2026, with employment types broken down into 67% Full Time, and 33% Part Time. Highlights an 100% In-person job distribution, with an average salary of $69,023 per year, or $33.2 per hour.

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 3 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.