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Cell Process Development Scientist Jobs (NOW HIRING)

Process Development Scientist

Denver, CO · On-site

$110K - $150K/yr

Process Development Scientist Location: Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of industrial biocatalysts and is seeking a hands-on Process ...

Process Development Scientist Location: Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of industrial biocatalysts and is seeking a hands-on Process ...

Work within a team of process scientists and/or engineers to design, execute, document, and generate primary data packages related to process development and technology transfer, while applying their ...

Work within a team of process scientists and/or engineers to design, execute, document, and generate primary data packages related to process development and technology transfer, while applying their ...

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Cell Process Development Scientist information

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

As of Sep 13, 2026, the average hourly pay for cell process development scientist in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What does a cell process development scientist do?

A Cell Process Development Scientist designs and optimizes methods for growing and manipulating cells, often for biopharmaceutical production, cell therapy, or research purposes. They work on scaling up cell cultures, improving yields, and ensuring reproducibility and quality throughout the development process. Their responsibilities may include developing protocols, troubleshooting technical issues, and collaborating with cross-functional teams to transfer processes to manufacturing. This role is critical for advancing new therapies and products from the lab to clinical and commercial production.

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

To thrive as a Cell Process Development Scientist, you need a solid background in cell biology, biotechnology, and bioprocess engineering, typically with an advanced degree (MS or PhD) in a related field. Familiarity with laboratory automation, bioreactor systems, and analytical tools like flow cytometry and qPCR, as well as experience with GMP regulations, is crucial. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills distinguish top performers in this role. These competencies are essential for developing robust, scalable cell manufacturing processes that ensure product quality and compliance in the biopharmaceutical industry.

What are some typical challenges faced by cell process development scientists when scaling up cell-based manufacturing processes?

Cell Process Development Scientists often encounter challenges related to maintaining cell quality and consistency during scale-up from laboratory to production scale. Factors such as changes in bioreactor conditions, nutrient supply, and process variability can affect cell growth and product yield. Addressing these issues requires close collaboration with cross-functional teams, including quality assurance and manufacturing, to optimize protocols and ensure compliance with regulatory standards. Adaptability and problem-solving skills are essential to troubleshoot and refine processes as they transition to larger-scale operations.

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

AspectCell Process Development Scientist

The Cell Process Development Scientist focuses on designing, optimizing, and scaling up cell culture processes for biopharmaceutical production. They typically hold advanced degrees in biological sciences and work in R&D or process development labs. The role involves method development, process validation, and collaboration with manufacturing teams. In contrast, a Cell Manufacturing Associate primarily executes established manufacturing procedures on the production floor, often with less emphasis on process design. Both roles are essential in biopharma, but the Scientist is more involved in process innovation, while the Associate handles day-to-day production tasks.

What are popular job titles related to Cell Process Development Scientist jobs?

For Cell Process Development Scientist jobs, the most frequently searched job titles are:

Process Development Scientist

San Francisco, CA • On-site

University of California, San Francisco
Colleges, Universities, and Professional Schools • 10K+ employees

Full-time

Re-posted 5 days ago


Key responsibilities

  • Design and execute complex process development efforts using genomic and epigenomic engineering tools and platforms.

  • Analyze, interpret, organize, and present data to internal and external groups in clear and concise manner.

  • Work closely with internal and external partners to support technology transfers and implementation of new process technologies.


University Of California San Francisco rating

7.8

Company rating: 7.8 out of 10

Based on 13 frontline employees who took The Breakroom Quiz


Job description

Application Window
Open date: March 13, 2026
Most recent review date: Friday, Apr 17, 2026 at 11:59pm (Pacific Time) Applications received after this date will be reviewed by the search committee if the position has not yet been filled.
Final date: Monday, Sep 13, 2027 at 11:59pm (Pacific Time) Applications will continue to be accepted until this date, but those received after the review date will only be considered if the position has not yet been filled.
Position description
Process Development Scientist
The Department of Laboratory Medicine at the University of California, San Francisco(UCSF) is seeking a motivated Process Development Scientist to join our Investigational Cellular Therapy (ICT) group . The ICT program aims to accelerate the development and delivery of promising new cell and gene therapies targeting cancer, autoimmunity, infectious disease, and inherited hematologic and immune disorders. ICT has established collaborations with UCSF research groups and a variety of academic and industrial partners to develop new cell and gene therapy technologies, platforms, and products.
The successful candidate will lead cellular engineering activities within a highly skilled process development team and collaborate closely with partner functions such as pre-clinical research, GMP manufacturing, analytical development, quality control, quality assurance, operations/facilities, and regulatory affairs to advance pipeline programs.
Key Responsibilities:
• Design and execute complex process development efforts using genomic and epigenomic engineering tools and platforms.
• Analyze, interpret, organize, and present data to internal and external groups in clear and concise manner.
• Author and review experimental proposals, SOPs, and technical reports for scientific publications and regulatory filings.
• Ensure data integrity, maintain laboratory record and prepare protocols and reports in a GMP-compliant manner.
• Work closely with internal and external partners to support technology transfers and implementation of new process technologies.
• Collaborate with and participate in teams to facilitate IND-enabling studies.
• Participate in GMP manufacturing campaigns for in-house products.
This position will occasionally involve long hours and some weekends and holidays. Scientific independence and attention to detail are critical to success in this position. The candidate will have the opportunity to contribute to scientific publications.
Required Qualifications:
• For Associate Specialists - A Master's degree (or equivalent degree) in Immunology, Biological Sciences, Biomedical Engineering, or related field or five to ten years of relevant experience is required.
• For Full Specialist - A PhD (or equivalent degree) in Immunology, Biological Sciences, Biomedical Engineering, or related field or ten or more years of relevant experience is required.
• Working knowledge of basic scientific principles and methods in order to independently design and perform experiments of moderate scope and complexity.
• Hands-on experience with aseptic tissue culture techniques and flow cytometry.
• Experience with genome editing techniques (e.g. CRISPR/Cas9 editing, base editing, prime editing, etc.)
• Experience working with GMP-compatible or automated cell processing platforms and equipment (e.g., electroporation systems, closed-system cell processing devices, automated cell culture or cell washing platforms).
• Organizational abilities and decision-making to prioritize work assignments.
• Effective written and verbal communication skills with internal and external collaborators.
• Ability to work in a collaborative manner, to assist in identifying any challenges or barriers.
Preferred Qualifications:
• Familiarity with Design of Experiments (DoE) approaches for process optimization.
• Experience working in regulated environments supporting IND-enabling studies, process qualification, or clinical manufacturing.
• Experience with analytical methods such as flow cytometry, ddPCR/qPCR, or next-generation sequencing for characterization of edited cells.
Applicants must apply online with a CV, cover letter, and the contact information of 3 references. Applicants' materials must list pending qualifications. Candidates must have required qualifications by time of hire.
See Table 24B for the salary range for this position. A reasonable estimate for this position is $75,600 - $194,800.
Application Requirements
Document requirements
  • Curriculum Vitae - CV must clearly list current and/or pending qualifications (e.g. board eligibility/certification, medical licensure, etc.).
  • Cover Letter

Reference requirements
  • 3 required (contact information only)

About UC San Francisco
As a University employee, you will be required to comply with all applicable University policies and/or collective bargaining agreements, as may be amended from time to time. Federal, state, or local government directives may impose additional requirements.
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
UCSF is committed to welcoming and serving all people, honoring the dignity of every individual without preference or prejudice, in support of its public mission and in alignment with our PRIDE values and Principles of Community.
As a condition of employment, the finalist will be required to disclose if they are subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct.
• "Misconduct" means any violation of the policies or laws governing conduct at the applicant's previous place of employment, including, but not limited to, violations of policies or laws prohibiting sexual harassment, sexual assault, or other forms of harassment, or discrimination, as defined by the employer.
• UC Sexual Violence and Sexual Harassment Policy
• UC Anti-Discrimination Policy
• APM - 035: Affirmative Action and Nondiscrimination in Employment
Job location
San Francisco, CA

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