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 ...
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 ...
Downstream Process
Tustin, CA · On-site
This role will partner with Manufacturing, Process Development, Quality, and MSAT teams to analyze downstream purification process data, identify trends, optimize manufacturing performance, and ...
Downstream Process
Tustin, CA · On-site
This role will partner with Manufacturing, Process Development, Quality, and MSAT teams to analyze downstream purification process data, identify trends, optimize manufacturing performance, and ...
Lead and mentor a team of downstream process development scientists and engineers * Set the technical direction and strategic priorities for the Downstream Processing function. * Define and track key ...
Lead and mentor a team of downstream process development scientists and engineers * Set the technical direction and strategic priorities for the Downstream Processing function. * Define and track key ...
Process Development Scientist - San Diego
San Diego, CA · On-site
$90 - $115/hr
Process Development Scientist Location: San Diego, CA | Employment Type: Full-Time Help bring ... Experience with peptide chemistry and downstream purification preferred * Ability to interpret ...
Process Development Scientist - San Diego
San Diego, CA · On-site
$90 - $115/hr
Process Development Scientist Location: San Diego, CA | Employment Type: Full-Time Help bring ... Experience with peptide chemistry and downstream purification preferred * Ability to interpret ...
Process Development Scientist
San Francisco, CA · On-site
$170K - $190K/yr
As a Process Development Scientist, you will own that transition. You will identify bottlenecks, failure modes, and scaling challenges in our sequencing workflows-starting with RNA sequencing-and ...
Process Development Scientist
San Francisco, CA · On-site
$170K - $190K/yr
As a Process Development Scientist, you will own that transition. You will identify bottlenecks, failure modes, and scaling challenges in our sequencing workflows-starting with RNA sequencing-and ...
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$108.50 - $222.30/hr
Principal Scientist I/II - Onsite, San Diego, CA. Responsible for developing downstream ... Lead a 3‑5 person downstream process team. Key Responsibilities * Lead and manage a 3‑5 person ...
New
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$108.50 - $222.30/hr
Principal Scientist I/II - Onsite, San Diego, CA. Responsible for developing downstream ... Lead a 3‑5 person downstream process team. Key Responsibilities * Lead and manage a 3‑5 person ...
New
Biologic Process Development Scientist
Irvine, CA · On-site
$111K/yr
Additionally, the Biologic Process Development Scientist will review, revise, and develop standard operating procedures (SOPs) as needed. Maintain up-to-date knowledge of regulatory requirements, lab ...
Biologic Process Development Scientist
Irvine, CA · On-site
$111K/yr
Additionally, the Biologic Process Development Scientist will review, revise, and develop standard operating procedures (SOPs) as needed. Maintain up-to-date knowledge of regulatory requirements, lab ...
Associate Director / Director, CMC Process Development
South San Francisco, CA · Hybrid
$180K - $220K/yr
Provide technical oversight of CDMOs for upstream/downstream process optimization, scale-up, cGMP ... Strong scientific problem-solving and root-cause analysis skills. * Extensive knowledge of GMP ...
Associate Director / Director, CMC Process Development
South San Francisco, CA · Hybrid
$180K - $220K/yr
Provide technical oversight of CDMOs for upstream/downstream process optimization, scale-up, cGMP ... Strong scientific problem-solving and root-cause analysis skills. * Extensive knowledge of GMP ...
Associate Director / Director, CMC Process Development
South San Francisco, CA · On-site
$180K - $220K/yr
Provide technical oversight of CDMOs for upstream/downstream process optimization, scale-up, cGMP ... Strong scientific problem-solving and root-cause analysis skills. * Extensive knowledge of GMP ...
Associate Director / Director, CMC Process Development
South San Francisco, CA · On-site
$180K - $220K/yr
Provide technical oversight of CDMOs for upstream/downstream process optimization, scale-up, cGMP ... Strong scientific problem-solving and root-cause analysis skills. * Extensive knowledge of GMP ...
Scientist, Biologics Formulation Development
Costa Mesa, CA · On-site
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
Scientist, Biologics Formulation Development
Costa Mesa, CA · On-site
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
Scientist, Biologics Formulation Development
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
Scientist, Biologics Formulation Development
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
Scientist, Biologics Formulation Development
Costa Mesa, CA · On-site
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
Scientist, Biologics Formulation Development
Costa Mesa, CA · On-site
$85K - $107K/yr
The Scientist, Biologics Formulation Development will establish and lead formulation development ... Additional responsibilities include designing downstream purification processes for protein-based ...
This individual will serve as a subject matter expert in downstream processing, assisting a team of scientists and engineers through process development at bench, pilot, and manufacturing scale. The ...
This individual will serve as a subject matter expert in downstream processing, assisting a team of scientists and engineers through process development at bench, pilot, and manufacturing scale. The ...
Principal Engineer I/II, MSAT / Viral Vector Downstream
Berkeley, CA · On-site
$170 - $215/hr
This person will work closely with the internal process development teams to define priorities ... maintaining scientific rigor and documentation quality. * Contributes clear downstream ...
New
Principal Engineer I/II, MSAT / Viral Vector Downstream
Berkeley, CA · On-site
$170 - $215/hr
This person will work closely with the internal process development teams to define priorities ... maintaining scientific rigor and documentation quality. * Contributes clear downstream ...
New
Staff Process Engineer
San Diego, CA · On-site
This individual will serve as a subject matter expert in downstream processing, assisting a team of scientists and engineers through process development at bench, pilot, and manufacturing scale. The ...
Staff Process Engineer
San Diego, CA · On-site
This individual will serve as a subject matter expert in downstream processing, assisting a team of scientists and engineers through process development at bench, pilot, and manufacturing scale. The ...
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$119K - $222K/yr
Principal Scientist I/II Position Location: Onsite, San Diego, CA Key Responsibilities ... Lead and manage a 3-5 person downstream process team and provide technical support, training, and ...
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$119K - $222K/yr
Principal Scientist I/II Position Location: Onsite, San Diego, CA Key Responsibilities ... Lead and manage a 3-5 person downstream process team and provide technical support, training, and ...
Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... downstream processing for oral solid dosage forms. * Experience supporting oral solid dosage form ...
Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... downstream processing for oral solid dosage forms. * Experience supporting oral solid dosage form ...
... downstream process development efforts within the Genetics Research and Delivery Group ... Partner with the Upstream and Analytical leads in Research and Process Sciences to build effective ...
... downstream process development efforts within the Genetics Research and Delivery Group ... Partner with the Upstream and Analytical leads in Research and Process Sciences to build effective ...
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$119K - $222K/yr
Principal Scientist I/II Position Location: Onsite, San Diego, CA Key Responsibilities ... Lead and manage a 3-5 person downstream process team and provide technical support, training, and ...
Principal Scientist, Early Pipeline Development
San Diego, CA · On-site
$119K - $222K/yr
Principal Scientist I/II Position Location: Onsite, San Diego, CA Key Responsibilities ... Lead and manage a 3-5 person downstream process team and provide technical support, training, and ...
Process Development Senior Scientist
Thousand Oaks, CA · On-site
$96K - $131K/yr
Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... downstream processing for oral solid dosage forms. * Experience supporting oral solid dosage form ...
Process Development Senior Scientist
Thousand Oaks, CA · On-site
$96K - $131K/yr
Process Development Senior Scientist What you will do Let's do this. Let's change the world. In ... downstream processing for oral solid dosage forms. * Experience supporting oral solid dosage form ...
Internship Downstream Process Development Scientist information
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Full-time
Re-posted 9 days ago
University Of California San Francisco rating
7.8
Based on 13 frontline employees who took The Breakroom Quiz
229th of 619 rated colleges and universities
Job description
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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Headquarters location
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