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Biotech Process Development Jobs in Oakland, CA (NOW HIRING)

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

This position is responsible for supporting the activities involved in the development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$125K - $161K/yr

This position is responsible for supporting the activities involved in the development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$90K - $210K/yr

This position is responsible for supporting the activities involved in the development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...

Cellares

Senior Process Engineer

South San Francisco, CA · On-site

$90 - $210/hr

This position is responsible for supporting the activities involved in the development, process ... A minimum of 5+ years of experience within the biotech/biopharma industry in cGMP Operations ...

Ohalo

Biotech Program Manager

South San Francisco, CA · On-site

$160K - $210K/yr

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... Own program success for one or more programs focused on discovery, process development, or ...

Ohalo

Biotech Program Manager

South San Francisco, CA

$160K - $210K/yr

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... Own program success for one or more programs focused on discovery, process development, or ...

Ohalo

Biotech Program Manager

South San Francisco, CA · On-site

$160K - $210K/yr

Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech ... Own program success for one or more programs focused on discovery, process development, or ...

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Showing results 21-40

All JobsBiotech Process Development JobsBiotech Process Development Jobs in Oakland, CA

Biotech Process Development information

See Oakland, CA salary details

$21

$38

$56

How much do biotech process development jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for biotech process development in Oakland, CA is $38.68, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $47.50 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in biotech process development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in biotech process development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Oakland, CA? For Biotech Process Development jobs in Oakland, CA, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Oakland, CA look for? The top searched job categories for Biotech Process Development jobs in Oakland, CA are:
What cities near Oakland, CA are hiring for Biotech Process Development jobs? Cities near Oakland, CA with the most Biotech Process Development job openings:
Biotech Process Development jobs near you

Sr. Scientist, Gene Editing Materials Process Development(temp)

Allogene Therapeutics

South San Francisco, CA • On-site

$60 - $70/hr

Contractor

Medical

Posted 6 days ago

Job description

Job Description
About Allogene:
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of "off-the-shelf" CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients.
Job Description:
We are seeking a highly motivated, self-driven and collaborative individual to join the Process and Product Development organization. The successful candidate will serve as a technical lead working with internal teams and external CDMOs focused on development and continued improvement of the manufacturing processes of gene delivery and/or gene editing materials used in allogeneic cell therapies. This individual will provide technical leadership across the product lifecycle, from early-stage process development through late-stage process characterization, control strategy development and commercial manufacturing readiness to support BLA submission and commercialization. This position will also provide technical oversight to support the production and re-supply of gene delivery and gene editing materials, as appropriate. This position is based in South San Francisco.
Responsibilities include, but are not limited to:
  • Serve as technical subject matter expertise supporting CDMOs to provide process and assay development expertise for gene editing and/or gene delivery materials
  • Partner with internal and external R&D, External Manufacturing, MSAT, and Quality to ensure cross-functional alignment
  • Contribute to process development, process characterization, control strategy development and PPQ planning activities
  • Work with internal and external partners to assess impact to process and method change for gene editing and/or gene delivery materials
  • Support planning, execution and troubleshooting deviations of Process Development and GMP runs at CDMOs
  • Develop and execute experiments to assess impact of gene editing and/or gene delivery materials on CART production process
  • Develop analytical assays and provide testing for gene editing and/or gene delivery materials, as needed
  • Engage with broader Process and Product Development team to contribute to achievement of Department goals
  • Other duties as assigned

Position Requirements & Experience:
  • PhD in biological sciences, engineering or related discipline with 5+ years of relevant experience in gene editing or gene delivery related field required (or MS with 10+ years, BS with 12+ years of industry experience)
  • Direct experience developing, characterizing, scaling, or supporting GMP manufacturing processes for gene editing materials (e.g., mRNA, nucleases) and/or gene delivery materials (e.g., AAV, lentiviral vectors, non-viral delivery systems) is strongly preferred. Experience solely using these materials for gene editing applications without involvement in process development or manufacturing is unlikely to meet the requirements of this role.
  • Strong knowledge background and hands-on experience with process and analytical development or manufacturing of gene editing material and/or viral/non-viral gene delivery material are required
  • Experience with applying Design of Experiments (DOE), statistical analysis, and data visualization tools (JMP, Spotfire, or equivalent) for process development or characterization studies
  • Prior experience serving as technical support for internal and external teams to manage process development and manufacturing at CDMOs is a plus
  • Familiarity with cGMP manufacturing and regulatory expectations for biologics gene editing material or cell therapy products is a plus
  • Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment
  • Ability to work independently and in a matrixed environment
  • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines
  • Ability to travel up to 10%
  • Candidates must be authorized to work in the U.S
  • This is a 1-year contract opportunity with the possibility of extension or contract-to-hire.

We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected hourly range for this role is $60 to $70 per hour. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients.
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