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Director Gene Synthesis Jobs (NOW HIRING)

GeneFab

Program Manager, CRDMO

Alameda, CA

$140K - $200K/yr

... and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 ... directed evolution of small molecule-regulated gene switches, and the engineering of highly ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

... and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 ... directed evolution of small molecule-regulated gene switches, and the engineering of highly ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$150 - $200/hr

... and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 ... directed evolution of small molecule-regulated gene switches, and the engineering of highly ...

GeneFab

Bioprocess Specialist - CONTRACT

Alameda, CA

$40 - $50/hr

... and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 ... directed evolution of small molecule-regulated gene switches, and the engineering of highly ...

GeneFab

Program Manager, CRDMO

Alameda, CA · On-site

$140K - $200K/yr

... and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 ... directed evolution of small molecule-regulated gene switches, and the engineering of highly ...

GeneFab

Senior Process Engineer, MSAT

Alameda, CA · On-site

$150 - $200/hr

... directed evolution of small molecule-regulated gene switches, and the engineering of highly ... About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell ...

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Director Gene Synthesis information

What does a director of gene synthesis do?

A Director of Gene Synthesis oversees the design, production, and quality control of synthetic genes within a biotechnology company or research institution. They manage teams responsible for DNA synthesis, optimize laboratory workflows, and ensure that projects comply with regulatory and safety standards. Additionally, they collaborate with scientists and clients to deliver custom genetic constructs and drive innovation in gene synthesis technologies.

What are some typical challenges faced by a director of gene synthesis, and how can they be addressed?

Directors of Gene Synthesis often encounter challenges such as optimizing workflow for high-throughput projects, maintaining quality control standards, and managing cross-functional teams that include scientists, technicians, and project managers. Balancing rapid turnaround times with accuracy and regulatory compliance is crucial. Addressing these challenges involves implementing robust process automation, fostering strong communication across departments, and staying updated with the latest technology advancements in synthesis methods.

What are the key skills and qualifications needed to thrive as a director of gene synthesis, and why are they important?

To thrive as a Director of Gene Synthesis, you need advanced expertise in molecular biology, genetics, and biotechnology, typically supported by a Ph.D. and years of leadership experience in related fields. Familiarity with DNA synthesis technologies, automation platforms, LIMS, and bioinformatics tools is essential, as well as knowledge of regulatory standards. Strong leadership, project management, and communication skills are critical for guiding teams, managing complex projects, and collaborating with stakeholders. These skills ensure the efficient delivery of high-quality gene synthesis products while driving innovation and compliance within the organization.

What are popular job titles related to Director Gene Synthesis jobs?

For Director Gene Synthesis jobs, the most frequently searched job titles are:

Infographic showing various Director Gene Synthesis job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, 1% Temporary, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Senior Analyst, Quality Control Analytical

Alameda, CA • On-site

GeneFab
See more jobs at GeneFabexternal

$60 - $80/hr

Other

Posted 29 days ago

Job description

Genefab is seeking an experienced analyst to join its Quality Control Analytical group. In this role, you will support the GMP QC testing at GeneFab, with a focus on testing, method transfer, qualification, troubleshooting and investigations.

Responsibilities
  • Provide technical expertise (SME).
  • Provide technical support to Analytical Development and QC Analytical Operations as needed.
  • Develop, implement, and update all Quality Control SOPs, testing records and other documentation needed for cGMP compliance.
  • Perform QC testing on in-process and final product samples to support release and stability testing.
  • Lead and perform technical root-cause investigations for aberrant results and deviations relating to analytical methods.
  • Lead and train junior employees to ensure testing procedures and practices comply with all applicable regulations and procedures.
  • Plan, lead, and execute analytical method transfers, qualifications, and validations.
  • Draft, Review, and Approve Method Transfer Protocols and Reports
  • Generate and review procedures, protocols and reports.
  • Proactively identify areas for continuous improvement in processes and procedures and lead these initiatives.
  • Collaborate closely with Interdepartmental MSAT, ASAT, and Manufacturing groups to support, execute, and/or provide oversight in the execution of method optimization, characterization, troubleshooting, transfer, and qualification
  • Perform additional duties as assigned
Requirements
  • B.S. degree in biology or related field with experience in cell therapy, immunology, cancer biology, or a closely related field.
  • Minimum of 5+ years of GMP/QC Laboratory experience.
  • Demonstrated ability to collaborate and work in cross-functional teams.
  • Strong organizational skills and attention to detail
  • Strong time management skills with a proven ability to meet deadlines
  • Strong analytical and problem-solving skills
  • Experience with relevant technologies such as: multicolor flow cytometry, cell culture (e.g., aseptic techniques, cell line expansion), multiplexed immunoassay, qPCR, and dPCR methods, Luminex, and ELISA.
  • Experience in GMP.
  • Experience with contract laboratories and or CDMO is a plus
  • Knowledge related to laboratory information management systems (LIMS) and electronic lab notebook record keeping (ELN) is a plus
  • Proficient in MS Word, Excel, Project, and PowerPoint
  • Experience with cell therapy or gene therapy is a plus
  • Availability to work extended hours such as evenings or weekends to meet deadlines when necessary
  • Comfortable in a fast-paced environment with minimal direction and able to adjust workload based on changing priorities
  • Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of the initial job description
  • Able to lift up to 40 pounds

$45 - $55 an hour

About GeneFab

GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.

We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.

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