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Associate Editor Jobs in San Ramon, CA (NOW HIRING)

Critical Mass

Associate Creative Engineer

San Jose, CA · On-site

As an Associate Creative Engineer, you are skilled in digital design at high scale. You will work ... Working knowledge of building and editing Keynote & PowerPoint decks * A hands-on, execution driven ...

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All JobsAssociate Editor JobsAssociate Editor Jobs in San Ramon, CA

Associate Editor information

See San Ramon, CA salary details

$15

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$53

How much do associate editor jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for associate editor in San Ramon, CA is $30.46, according to ZipRecruiter salary data. Most workers in this role earn between $24.42 and $34.13 per hour, depending on experience, location, and employer.

What are some common challenges an Associate Editor might face when balancing multiple projects and deadlines?

Associate Editors often juggle several articles or publications at once, each with its own timeline and set of contributors. A common challenge is prioritizing tasks effectively to meet tight deadlines while maintaining editorial quality and accuracy. This role requires strong organizational skills and clear communication with writers, senior editors, and other team members to ensure everyone is aligned. Developing efficient workflows and being adaptable to sudden changes—such as urgent revisions or shifting editorial calendars—are essential for success in this fast-paced environment.

What is the difference between Associate Editor vs Copy Editor?

AspectAssociate EditorCopy Editor
Required CredentialsBachelor's degree, experience in editing or publishingBachelor's degree, strong language and grammar skills
Work EnvironmentEditorial teams in publishing, media, or academic settingsPublishing houses, magazines, online media
Employer & Industry UsageUsed in publishing, journalism, academic publishingCommon in editing, publishing, media industries
Primary FocusContent acquisition, editorial decision-making, overseeing projectsGrammar, style, clarity, and correctness of text

While both roles are vital in publishing, an Associate Editor typically handles content selection and editorial oversight, whereas a Copy Editor focuses on refining language, grammar, and style. The Associate Editor often manages multiple projects and collaborates with writers, while the Copy Editor ensures the final text is polished and error-free.

What does an Associate Editor do?

An Associate Editor is responsible for supporting the editorial process at a publication or media outlet. Their tasks usually include reviewing submissions, editing articles for clarity and accuracy, coordinating with writers and contributors, and helping manage deadlines. Associate Editors often assist in shaping content strategy and may contribute their own writing as well. They work closely with senior editors to ensure the quality and consistency of published materials.

What are the key skills and qualifications needed to thrive as an Associate Editor, and why are they important?

To excel as an Associate Editor, you need strong writing, editing, and research skills, often backed by a degree in English, journalism, or a related field. Familiarity with content management systems (CMS), style guides (like AP or Chicago), and editing software is typically required. Attention to detail, organization, and effective communication are crucial soft skills for managing deadlines and collaborating with writers. These abilities ensure content accuracy, quality, and timely publication in a fast-paced editorial environment.
What are the most commonly searched types of Editor jobs in San Ramon, CA? The most popular types of Editor jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Associate Editor jobs? Cities near San Ramon, CA with the most Associate Editor job openings:
Associate Editor jobs near you
Infographic showing various Associate Editor job openings in San Ramon, CA as of June 2026, with employment types broken down into 56% Full Time, 28% Part Time, and 16% Contract. Highlights an 84% In-person, and 16% Remote job distribution, with an average salary of $63,351 per year, or $30.5 per hour.

Scientist II, mRNA Research & Production

Profluent

Emeryville, CA

Other

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

Job description

Profluent is seeking a highly motivated Scientist II to drive mRNA production and process development for our customized base editor programs. This is a hands-on, lab-based role focused on the synthesis, purification, characterization, and optimization of research-grade mRNA for high-throughput screening, cell-based assays, and scaled production for mouse studies.

This individual will serve as the technical lead for Profluent's internal mRNA production core function, bridging molecular design and high-quality material generation for in vitro and in vivo studies. The successful candidate will bring strong experience with IVT-based mRNA production, template preparation, purification, analytics, troubleshooting, and workflow optimization, as well as the ability to coordinate and mentor a small team executing routine production and analytical workflows.

The role will initially focus on customized base editor mRNAs and will expand over time to support additional programmable genome engineering modalities, including engineered recombinases and other RNA-delivered therapeutic systems.

Responsibilities 

  • Lead and execute end-to-end research-grade automated mRNA production workflows, including template preparation, plasmid DNA sequencing data analysis, linearization, IVT, capping or cap analog workflows, nucleotide modification, purification, buffer exchange, storage, and batch release for research use
  • Design mRNA (5'/3' UTR, coding sequence, modifications, etc.) to improve protein yield, activity, and specificity using established and cutting-edge methodology 
  • Manage and mentor a small mRNA production core function, helping coordinate production schedules, train team members, review batch quality, and maintain reliable material delivery to R&D teams
  • Partner with payload engineering, delivery, in vivo pharmacology, bioanalytics, and translational teams to ensure mRNA materials are fit-for-purpose for platform and program needs
  • Produce high-quality mRNA for rapid screening of customized base editors in cell-based assays, as well as scaled batches to support mouse studies, assay development, and early translational experiments
  • Improve IVT and purification workflows to increase yield, purity, consistency, turnaround time, and functional performance while minimizing impurities such as dsRNA, abortive transcripts, truncated products, residual template DNA, endotoxin, and other process-related contaminants
  • Implement and interpret fit-for-purpose mRNA analytical assays, including concentration, integrity, transcript purity, size distribution, dsRNA, residual DNA, endotoxin, and functional expression or potency readouts
  • Use analytical platforms such as Fragment Analyzer, TapeStation, Bioanalyzer, gel or capillary electrophoresis, HPLC/UPLC, dsRNA ELISA, endotoxin assays, qPCR/ddPCR, and cell-based assays to characterize mRNA quality
  • Engage and coordinate CROs for production and analytics
  • Maintain clear SOPs, batch records, analytical summaries, sample inventories, and production documentation to support reliable material handoff and reproducible workflows
  • Analyze production and analytical data to troubleshoot batch failures, identify process trends, and recommend improvements to quality, speed, and robustness
  • Support mRNA production workflows for emerging programmable genome engineering modalities, including engineered recombinases, as Profluent's platform and portfolio evolve

Qualifications 

  • PhD, MS, or BS in molecular biology, biochemistry, chemical engineering, bioengineering, biotechnology, pharmaceutical sciences, or a related discipline, with relevant industry experience in mRNA production, RNA process development, nucleic acid manufacturing, or related areas
  • PhD with 2-3 years relevant experience, MS with 10+ years, or BS with 12+ years of relevant experience 
  • Deep hands-on experience with IVT-based mRNA production and the technical challenges of generating high-quality RNA for in vitro and in vivo studies
  • Experience with plasmid or DNA template preparation, linearization, IVT, capping or cap analog workflows, nucleotide modification, mRNA purification, and product characterization
  • Strong understanding of mRNA quality attributes, process-related impurities, IVT performance, purification strategies, stability, storage, and the relationship between mRNA quality and biological performance
  • Experience producing mRNA for discovery-stage screening and scaling for in vivo preclinical rodent studies
  • Experience with modified nucleotides, cap analogs, enzymatic capping, polyA strategies, UTR/codon/design-variable screening, or RNA design-for-potency and manufacturability
  • Experience coordinating, training, mentoring, or managing research associates or technical team members in a production, process development, core-lab, or high-throughput R&D environment
  • Experience with preparative chromatography, TFF, bead-based purification, buffer exchange, or other mRNA purification approaches
  • Strong technical judgment, attention to detail, and ability to independently troubleshoot production and analytical workflows
  • Excellent organizational and communication skills, including experience maintaining SOPs, batch records, analytical summaries, and clear technical documentation
  • Ability to work effectively with cross-functional teams in a fast-paced R&D environment

Preferences

  • Experience supporting genome editing, base editing, gene writing, engineered recombinases, mRNA/LNP therapeutics, RNA medicines, gene therapy, cell therapy, or other advanced therapeutic modalities
  • Experience with automation-compatible workflows, including deep-well plates, magnetic bead cleanup, KingFisher instruments, liquid handlers, or LIMS-like sample tracking systems
  • Familiarity with LNP formulation interfaces, RNA buffer compatibility, freeze-thaw considerations, storage stability, and downstream delivery-performance impacts
  • Familiarity with GMP readiness, IND-enabling supply strategy, raw material strategy, plasmid supply, enzyme/cap/nucleotide sourcing, quality systems, or CMC planning for RNA therapeutics

What We Offer

  • High-growth opportunity with meaningful impact on the future of protein design
  • Competitive compensation package with equity participation
  • 401(k) with a strong employer match
  • Comprehensive benefits including health/dental/vision insurance
  • Generous PTO policy and commitment to work-life balance
  • Professional development opportunities in a cutting-edge field at the intersection of AI and biology

Profluent Bio, Inc is an equal opportunity employer promoting diversity and inclusion in the workspace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical conditions, veteran status, sexual orientation, gender (including gender identity and gender expression), sex (which includes pregnancy, childbirth, and breastfeeding), genetic information, taking or requesting statutorily protected leave, or any other basis protected by law.

Work Authorization Requirement

Applicants must have ongoing work authorization in the United States that does not require employer sponsorship. Sponsorship will not be provided now or at any time in the future for this position.

Employment Eligibility Verification

Legal authorization to work in the United States is required. In compliance with federal law, all persons hired must verify their identity and work eligibility and complete the required employment verification form upon hire.

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