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Chemistry Editor Jobs (NOW HIRING)

GSK

Scientist, Oligonucleotide Synthesis

Cambridge, MA · On-site

$96K - $160K/yr

ASO, siRNA, SSO, RNA Editors). Preferred Qualification If you have the following characteristics, it would be a plus: * MS with 2+ years or above in Oligonucleotide synthesis and/or Chemistry and/or ...

bakelite

QA Chemist - Taylorsville

Taylorsville, MS · On-site

PowerPoint - presentation creation/editing). * Experience working as part of a multifunctional team ... Bachelor's degree or higher in chemistry. * Strong knowledge and skills in organic and polymer ...

bakelite

QA Chemist - Taylorsville

Taylorsville, MS · On-site

PowerPoint - presentation creation/editing). * Experience working as part of a multifunctional team ... Bachelor's degree or higher in chemistry. * Strong knowledge and skills in organic and polymer ...

bakelite

QA Chemist - Taylorsville

Taylorsville, MS · On-site

PowerPoint - presentation creation/editing). * Experience working as part of a multifunctional team ... Bachelor's degree or higher in chemistry. * Strong knowledge and skills in organic and polymer ...

bakelite

QA Chemist - Taylorsville

Taylorsville, MS · On-site

PowerPoint - presentation creation/editing). * Experience working as part of a multifunctional team ... Bachelor's degree or higher in chemistry. * Strong knowledge and skills in organic and polymer ...

Mass General Brigham

Postdoctoral Fellows

Boston, MA · On-site

$53K - $72K/yr

D. or equivalent in chemistry, bioengineering, chemical engineering, materials science, polymer ... In vitro and in vivo efficacy studies, including expression, knockdown, or editing readouts

Massgeneralbrigham

Postdoctoral Fellows

Boston, MA · On-site

$53K - $72K/yr

D. or equivalent in chemistry, bioengineering, chemical engineering, materials science, polymer ... In vitro and in vivo efficacy studies, including expression, knockdown, or editing readouts

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$47K

$109.9K

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How much do chemistry editor jobs pay per year?

As of Aug 16, 2026, the average yearly pay for chemistry editor in the United States is $109,863.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $142,000.00 per year, depending on experience, location, and employer.

What does a chemistry editor do?

A Chemistry Editor reviews, edits, and manages scientific content related to chemistry for accuracy, clarity, and consistency. They work with researchers, writers, and publishers to refine manuscripts, ensure proper use of scientific terminology, and adhere to editorial guidelines. Their role may also involve fact-checking, formatting references, and staying updated on scientific advancements.

What are the key skills and qualifications needed to thrive as a chemistry editor?

To thrive as a Chemistry Editor, you need a comprehensive understanding of chemical sciences, excellent written communication skills, and a degree in chemistry or a related field, often at the graduate level. Familiarity with reference management software, manuscript submission platforms, and scientific style guides such as ACS or APA is typically required. Strong attention to detail, critical thinking, and effective collaboration make a candidate stand out. These skills are essential to ensure the accuracy, clarity, and integrity of scientific content while facilitating smooth communication between authors, reviewers, and publishers.

What are some common challenges faced by chemistry editors in their daily work?

Chemistry Editors often face the challenge of balancing tight publication deadlines with the need to thoroughly review and edit complex scientific manuscripts. Interpreting technical jargon, addressing inconsistencies, and ensuring compliance with journal or publisher guidelines can be demanding, especially when working with international contributors. Editors must also mediate between authors and peer reviewers to resolve conflicting feedback or requests for clarification. Successfully managing these challenges requires a blend of subject matter expertise, diplomacy, and organizational skills, but it also offers the rewarding experience of contributing to the advancement of scientific knowledge.

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Chemistry Editor jobs near you
Infographic showing various Chemistry Editor job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 72% Full Time, 22% Part Time, 1% Temporary, and 3% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $109,863 per year, or $52.8 per hour.

Senior Scientist / Senior Engineer, LNP Process Development

Prime Medicine

Cambridge, MA

$100K - $136K/yr

Full-time

Posted 28 days ago

Job description

Prime Medicine was founded to bring the promise of gene editing to patients. We use Prime Editing, a next-generation technology that can "search and replace" to restore normal genetic function almost anywhere in the genome. Prime Editing searches to find the precise place in the genome to edit and replace the segment of faulty DNA with a correct copy of DNA. A single Prime Editor can correct the individual mutations found across patients, meaning Prime Editing can potentially address more than 90 percent of known disease-causing genetic mutations.

We envision a world where this technology can cure, halt, and ultimately prevent genetic diseases, providing lifelong benefits to patients. Prime Medicine offers the opportunity to shape the future of gene editing and transform how medicines are used to treat disease.

Position Summary

The Senior Scientist / Senior Engineer, LNP Process Development will provide technical leadership for the development, characterization, and scale-up of robust, scalable lipid nanoparticle (LNP) formulation and drug product manufacturing processes. This individual will be responsible for driving LNP process development - spanning formulation, process optimization and characterization, scale-up, and technology transfer support for key pipeline assets.

Key Responsibilities

Technical Leadership & Process Development

  • Lead the design, execution, and optimization of LNP processes to accommodate novel formulations and drug product manufacturing processes (LNP mixing and tangential flow filtration [TFF]) from bench through GLP/GMP scale, with emphasis on developing robust and scalable processes
  • Serve as a subject matter expert for LNP process development across programs and therapeutic areas, partnering with Research, Platform, Hematology, and other teams to translate novel modalities into developable drug products
  • Evaluate and implement emerging technologies, novel materials, delivery and process innovations that continuously improve delivery efficiency, drug product quality, manufacturability, and cost of goods
  • Support technology transfer activities to external contract development and manufacturing organizations (CDMOs), including preparation of tech transfer packages, on-site execution support (Person-in-Plant), and process troubleshooting
  • Author and contribute to Chemistry, Manufacturing, and Controls (CMC) sections of regulatory filings, briefing books, and regulatory responses related to LNP drug product
  • Maintain impeccable documentation using electronic lab notebooks (ELNs); generate experimental protocols, development reports, technology transfer packages, SOPs, and technical reports to support clinical development
  • Communicate complex technical information clearly through presentations, written reports, and everyday collaboration to diverse audiences including cross-functional stakeholders and external partners

Qualifications & Experience

  • Ph.D. in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences, Materials Science, or a related discipline with 8+ years of relevant industrial experience in LNP process development and formulation development; M.S. with 12+ years
  • Demonstrated expertise in LNP formulation processes, TFF operations, and related characterization methods
  • Hands-on experience with LNP delivery and formulation development, process scale-up from bench to GLP/GMP scale, and technology transfer to GMP facilities and/or CDMOs
  • Strong proficiency in analytical characterization techniques (HPLC/UPLC, DLS/SLS, TEM, DSC, SAXS, UV-Vis, fluorescence spectrophotometry) to support process development
  • Experience with statistical design of experiments (DoE) and knowledge of Quality by Design (QbD) methodologies
  • Hands-on experience with defining and setting up equipment systems for LNP and TFF processes
  • Knowledge of CMC regulatory requirements and experience contributing to IND/CTA submissions
  • Excellent communication skills, with the ability to effectively collaborate cross-functionally, prioritize activities to meet program goals, and present complex technical information to diverse audiences
  • Highly self-motivated with strong organizational skills, the ability to manage competing priorities, and a hands-on approach to problem-solving

Apply