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Senior Scientific Editor Jobs in Riverside, CA (NOW HIRING)

Our specialized experience includes design for data centers, healthcare, science and technology ... Review and editing of project specifications with minor assistance. * Proficient knowledge of ...

Mid-Level Plumbing Engineer

Tustin, CA · On-site

$93K - $117K/yr

Our specialized experience includes design for data centers, healthcare, science and technology ... Review and editing of project specifications with minor assistance. * Proficient knowledge of ...

Mid-Level Plumbing Engineer

Tustin, CA · On-site

$93K - $117K/yr

Our specialized experience includes design for data centers, healthcare, science and technology ... Review and editing of project specifications with minor assistance. * Proficient knowledge of ...

Mechanical Engineer

Tustin, CA · On-site

$70K - $110K/yr

Our specialized experience includes design for data centers, healthcare, science and technology ... General knowledge of project specifications and editing techniques. * General knowledge of ...

Mechanical Engineer

Tustin, CA · On-site +1

$70K - $110K/yr

Our specialized experience includes design for data centers, healthcare, science and technology ... General knowledge of project specifications and editing techniques. * General knowledge of ...

Showing results 21-40

Senior Scientific Editor information

See Riverside, CA salary details

$38.6K

$86.7K

$125.7K

How much do senior scientific editor jobs pay per year?

As of Aug 22, 2026, the average yearly pay for senior scientific editor in Riverside, CA is $86,706.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,800.00 and $109,000.00 per year, depending on experience, location, and employer.

What does a senior scientific editor do?

A Senior Scientific Editor reviews, edits, and manages scientific manuscripts to ensure clarity, accuracy, and adherence to publication standards. They work closely with authors, peer reviewers, and editorial teams to guide manuscripts through the publication process. Their responsibilities may include evaluating scientific content, providing feedback to improve research presentation, overseeing journal sections, and maintaining high editorial standards. Senior Scientific Editors often have advanced degrees in scientific fields and significant experience in academic publishing. They play a critical role in ensuring the quality and integrity of scientific literature.

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

To thrive as a Senior Scientific Editor, you need a strong background in scientific research, excellent editing and writing skills, and typically an advanced degree (such as a PhD) in a relevant scientific field. Familiarity with reference management software, manuscript tracking systems, and publication standards (like AMA, APA, or journal-specific guidelines) is essential. Outstanding attention to detail, critical thinking, and the ability to communicate complex concepts clearly are vital soft skills for this role. These skills ensure the accuracy, clarity, and integrity of scientific publications, contributing to effective communication within the scientific community.

What are some common challenges faced by senior scientific editors when managing the peer review process?

Senior Scientific Editors often encounter challenges such as balancing timely manuscript decisions with maintaining high editorial standards. Coordinating communication among authors, reviewers, and editorial board members can require strong organizational skills and diplomacy, especially when handling conflicting reviewer feedback or sensitive revisions. Additionally, staying current with developments in the relevant scientific field and ensuring ethical guidelines are upheld throughout the review process are key responsibilities that demand continuous learning and attention to detail.

What is the difference between Senior Scientific Editor vs Scientific Writer?

AspectSenior Scientific EditorScientific Writer
CredentialsAdvanced degree in science, editing experienceDegree in science or related field, writing skills
Work EnvironmentAcademic, publishing, research organizationsPharmaceutical, biotech, research institutions
Employer & IndustryScientific journals, publishers, research institutesPharmaceutical companies, research firms, agencies
Primary FocusEditing, ensuring scientific accuracy, quality controlCreating scientific content, reports, manuscripts

While both roles require scientific knowledge, Senior Scientific Editors focus on reviewing and refining scientific content for accuracy and clarity, often overseeing publication quality. Scientific Writers primarily produce scientific documents, reports, and articles. The roles complement each other but differ in responsibilities and focus areas within the scientific communication process.

What are the most commonly searched types of Scientific Editor jobs in Riverside, CA?

The most popular types of Scientific Editor jobs in Riverside, CA are:

What are popular job titles related to Senior Scientific Editor jobs in Riverside, CA?

For Senior Scientific Editor jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Senior Scientific Editor jobs in Riverside, CA look for?

The top searched job categories for Senior Scientific Editor jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Senior Scientific Editor jobs?

Cities near Riverside, CA with the most Senior Scientific Editor job openings:

Infographic showing various Senior Scientific Editor job openings in Riverside, CA as of June 2026, with employment types broken down into 100% Full Time. Highlights an 71% In-person, and 29% Remote job distribution, with an average salary of $86,706 per year, or $41.7 per hour.

Sr. Specialist, Quality Systems

Avid Bioservices

Tustin, CA • On-site

$42.69 - $53.36/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 27 days ago


Job description

Description
Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The role of the Sr. Specialist, Quality Systems, is to provide technical review of Quality Management System discrepancy reports and CAPAs. In this role, you will participate in the generation and revision of controlled and project documents, perform assigned tasks and work to achieve company goals and department objectives and provide visible leadership to the organization that will instill operational best practices, a team-oriented work environment and productive results to the organization.
  • Author, review, edit, and approve discrepancy reports including, but not limited to, reports for deviations, calibration exceptions, out-of-specification (OOS) results, and out-of-limit (OOL) results; ensure discrepancy reports meet procedural and regulatory requirements, including requirements for root cause analysis and impact assessment.
  • Author, review, edit, and approve CAPA records; ensure CAPA records meet procedural and regulatory requirements.
  • Author, review, edit, and approve controlled documents including, but not limited to, standard operating procedure (SOPs), forms, and BPRs.
  • Participate in the generation and revision of controlled and project documents; author, review, edit, and approve controlled documents (including procedures, methods, and forms related to quality systems and to manufacture and testing of product) and project documents (including protocols and reports related to development, validation, and stability).
  • Interact with interdepartmental contacts on discrepancy reports, CAPA records, controlled documents, and other Quality topics; represent Quality on multi-disciplinary teams.
  • Maintain a state of inspection readiness; participate in inspection preparation activities.
  • Provide assistance to internal and external customers in support of departmental functions.
  • Collaborate with Management to establish and meet targets and timelines.
  • Independently manage competing priorities with limited instruction.
  • Follow company policies and procedures.
  • Perform other duties as assigned by management.

Minimum Qualifications:
  • B.A. or B.S. degree (preferably in a life sciences field)
  • Minimum of 4-5 years of experience in the biopharmaceutical industry (preferably with biologics).
  • Knowledge of cGMPs or equivalent regulations.
  • Ability to interpret Quality standards for implementation.
  • Skills to independently evaluate situations and propose potential solutions.
  • Ability to interpret Quality standards for implementation.
  • Excellent technical writing and editing skills.
  • Progressive experience with deviation records.
  • Experience using quality systems software (quality management systems and/or electronic document management systems)

Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days of work are Monday through Friday, 8:00am to 5:00pm PST unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $42.69 to $53.36 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.