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Remote Document Control Jobs in Temecula, CA (NOW HIRING)

ABB

Protection and Control Engineer

Carlsbad, CA · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

While this is a full remote position, there is preference for candidates located in the Northern ... Develop engineering documentation and perform analyses-such as schematics, logic diagrams, layouts ...

RQ Construction

Project Architect

Carlsbad, CA · On-site +1

$100K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... documentation, code compliance, quality control, and project coordination. Experience with DoD ... Hybrid schedule (in-office Monday-Wednesday; optional remote (Thursday-Friday) * Comprehensive ...

Dudek

As-Needed Land Surveying CAD Technician

Encinitas, CA · On-site +1

$38 - $47.50/hr

Follow written instructions, technical documentation, and QA/QC standards accurately * Adapt to ... This job operates in a remote or office-based environment and this role routinely uses standard ...

Dudek

Land Surveying CAD Technician

Encinitas, CA · On-site +1

$38 - $47.50/hr

Follow written instructions, technical documentation, and QA/QC standards accurately * Adapt to ... This job operates in a remote or office-based environment and this role routinely uses standard ...

Dudek

Land Surveying CAD Technician

Encinitas, CA · On-site +1

$38 - $47.50/hr

Follow written instructions, technical documentation, and QA/QC standards accurately * Adapt to ... This job operates in a remote or office-based environment and this role routinely uses standard ...

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Remote Document Control information

See Temecula, CA salary details

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How much do remote document control jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for remote document control in Temecula, CA is $21.59, according to ZipRecruiter salary data. Most workers in this role earn between $17.21 and $24.86 per hour, depending on experience, location, and employer.

What does a remote document control do?

As a Remote Document Control specialist, you can expect to be responsible for maintaining and organizing digital files, ensuring proper version control, and distributing documents to relevant stakeholders on schedule. You'll frequently review documents for accuracy and compliance with company or industry standards, manage access permissions, and keep detailed records of document revisions. Collaboration with project managers, engineers, or other departments is common, often requiring proactive communication via email or project management platforms. This role demands a high degree of organization and the ability to adapt quickly to changing priorities in a virtual team environment.

What is a remote document control?

A Remote Document Control job involves managing, organizing, and maintaining digital documents and records for a company while working from a remote location. Responsibilities typically include document version control, ensuring compliance with company policies and regulatory requirements, and facilitating document access for relevant teams. Professionals in this role use document management systems (DMS) and collaboration tools to streamline workflows and maintain data integrity. Strong attention to detail, organizational skills, and knowledge of industry-specific regulations are essential. This role is common in industries such as healthcare, engineering, manufacturing, and legal services.

What are the key skills and qualifications needed to thrive in remote document control, and why are they important?

To excel as a Remote Document Control professional, you need strong organizational abilities, attention to detail, and experience with document management procedures, often supported by relevant experience or a degree in business administration or a related field. Familiarity with document control software (such as SharePoint, DocuSign, or Aconex) and knowledge of regulatory standards or ISO certifications are commonly required. Excellent communication, time management, and problem-solving skills are essential soft skills for collaborating across remote teams and meeting deadlines. These competencies ensure accurate document processing, regulatory compliance, and smooth coordination in distributed work environments.

What are the most commonly searched types of Document Control jobs in Temecula, CA?

The most popular types of Document Control jobs in Temecula, CA are:

What are popular job titles related to Remote Document Control jobs in Temecula, CA?

For Remote Document Control jobs in Temecula, CA, the most frequently searched job titles are:

What job categories do people searching Remote Document Control jobs in Temecula, CA look for?

The top searched job categories for Remote Document Control jobs in Temecula, CA are:

What cities near Temecula, CA are hiring for Remote Document Control jobs?

Cities near Temecula, CA with the most Remote Document Control job openings:

Remote Document Control jobs near you
Infographic showing various Remote Document Control job openings in Temecula, CA as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% Remote job distribution, with an average salary of $44,908 per year, or $21.6 per hour.

Senior Scientist, Analytical Development & Quality Control (ADQC)

Ionis Pharmaceuticals

Carlsbad, CA • On-site, Remote

$113K - $150K/yr

Full-time

Re-posted 6 days ago

Job description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We’re pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs.  With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.

At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees. 

With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive. 

We’re building on our rich history, and we believe our greatest achievements are ahead of us. If you’re passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!

SENIOR SCIENTIST, ANALYTICAL DEVELOPMENT & QUALITY CONTROL (ADQC)

SUMMARY: 

Seeking an experienced analytical chemist to join our Analytical Development & Quality Control (ADQC) group at the Senior Scientist level. The ideal candidate will be familiar with a broad range of analytical chemistry techniques, possess a strong work ethic and strong technical background, demonstrate excellent oral and written communication skills, and have experience working in a GMP environment. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail.

RESPONSIBILITIES:

  • Develop and validate analytical methods for Starting Materials and peptides
  • Characterize new reference standards by a variety of analytical techniques
  • Conduct routine and non-routine analysis of Raw and Starting Material samples
  • Document and compile data for quality review
  • Review data for compliance to specifications
  • Conduct analytical investigations
  • Author scientific reports and portions of the CMC section of regulatory filings
  • Author SOPs as needed (e.g., analytical methods, equipment procedures, and material specifications)
  • Present at internal and cross-functional scientific meeting

REQUIREMENTS:

  • Ph.D. in Analytical Chemistry or related discipline with at least 2 years of industry experience
  • Skilled in developing methods using LC-MS, HPLC, and GC
  • Good understanding of the drug development process
  • Practical knowledge of GMP requirements, with hands-on GMP experience preferred
  • Familiarity with ICH and FDA method validation guidelines, including phase-appropriate strategies
  • Ability to problem solve, manage priorities and maintain aggressive timelines for multiple projects
  • Ability to work productively and independently within a team or matrix environment
  • Excellent written and verbal communication skills

Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition #IONIS003987

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits

Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits

The pay scale for this position is $113,856 to $150,241

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

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