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Remote Gxp Systems Jobs in California (NOW HIRING)

Remote Gxp Systems information

What are the key skills and qualifications needed to thrive as a Remote GxP Systems Specialist, and why are they important?

To thrive as a Remote GxP Systems Specialist, you need a strong understanding of GxP regulations (such as GMP, GLP, and GCP), quality assurance principles, and experience in life sciences or pharmaceutical environments, often supported by a relevant degree. Familiarity with validated computerized systems, compliance software (e.g., Veeva Vault, TrackWise), and certifications like Certified Quality Auditor (CQA) are highly valuable. Excellent attention to detail, problem-solving skills, and strong remote communication abilities help you effectively manage compliance tasks and collaborate with global teams. These skills ensure that regulated systems meet stringent quality standards and regulatory requirements, minimizing compliance risks for the organization.

What are some common challenges faced by professionals working in remote GxP systems roles, and how can they be addressed?

One common challenge in remote GxP systems roles is maintaining clear communication and coordination across distributed teams, especially when ensuring compliance with regulatory standards. Professionals often need to navigate time zone differences, secure data handling, and remote validation processes. These challenges can be addressed by using robust project management tools, regular virtual meetings, and secure collaboration platforms. Establishing clear documentation and protocols also helps ensure compliance and smooth workflows while working remotely.

What is the difference between Remote Gxp Systems vs Remote Quality Assurance Specialist?

AspectRemote Gxp SystemsRemote Quality Assurance Specialist
CertificationsGxP-related certifications (e.g., GxP, CSV)ISO, GxP, or QA certifications
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, or healthcare sectors
Industry UsageCommon in pharmaceutical and biotech companiesWidespread in healthcare, manufacturing, and software
Job FocusEnsuring GxP compliance in systems and processesQuality assurance and process validation

Remote Gxp Systems roles focus on maintaining GxP compliance within regulated industries, while Remote Quality Assurance Specialists concentrate on overall quality processes across various sectors. Both roles require similar certifications and often overlap in industry usage, but their primary focus differs: Gxp Systems emphasizes system compliance, whereas QA Specialists focus on quality assurance practices.

What are Remote GxP Systems?

Remote GxP systems refer to software or technological platforms used to manage Good Practice (GxP) compliance activities—such as Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and Good Manufacturing Practice (GMP)—from a remote or offsite location. These systems enable organizations in regulated industries, like pharmaceuticals and biotechnology, to securely access, monitor, and control quality and compliance data without being physically present on site. Remote GxP systems often include features for electronic records, audit trails, and real-time collaboration to ensure regulatory standards are consistently met, even when teams are distributed.
What are the most commonly searched types of Gxp Systems jobs in California? The most popular types of Gxp Systems jobs in California are:
What are popular job titles related to Remote Gxp Systems jobs in California? For Remote Gxp Systems jobs in California, the most frequently searched job titles are:
What job categories do people searching Remote Gxp Systems jobs in California look for? The top searched job categories for Remote Gxp Systems jobs in California are:
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Infographic showing various Remote Gxp Systems job openings in California as of July 2026, with employment types broken down into 5% Locum Tenens, 10% Internship, 14% As Needed, 61% Full Time, 4% Part Time, and 6% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution.

Manager/ QA Associate, GxP Quality Systems

Ionis Pharmaceuticals

Carlsbad, CA • On-site, Remote

$70K - $102K/yr

Full-time

Posted 10 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!

MANAGER/ QA ASSOCIATE, GxP QUALITY SYSTEMS

SUMMARY: 

Ionis is seeking a Manager / QA Associate, GxP Quality Systems, to support compliance across Ionis quality systems. This role is responsible for supporting the planning, execution, and oversight of GMP and GxP quality assurance activities and ensuring alignment with applicable domestic and international regulatory requirements, industry guidelines, and Ionis quality management system procedures.

CORE RESPONSIBILITIES: 

  • Support QMS processes and workflows to ensure procedures, records, and practices remain aligned with applicable regulatory requirements, GMP and GxP expectations, and Ionis policies and SOPs.
  • Generate, trend, and present QMS metrics to management and cross-functional stakeholders; identify compliance risks, performance gaps, and continuous improvement opportunities.
  • Lead and participate in cross-functional initiatives that strengthen quality system compliance, effectiveness, inspection readiness, and operational efficiency.
  • Support Quality Management Review activities, including data collection and analysis, development of presentation materials, facilitation support, documentation of actions, and follow-up on commitments.
  • Support inspection readiness activities, including coordination of preparation efforts, review of inspection support materials, response tracking, and follow-up on regulatory commitments.
  • Support execution of the vendor management program, including supplier, CMO, and CTL audit support, internal audit activities, and vendor change notifications.
  • Support new quality initiatives and company-wide projects that require significant QA partnership and resources.
  • Contribute to the design and implementation of corporate quality and continuous improvement programs.

REQUIREMENTS: 

  • Bachelor’s degree in a science-related or other relevant discipline required.
  • Strong understanding of quality assurance and quality management, with 3+ years of relevant experience required.
  • Strong understanding of quality systems guidelines and regulatory requirements applicable to the pharmaceutical or biotechnology industry required.
  • Familiarity with artificial intelligence applications in a GxP quality assurance or quality systems environment is highly desirable.
  • Strong customer orientation, written and verbal communication skills, and pragmatic problem-solving skills required.

Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS004063

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 $70,844 to $102,371

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

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