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Remote Quality Control Auditor Jobs in California

Prismatik

Document Control Specialist

Irvine, CA · On-site +1

$23 - $25/hr

Working closely with Engineering, Quality, Regulatory, and Manufacturing, you'll help drive ... Ensures accurate and timely input of database entries; implements a self-auditing system to verify ...

Fieldguide

Audit Methodology Lead

San Francisco, CA · On-site +1

$185K - $230K/yr

Ensure methodologies and customizations are implemented with appropriate quality control rigor ... Strong expertise in AICPA auditing standards (GAAS), PCAOB and audit methodology * Experience with ...

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Remote Quality Control Auditor information

What does a remote quality control auditor do?

A Remote Quality Control Auditor is responsible for evaluating and ensuring the quality of products, services, or processes from a remote location. They review documents, data, or recorded transactions to verify compliance with company standards and regulatory requirements. Using digital tools, they identify discrepancies, recommend improvements, and report findings to management. This role is essential in maintaining high-quality standards while allowing flexibility to work from home or other remote locations.

What are the key skills and qualifications needed to thrive as a remote quality control auditor?

To thrive as a Remote Quality Control Auditor, you need a solid understanding of quality assurance principles, auditing procedures, and typically a relevant degree such as in business, engineering, or a related field. Familiarity with quality management systems (like ISO 9001), audit software, and data analysis tools is often essential, along with industry-recognized certifications such as Certified Quality Auditor (CQA). Critical thinking, attention to detail, and effective written and verbal communication are standout soft skills for this role. These skills ensure accurate assessments, consistent compliance, and clear reporting while working independently in a remote setting.

How do remote quality control auditors typically collaborate with on-site teams to ensure compliance and accuracy?

Remote Quality Control Auditors often work closely with on-site teams through virtual meetings, shared documentation systems, and regular progress updates. While they may not be physically present, auditors use digital tools to review process data, monitor compliance, and provide feedback. Establishing clear communication channels and building relationships with on-site personnel are key to resolving discrepancies and upholding quality standards. Regular collaboration ensures that audits are thorough and any issues are addressed promptly, maintaining the integrity of quality control processes.

What is the difference between Remote Quality Control Auditor vs Remote Quality Assurance Specialist?

AspectRemote Quality Control AuditorRemote Quality Assurance Specialist
CertificationsISO, Six Sigma, industry-specific auditsISO, Six Sigma, process improvement certifications
Work EnvironmentAuditing products/services remotely, reviewing complianceDeveloping and implementing quality processes remotely
Industry UsageManufacturing, healthcare, software testingManufacturing, healthcare, software development

Both roles focus on quality but differ in scope. Remote Quality Control Auditors primarily verify compliance through audits, while Remote Quality Assurance Specialists develop and improve quality systems. Understanding these distinctions helps job seekers target the right position based on their skills and career goals.

What cities in California are hiring for Remote Quality Control Auditor jobs?

Cities in California with the most Remote Quality Control Auditor job openings:

Senior Scientist, Analytical Development & Quality Control (ADQC)

Carlsbad, CA • On-site, Remote

Ionis Pharmaceuticals
Biotechnology Research and Development • 201 - 500 employees
Learn more about Ionis Pharmaceuticalsexternal

$113K - $150K/yr

Full-time

Re-posted 3 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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