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Remote Pharmaceutical Quality Control Jobs (NOW HIRING)

Hui Huliau

Construction Quality Control Manager

OK · Remote

$85.50K - $113.60K/yr

The QC Manager is also required to attend all partnering meetings, conduct the QC meetings, perform ... remote work-sharing tools. Must be able to sit, stand, and work at a computer for long periods of ...

W3Global Inc.

Quality Control Inspector

Washington, DC · On-site +1

$90K - $125K/yr

Remote work may be considered for the right candidate, preferably within the Mid-Atlantic region. Most structural steel projects are located between New York and Virginia, so candidates within ...

Xometry

Virtual Quality Control Inspector

Lexington, KY · On-site +1

The successful candidate will interact with DFM Engineering, Manufacturing, Quality Control, Case ... Previous remote work experience a plus #LI-Hybrid Xometry is an equal opportunity employer. All ...

SANS Institute

PT Quality Control Analyst

Bethesda, MD · On-site +1

$41K - $46K/yr

What You'll Achieve at SANS We are seeking a Quality Control Analyst to join our Courseware ... Ability to communicate with remote team members clearly and precisely * Unrestricted authorization ...

SANS Institute

PT Quality Control Analyst

Bethesda, MD · Remote

What Youll Achieve at SANS We are seeking a Quality Control Analyst to join our Courseware ... Ability to communicate with remote team members clearly and precisely * Unrestricted authorization ...

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How much do remote pharmaceutical quality control jobs pay per hour?

As of May 30, 2026, the average hourly pay for remote pharmaceutical quality control in the United States is $45.67, according to ZipRecruiter salary data. Most workers in this role earn between $44.47 and $46.88 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Pharmaceutical Quality Control Specialist, and why are they important?

To thrive as a Remote Pharmaceutical Quality Control Specialist, you need a strong background in chemistry, biology, or pharmaceutical sciences, typically supported by a relevant degree and experience in quality assurance or laboratory settings. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practice (GMP) guidelines, and regulatory compliance certifications is essential. Attention to detail, strong analytical skills, and effective remote communication set outstanding professionals apart in this field. These skills ensure accurate product testing, regulatory compliance, and seamless collaboration across distributed teams, which are critical for patient safety and product integrity.

What are some common challenges faced by professionals working in remote pharmaceutical quality control roles?

One common challenge in remote pharmaceutical quality control is maintaining clear and consistent communication with on-site teams, especially when reviewing documentation or addressing deviations. Remote professionals may also encounter difficulties accessing physical samples or equipment, requiring strong coordination with in-house staff and effective use of digital tools. Staying updated on evolving regulatory standards and ensuring data security when handling sensitive information are also critical responsibilities. Successful remote quality control specialists often develop strong self-management and collaboration skills to overcome these challenges.

What is a Remote Pharmaceutical Quality Control specialist?

A Remote Pharmaceutical Quality Control specialist is a professional responsible for ensuring that pharmaceutical products meet required quality standards, but works from a location outside of the physical laboratory or manufacturing site. They typically analyze data, review documentation, and monitor compliance with regulations using digital tools and remote access to laboratory information systems. Their role may also include coordinating with on-site teams to address quality issues, conducting virtual audits, and maintaining records for regulatory agencies. Working remotely allows these specialists to contribute to product safety and efficacy while leveraging technology for efficient collaboration.

What is the difference between Remote Pharmaceutical Quality Control vs Remote Pharmaceutical Quality Assurance?

AspectRemote Pharmaceutical Quality ControlRemote Pharmaceutical Quality Assurance
CertificationsQC certifications, GMP trainingQA certifications, GMP compliance training
Work EnvironmentLaboratory testing, sample analysisProcess audits, documentation review
Industry UsageQuality testing roles in pharma companiesProcess and system oversight roles

Remote Pharmaceutical Quality Control focuses on testing and analyzing pharmaceutical samples to ensure product quality, while Remote Pharmaceutical Quality Assurance emphasizes overseeing processes, documentation, and compliance to maintain quality standards. Both roles require similar certifications and are integral to pharmaceutical manufacturing, but they differ in daily tasks and focus areas.

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Remote Pharmaceutical Quality Control jobs near you
Research Associate II, Analytical Development & Quality Control (ADQC)

Research Associate II, Analytical Development & Quality Control (ADQC)

Ionis Pharmaceuticals

Carlsbad, CA • On-site, Remote

$71.22K - $90.45K/yr

Full-time

Posted 19 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!

RESEARCH ASSOCIATE II, ANALYTICAL DEVELOPMENT & QUALITY CONTROL (ADQC)

SUMMARY: 

Seeking an experienced analytical chemist to join our Analytical Development & Quality Control (ADQC) group at the Research Associate II level. The ideal candidate will be familiar with HPLC and other 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:

  • Conduct routine and non-routine analysis of Raw and Starting material samples
  • Review analytical data for compliance to SOPs
  • Assemble and document data for quality review
  • Present and participate in internal and external scientific meetings
  • Revise and update SOPs as needed (e.g., analytical methods, equipment procedures, and material specifications)
  • Conducts analytical investigations
  • Applies knowledge of cGMP and GLP
  • May develop and/or optimize analytical methods
  • May author sections of scientific reports

REQUIREMENTS:

  • BS or MS degree in Chemistry or related field
  • 2+ years of experience in analytical development and quality control role
  • Practical knowledge of HPLC, MS, and GC, including operation of instrumentation
  • Familiarity with GMP requirements, with hands-on GMP experience preferred
  • Experience following SOPs and recording data in laboratory notebooks or data collection forms
  • Ability to interpret experimental results and demonstrate good judgement in resolving issues / making recommendations
  • Detail oriented with strong organizational skills
  • Excellent written and verbal communication skills
  • Ability to manage priorities and maintain aggressive timelines for multiple projects

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 $71,219 to $90,448

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

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

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