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Quality Control Stability Analyst Jobs (NOW HIRING)

DISCGENICS INC

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP ... Qualifies, maintains, and monitors stability chambers. * Qualified trainer for test methods

DISCGENICS INC

Quality Control Analyst

Salt Lake City, UT · On-site

$23 - $31/hr

The QC Analyst performs quality control analysis of raw material, and finished product using USP ... Qualifies, maintains, and monitors stability chambers. * Qualified trainer for test methods

Moderna Therapeutics

$25.50 - $34.50/hr

This role sits at the intersection of Quality Control Chemistry and global stability programs, driving the analytical backbone that ensures product quality and compliance. It combines hands-on ...

Lonza

QC Specialist III-Stability

Portsmouth, NH · On-site

The QC Specialist III serves as the primary Stability representative on Analytical Project Teams and works directly with customers, contract laboratories, and internal cross-functional teams. This ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$24.50 - $33/hr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

Cellares

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... analyzing resumes, or assessing responses. These tools assist our recruitment team but do not ...

Lonza

QC Specialist III-Stability

Portsmouth, NH

The QC Specialist III serves as the primary Stability representative on Analytical Project Teams and works directly with customers, contract laboratories, and internal cross-functional teams. This ...

Intellectt INC

QC Analyst

Lebanon, IN · On-site

$23 - $31/hr

Please feel free to share your updated resume at vyshnavi.t@intellectt.com Job Title: QC Analyst ... Experience with COAs, stability reports, SOPs * Good technical writing and communication skills ...

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How much do quality control stability analyst jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for quality control stability analyst in the United States is $27.92, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $31.01 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Quality Control Stability Analyst, and why are they important?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

What are some typical challenges faced by Quality Control Stability Analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.

What are Quality Control Stability Analysts?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What is the difference between Quality Control Stability Analyst vs Quality Control Analyst?

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

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Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in the United States as of May 2026, with employment types broken down into 97% Full Time, 1% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

Scientist, Quality Control Operation

WuXi Biologics

Cranbury, NJ • On-site

Full-time

Posted 14 days ago

Job description

Job Title - Scientist, Quality Control
Work Location - Cranbury, NJ
Job Summary:
The Scientist-QC Operations will be responsible for QC sample management, RS management, and QC stability study program to support QC GMP activities, including but not limited to in-time and properly sample/RS receiving, aliquoting, storage, and distribution for testing, and stability study protocol writing/reviewing/revising, stability sample receiving, aliquoting for stability study initiation, storage, pulling, aliquoting and distribution for testing in time and correctly to ensure on-time delivery of test results, validation data and other QC deliverables to internal and external clients. Also as inventory management QC GMP documentation archive backup to support QC inventory management and QC GMP documentation archive as needed. Strong communication, detail orientation, and time management skills are desired.
Responsibilities:
  • Responsible for QC sample management, including but not limited to receiving, storage, aliquoting, distributing, tracking, and disposing of QC testing sample and reference standards.
  • Responsible for stability sample management, including but not limited to sample receiving, aliquoting, distributing, tracking, and disposing of stability backup sample.
  • Responsible for reference standard (RS) management, including RS receiving, aliquoting, storage, and distribution.
  • Perform technical review of sampling plans, stability study protocols, RS aliquoting, qualification and re-qualification protocols.
  • Perform RS, regulatory retain sample, and stability samples annual inventory checking.
  • Coordinate with QC Functional Leads (QCFL) to ensure timely cleanup, reconciliation, and disposal of project-related stability and RS samples upon project completion.
  • Support QC lab inventory management, including but not limited to QC lab inventory ordering, receiving, storage, distribution, inventory tracking.
  • Ensure compliance with QC operation related documentation and training for company's requirements
  • Request sample/RS and stability management-related control paper forms and logbooks for sample storage refrigerators, freezers and chambers from QA as needed.
  • Responsible for maintenance of all refrigerators/freezers used for sample/RS/stability sample storage well organized and clean and responding to alarms and executing corrective actions to protect sample integrity.
  • Responsible for weekly in-process sample clean up and disposal.
  • Perform all activities in compliance with applicable safety policies, quality systems, and cGMP requirements.
  • Mentor junior QC operation staff and provide technical guidance and support.
  • Perform other duties assigned by management to support overall QC operations.
  • Qualifications:
  • Bachelor's degree: 4+ years of experience in the related professional field. Master's degree and above: 2+ years of experience in the related professional field.
  • Full-time undergraduate degree or above, majoring in biology, chemical engineering, chemistry, pharmacy or related majors.
  • Be skilled at reading, writing, and understanding GMP documentation.
  • Strong attention to detail and organizational skills
  • Good computer operation skills in Microsoft Word, Excel, PowerPoint etc.
  • Broad knowledge and experience in GMP regulations.
  • High awareness of confidentiality and responsibility.
  • Detail oriented and effective time management.
  • Critical thinking, scientific reasoning, planning and problem-solving skills.
  • Experience with a wide variety of software and information systems (e.g. LIMS, TrackWise, MC, etc.).
  • Be able to work independently as well as a good team player.

Salary range for this position is 60,200-96,300
Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

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