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Quality Control Stability Analyst Jobs (NOW HIRING)

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 ...

Quality Control Analyst

Monroe, NC · On-site

$22.25 - $30/hr

Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in ... Provide information, data for evaluation and execution of stability study as per Quality and ...

Quality Control Analyst

Bridgewater, NJ

$24.50 - $33/hr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

Quality Control Analyst

Bridgewater, NJ · On-site

$90K - $210K/yr

Write stability protocol and stability reports * Write and revise Quality Control Standard ... reviewing applications, analyzing resumes, or assessing responses and identifying potential ...

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 ...

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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QC Analyst

Miami, FL

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

QC Analyst

Miami, FL · On-site

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

QC Analyst

Miami, FL

$23 - $30.75/hr

The QC Analyst I - is an entry-level role in the analytical Quality Control responsible for ... stability, cleaning verification samples following written procedures and applicable SOPs, to ...

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Quality Control Stability Analyst information

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

As of Jul 1, 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 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 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 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.

Is QC analyst a stressful job?

A Quality Control Stability Analyst role can be stressful due to strict regulatory standards, the need for precision, and tight deadlines. The job often requires attention to detail, analytical skills, and familiarity with laboratory tools, which can contribute to work pressure but also offers a structured environment.

Is QC a high paying job?

Quality Control Stability Analysts typically earn salaries that are competitive within the manufacturing and pharmaceutical industries, with pay often increasing with experience and certifications. While not usually among the highest-paying roles, it can offer a stable income, especially for those with specialized skills or in regulated environments.

What does a quality control analyst do?

A quality control stability analyst monitors and evaluates the stability of pharmaceutical or manufacturing products over time to ensure they meet quality standards. They perform tests, analyze data, and document results, often using laboratory equipment and software, to confirm product consistency and compliance with regulations.

How much is the salary of a QA analyst?

The salary of a Quality Control Stability Analyst typically ranges from $50,000 to $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. The role often requires knowledge of laboratory testing, stability studies, and regulatory compliance.

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.
More about Quality Control Stability Analyst jobs
What cities are hiring for Quality Control Stability Analyst jobs? Cities with the most Quality Control Stability Analyst job openings:
What states have the most Quality Control Stability Analyst jobs? States with the most job openings for Quality Control Stability Analyst jobs include:
Infographic showing various Quality Control Stability Analyst job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 91% Full Time, 3% Part Time, and 4% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $58,065 per year, or $27.9 per hour.

Specialist, Quality Control Analytical

NKW NantKwest Inc

El Segundo, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
Work with a collaborative team with the ability to work across different areas of the company.
Ability to join a growing company with professional development opportunities.

Position Summary

The Specialist, Quality Control Analytical will serve as Subject Matter to advise testing laboratories on method development, method validation, method transfer, and quality investigations. Primary duties will include data review and troubleshooting of analytical test methods.

Essential Functions

  • Author, review and revise documentation (SOPs, test methods, analytical method development, method validation, method transfer protocols/ reports, product specifications)
  • Review QC stability and lot release data (data integrity check) and CoAs issued by contract testing laboratories and create batch release certificate of analysis
  • Author and review laboratory OOS investigation and invalid laboratory test result, including filing internal Quality Systems reports as applicable.
  • Issue ImmunityBio release Certificates of Analysis (CoAs) to support QA lot disposition activities.
  • Author, review and revise Analytical Section of documents such as the IND, BLA for regulatory CMC submission
  • Provide technical expertise to troubleshoot analytical methods
  • Mange suppliers change notifications and change controls
  • Generate Purchase Requests and Purchase Orders for contract testing laboratories projects
  • Ensure timely escalation of quality control related issues
  • Assist QC-Analytical management in tracking and trending data
  • Collaborate with other departments (e.g. QA and Regulatory) for quality control related duties
  • Attend QC-Analytical internal meetings and external meetings with contract testing laboratories
  • May conduct other duties, as assigned
  • Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.

Education & Experience

  • Bachelor's degree with 6+ years relevant experience in Analytical Chemistry or related discipline required; or
  • Master's degree with 4+ years of experience in Analytical Chemistry or related discipline required.
  • Experience in method development, method validation, method transfer, lot release tests, stability programs and specification development required

Knowledge, Skills, & Abilities

  • Strong knowledge of quality control analytical method development, method validation and method transfer.
  • Strong technical writing skills to author SOPs, analytical tests methods, qualification/validation protocols/ reports.
  • Knowledge and understanding of USP, EP and ICH guidelines.
  • In-depth knowledge of GMPs and pharmaceutical regulations.
  • Ability to communicate effectively with internal functions both in writing and verbally.
  • Ability to collaborate with contract testing laboratories, consultants, ensuring compliance with company procedures.
  • Ability to multi-task and prioritize.
  • Strong problem solving and computer skills.

Working Environment / Physical Environment

  • This position works on-site.
  • Regular work schedule is Monday - Friday, within standard business hours. Flexibility is available with manager approval.
  • Flexibility in working schedule, i.e., off-hours, second shift, and weekends.
  • Exposure to onsite in-lab environment.
  • Must be able to don and wear Personal Protective Equipment (PPE) as required.
  • Lifting, standing, climbing, bending, grasping, sitting, pulling, pushing, stooping, stretching, and carrying are generally required to perform the functions of this position.
  • Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
  • Must be able to lift frequently lift up to 35 pounds and occasionally lift/move 50 pounds.

This position is eligible for a discretionary bonus and equity award. The hourly base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$42.85 (entry-level qualifications) to $47.12 (highly experienced) per hour

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability Healthcare and Dependent Care Flexible Spending Accounts 401(k) Retirement Plan with Company Match 529 Education Savings Program Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks Paid Time Off (PTO) includes: 11 Holidays Exempt Employees are eligible for Unlimited PTO Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.