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Stability Analyst Jobs (NOW HIRING)

Moderna Therapeutics

$25.50 - $34.50/hr

As a QC Analyst, you will also support global GMP stability programs through a variety of operational and technical activities, including sample set downs, pulls, shipments, data trending and ...

Ercot

Operations Stability Engineer 3

Taylor, TX

$70K - $94K/yr

... stability issues, and appropriately reports findings and recommendations ... Level 3: * Designs and performs steady-state analyses and dynamic contingency analyses using power ...

Moderna Therapeutics

$25.50 - $34.50/hr

Perform routine and advanced analytical chemistry and stability testing, including HPLC, UPLC, GC, UV, Dynamic Light Scattering (particle analysis), and Karl Fischer (KF) * Execute HPLC (AEX) and ...

Ercot

Operations Stability Engineer 2

Taylor, TX · On-site

$70K - $94K/yr

... stability issues, and appropriately reports findings and recommendations ... Level 3: * Designs and performs steady-state analyses and dynamic contingency analyses using power ...

Vaxcyte

Stability Manager

San Carlos, CA

$147K - $171K/yr

Summarize vaccine stability results by applying analytical testing expertise to ensure scientific and technical excellence. Utilize statistical software like JMP to perform rigorous statistical ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

Summarize vaccine stability results by applying analytical testing expertise to ensure scientific and technical excellence. Utilize statistical software like JMP to perform rigorous statistical ...

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Stability Analyst information

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$73.3K

$130K

How much do stability analyst jobs pay per year?

As of Jun 8, 2026, the average yearly pay for stability analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

What is a Stability Analyst?

A Stability Analyst is a professional who evaluates the stability and shelf life of pharmaceutical products, chemicals, or other materials. They design, conduct, and analyze stability studies to ensure products remain effective and safe throughout their intended shelf life. Their work involves monitoring changes in physical, chemical, and microbiological properties under various environmental conditions. Stability Analysts play a critical role in regulatory compliance and product quality assurance.

What jobs make $1,000,000 a year?

In the field of stability analysis, high-paying roles such as senior risk managers, quantitative analysts, or chief risk officers in finance or large corporations can earn close to or exceeding $1,000,000 annually, especially with bonuses and incentives. These positions typically require advanced degrees, extensive experience, and strong analytical skills, often involving complex modeling and regulatory compliance.

What are some common challenges faced by Stability Analysts in coordinating cross-functional teams during product stability studies?

Stability Analysts often work closely with teams from quality control, manufacturing, and regulatory affairs to ensure accurate and timely stability testing. A common challenge is aligning schedules and priorities among different departments, especially when handling multiple projects simultaneously. Effective communication and proactive project management are essential to minimize delays and ensure compliance with regulatory guidelines. Building strong working relationships and maintaining clear documentation can help Stability Analysts navigate these challenges successfully.

What jobs pay $3,000 a day?

High-paying jobs that can reach $3,000 a day often include specialized roles such as senior financial analysts, certain consulting positions, or highly experienced software engineers, especially those working as contractors or in freelance capacities. These roles typically require advanced skills, certifications, or extensive experience, and may involve project-based or contract work with high hourly or daily rates.

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

To thrive as a Stability Analyst, you need a solid background in chemistry, pharmaceutical sciences, or a related field, typically supported by a relevant degree and experience in laboratory environments. Familiarity with analytical techniques such as HPLC, GC, and stability testing protocols, along with knowledge of regulatory guidelines like ICH, is essential. Strong attention to detail, problem-solving abilities, and clear documentation skills help ensure accuracy and regulatory compliance. These competencies are important for reliably assessing product stability, maintaining quality standards, and supporting the safe release of pharmaceutical products.
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Stability Analyst jobs near you

Stability Associate

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

Job description

Job Description Header:
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Stability Associate in Boca Raton, FL!
Job Title: Stability Associate
Job Description:
Position Summary:
The Stability Associate is responsible for executing stability studies of plasma-derived biopharmaceutical products in a cGMP environment. Areas of focus are planning and executing studies, managing study inventory, and scheduling and performing stability pulls. Additional stability related support activities include writing protocols, monitoring and trending data, and writing stability reports.
Essential Functions (ES) and Responsibilities:
  • Responsible for all day-to-day activities of the Quality Control Stability program:
    • Plans and executes stability studies.
    • Manages stability inventories.
    • Schedules and performs stability pulls.
    • Monitors the completion of test data.
    • Performs data verification for stability reports.
    • Supports the management of temperature-controlled chambers.
  • Supports and assists in all other aspects of the Quality Control Stability program as needed:
    • Preparation and revision of technical documentation for department areas of responsibility such as Procedures, Stability Protocols, Specifications, etc.
    • Perform and interpret statistical analysis of trends by linear regression, ANCOVA, and control charting using appropriate data analysis software.
    • Preparation and revision of stability data reports with adherence to regulatory and company guidelines.
    • Preparation of thorough change controls and investigations for quality systems.
  • Possesses expertise and guides others in cGMP and cGDP practices in documentation and execution of job functions.

Competencies
Ability to follow the cGMP's and procedures with great attention to detail
Able to work in high-pressure, deadline-driven environment
Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
Possess time management skills and be able to balance multiple job assignments at once
Possesses excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations
Education & Experience Requirements:
Education Requirements:
A bachelor's or master's degree in Biology, Chemistry, Mathematics, or a related scientific field is required.
Experience Requirements:
  • Requires at least 1 - 3 years of experience in a regulated laboratory setting, and previous work experience in a regulated environment (FDA, EPA, etc.).
  • Must be familiar with GLP and GMP guidelines.
  • Must have working knowledge of trending and/or stability analysis in a regulated environment.
  • Ensures compliance with all regulatory requirements by verifying procedures are being followed, all recordkeeping is current, proper maintenance occurs, and new requirements are identified as they arise.
  • Effectively communicates critical stability and quality related information to appropriate teams.
  • Is a subject matter expert for areas of responsibility for internal and external customers and participates in internal and external audits.
  • Identifies opportunities for and participates in continuous improvements to increase efficiency and compliance.
  • Performs, reviews, and trains on processes performed within the QC department.
  • Assists in other QC, regulatory support, and data analysis functions, as assigned by the Manager.
  • Analyzes issues and exercises judgment within defined procedures to determine appropriate resolution to problems.
  • Reports on non-standard problems with area management.
  • Is familiar with Standard Operating Procedures (SOP) writing procedures.

Preferred Experience:
Working knowledge of stability program requirements in a regulated environment preferred.
Compliance Requirements (ES):
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
Job Description Footer:
In addition to competitive compensation, we offer a comprehensive benefits package including:
  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance
  • Company paid STD and LTD
  • Company Paid Holidays
  • 3 Weeks' Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)
  • Easily accessible to Tri-RailFree shuttle to the Boca Tri-Rail station

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
ADMA Biologics is an Equal Opportunity Employer.

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