ZipRecruiter

Log In

1

Stability Biologics Jobs (NOW HIRING)

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$134K - $162K/yr

We embody our collectively audacious goal to courageously make the most complex biologics ever ... Primary responsibility will include managing stability studies for individual projects and ...

Vaxcyte

Stability Manager

San Carlos, CA · On-site

$147K - $171K/yr

Demonstrated proficiency and expertise in various analytical methodologies, particularly in the context of stability testing and assessment of biologics or vaccines. * Solid understanding of relevant ...

Abzena Inc.

QC Stability Manager

San Diego, CA · On-site

With extensive experience in developing biologics and bioconjugates, we offer a seamless service ... The QC Stability Manager is responsible for leading and supporting GMP large-molecule stability ...

Novartis

Senior Expert Stability

East Hanover, NJ

$118K/yr

Knowledge of Biologics and/or Gene therapy testing methods, validation and qualification. * Knowledge of ICH, specifically stability guidelines. * Excellent oral and written communication skills with ...

next page

Showing results 1-20

All JobsStability Biologics Jobs

Stability Biologics information

See salary details

$14

$25

$48

How much do stability biologics jobs pay per hour?

As of Jun 19, 2026, the average hourly pay for stability biologics in the United States is $25.47, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $29.57 per hour, depending on experience, location, and employer.

What are the risks of stability biologics?

Stability biologics professionals handle biologic products that can pose risks such as contamination, degradation, or instability during storage and handling. These risks can lead to reduced efficacy or safety issues if proper quality control, aseptic techniques, and storage conditions are not maintained. Ensuring compliance with regulatory standards and proper training helps mitigate these risks in the role.

What is stability biologics used for?

Stability biologics involves studying the stability and shelf life of biological products such as vaccines, proteins, and antibodies. It helps ensure these products remain effective and safe during storage and transportation, often requiring specialized testing and quality control measures. Professionals in this field analyze factors like temperature, pH, and formulation to optimize product stability.

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

To thrive as a Stability Biologist, you need a solid background in biology, chemistry, or pharmaceutical sciences, often with a relevant degree. Familiarity with laboratory equipment, stability testing protocols, and regulatory guidelines such as ICH is crucial, along with experience using LIMS (Laboratory Information Management Systems). Strong analytical thinking, attention to detail, and effective communication skills help ensure accurate data interpretation and reporting. These competencies are vital for maintaining product quality and compliance with regulatory standards in pharmaceutical development.

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

AspectStability BiologicsQuality Control Analyst
Required CredentialsBachelor's degree in biology, biochemistry, or related field; experience in biologics manufacturingBachelor's degree in life sciences; experience in lab testing and quality assurance
Work EnvironmentBiotech manufacturing facilities, laboratories, quality assurance teamsLaboratories, testing facilities, quality assurance departments
Employer & Industry UsageBiotech companies, biologics manufacturing firmsPharmaceutical companies, biotech firms, contract labs

Stability Biologics professionals focus on product stability testing and formulation, while Quality Control Analysts primarily perform lab testing to ensure product quality. Both roles require similar educational backgrounds and work in biotech or pharmaceutical environments, but their specific responsibilities differ within the product development and quality assurance processes.

What jobs pay 2000 a day?

Jobs in highly specialized fields such as certain consulting roles, executive positions, or freelance professionals like surgeons, anesthesiologists, or top-tier lawyers can pay around $2,000 per day. These roles typically require advanced skills, certifications, or extensive experience, and often involve high-pressure environments or significant responsibility.

What are Stability Biologics?

Stability Biologics refers to a company that specializes in the development, manufacturing, and distribution of biologic products, particularly those used for tissue repair and regenerative medicine. These biologics include allografts and tissue-based products that support healing in orthopedic, spine, and wound care applications. The company ensures that these products maintain their safety, efficacy, and integrity through rigorous quality control and stability testing processes. Stability Biologics works closely with healthcare providers to supply innovative solutions that enhance patient outcomes.

What are some common challenges faced by professionals working in stability biologics, and how can they be addressed?

Professionals in stability biologics often encounter challenges such as managing complex testing protocols, adhering to strict regulatory requirements, and handling the variability of biological samples over time. Ensuring accurate data collection and interpretation is critical, particularly when products may behave unpredictably under different storage conditions. These challenges can be addressed by maintaining clear documentation, staying up-to-date with regulatory guidance, collaborating closely with quality assurance teams, and leveraging validated analytical methods to ensure consistency and compliance throughout the stability study process.

What is the most stable job to have?

In the field of stability biologics, roles such as process development scientists and quality assurance specialists tend to be more stable due to the ongoing demand for biologic therapies and regulatory compliance. These positions often require specialized skills, certifications, and consistent industry growth, contributing to job stability.
More about Stability Biologics jobs
What cities are hiring for Stability Biologics jobs? Cities with the most Stability Biologics job openings:
What states have the most Stability Biologics jobs? States with the most job openings for Stability Biologics jobs include:
What job categories do people searching Stability Biologics jobs look for? The top searched job categories for Stability Biologics jobs are:
Stability Biologics jobs near you
Infographic showing various Stability Biologics job openings in the United States as of June 2026, with employment types broken down into 3% Internship, 77% Full Time, 7% Part Time, 3% Temporary, 7% Contract, and 3% Nights. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $52,986 per year, or $25.5 per hour.

Stability Associate

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 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.

Apply