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Stability Biologics Jobs (NOW HIRING)

Stability Manager

San Carlos, CA ยท 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 ...

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 ...

Scientist 2 - Stability

Rockville, MD ยท On-site

$71K - $132K/yr

As a Stability Scientist 2, your activities will support stability programs for a wide set of ... D. in scientific discipline (e.g., Chemistry, Biochemistry, Biology, etc.) with 1+ years of ...

QC Stability Manager

San Diego, CA ยท On-site

$120K - $150K/yr

With extensive experience in developing biologics and bioconjugates, we offer a seamless service ... As the QC Stability Manager , you will lead a high-performing Quality Control team responsible for ...

Associate degree in Chemistry, Biology, or a related scientific discipline, or equivalent laboratory experience. * 1 to 3 years of laboratory experience supporting analytical testing or stability ...

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Stability Biologics information

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How much do stability biologics jobs pay per hour?

As of Jul 9, 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 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 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.
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:
Infographic showing various Stability Biologics job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $52,986 per year, or $25.5 per hour.
Stability Manager

Stability Manager

Vaxcyte

San Carlos, CA โ€ข On-site

$134K - $162K/yr

Full-time

Re-posted 21 days ago


Job description

Join our Mission to Protect Humankind!
Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance.
WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values:
*RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered.
*AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind.
*LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives.
*MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making.
Summary:
Vaxcyte is looking for an energetic and talented individual to join Vaxcyte's Vaccine Product Development organization as a Stability Manager within the Quality Control Unit. The primary function of this level position is to manage the stability program for various projects in preclinical and clinical development.
The position will be an integral part of the team implementing and maintaining cGMP Stability for all phases of clinical development. Primary responsibility will include managing stability studies for individual projects and stability data analysis. This individual will collaborate with QC members in a highly collaborative and cross-functional environment. The ideal candidate will apply strong stability experience, ensure compliant operations and documentation, foster open communication, and pursue data-driven approaches.
Essential Functions:
  • Designs, coordinate, and execute stability studies for early and late-stage vaccine products according to regulatory guidelines and company protocols.
  • Summarize vaccine stability results by applying analytical testing expertise to ensure scientific and technical excellence. Utilize statistical software like JMP to perform rigorous statistical analyses, ensuring robust interpretation of data and adherence to regulatory standards.
  • This includes, but not limited to, creating, implementing, and managing stability databases, performing data trending and statistical analysis, study and testing forecasting and reporting of metrics, creation, revision and approval of SOP's, stability protocols and reports in accordance with current GMP, FDA, EU, Global and ICH guidelines and regulations.
  • Produce impactful PowerPoint presentations to effectively communicate stability data to diverse project team members. Support the attainment of project milestones by facilitating stability monitoring and determining expiration dates for clinical and in-process materials.
  • Authors, reviews, revises, and approves SOP's, stability protocols and reports, memo's, regulatory and specification documents (as required).
  • The Stability Manager will also assist with leading the functionality and maintenance of stability related processes and systems.
  • Drives continuous improvement activities for the clinical stability programs.
  • Ensures that the GMP stability program continuously aligns with FDA, ICH and other international agencies.
  • Manages Quality Systems records for QC Stability- creates, assesses, reviews Deviations, Change Controls, CAPA's and other applicable stability-related investigations and events.
  • Guide and work with others to identify opportunities for continuous improvement and implement/maintain solutions.
  • Provide strong teamwork in establishing a quality culture and shared accountability. Ensure GMP compliance is built into the design and implementation of processes and systems, including tracking metrics to monitor and improve performance.

Requirements:
  • MS or BS with minimum of 8 years of industry experience in Pharma / Biotech industry required.Other combinations of education and/or experience may be considered.
  • Strong understanding of vaccine stability principles, including degradation pathways, accelerated stability testing, and shelf-life determination.
  • 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 FDA, EU, and ICH regulatory guidelines and pharmacopeia as applicable to stability study design, expiry dating, and analytical method qualification/validation for biologics and vaccines.
  • Solid understanding and hands-on experience of applying basic statistical tools for stability data trending and rate analysis to support retest period/ shelf-life proposals.
  • Attention to detail and excellent skills in record keeping / documentation.
  • Experience in IND, NDA and BLA submission is highly preferred.
  • Experience working in a regulated (GLP / GMP) environment.
  • Extensive technical writing experience.
  • Strong interpersonal skills; ability to communicate effectively both verbally and in written formats.
  • Solid understanding of product development activities in biotech/drug/vaccine development, including key interdependencies, and knowledge of proven development strategies and tactics.
  • Ability to work globally with CMOs in different countries and continents.

Reports to: Director, Stability
Location: San Carlos, CA
Compensation: The compensation package will be competitive and includes comprehensive benefits and an equity component.
Salary Range: $147,000 - $171,000 *(SF Bay Area). Salary ranges for non-California locations may vary.
We are 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, disability or veteran status.

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About Vaxcyte

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

San Carlos, CA, US

Year founded

2013