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Stability Biologics Jobs (NOW HIRING)

Integrated Resources

Stability Associate

Waltham, MA · On-site

Minimum 2 years of direct experience in stability/formulation of biological and/or small molecule products in the Pharmaceutical industry, with 5-8 years industry experience. Skills Required:

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 ...

WuXi Biologics

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have ... Supports the QC Operations group in RS/Stability/inventory management. Essential Job Functions

WuXi Biologics

Scientist I, QC

Cranbury, NJ · On-site

$60K - $96K/yr

WuXi Biologics' achievements are a direct result of the efforts made by our employees. We have ... Supports the QC Operations group in RS/Stability/inventory management. Essential Job Functions

Herbalife

Manager, Stability

Torrance, CA · On-site

Education • Bachelor of Science degree in Chemistry, Biochemistry, Biology, Microbiology, or a related scientific discipline. Experience • 7+ years • Demonstrated experience with stability ...

Herbalife

Manager, Stability

Torrance, CA · Hybrid

Education • Bachelor of Science degree in Chemistry, Biochemistry, Biology, Microbiology, or a related scientific discipline. Experience • 7+ years • Demonstrated experience with stability ...

Herbalife

Manager, Stability

Torrance, CA · Hybrid

Education Bachelor of Science degree in Chemistry, Biochemistry, Biology, Microbiology, or a related scientific discipline. Experience 7+ years Demonstrated experience with stability protocol ...

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How much do stability biologics jobs pay per hour?

As of Sep 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 is 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 the key skills and qualifications needed to thrive as a stability biologist?

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 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 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.

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Stability Biologics jobs near you
Infographic showing various Stability Biologics job openings in the United States as of September 2026, with employment types broken down into 75% Full Time, and 25% Temporary. Highlights an 100% In-person job distribution, with an average salary of $52,986 per year, or $25.5 per hour.

Stability Associate

Waltham, MA • On-site

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Full-time

Re-posted 19 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Title: Stability Associate

Duration: 6 Months (Temp to perm)

Location: Waltham, MA. 02451

Position Summary:

  • Support operational and technical aspects of clinical/commercial drug substance, drug product, reference standard, and placebo GMP stability programs.
  • Ensure compliance and support of company Standards, Practices, and SOPs as well as ICH and FDA guidelines.
  • This includes design of stability protocols, expiry dating for clinical/commercial products, providing stability sections for regulatory submissions, technical assessment of stability data, specification changes and investigations, routinely working with CMO/CLOs to ensure timelines are met for release and stability testing of product.

Key Responsibilities:

  • Designs and manages studies. Collaborates with CLOs to ensure proper testing and reporting of stability samples.
  • Assigns expiry to drug substance, drug product, and reference standard
  • Trends and evaluates stability data proactively.
  • Authors' stability reports for regulatory submissions.
  • Participates in meetings and contributes toward the goals of the CMC. Contributes to major/critical manufacturing and leads stability investigations (deviations, OOS, cross-site and cross-functional).
  • Authors stability assessments writing for basic Anomalous Results (ARs) and Out of Trend (OOT) stability results.
Qualifications

Minimum Qualifications:

  • BS or MS degree in science (Analytical Chemistry, Biochemistry, Biology, Chemistry, Organic Chemistry, Pharmaceutical Chemistry, Protein Chemistry) or related technical field.
  • Minimum 2 years of direct experience in stability/ formulation of biological and/or small molecule products in the Pharmaceutical industry, with 5-8 years industry experience.

Skills Required:

  • Knowledge of analytical methods, ICH Guidelines, and strong ability to analyze data.
  • Good understanding of statistical analysis and interpretation of data.
  • Proficiency with cGMPs and experience with Microsoft Office (Word, Excel, and PowerPoint) and SAS JMP are required.
  • Strong technical writing skills and communication skills are essential
Additional Information

Kind Regards,

Sabanaaz Shaikh

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Gold Seal JCAHO Certified for Health Care Staffing

"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)


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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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