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Stability Biologics Jobs (NOW HIRING)

Moderna, Inc.

Sr. Manager, CMC Stability

Norwood, MA · On-site

Experience supporting stability programs for biologics, vaccines, or other complex drug products in either development/clinical or commercial settings. * Experience authoring or contributing to ...

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $140K/yr

Manage stability studies, draft stability protocols and report, coordinate and perform sample ... biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and ...

Forge Biologics

Statistician (Scientist I)

Columbus, OH · On-site

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is ... stability studies through trend analysis, control charting, and regression modeling Assist in data ...

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Stability Biologics information

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How much do stability biologics jobs pay per hour?

As of Jun 18, 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.
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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.
Sr. Scientist, Downstream and Biologics Formulation Development

Sr. Scientist, Downstream and Biologics Formulation Development

Avid Bioservices

Tustin, CA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
Avid is seeking a highly motivated and technically strong Sr. Scientist, Downstream and Biologics Formulation Development to lead biologics formulation development while contributing to integrated downstream process development within a fast-paced, client-facing environment. This role is responsible for defining formulation strategies, executing technical studies, and supporting cross-functional integration as the capability expands. Additional responsibilities include designing downstream purification processes for protein-based biologics, viral clearance studies, scale-down and scale-up activities, and technology transfer to manufacturing. The individual will collaborate closely with Cell Line Development, Upstream Process Development, Analytical Sciences, MSAT, DS/DP Manufacturing, Program Management, and external partners to support client programs.
Key Responsibilities:
  • Lead formulation development for biologics, including pre-formulation assessments, excipient screening, and stability studies. Demonstrated experience in formulation development for complex biologic modalities-including antibody-drug conjugates (ADCs)-with understanding of modality-specific stability and developability challenges is highly advantageous.
  • Lead downstream process development for biologics, including capture chromatography, polishing chromatography, viral inactivation/filtration, and tangential flow filtration (TFF).
  • Extensive hands-on experience with analytical techniques for protein characterization, including DLS, DSF, SEC, CE, rheology, and spectroscopy. Design and interpret analytical testing strategies including HPLC (SEC & IEX), CE-SDS, SDS-PAGE, UV spectroscopy, and other biophysical assays to support process development and formulation studies.
  • Expertise in developing high concentration protein formulations and resolving issues such as aggregation, viscosity, and solubility. Able to identify and mitigate formulation risks including precipitation and chemical degradation.
  • Design experiments, analyze data, and prepare technical protocols, reports, and development summaries.
  • Establish and drive scientific strategy, workflows, and best practices for early- to late-stage biologics formulation development, with the ability to operate independently in a dynamic, fast-paced, client-facing environment with evolving priorities.
  • Serve as a technical subject matter expert (SME) in client engagements, including proposals, presentations, and project reviews; prior line management or informal leadership experience is advantageous.
  • Collaborate effectively with cross-functional teams to align project timelines, priorities, and resource planning.
  • Mentor and develop junior scientists and technical staff, and support onboarding of new team members.
  • Evaluate and implement new technologies and platform approaches to enhance internal capabilities and drive innovation.
  • Ensure compliance with applicable quality, regulatory, and safety standards.
  • Perform additional responsibilities as required to support evolving business and project needs.
  • Occasional travel may be required (by land or air) to attend conferences, seminars, off-site client meetings, and marketing events as needed.
Minimum Qualifications:
  • Master's degree/PhD degree in Biochemistry, Chemistry, or related field and minimum 4-6 years of relevant experience and demonstrated working knowledge of scientific principles.
  • Prior experience in formulation development, stability studies, and analytical characterization of biologics or strong background in biochemical and biophysical characterization of proteins with deep understanding of protein structure and function.
  • Experience in development of ultra-high concentration and pre-developability assessment
  • Proven record of strong technical writing and communication skills.
  • Ability to thrive in a dynamic, cross-functional environment.
Preferred Qualifications:
  • Ph.D. in Biochemistry, Chemistry, or related field with 4-6 years of industry experience, or M.S. with 6-10 years of experience.
  • Prior experience in formulations process development and/or downstream process development of biologics is a plus.
  • Experience mentoring or leading scientific staff preferred.
  • Candidates with strong expertise in either biologics formulation development or downstream process development will be considered, with opportunities to contribute across both areas.
Position Type/Expected Hours of Work:
This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00am to 5:00pm PST unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.
Compensation:
We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
The compensation range for this role is $147,200-$184,000annually depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
Who you are:
  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Physical Demands & Work Environment:
In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.
Employment Type: Full-Time

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