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Origin Biologics Jobs (NOW HIRING)

Eocene Environmental Group

Senior Biologist

Chico, CA · On-site

$43/hr

... origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

Eocene Environmental Group

Senior Biologist

Ukiah, CA · On-site

$43/hr

... origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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Showing results 41-60

All JobsOrigin Biologics Jobs

Origin Biologics information

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$29.5K

$100.5K

$117.5K

How much do origin biologics jobs pay per year?

As of Jul 24, 2026, the average yearly pay for origin biologics in the United States is $100,501.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,500.00 and $116,500.00 per year, depending on experience, location, and employer.

What jobs can I get with bioscience?

With a background in bioscience, you can pursue roles such as research scientist, laboratory technician, quality control analyst, or bioprocess engineer. These positions often require knowledge of laboratory techniques, data analysis, and sometimes specialized certifications or advanced degrees.

What does a typical workday look like at Origin Biologics?

A typical workday at Origin Biologics may involve conducting laboratory experiments, analyzing samples, documenting results, and collaborating closely with research scientists and quality assurance teams. The role often requires adherence to strict protocols and good laboratory practices to ensure safety and product reliability. You may also participate in team meetings to discuss project progress or troubleshoot technical issues. This dynamic environment encourages ongoing learning and teamwork, providing opportunities to develop new skills and contribute to innovative biologic products.

What is an Origin Biologics job?

An Origin Biologics job typically involves working with biological materials, such as human or animal-derived cells, tissues, or proteins, for medical and research applications. Employees in this field may engage in roles related to manufacturing, quality control, regulatory compliance, or research and development. These jobs require knowledge of biotechnology, laboratory procedures, and industry regulations to ensure the safety and efficacy of biological products.

What is a bioscience job?

A bioscience job involves working in the field of biological sciences, often focusing on research, development, or manufacturing related to health, medicine, or biotechnology. These roles typically require knowledge of laboratory techniques, scientific analysis, and sometimes specialized certifications or degrees in biology, biochemistry, or related fields.

What are the key skills and qualifications needed to thrive in the Origin Biologics position, and why are they important?

To thrive at Origin Biologics, you generally need a background in life sciences such as biology, biochemistry, or biotechnology, along with relevant laboratory experience. Familiarity with lab equipment, aseptic techniques, Good Manufacturing Practice (GMP), and industry-specific software or certifications like ISO 13485 is highly valued. Attention to detail, strong problem-solving abilities, and effective teamwork and communication skills are also essential. These competencies ensure accuracy, compliance, and efficiency while contributing to high-quality biologics research, development, or production.

More about Origin Biologics jobs
What cities are hiring for Origin Biologics jobs? Cities with the most Origin Biologics job openings:
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What states have the most Origin Biologics jobs? States with the most job openings for Origin Biologics jobs include:
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Origin Biologics jobs near you
Infographic showing various Origin Biologics job openings in the United States as of July 2026, with employment types broken down into 33% Full Time, 17% Part Time, 17% Temporary, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $100,501 per year, or $48.3 per hour.
Scientific Program Manager & Biologics SME

Scientific Program Manager & Biologics SME

Frontage Laboratories

Exton, PA • On-site

$60K - $66K/yr

Full-time

Medical, Dental, Life, Retirement

Posted 2 days ago

Job description

Scientific Program Manager & Biologics SME (Subject Matter Expert)

Fulltime

Exton, PA

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position Summary

The Scientific Program Manager & Biologics SME will serve as the primary scientific liaison for large molecule bioanalytical programs, including PK, immunogenicity (ADA), cell-based and non-cell-based neutralizing antibody (NAb) assays, and other complex ligand-binding and cell-based assay platforms.

This role combines scientific expertise and client-facing communication to drive successful execution of GLP, non-GLP, and clinical support studies within the Biologics Service group.

The position works closely with laboratory operations, quality assurance, program management, and business development teams to ensure technical excellence, regulatory compliance, and efficient delivery of high-quality data to sponsors.

Key Responsibilities:

Scientific Liaison & SME Support:

  • Present and introduce Biologics services to clients, including LBA-based assays for PK, ADA, NAb, and cell-based functional assays.
  • Provide scientific consultation during pre-clinical and clinical program design, including assay selection, format, feasibility, and method development strategy.
  • Serve as subject matter expert on large molecule assay performance, MRD, analytical range, cut-point strategy, validation parameters, and sample analysis workflow.

Program Management & Client Engagement:

  • Act as scientific point-of-contact for assigned programs; attend kickoff, alignment, troubleshooting, and result review meetings.
  • Coordinate with Program Management to ensure timelines, deliverables, and sponsor expectations are clearly communicated and met.
  • Prepare or review scientific sections of proposals, protocols, validation plans, and study reports.
  • Collaborate with lab supervisors and technical teams to troubleshoot assay challenges and implement scientific improvements.

Regulatory & Quality Compliance:

  • Familiar with appropriate regulatory frameworks, including FDA 21 CFR Part 58 (GLP)
  • Non-GLP discovery and early development programs.
  • Clinical sample testing requirements (GCP interface).
  • Partner with QA and Compliance on audits, data integrity requirements, documentation accuracy, and deviation investigations.

Qualifications:

Required

  • Master’s degree or higher in Biology, Biochemistry, Pharmaceutical Sciences, Immunology, or related field (PhD preferred but not required).
  • 5+ years of hands-on experience developing, validating, and troubleshooting large molecule assays, including PK (ligand-binding assays), ADA (screening, confirmatory, titration). Cell-based NAb assays.
  • Other functional / MOA-based cell assays.
  • Demonstrated knowledge of GLP regulations (21 CFR Part 58) and experience supporting non-GLP and clinical programs.
  • Strong ability to interpret complex scientific data and communicate clearly with internal teams and external sponsors.
  • Experience working in a CRO or regulated bioanalytical environment strongly preferred.

Preferred

  • Experience in a leadership or supervisory role.
  • Familiarity with BioA reporting structures, immunogenicity risk assessments, and cut-point strategies.
  • Experience interacting with regulatory agencies or contributing to submissions.

Competencies

  • Strong scientific communication and presentation skills.
  • Ability to lead projects cross-functionally and coordinate with operations, PM, BD, and QA.
  • Strategic problem-solving mindset with attention to detail.
  • Client-focused, collaborative, and able to operate in a fast-paced CRO environment.

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.