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Viral Vector Jobs (NOW HIRING)

Jj

Senior Manager, Vector Biology

Cambridge, MA · On-site

Manage a team of scientists and engineers focused on viral vector biology, vector design, and assay development * Oversee the team's work to improve lentiviral vector design and performance for in ...

Jj

Senior Scientist, Vector Biology

Cambridge, MA · On-site

$100K - $136K/yr

Take part in designing,modifying,optimizing,and screening viral envelopes/proteins to target ... Support the development of innovative vector analytical and characterization assays. * Contribute ...

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$30.5K

$102.3K

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How much do viral vector jobs pay per year?

As of Jun 19, 2026, the average yearly pay for viral vector in the United States is $102,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,000.00 and $135,500.00 per year, depending on experience, location, and employer.

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

To excel as a Viral Vector Scientist, you typically need a strong background in molecular biology, virology, or related life sciences, often supported by a relevant advanced degree. Familiarity with laboratory techniques such as cloning, cell culture, qPCR, viral purification, and use of tools like flow cytometry and bioreactors is essential, with certifications in biosafety being advantageous. Strong attention to detail, problem-solving skills, and effective teamwork are key soft skills for success in this field. These competencies are crucial for ensuring the safe, efficient, and reliable development of viral vectors used in gene therapy and biomedical research.

What is a Viral Vector job?

A Viral Vector job typically involves the development, production, and optimization of viral vectors used in gene therapy and vaccine applications. Professionals in this field work in biotechnology or pharmaceutical companies, focusing on designing and engineering viruses to deliver genetic material into cells safely and efficiently. Responsibilities may include cell culture, molecular cloning, vector purification, and quality control. This role is critical in advancing treatments for genetic disorders, cancer, and infectious diseases.

What jobs does vector offer?

A viral vector specialist or researcher typically works in biotechnology or pharmaceutical companies, focusing on developing and producing viral vectors for gene therapy and vaccine delivery. These roles often require knowledge of molecular biology, virology, and laboratory techniques, with positions available in research, manufacturing, and quality control environments.

What is the highest paying job in virology?

In virology, senior research directors, principal investigators, and biotech executives tend to have the highest salaries, often exceeding six figures annually. These roles typically require advanced degrees, extensive experience, and leadership skills in research or industry settings.

What job makes $10,000 a month without a degree?

A viral vector specialist in the biotech or pharmaceutical industry can earn around $10,000 or more per month, especially with experience and specialized skills in gene therapy or vaccine development. These roles often require technical knowledge of laboratory procedures, quality control, and sometimes certifications, but may not always require a formal degree if complemented by relevant experience or training.

What does a viral vector do?

A viral vector is used in gene therapy and research to deliver genetic material into cells. Viral vectors are engineered viruses that can efficiently transfer DNA or RNA, enabling the modification or regulation of gene expression in target cells. Working with viral vectors requires knowledge of molecular biology techniques and safety protocols to prevent unintended exposure.

What are some common challenges faced by professionals working in viral vector development?

Professionals in viral vector development often encounter challenges such as troubleshooting low viral yields, maintaining strict contamination controls, and optimizing protocols for efficient gene delivery. The work environment is highly regulated, requiring close attention to safety and compliance standards, and frequent collaboration with cross-functional teams like quality assurance and manufacturing. Staying updated with emerging technologies and evolving regulatory requirements is also crucial. These challenges help foster advanced technical expertise and provide valuable problem-solving experience that contribute to long-term career growth in gene therapy and biotechnology.

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Viral Vector jobs near you
Senior Scientist, Viral Upstream Process Development

Senior Scientist, Viral Upstream Process Development

CEDENT

Philadelphia, PA

$92K - $126K/yr

Full-time

Posted 26 days ago

Job description

Reporting to the Associate Director, Upstream Process Development, the Senior Scientist will contribute to upstream viral process development to bring Client's pipeline of T cell and viral vector-based products to the clinic. Responsibilities will include, but are not limited to, performing the day-to-day activities of the viral process development lab, building Client's viral manufacturing capabilities, and executing experiments to support viral process development/characterization. This role will collaborate significantly with research and analytical development teams, as well as contract development and manufacturing organizations.
Key responsibilities:
  • Contribute to the setup and organization of the Client's vector process development capabilities.
  • Develop bench scale suspension culture processes for viral vector generation within shake flasks and bioreactors through design and execution of experiments to support process characterization, and process transfer activities between the research team, TechOps, and external partners.
  • Provide experimental execution, data review and analysis, and maintenance of accurate and detailed lab notebooks.
  • Perform day-to-day activities in the vector process development lab including maintaining equipment, ordering materials and managing inventory, and preparing buffers and process aids.
  • Author and review technical documents, including but not limited to batch records, SOPs, development reports and process specific sections of regulatory documents.
  • Represent Client externally at meetings (professional associations, with regulatory bodies, etc.).
  • Serve as a PD subject matter expert on both internal and external teams (CDMO, material & equipment suppliers, etc.).
Required experience & skills:
  • Bachelor’s Degree with 10 years, Master’s Degree with 8 years or Ph.D. with 5 years in chemical engineering, biochemical engineering/bioengineering, biotechnology or related discipline
  • Hands-on experience with viral vector upstream processing, including excellent small-scale aseptic technique and expert understanding of bioreactor operation and control loops.
  • Experience implementing processes in clinical and commercial manufacturing of cell and gene therapy / biopharma products
  • Demonstrated ability to apply knowledge of cell biology, chemical engineering, or bioengineering toward process development, scale-up /scale-down and troubleshooting
  • Strong scientific reasoning, problem-solving, and applied mathematics and statistics skills, including the ability to break down complex problems into manageable hypotheses
  • Proven experience collaborating with internal and external partners
  • Ability to balance individual contributions while training and informally mentoring junior colleagues.
  • Working knowledge of GMP guidelines for clinical and commercial manufacturing
  • Proficiency in using Microsoft Word, Excel, Power Point and data analysis/presentation software such as JMP and/or GraphPad
  • Excellent interpersonal, verbal and written communication skills
  • Strong organizational & problem-solving skills, with excellent attention to detail and the proven ability to collaborate in a dynamic team environment
Preferred experience & skills:
  • End-to-end experience in plasmid and Lentivirus development and manufacturing
  • Experience with high-throughput bioreactors systems, namely AMBR, but others will be considered
  • Experience drafting CMC sections for INDs
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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