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Viral Vector Scientist Jobs in Raleigh, NC (NOW HIRING)

Duke University

Postdoctoral Associate

Durham, NC · On-site

Support viral vector delivery and molecular, biochemical, histological, and cellular experiments ... Advance Scientific Discovery * Collaborate on manuscripts, scientific publications, conference ...

AskBio

Sr. Scientist, DNA Development

Durham, NC

This role drives process understanding by linking DNA design to process performance and vector ... Expertise in viral gene therapy, including recombinant adeno-associated virus systems * Strong ...

AskBio

Sr. Scientist, DNA Development

Durham, NC · On-site

This role drives process understanding by linking DNA design to process performance and vector ... Expertise in viral gene therapy, including recombinant adeno-associated virus systems * Strong ...

Novartis

Scientist - Upstream Cell Culture

Durham, NC

$93K - $174K/yr

... and vector production processes. Executes experiments and troubleshoot process and equipment ... Organized and systematic approach to viral or biologic production. * Ability to multi-task and meet ...

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Showing results 21-40

All JobsViral Vector Scientist JobsViral Vector Scientist Jobs in Raleigh, NC

Viral Vector Scientist information

See Raleigh, NC salary details

$36.5K

$119.3K

$191K

How much do viral vector scientist jobs pay per year?

As of Sep 4, 2026, the average yearly pay for viral vector scientist in Raleigh, NC is $119,312.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,800.00 and $132,200.00 per year, depending on experience, location, and employer.

What is the difference between Viral Vector Scientist vs Gene Therapy Research Scientist?

AspectViral Vector ScientistGene Therapy Research Scientist
Required CredentialsBachelor's or Master's in Molecular Biology, Biotechnology, or related fields; experience in vector developmentBachelor's or Master's in Molecular Biology, Genetics, or related fields; focus on gene delivery systems
Work EnvironmentLaboratories developing viral vectors for gene delivery, often in biotech or pharma companiesResearch labs focused on gene therapy applications, including vector design and preclinical testing
Employer & Industry UsageBiotech, pharmaceutical companies, research institutionsGene therapy companies, biotech firms, academic research centers

The Viral Vector Scientist specializes in designing and producing viral vectors used for gene delivery, while the Gene Therapy Research Scientist focuses on developing and testing gene therapy strategies, often utilizing viral vectors. Both roles require similar educational backgrounds and work environments but differ in their specific focus within gene therapy development.

What are popular job titles related to Viral Vector Scientist jobs in Raleigh, NC?

For Viral Vector Scientist jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Viral Vector Scientist jobs in Raleigh, NC look for?

The top searched job categories for Viral Vector Scientist jobs in Raleigh, NC are:

Viral Vector Scientist jobs near you
Infographic showing various Viral Vector Scientist job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 89% Full Time, 6% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $119,312 per year, or $57.4 per hour.

Director/Assoc. Director, Quality Assurance (Site Quality Head)

Encoded Therapeutics

Morrisville, NC • On-site

Full-time

Medical, Life, PTO

Posted 14 days ago

Job description

Encoded Therapeutics Inc. is a biotechnology company advancing precision medicines for a broad range of genetic disorders. Our mission is to unlock new opportunities for viral gene therapy through genomics-driven discovery. We focus on delivering life-changing advances for individuals with genetic disorders not addressable with current approaches. For more information, please visit www.Encoded.com.
Encoded Therapeutics is seeking an experienced and vision-driven Associate Director/Director, Quality Assurance to serve as the Site Quality Head for our Research Triangle Park (RTP) clinical manufacturing facility. In this critical leadership position, you will establish, maintain, and oversee all Site Quality Operations, ensuring phase appropriate Quality oversight and compliance with CGMP regulations, internal standards, and global regulatory expectations.
Responsibilities
Site Quality Leadership & Strategy
  • Represent QA in cross-functional team meetings and interacts with Manufacturing, Process Sciences, Facilities & Engineering, Supply Chain, Analytical Sciences, Regulatory, etc. applying strong communication and collaboration skills.
  • Maintain updated and relevant knowledge of the GMP landscape, regulations, and guidelines.
  • Drive risk-based quality decision-making, and lead escalation and resolution of critical quality events that may impact product supply, data integrity, or patient safety.
  • Author, review, and provide technical QA support for site-related sections of regulatory filings and agency interactions.
  • Support any site or regulatory body inspections.
  • Manage QA team activities to support internal operations, supply chain, quality control, and facilities.
  • Lead, mentor, and build a high-performing local Quality Assurance team.
  • Trends and reports key quality metrics to the leadership team.
Quality Operations and Product Disposition
  • Provide quality leadership and operational oversight for environmental monitoring, clinical manufacturing (AAV/Gene Therapy), analytical testing, stability, batch record review, and disposition.
  • Provide guidance and recommendations to ensure material is manufactured in accordance with established procedures, CGMPs, and appropriate regulations.
  • Lead QA oversight for analytical method data review, method validation QA approvals, tech transfer protocol/report reviews, and product specifications.
  • Author and revise QA related standard operating procedures and provides guidance for generation, review, and approval of process, equipment, test method, and other SOPs.
  • Reviews and approves all GMP related documentation including internal protocols, reports, test records, batch records, labels, specifications and other documents for drug substance.
  • Provide oversight and support staff to ensure executed batch records and associated documents to are in compliance with approved procedures and CGMP expectations to determine acceptability of product disposition.
  • Review and approve change controls related to the implementation or revision of process, method, and/or equipment changes.
  • Provide quality oversight of root-cause analysis and product impact assessment for investigations as a result of deviations, OOS, and OOT investigations ensuring appropriate CAPA actions are identified.
  • Support and lead risk assessments to proactively identify, assess, and mitigate site risks.
  • Support and maintain the site Contamination Control Strategy (CCS) to mitigate cross-contamination and environmental risks.
Material and Supply Chain Quality
  • Provide quality leadership and operational oversight for raw materials and reagent release, specifications, incoming controls, and storage.
  • Lead teams to resolve any non-conforming materials and site supply chain risks.
Facility and Validation Oversight
  • Direct Quality oversight for commissioning, qualification, and validation (CQV) of site facilities, process equipment, automated systems, and analytical instrumentation.
  • Oversee site computer system validation (CSV) and data integrity initiatives to comply with 21 CFR Part 11 and global guidelines.
  • Provide Quality oversight for facilities, utilities, equipment, and instrument maintenance and management.
  • Prioritize projects appropriately and with flexibility to accommodate changing program objectives.
  • Identifies opportunities for improvement and drives continuous improvement initiatives.
  • Perform other duties and projects as assigned by management.

Requirements
  • Education: Bachelor's degree in Life Sciences or a related discipline, or Master's degree in Life Sciences or a related discipline.
  • Experience: Minimum of 12+ years of progressive Quality Assurance experience in the pharmaceutical, biotechnology, or biologics industry, with at least 5+ years in a senior Quality management leadership role.
  • Direct experience in Gene Therapy, Cell Therapy, Viral Vector (AAV), or Advanced Therapy Medicinal Products (ATMPs) is strongly preferred.
  • Strong understanding of applicable regulatory requirements and guidance documents (21 CFR, USP, EP, ICH).
  • Demonstrated track record of leading successfully through regulatory inspections (FDA, EMA, etc.).
  • Demonstrated knowledge of batch disposition, deviation/CAPA management, change control, validation, raw material quality oversight, and environmental monitoring.
  • Knowledge of Six Sigma and LEAN, and experience using root cause analysis tools to identify and correct deviations, are a plus.
  • Eligible to work in the United States.
  • Able to work on-site.

Benefits
  • Comprehensive benefits package, including competitive employer premium contributions
  • Meaningful stock option grants
  • PTO, sick time, and holiday pay
  • Generous Parental Leave program
  • Pre-tax medical and dependent care programs
  • STD, LTD, Life and AD&D
  • Professional development opportunities
  • Team-building events
  • Stocked micro-kitchen with drinks and snacks
  • Wellness Resources

Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages.

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