Scientist, Virology

Solvias; Morrisville (NC); On-site; USD 90,000 - 140,000; Full time

Job summary

Solvias North America in RTP, North Carolina, is seeking a Scientist, Virology with strong viral and cell culture maintenance and quantification expertise. This on-site role sits in the GMP-regulated Large Molecule & Advanced Therapy laboratory environment at the new RTP headquarters.

You will perform viral culture and gene editing tasks, coordinate daily lab activities with the Sr. Scientist or Team Lead, assist method development and validation, and ensure timely, high‑quality data delivery to

Qualifications

• M.S. or Ph.D. Life Sciences with 5+ years relevant experience or B.A./B.S. with 10+ years relevant experience.
• Experience with viral & cell culture, vector design, cell line development, and gene editing in GMP/GLP/GCP settings.
• Experience in method development, qualification & validation of CGT, biologics, and emerging technologies.

Responsibilities

• Ensure GMP regulatory compliance and SOP adherence.
• Process client samples, qualify controls, document in LIMS/ELN, review protocols.
• Participate in investigations of deviations and change controls.
• Contribute to process improvements for efficient lab workflows.
• Maintain inventory and instrument maintenance.
• Collaborate with cross‑functional teams and customers.

Skills

Viral culture

Cell culture

Vector design

Cell line development

Gene editing

GMP/GLP/GCP

Data analysis

Communication

Team collaboration

Lean Six Sigma

Education

M.S. or Ph.D. Life Sciences

B.A./B.S. Life Sciences with 10+ years experience

Tools

LIMS

ELN

Automation

Statistics & programming

Slide deck creation

Job description

Job Description

Located at our US headquarters in RTP, North Carolina, the Scientist, Virology position will be experienced and well versed in various technical aspects related to viral and cell culture maintenance and viral quantification methods. Additionally, experience with vector design, cell line development, and gene editing technologies are desirable skills. This position is on‑site based in the newly built US headquarters in RTP and is part of the Large Molecule & Advanced Therapy Medicinal Products Services laboratory environment, following Good Manufacturing Practices (GMP).

Critical Performance Areas

• Perform viral & cell culture, vector design, cell line development, and gene editing technologies with minimal supervision while performing ancillary lab activities to maintain optimal laboratory function/performance.
• Coordinate with the Sr. Scientist &/or Team Lead to execute daily laboratory tasks, such as processing client samples, assay development, and training activities.
• Assist in the development, validation, and transfer of analytical methods for the analysis of drug products via cell & gene therapy according to GMP requirements.
• Manage multiple tasks at the same time and ensure on‑time testing and delivery of the highest quality results to clients.
• Generate and assess data generated, record assay metrics, and proactively implement performance improvements.
• Communicate effectively with the Virology Sr. Scientist, Virology Team Lead, and across various teams at RTP.

Responsibilities

Essential Job Functions

• Ensure compliance with GMP regulatory requirements and SOPs.
• Process client samples, qualify controls/standards, document all processes in LIMS/ELN, review draft protocols, and other aspects of a laboratory operations regulated environment.
• Participate in investigations of processing deviations, non‑conformity, OOS, change controls and other quality events as applicable.
• Contribute to process improvements for effective and efficient workflows in the lab.
• Maintain inventory, ordering of laboratory supplies, and instrument maintenance.
• Work collaboratively with cross‑functional teams and customers.

Requirements

Qualifications

• M.S. or Ph.D. Life Sciences with 5+ years relevant experience or B.A./B.S. with 10+ years relevant experience.
• Experience working on viral & cell culture, vector design, cell line development, and gene editing technologies in a GMP, GLP, or GCP environment.
• Experience in method development, qualification & validation of CGT, biologics, and emerging technologies.

Other Desired Skills/Abilities

• Experience in a CRO or CDMO strongly preferred.
• Excellent organizational skills, ability to work independently and collaboratively in a team environment.
• Strong written and verbal communication skills.
• Experience working with LIMS, automation, databases, statistics/programming, and building slide decks for client presentation.
• Lean 6Sigma.
• Able to multitask and adjust prioritization as necessary.
• Bioinformatics experience is desirable, but not a requirement.

Disclaimer

Solvias North America does not currently offer relocation packages or sponsor work visas. All applicants must have the legal right to work in the location of the job posting.

NOTE

This job description is not intended to be all-inclusive. Individuals may perform other related duties to meet the ongoing needs of the organization.