Scientist, Virology

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).

• 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.

• 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.

• 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.

• 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 6
  
  Sigma.
• Able to multitask and adjust prioritization as necessary.
• Bioinformatics experience is desirable, but not a requirement.

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.

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