Senior Vector Scientist (MSAT) — Tech Transfer Leader

USWM, LLC; Philadelphia (Philadelphia County); On-site; USD 104,000 - 148,000; Full time

Job summary

USWM, LLC in Philadelphia, PA is seeking a Principal Scientist (Vector) to lead MSAT activities, drive technology transfer, and oversee validation campaigns for viral vector production. This role requires deep vector knowledge and a strong track record in cGMP environments.

The candidate will collaborate with QA, Regulatory Affairs, Analytical Sciences, and Manufacturing to ensure quality, regulatory readiness, and successful external partnerships while mentoring junior staff and guiding

Qualifications

• Advanced degree with 4+ years (PhD) or 8+ years (MS) or 10+ years (BS) of industry experience.
• Knowledge of aseptic techniques and regulatory guidelines (FDA/EU) for validation.
• Experience with cGMP, Annex 1, ATMP guidance and process transfers.
• Proven ability to manage cross-functional teams and CRO/CMO oversight.
• Strong data analysis and QbD/statistical skills.

Responsibilities

• Provide technical leadership for technology transfer, process optimization, and evaluation to support development and commercialization of products.
• Lead phase-appropriate studies for characterization and development of pipeline products.
• Oversee process lifecycle management for CGT programs and technology transfer.
• Coordinate with QA, Regulatory, Analytical Sciences, Supply Chain, and Facilities to align priorities and timelines.
• Mentor junior scientist and oversee cross-functional collaboration.
• Represent MS&T in cross-functional meetings and drive aseptic validation activities.

Skills

Aseptic techniques

Regulatory understanding

Project management

Cross-functional collaboration

Vector biology knowledge

Education

PhD in relevant field

MS in relevant field

BS in relevant field

Job description

USWM, LLC in Philadelphia, PA is seeking a Principal Scientist (Vector) to lead MSAT activities, drive technology transfer, and oversee validation campaigns for viral vector production. This role requires deep vector knowledge and a strong track record in cGMP environments.

The candidate will collaborate with QA, Regulatory Affairs, Analytical Sciences, and Manufacturing to ensure quality, regulatory readiness, and successful external partnerships while mentoring junior staff and guiding