Cell Therapy GMP Manufacturing Associate II — Onsite

Beam Therapeutics; Durham (NC); On-site; USD 65,000 - 90,000; Full time

Job summary

Beam Therapeutics is seeking a Manufacturing Associate II / Senior Manufacturing Associate I to support scaling of cGMP manufacturing at our RTP site. You will work on GMP production, interfacing with cross-functional teams, and ensuring training qualifications are maintained.

The role requires onsite work in RTP area, with flexibility during peak times, and preferred experience in SAP, Veeva, and Cell Therapy operations within a GMP environment.

Qualifications

• BS/MS in Life Sciences or Engineering required or a plus with 4-6 years of relevant experience.
• Experience in SAP, Veeva, and Cell Therapy operations strongly preferred.
• Results oriented with the ability to demonstrate resiliency, ownership, and drive.
• Team oriented with excellent collaboration skills.
• Must be able to work onsite daily and have a flexible schedule during peak times, including outside normal hours.

Responsibilities

• Support multiple areas of GMP production, and lead most operations as needed.
• Establish and maintain strong relationships at the site and cross-functionally.
• Manages and maintains training qualifications for assigned operations, operates as lead trainer on most operations.
• Identifies and revises manufacturing documents (Equipment SOPs) as required.
• Drafts change controls as required and manages small projects for area.
• Performs limited CQV required tasks when needed for any new plant expansions or upgrades.
• Operate in up to an ISO 5/Grade B environment.

Skills

Leadership

Team collaboration

GMP experience

Education

BS/MS in Life Sciences or Engineering

Tools

SAP

Veeva

Job description

Beam Therapeutics is seeking a Manufacturing Associate II / Senior Manufacturing Associate I to support scaling of cGMP manufacturing at our RTP site. You will work on GMP production, interfacing with cross-functional teams, and ensuring training qualifications are maintained.

The role requires onsite work in RTP area, with flexibility during peak times, and preferred experience in SAP, Veeva, and Cell Therapy operations within a GMP environment.