Manufacturing Associate l/II Job at Beam Therapeutics (Durham, NC)

Job Description

Beam Therapeutics is looking for a highly energetic Manufacturing Associate/Sr. Manufacturing Associate to support GMP operations in 2026 at our site in Research Triangle Park, NC. Reporting to Sr Leadership in Manufacturing, the successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and routine GMP Operations.

Job Responsibility

Cultivate Beam’s culture and our values-driven organization focused on people
Execute against the mission, vision, and strategy for Beam internal cGMP Manufacturing
Ensure safety, compliance, efficiency, and sustainability throughout cGMP operations
Lead and coordinate resources to ensure quality standards are met and products are delivered on time and within budget
Champion development of a learning culture that embraces innovation and continuous improvement
Support up to but not limited to multiple areas of GMP production as needed
Support department during audits and regulatory inspections
Establish and maintain strong relationships at the site and cross-functionally
Assures alignment of internal manufacturing schedules with product supply forecasts and program timelines
Develops and maintains detailed manufacturing project plans, defines risks, and establishes contingency plans to ensure projects are delivered on time, within budget, and adhere to high quality standards
Support facility /equipment qualification and training for the ability of meeting process and regulatory expectations
Contributes to development and implementation of manufacturing documents (batch records, procedures, and technical reports)
Assist MFG support functions in relation to manufacturing deviation investigations and change controls / CAPAs

Requirements

BS, MS a plus, in Life Sciences or Engineering with minimum of 0-10 years of relevant experience
Must be willing to have a flexible schedule to support a multi-shift operation that covers nights and weekends as needed
Proven experience as a contributor in a cGMP manufacturing operation
experience leading cell/gene therapy manufacturing operations strongly preferred
Demonstrated deep technical knowledge of facility design considerations, process strategies, technology transfer, and manufacturing operations in a biotech/pharmaceutical environment
Outstanding written and verbal written communication skills, with the ability to convey strategies and results to a diverse audience
Demonstrated entry level business acumen
Dynamic interpersonal skills and the ability to manage through influence, while being part of a team
Ability to juggle multiple projects and priorities and adapt quickly to changing circumstances
High degree of customer focus (internal/external) and demonstrated collaboration in a team environment
Results oriented with the ability to demonstrate resiliency, ownership, and drive
Travel for in-person interactions with cross-functional stakeholders to ensure tech transfer is on track as needed
Must be able to work onsite daily and willing to have a flexible schedule during peak times, which may include supporting critical operations outside of normal work hours, as needed

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Manufacturing Associate l/II

Job Description

Job Responsibility

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