Manufacturing Associate l/II

Beam Therapeutics•Durham, NC

2d•$34 - $45•Onsite

About The Position

Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Position Overview: 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. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment.

Requirements

BS, MS a plus, in Life Sciences or Engineering with minimum of 0-10 years of relevant experience. Level will be determined based on a combination of experience and education.
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.

Responsibilities

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.