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Manufacturing Associate l/II

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Beam Therapeutics

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Location:
United States , Durham, NC

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Category:
Manufacturing

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Contract Type:
Not provided

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Salary:

34.00 - 45.00 USD / Hour
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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

Additional Information:

Job Posted:
March 04, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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