Engineer/Sr Engineer, Manufacturing Sciences & Technology; mRNA/LNP
Listed on 2025-12-27
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Engineering
Manufacturing Engineer, Process Engineer, Validation Engineer, Quality Engineering
Engineer / Sr Engineer, Manufacturing Sciences & Technology (mRNA/LNP)
Join to apply for the Engineer / Sr Engineer, Manufacturing Sciences & Technology (mRNA/LNP) role at Beam Therapeutics.
Company OverviewBeam 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‑strand 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.
$/yr - $/yr
Responsibilities- Supports MS&T activities related to mRNA and LNP programs
- Supports the technology transfer and implementation of mRNA and LNP GMP manufacturing processes, collaborates with sending and receiving site cross‑functional team members
- Supports bulk drug substance and bulk drug product manufacturing across the full product lifecycle, including process design, process performance qualification (PPQ), commercial production, and continued process verification (CPV)
- Authors technical documentation, including technology transfer plans, facility fit and gap analysis reports, manufacturing study protocols and reports, and risk assessments
- Supports equipment design to meet process needs and compliance/regulatory expectations; supports Engineering and Validation departments with subsequent procurement, qualification, and GMP readiness
- Supports regulatory submissions, responses, on‑site audits, and inspections
- Represents MS&T in cross‑functional teams related to mRNA/LNP programs and manufacturing operations
- Provides person‑in‑plant (PIP) support in manufacturing at Beam Durham
- Supports MS&T lab and non‑GMP analytical testing of in‑process intermediates, as needed
- Establishes trusting and collaborative work relationships across and between Beam sites
- Accommodates a flexible schedule during GMP manufacturing, which may include PIP support for critical operations outside of normal business hours
- Ph.D. in Chemical Engineering, Bioengineering, Biochemistry, or equivalent with minimum 6 years of relevant work experience, or an M.S. degree with a minimum of 8 years of relevant work experience, or a B.S. degree with a minimum 10 years of relevant work experience. Level will be commensurate with experience and academic background.
- Demonstrated experience in technology transfer, scale‑up, and implementation of downstream unit operations, such as tangential flow filtration, normal flow filtration, and chromatography; direct experience in downstream process development is preferred
- Experience in executing Process Validation lifecycle approach; i.e. process design, PPQ, and CPV
- Experience in leading cross‑functional teams for non‑conformance event investigations, Root Cause Analyses (RCAs), and CAPAs
- Experience with DLS, UV spectroscopy, and UPLC/HPLC analytical testing methods is a plus
- Outstanding written, verbal, and presentation skills; ability to communicate strategies, plans, and results to a diverse audience
- Ability to simultaneously manage multiple projects and priorities and adjust quickly to dynamic situations
- High degree of customer focus and collaboration in a team environment
Mid‑Senior level
Employment TypeFull‑time
Job FunctionBiotechnology Research and Pharmaceutical Manufacturing
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