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Beam is looking for a highly motivated Engineer/Senior Engineer to join our growing Manufacturing Sciences & Technology (MS&T) team. The MS&T Engineer will be responsible for supporting process technology transfers and GMP manufacturing at the Beam Durham facility. Support includes technical support and subject matter expertise for bulk drug substance and bulk drug product GMP clinical, PPQ, and commercial manufacturing. This role supports the execution of the CMC program strategy through strong collaboration and partnership with cross-functional team members in Process Development (PD), Analytical Research and Development (ARD), Manufacturing, Supply Chain, Quality Control, and Quality Assurance.
Job Responsibility:
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
Requirements:
Ph.D. in Chemical Engineering, Bioengineering, Biochemistry, or equivalent with minimum 6 years of relevant work experience
M.S. degree with a minimum of 8 years of relevant work experience
B.S. degree with a minimum 10 years of relevant work experience
Demonstrated experience in technology transfer, scale-up, and implementation of downstream unit operations, such as tangential flow filtration, normal flow filtration, and chromatography
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
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
Nice to have:
Direct experience in downstream process development is preferred
Experience with DLS, UV spectroscopy, and UPLC/HPLC analytical testing methods is a plus
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