ElevateBio

Biotechnology

SeniorAssociateProcessEngineer(Contract)

$0–0k Waltham, Massachusetts, United States CONTRACT
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“Senior Associate Process Engineer (Contract) at ElevateBio. Skills: Process engineering, GMP manufacturing. Provide process science support. Support GMP manufacturing”

Industry & Context.

Biotechnology
Problems you'll solve

Scientific methodology; Technical reasoning

What You'll Do.

Provide process science support

Support GMP manufacturing

Support technology transfers

Support development studies

Support characterization

Support continuous improvement

Write product impact assessments

Write root-cause analysis reports

Write technical reports

Support data collection

Author technical documentation

Review technical documentation

Support quality events

Assist in root cause determination

How You'll Work.

Team & Collaboration

Cross-functional teams; Process Development; Manufacturing; Quality; Supply Chain

Communication Scope

Technical documentation

Process & Methodology

CAPA, Change Controls

Full Job Description

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently. The Role: ElevateBio is looking for a Senior Associate Process Engineer within the Manufacturing Science and Technology (MSAT) organization. As a Senior Associate Process Engineer in MSAT, you will provide process science support for GMP manufacturing, technology transfers, development studies, characterization, validation, and continuous improvement projects within a highly matrixed cross-functional team for ElevateBio programs. As part of support, you will write protocols, product impact assessments, root-cause analysis reports, and technical reports. You will additionally support data collection and charting for non-GMP and GMP batches. This position is a 6-month contract. Here’s What You’ll Do: Work cross-functionally across Process Development, Manufacturing, Quality, and Supply Chain to provide support for technology transfers and cGMP manufacturing for both clinical and commercial stage programs across modalities including cell and gene therapy, mRNA and viral vector. Authoring and reviewing technical documentation related to manufacturing activities including protocols, technical reports, work instructions, SOPs. Own and support quality events such as deviations, investigations, CAPAs, and Change Controls. Assist in the root cause determination of process-related deviations in a timely and complete manner. The candidate will work with a cross-functional team to resolve complex problems using experience and efficient application of scientific methodology and technical reasoning, then propose comprehensive process solutions and improvements. Support gap analyses and risk assessments to support the capital projects and

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