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AtAldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers.As a member of our team,youllhelp bring life-changing innovations to lifeimpactingmillions around the world. We bring together deep scientificexpertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whetheryou'relaunching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potentialone discovery at a time.

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TheEngineerII, LNPProcess Developmentleads technology transfer activities across Drug Substance and Drug Product life cyclesfrom latestage process development through clinical and commercial manufacturing. This roledrivesprocess design, scaleup, and optimization with a focus on LNP Drug Product delivery systems. The position applies strong technical skills and independent problemsolving to help ensure manufacturing processes are robust, efficient, and compliant for both internal development programs and external client transfers.

This position reports to the Manager of LNP Technical Operations and is part of the Technical Operations Departmentlocatedin Fargo, ND. This is an on-site role.

In this role, you will have the opportunity to:

• Drivetechnical activities that support robust, compliant processes aligned with client expectations and regulatory requirements.

• Execute and help shapeprocess design, evaluation, and optimization work for LNPbased Drug Product processes, including technical documentation, equipment fit assessments, and execution of studies that support scalable and reliable GMP operations.

• Provide handson technical support during manufacturing campaigns,assistingwith troubleshooting, deviation management, and crossfunctional alignment tomaintainstrong process understanding through final product release.

• Develop growing subjectmatterexpertisein LNP formulation science, process development, and technology transfer, and provide clear, dependable technical input during client discussions and internal reviews. Inform technical and operational decisions by contributing datadriven insights to evaluations ofnew technologies, capital investments, and process improvements.

• Supportdevelopmentof junior team members by sharing technical learnings,participatingin crossfunctional efforts, and promoting best practices in scientific and operational execution.

The essential requirements of the job include:

• BS degree in Chemical Engineering, Bioengineering, Chemistry, or a related field with 4+ years of relevant industry experience in biopharma, drug product development, or LNP/mRNAbased manufacturing, supporting process development, scaleup, or GMP technical operations.OR

• MS degree in a relevant scientific or engineering discipline with 2+ years of experience supporting process development, scaleup, or GMP technical operations.OR

• PhD in a related field with 1+yearof handson experience in LNP formulation, RNA therapeutics, or parenteral drug product manufacturing.

• Foundational experience with LNP formulation, microfluidicsbased mixing, and technology transfer, including involvement in GMP batch support, process troubleshooting, deviation investigations, or data analysis.

• Effective crossfunctional communication and collaboration skills, including partnering with Manufacturing, QA, QC, MSAT, and clientfacing teams, preparing technical documentation, presenting data, and supporting datadriven decisions and continuous improvement.

It would be a plus if you alsopossesspreviousexperience in:

• Supporting mRNA or LNP development and scaleup activities, including exposure to CMC expectations or regulatoryrelevant documentation.

• Working with formulation or microfluidic mixing systems and helping adapt or troubleshoot these platforms during process development or tech transfer.

• Performing or interpreting routine analytical characterization to assess LNP or drug product quality and contribute to datadriven process decisions.

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