RNA Process Scientist I - GMP Transfer & Ops

Aldevron

Fargo (ND)

On-site

USD 70,000 - 90,000

Full time

9 days ago

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Job summary

Aldevron in Fargo, ND is seeking a Scientist I to onboard RNA technical transfers from development through clinical and commercial stages. You will help ensure robust, compliant GMP manufacturing processes and work with internal teams to enable on-time, right-first-time delivery.

Reporting to the Manager of RNA Technical Operations, this on-site role emphasizes hands-on process review, technical writing, and data analysis in support of drug substance programs and external client transfers.

Qualifications

  • BS degree with 2+ years in biopharma/drug substance or RNA manufacturing.
  • MS degree with 1+ year in scale-up or technical operations in biopharma.
  • PhD with 0+ years in process development or RNA/LNP manufacturing.

Responsibilities

  • Assist in execution of working plans or studies in RNA work streams, including technical writing and documentation.
  • Execute and aid in onboarding of RNA technical transfers through product life cycle.
  • Work collaboratively across manufacturing, quality, and validation as a SME to support on-time delivery and right-first-time metrics.
  • Execute change controls and assist in quality investigations and technical writing with oversight.
  • Align with evolving business priorities by supporting other critical functional areas as needed.

Skills

RNA manufacturing
Technical operations
Data analysis
Technical writing
GMP operations

Education

BS degree in chemical engineering / bioengineering / biology / molecular biology / biochemistry / chemistry
MS degree in chemical engineering / bioengineering / biology / molecular biology / biochemistry / chemistry
PhD in chemical engineering / bioengineering / biology / molecular biology / biochemistry / chemistry

Tools

AKTA systems
KrosFlo systems
Unicorn
Repligen Recipe Editor

Job description

Aldevron in Fargo, ND is seeking a Scientist I to onboard RNA technical transfers from development through clinical and commercial stages. You will help ensure robust, compliant GMP manufacturing processes and work with internal teams to enable on-time, right-first-time delivery.

Reporting to the Manager of RNA Technical Operations, this on-site role emphasizes hands-on process review, technical writing, and data analysis in support of drug substance programs and external client transfers.

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