Associate Scientist, mRNA Platform Process Development

TechDigital Group; Seattle (WA); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a motivated Associate Scientist to join their dynamic team in Seattle. This role focuses on the development of mRNA processes, utilizing advanced purification techniques and analytical methods. The ideal candidate will engage in the generation, purification, and characterization of mRNA molecules, contributing to groundbreaking gene editing therapies. If you thrive in a fast-paced environment and are passionate about advancing biotechnological innovations, this opportunity is perfect for you. Join a collaborative team dedicated to pushing the boundaries of science and making a meaningful impact in the field.

Qualifications

• 2+ years of relevant industry experience in mRNA process development.
• Hands-on experience with purification techniques and molecular cloning.

Responsibilities

• Generate purified mRNA and execute downstream process development experiments.
• Maintain lab documentation and present data in group meetings.

Skills

Downstream purification of biological molecules

Molecular cloning

Analyzing purified nucleic acids

Technical writing

Clear communication

Education

STEM degree

Degree in biological or chemical engineering

Tools

AKTA

HPLC

JMP

Job description

Associate Scientist, mRNA Platform Process Development

Job Title– Associate Scientist, mRNA Platform Process Development
Location: Seattle, WA * 100% Onsite
Top Skills:

1. Hands-on experience with the downstream purification of biological molecules (AKTA, chromatography, TFF, viral filtration, etc.)
2. Experience with molecular cloning, PAGE, and agarose gels
3. Experience working with, storing, and analyzing purified nucleic acids

Seeking a highly motivated Associate, or Sr. Associate, Scientist to work in a fast-paced PD environment applying rigorous scientific principles towards developing a platform process for producing mRNA. As a part of the Gene Delivery and Editing Process Development (GDEPD) organization, the ideal Associate will possess sufficient experience in the downstream process development of biological molecules, with a high preference for any experience with developing processes with nucleic acids. The Associate will also gain familiarity with mRNA analytical methods and their interpretation in the context of mRNA attributes and function in gene editing applications.

A successful Associate will directly employ purification principles and biochemistry techniques to develop our next-generation gene edited therapies. In this capacity, the Associate will produce, purify, and characterize mRNA molecules to enable robust ex vivo studies. This candidate will use recombinant enzymes to produce and functionalize mRNA, AKTA systems to purify mRNA via affinity and other chromatography methods, TFF to further purify and formulate mRNA, as well as use HPLCs and other biochemical analytical techniques for characterization. An outstanding candidate will be driven by a desire to create, optimize, and define processes with speed in a collaborative environment.
Key Responsibilities:

1. Material generation of purified mRNA
2. Execute and troubleshoot IVT and downstream process development experiments
3. Manage the flow of samples and data with various downstream users of mRNA
4. Assist in the design of experiments and interpretation of data
5. Actively participate and support lab maintenance and continuous improvement initiatives
6. Maintain accurate and detailed laboratory notebook and documentation
7. Summarize and present data in group meetings and contribute to group discussions
8. Author technical reports, study memos, and protocols

Basic Qualifications:

1. STEM degree with 2+ years of relevant industry experience; title/compensation will be commensurate with education, experience, and skillset
2. Hands-on experience with the downstream purification of biological molecules (AKTA, chromatography, TFF, viral filtration, etc.)
3. Experience with molecular cloning, PAGE, and agarose gels
4. Experience working with, storing, and analyzing purified nucleic acids
5. Independently motivated with the ability to work in teams
6. Ability to communicate clearly and concisely through oral presentation and technical writing
7. Ability to leverage literature, internal and external resources to solve problems and develop new technologies

Preferred Qualifications:

1. Degree in biological or chemical engineering, biochemistry, or bio-related field
2. Experience with JMP for DoE design and analysis
3. Experience with IVT of mRNA, including successful transfer for GMP manufacturing
4. Experience with recombinant nucleic acid processing enzymes
5. Experience with interpreting qPCR, HPLC, NGS, and mass spec data sets
6. Experience interacting and collaborating with vendors