Strand Therapeutics

Scientist / Senior Scientist, Analytical Development

Strand Therapeutics$120K — $142K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • B.S. or advanced degree in a relevant scientific discipline.
  • 7+ years of experience in liquid chromatography and method development.
  • Proficient in HPLC/UPLC techniques and mass spectrometry.
  • Experience with biochemical assays related to nucleic acid therapies.
  • Detail-oriented with strong documentation and writing skills.
  • Knowledge of regulatory aspects in mRNA-LNP products is advantageous.
  • Capable of thriving in a fast-paced, entrepreneurial environment.

Responsibilities

  • Leads the development and validation of analytical methods for mRNA and LNP formulations.
  • Analyzes data to influence process development and optimization.
  • Acts as a subject matter expert in analytical chemistry and mass spectrometry.
  • Collaborates with external research organizations for compliance to timelines.
  • Mentors junior scientists in analytical techniques and theory.
  • Develops proprietary software for oligonucleotide analysis.
  • Maintains documentation and contributes to regulatory submissions.
  • Keeps updated on advancements in RNA and LNP technologies.

Benefits

  • Comprehensive health, dental, and life insurance.
  • Flexible open PTO policy.
  • Onsite lunch catering for employees.
  • Support for commuting expenses.
  • Emphasis on professional development in a collaborative environment.
Full Job Description
Job Summary:

Strand is looking for people who have the enthusiasm and motivation to be a highly contributing member of a small but extremely productive team. This opportunity will offer the employee the ability to work in a matrix-based environment and be a part of the future strategy of the company.

We are looking for a highly motivated and innovative candidate for the role of Scientist / Senior Scientist of Analytical Development. The expectation is that the Scientist / Senior Scientist will have experience independently executing analytical experiments using HPLC/UPLC techniques. Reporting to the Associate Director of Analytical Development, the right candidate will be a strategic thinker that brings a leadership presence and enthusiasm for Strand along with a desire to conquer new challenges.

Primary Responsibilities:
  • Leads development, execution, and validation of RP-IP/RP/IEX based analytical methods to establish identity, purity, potency, and stability criteria for early-stage mRNA and LNP formulations using UPLC-ESI-ToF, PDA, and CAD.
  • Analyzes data and draws conclusions which drive screening, optimization, and scale-up efforts in mRNA and LNP Process Development.
  • Serves as subject matter expert in analytical chemistry, mass spectrometry, and method qualification and transfer.
  • Interfaces with external contract research organizations to ensure compliance with internal timeline and quality requirements.
  • Mentors and develops junior scientists in analytical theory and in applications of analytical technology and software platforms.
  • Created proprietary ToF mass spec oligonucleotide mass target and predictive sequence library software to rapidly profile known and identify unknown oligonucleotide mass signals.
  • Maintains electronic notebook records and authors protocols.
  • Contributes to data packages for regulatory submissions.
  • Actively maintains current understanding of RNA and LNP landscape by attending conferences and other events.

Qualifications:
  • B.S. or Advanced Degree in Chemistry, Chemical Engineering, Biology, Biochemistry, Molecular Biology or other relevant scientific discipline.
  • 7+ years of experience with a focus on varying liquid chromatography modes (RP, RP-IP, AEX, SEC, etc), LC-MS, or capillary gel electrophoresis.
  • Working experience in HPLC/UPLC method development.
  • Experience with enzymatic and chemical reactions, PCR, plasmid processing, and standard analytical techniques for biologics or nucleic acid therapies.
  • This position requires conducting laboratory experiments, excellent documentation review and writing skills, and the flexibility to work on multiple projects as needed.
  • Understanding of process development, and/or regulatory aspects of mRNA-(lipid) nanoparticle products would be a plus.
  • Ability to quickly adapt to change and thrive in a dynamic and entrepreneurial early-stage environment.
  • A strong team player with excellent oral and written communication skills and a demonstrated ability to work independently.
  • Independently motivated, detail oriented and good problem-solving ability.

Strand offers a fast-paced, entrepreneurial, team-focused small company environment. We also offer a top-notch benefits package (health, dental, life, open PTO, onsite lunch catering, commuter support and more) and work/life flexibility and integration. Being part of the Strand team allows you to become part of a small team that supports professional development while working together to meet Strand's goals.

Job Type: Full-time

Salary: $120,000 - $142,000 annually plus bonus and equity incentives

Pay Transparency Base Salary Range

$120,000-$142,000 USD

About Strand Therapeutics

Strand Therapeutics is a biotechnology company that develops innovative therapies using messenger RNA (mRNA) technology. The company's proprietary platform enables the design of mRNA therapeutics that can target specific cells and tissues, providing a potential treatment for a wide range of diseases. Strand's lead program is focused on developing mRNA therapies for cancer, with a goal of creating personalized treatments that can be tailored to individual patients. The company was founded in 2016 and is headquartered in Cambridge, MA.
Learn more about Strand Therapeutics
Size
50 employees
Industry
Net Income
-$20 million
Founded
2016

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