Analytical Scientist

SystImmune Inc.; Redmond (WA); On-site; USD 80,000 - 110,000; Full time

Job summary

A leading biotechnology company is seeking an Analytical Scientist to contribute to the development of antibody-based therapeutics. This PhD-level position involves designing analytical methods and collaborating in a fast-paced environment, ideal for candidates passionate about contributing to innovative therapies and familiar with biopharmaceutical processes.

Qualifications

• 0-3 years of relevant industry experience in biotech/pharma.
• Strong background in HPLC/UPLC and binding assays.
• Comfortable in dynamic environments with shifting priorities.

Responsibilities

• Develop and execute robust analytical methods using UPLC, CE, and binding assays.
• Collaborate with cross-functional teams in an integrated CMC environment.
• Author technical reports and contribute to regulatory documentation.

Skills

Analytical Chemistry

Biochemistry

Pharmaceutical Sciences

Teamwork

Communication

Problem-solving

Education

PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences

Tools

JMP

Empower

SoftMax Pro

ForteBio Data Analysis

Job description

As an Analytical Scientist, the incumbent will be a core contributor to the development and characterization of antibody-based therapeutics. The scientist will design and implement analytical methods for early- to mid-stage development, with a focus on UPLC, CE, and binding assays. This is a hands-on lab role ideal for a PhD-level scientist who thrives in a dynamic, high throughput setting and is proficient in working cross-functionally.

Key Responsibilities

• Develop and execute robust analytical methods using UPLC (SEC, IEX, RP), CE (CE-SDS, cIEF), and binding assays (ELISA, BLI) to support antibody characterization. Maintain good documentation for all studies.
• Support cell line development, process development, formulation screening, comparability, and stability studies.
• Analyze, interpret, and communicate data to project teams in a timely and scientifically rigorous manner.
• Collaborate with upstream, downstream, and formulation scientists in an integrated CMC environment.
• Author high-quality technical reports, method protocols, and contribute to regulatory documentation.
• Evaluate new analytical technologies and help build internal capabilities as the company scales.
• Contribute to establishing a phase-appropriate analytical control strategy for lead candidates.
• Wear multiple hats, bring solutions, and help shape the analytical infrastructure as the company grows.

Qualifications

• PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.
• 0–3+ years of relevant industry experience (biotech/pharma) in biologics analytical development and demonstrate strong teamwork.
• Strong technical background in HPLC/UPLC and CE techniques for therapeutic proteins.
• Hands-on experience with antibody binding assays (e.g., ELISA, SPR or BLI).
• Solid understanding of antibody structure, post-translational modifications, and critical quality attributes (CQAs).
• Comfortable working in a dynamic environment with shifting priorities and evolving needs.
• Excellent communication, organization, and problem-solving skills.

Additionally, it’s desirable that the candidate has:

• Experience in tech transfer, method qualification, or early GMP readiness.
• Familiarity with software platforms like JMP, Empower, SoftMax Pro, or ForteBio Data Analysis.
• Passion for working in a mission-driven environment and building from the ground up.