Analytical Development Scientist II

Serán BioScience•Bend, OR

9h•Onsite

About The Position

Serán BioScience provides custom formulation, process development and clinical manufacturing services for a variety of pharmaceutical clients. The Scientist II role will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs. The work performed in this role will help to shape analytical strategy, collaboration across functions, and deliver high-quality data that enables the success of early/late phase clinical programs.

Requirements

Scientific curiosity and willingness to learn
Demonstrates intermediate expertise with analytical equipment (e.g. disso, KF, GC, LC, XRPD, or mDSC; preferred LC and GC)
Excellent verbal and written communication skills
Excellent organizational skills and attention to detail
Excellent time management skills with a proven ability to meet deadlines
Strong analytical and problem-solving skills.
Ability to prioritize tasks and to delegate them when appropriate
Ability to function well in a high-paced work environment
Demonstrated ability to collaborate and work in cross-functional teams
Accepts feedback and constructively manages conflict
Proficient with Empower
Proficient with Microsoft Office Suite or related software
Bachelor’s degree in chemistry or related field, with 4 years of hands-on lab experience preferred; or Master’s degree in chemistry or related field, with 2 years of hands-on lab experience preferred.
Requires 1 year of GMP experience.

Nice To Haves

intermediate expertise with analytical equipment (preferred LC and GC)
Bachelor’s degree in chemistry or related field, with 4 years of hands-on lab experience
Master’s degree in chemistry or related field, with 2 years of hands-on lab experience

Responsibilities

Perform analytical testing such as UHPLC/HPLC, KF, Water Activity, Dissolution to support small molecules drug product development in GMP environment
Develop and optimize methods for drug products across early phase and late phase clinical stages
Execute method transfers to QC or partner labs, ensuring robustness and compliance.
Plan, troubleshoot, and independently execute laboratory studies, generating high-quality data for CMC decision-making.
Prepare and review technical reports, analytical methods, and protocols, contributing to regulatory-ready documentation.
Collaborate with cross-functional teams (QC, QA, Process Development, Project Management) and communicate results to internal and external stakeholders.
Act as a subject matter expert (SME) in analytical development, providing technical leadership and supporting analytical strategy.
Initiate, draft, and perform testing for discrepancy reports; as necessary.
Maintain GMP training certification to be able to perform work in a GMP laboratory
Provide regular updates to senior management on project progress
Identify opportunities for process improvements and propose solutions
Identifies out of trend data.
Responsibilities may increase in scope to align with company initiatives.