Analytical Development Scientist II

Seranbio; Bend (OR); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

PTO accrual

Retirement plan

Health plans

Life insurance

Disability insurance

Employee assistance program

Pet insurance

Job summary

Serán BioScience seeks a Scientist II to support analytical method development, optimization, and validation for small molecule drug products in early and late phase clinical R&D. You will collaborate across QC, QA, Process Development, and Project Management to shape analytical strategy and deliver high-quality data for GMP Clinical Release and Stability programs.

The role emphasizes method development (HPLC/LC), transfer, documentation, and SME leadership in analytical development, with a

Qualifications

• Analytical method development experience (preferably HPLC) in a cGMP pharmaceutical lab (1–2 years).
• Scientific curiosity and willingness to learn.
• Experience with analytical equipment (e.g., Dissolution, KF, GC, LC; LC/GC preferred).

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 and APIs 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 management on projects
• Identify opportunities for process improvements and propose solutions
• Identifies out of trend data.
• Responsibilities may increase in scope to align with company initiatives.

Skills

Analytical method development

HPLC

Data analysis

Communication

Organization

Time management

Problem solving

Collaboration

Empower

Microsoft Office

Education

Bachelor’s degree in chemistry or related field

Master’s degree in chemistry or related field

Tools

LC

GC

KF

Dissolution

Dissolution tester

Empower

Microsoft Office Suite

Job description

Serán is seeking a Scientist II who 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.

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 and APIs 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 management on projects
• Identify opportunities for process improvements and propose solutions
• Identifies out of trend data.
• Responsibilities may increase in scope to align with company initiatives.

Qualifications

• Proven analytical method development experience (preferably HPLC) with at least 1-2 years in a cGMP pharmaceutical industry lab
• 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)
• Conveys general understanding of USP, ICH, and EP guidance as they pertain to method validation/qualification/transfer and general chapters for relevant instrumentation
• 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 function well in a fast‑pace 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

Education & Experience

• 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.

Physical Requirements

• Prolonged periods of sitting or standing at a desk and working on a computer.
• Prolonged periods of standing or sitting while monitoring laboratory equipment.
• Must be able to lift up to 15 pounds at times.
• Adheres to consistent and predictable in‑person attendance.

Visit https://www.seranbio.com/careers to learn more about company culture and the community of Bend, Oregon.

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Benefits Summary

• Serán employees accrue over four weeks of paid time off annually.
• Employer contributions to a retirement account begin after 90 days and do not require an employee match or vesting period.
• Various health plans allow employees to find the best coverage for their individual or family needs with minimal employee contributions.
• Serán covers each employee with basic life and long‑term disability, giving access to increase or add coverage.
• An Employee Assistance Program provides support for all things related to our employees’ wellbeing, along with access to pet insurance.

The Corporate Headquarters of Serán BioScience are located at 63047 Layton Ave, Bend, OR 97701.