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HomeCompaniesSeranbioAnalytical Development Scientist II

Analytical Development Scientist II

Seranbio · Bend, Oregon · On Site · Active · Lever

Job facts

FieldValue
CompanySeranbio
TitleAnalytical Development Scientist II
Normalized title-
Department / teamQuality / Analytical Development
LocationBend, OR, United States
Work modelOn Site
Employment typeFull Time Exempt
Salary-
Statusactive
ATS providerLever
Posted / first seen2026-04-23 / 2026-05-29
Changed / last seen2026-05-29 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Seranbio.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Lever.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Bend.Open
Department jobsActive postings in Quality.Open
Work model jobsActive On Site postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanySeranbio
Source7258d68f-d859-49ac-bb3f-5ad6545c3516
ATS providerLever

Description

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. Duties and 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. Required Skills/Abilities 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 Education and 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.

Full job record

Job IDaec53e4426698f4c40fc860298a8b5976a803760
Org ID9ca8059a-1734-4dba-aa9d-c1bdfa75aff8
Source ID7258d68f-d859-49ac-bb3f-5ad6545c3516
Board ID7258d68f-d859-49ac-bb3f-5ad6545c3516
Providerlever
Provider Job Key8664ab0e-15f1-409a-9e53-450a791678a3
TitleAnalytical Development Scientist II
Normalized Title
Statusactive
Activeyes
Location TextBend, Oregon
DepartmentQuality
TeamAnalytical Development
Employment TypeFull-time Exempt
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionOR
CityBend
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://jobs.lever.co/seranbio/8664ab0e-15f1-409a-9e53-450a791678a3
Apply URLhttps://jobs.lever.co/seranbio/8664ab0e-15f1-409a-9e53-450a791678a3/apply
First Seen At2026-05-29 07:00:37Z
Last Seen At2026-06-06 07:56:39Z
Last Checked At2026-06-06 07:56:39Z
Last Changed At2026-05-29 07:00:37Z
Inactive At
Source Posted At2026-04-23 00:05:42Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=lever/board=seranbio/date=2026-06-06/2026-06-06T07-56-39-120Z-0b3a16529c97b39ae8e980e7f69a33f53d119fe008917eea3878873eeb9d290c.json
Event Fields
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  "active_status": "active"
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Parsed Structured
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Extensions
{}
Native Structured
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    {
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    },
    {
      "text": "Physical Requirements",
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  "categories": {
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    "commitment": "Full-time Exempt",
    "department": "Quality",
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      "Bend, Oregon"
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  "salaryRange": null,
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