Senior Scientist II Biologics

Trident Consulting; Irvine (CA); On-site; USD 118,000 - 148,000; Full time

Job summary

Trident Consulting seeks a Sr. Scientist II, Biologics in Aliso Viejo, CA to lead analytical development for large molecules, validate assays, and drive technology transfer. You will partner with cross‑functional teams, oversee CRO/CMO activities, and contribute to regulatory submissions.

The role demands hands‑on lab work, troubleshooting, and ability to manage multiple projects with strong communication.

Qualifications

• Analytical method development for large molecules.
• Ability to collaborate with cross-functional teams.
• Experience engaging with CROs and CMOs.
• Familiarity with regulatory/GxP environments.

Responsibilities

• Develop, validate, and transfer analytical and potency assay methods for large molecules.
• Oversee stability studies and conduct trend analysis.
• Coordinate activities with CROs/CMOs to ensure timely results.
• Act as analytical lead on CMC project teams and communicate findings.
• Prepare technical reports and contribute to regulatory submissions.
• Provide training and guidance to scientists in the team.

Skills

Analytical method development

Team collaboration

CRO/CDMO collaboration

Education

Ph.D. in biochemistry or related field

M.S. in biochemistry or related field with 10+ years

Tools

HPLC

UPLC

LC-MS

ELISA

qPCR

ddPCR

Biacore/Octet

Job description

Trident Consulting is seeking an \" Sr. Scientist II, Biologics\" for one of our direct clients in “Aliso Viejo, CA\". A global leader in business and technology services.

Job Title: Sr. Scientist II, Biologics

Salary Range: $118,000 – $148,000 Annually

This is a very hands-on position working in a lab doing experiments running the instruments themselves. This is not an entry level role. Need someone to start and run the project and have the ability to troubleshoot and work with a team.

Must have

• 1) Analytical Methodical developments for large molecules
• 2) Able to collaborate with the team
• 3) Be able to engage and work with CRO and CDMO

Description

What You’ll Do: This position is within the Analytical Technologies team of the Applied Research department.

• This role focuses on developing, validating, and transferring analytical and biological potency assay and cell-based assay methods to support large molecule drug development and formulations from early-stage clinical studies through commercialization.
• The position also involves overseeing stability studies and conducting trending analysis.
• The position will establish, coordinate and monitor analytical related activities both internally and with CROs and CMOs to ensure quality and timeliness of projects.
• The ideal candidate works effectively and collaboratively with cross-functional groups and will represent as analytical lead on CMC project teams.
• This position is expected to communicate data both verbally at group meetings and through written documents and reports and be able to comfortably multitask across projects and disciplines.
• Provides technical expertise to design, conduct, and implement analytical and development activities for large and small molecules to support all stages of drug development. Troubleshoots and solves technical challenges independently in a timely manner and ensures generation of high-quality scientific data. Evaluates and interprets data from release and stability studies and provides scientific conclusions to support decision making.
• Maintains expertise in cutting-edge assay technologies and continuously develops excellent assay troubleshooting skills in analytical methodologies used for the characterization of drug delivery systems and protein formulations for drug release, potency, biological activity, stability, impurity testing and aggregation profile.
• Collaborate with protein/peptide engineering SMEs and contribute biological knowledge to the design of novel proteins with desired pharmacological characteristics.
• Prepares high quality experimental protocols and technical reports in support of regulatory submissions.
• Independently authors appropriate portions of CMC section of INDs, NDAs and prepares responses to regulatory questions.
• Provides training and guidance to scientists in the team.
• Provides regular and open communication to keep project teams, and management informed of direction, progress and strategic developments in supporting and meeting companies’ goals and objectives.
• Actively participates in departmental committees/meetings as an advisor in scientific, administrative and regulatory areas.
• Represents as analytical lead on CMC project teams, provides scientific solutions and contributes to team discussions.
• Support QC department with establishing robust methods, product specifications, method validations and method transfers.
• Proactively develops and maintains knowledge in current analytical and bioanalytical sciences and investigates new technologies, recommends and implements innovative techniques to the team.

Requirements

• Strong hands-on knowledge of chromatographic theory and technology.
• Working knowledge of HPLC, UPLC, IEX-HPLC, SEC-HPLC, LC-MS, CE techniques, cIEF, MSD, ELISA, ddPCR, qPCR, Octet, Biacore, and other common analytical and bioassay techniques used to determine potency, purity, and in‑vitro performance of drug substance and drug product for large molecules.
• Ability to independently lead investigations and troubleshoot technical problems at all stages of development, being detail oriented are important attributes.
• Excellent written and verbal communication skills; prior experience working within regulated environments (e.g., GxP, ICH, FDA) to ensure analytical activities meet compliance standards and support regulatory filings and inspections.
• Strong ability and knowledge to develop, validate and transfer methods.
• Experience in oversight of stability studies, conducting trend analysis and interpreting data.
• Strong scientific and leadership skills with the ability to be a subject matter expert at matrix teams and influence and collaborate.
• Ability to work within a diverse workforce, scientific participation and collaboration with colleagues in industry, academia and regulatory agencies.
• Experience in interacting with pharmaceutical CROs and CMOs and providing guidance.
• Project management skills including the ability to manage multiple projects and evaluate project resource requirements. Strong knowledge of Quality systems, Drug Product Manufacturing and Validation. Good knowledge of drug development and product regulations.
• Ph.D. (with 8+ years) or M.S. (10+ years) in biochemistry, immunoanalytical/analytical chemistry, or related scientific field and 6+ years of pharmaceutical industry experience in large molecule analytical development, drug product analysis and regulatory submissions.