Scientist I – Analytical Development

Grifols

. Plan and perform analytical techniques including SE-HPLC, SEC-MALS, CEX-HPLC, cIEF, SDS-PAGE, CE-SDS, ELISA, MSD, in vitro cell-based assays, and qPCR .

Posted 11/9/2026full-timeSan Carlos • California • United StatesJuniorMid-Level💰 $100,412 - $120,515 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in analytical method development and qualification for therapeutic antibody drug candidates, utilizing techniques such as SE-HPLC, ELISA, and qPCR. Proven ability to analyze and present data effectively while collaborating across functional teams and mentoring junior staff.

Highest-signal resume keywords

Analytical Method DevelopmentSE-HPLCELISAGMP KnowledgeProject Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

SE-HPLCSEC-MALSCEX-HPLCSDS-PAGECE-SDSELISAMSDQPCRAnalytical Method QualificationIn Vitro Cell-Based Assays

Soft Skills

Problem-SolvingCommunicationMentoringCollaborationFlexibility

Tools & Technologies

Microsoft OfficeGraphPad PrismOpenLabs CDS

Industry Keywords

Antibody Therapeutics DevelopmentLaboratory EnvironmentBiological FluidsInfectious OrganismsPersonal Protective Equipment

About the role

Key responsibilities & impact

Plan and perform analytical techniques including SE-HPLC, SEC-MALS, CEX-HPLC, cIEF, SDS-PAGE, CE-SDS, ELISA, MSD, in vitro cell-based assays, and qPCR
Analyze, interpret, and present analytical data to drive technical understanding, meet project objectives, troubleshoot, and make recommendations
Discuss experimental plans and results with project team members
Develop, write, and review analytical test methods, method qualification protocols, and method qualification reports
Collaborate across discovery, process development, project management, and other functional groups involved in antibody therapeutics development
Coordinate with external collaborators and CROs during method transfers
Lead assigned projects or teams as needed
Mentor and train other technical staff
Support development of recombinant therapeutic antibody drug candidates through analytical method development, optimization, qualification, and transfer

Requirements

What you’ll need

Bachelor's degree with 4+ years of experience, or master's degree with 2+ years of experience
Experience with several of the following analytical techniques: SE-HPLC, SEC-MALS, CEX-HPLC, SDS-PAGE, CE-SDS, ELISA, MSD, in vitro cell-based assays, qPCR
Proficiency in analytical method development and analytical method qualification/validation
Proficiency in Microsoft Office, GraphPad Prism or similar, OpenLabs CDS or similar
Working knowledge of GMPs
Strong scientific understanding and logical thinking
Ability to train others in basic laboratory techniques and equipment operation
Demonstrated flexibility and problem-solving abilities
Ability to work in a clinical and/or laboratory environment
Ability to handle exposure to biological fluids, infectious organisms, chemicals, and electrical office equipment with required personal protective equipment
Ability to perform required sitting, standing, bending, twisting, walking, squatting, reaching, and frequent hand movements
Ability to lift 15–30 lbs., with a maximum lift of 35 lbs.
Correctable near and far vision, color perception/discrimination
Ability to communicate complex information and understand spoken information
Ability to work with diverse groups to obtain consensus on complex issues
Ability to apply abstract principles to solve complex conceptual issues
Ability to perform complex tasks under variable and changing conditions

Benefits

Comp & perks

Up to 5% of the company bonus pool
Medical insurance
Dental insurance
Vision insurance
Life insurance
PTO
Paid holidays
Up to 5% 401(K) match
Tuition reimbursement
Professional growth and career progression opportunities