Sr. Research Associate II, Analytical Operations, Cell-based Assays Oceanside, CA

Compensation

: $164,410.00 - $164,410.00 /year *

Employment Type

: Full-Time

Industry

: Scientific Research



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Sr. Research Associate II, Analytical Operations, Cell-based Assays Oceanside, CA

Job Description

Specific Responsibilities and skills for position

A good understanding of Bioassay method development (ELISA, Receptor Binding, Flow Cytometry, and Cell-based) for early and late stage biotherapeutics is required. The successful candidate will be expected to demonstrate hands-on experimental responsibilities in the laboratory, independently champion technology development projects, be involved in new assay evaluation and optimization, and define GMP potency platforms.

The candidate will contribute to developing and validating potency assays, confirming the potency of final drug substance and drug product, and supporting lot release and stability QC testing. The candidate will also participate in structure activity relationship work as part of a team to characterize the molecule, degradation pathways and define critical quality attributes in a phase appropriate context. The candidate will also participate in process development and compatibility studies.

Works with Gilead internal researchers in the identification and selection of robust potency assays and optimization efforts for GMP applications. Identifies and deploys orthogonal characterization methods to aid in identifying critical quality attributes. Responsible for production and maintenance of all critical custom reagents and cell lines used in development and QC potency assays.

The applicant should be an effective communicator of ideas, project goals and results to team members across cross-functional roles/departments. Ability to proactively identify issues and develop solutions in a collaborative multidisciplinary environment. This is a highly collaborative environment where willingness and ability to communicate and work effectively with individuals across various project teams is essential.

Candidates should be self-motivated and organized, familiar with the relevant literature, and enjoy scientific investigation and thinking, proactively identify issues and develop solutions in a collaborative multidisciplinary environment. The applicant is also expected to exercise considerable latitude in determining objectives and approaches to assignments, and should be an effective communicator of ideas, project goals, and results to team members across cross-functional roles/departments.

Essential Duties and Job Functions

Under general supervision, develop and validate potency assays to support biological drug development.

Demonstrate hands-on experimental responsibilities in the laboratory including aseptic technique, routine cell culturing and performance of plate-based assays.

Operates scientific equipment, selects appropriate methods and techniques to perform experiments, and prepare related reports. Plans and organizes details of experiments with guidance.

Demonstrate good verbal communication skills and interpersonal skills. Be able to work in a fast-paced and highly collaborative working environment.

Knowledge of GMP, GLP or GxP is highly preferred.

Knowledge, Experience, and Skills

5 years of experience with B.S. degree, or 3 years of experience with M.Sc. or MS in biology or relevant scientific discipline.

Good communication skills (both verbal and technical) and interpersonal skills are required. Must be able to work in highly flexible and effective teams.

Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results. Demonstrates high attention to detail, ability to recognize anomalous and inconsistent results and interpret experimental outcomes. Demonstrates technical proficiency, scientific creativity, collaboration with others and independent thought in suggesting experimental design and research strategy. Experience with GMP validation and testing is preferred.

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As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ...@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the EEO is the Law poster.

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Associated topics: aseptic technique, bacteria, biopharma, health, healthcare, histotechnologist, immuno oncology, microbiological, pharmaceutical, pharmacometrics * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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