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Sr Research Associate I, Biologics Analytical Operations

Employer
Gilead Sciences, Inc.
Location
Foster City, California
Salary
See job description.
Closing date
Oct 17, 2021

View more

Sector
Science, Pharmaceutical
Hours
Full Time
Organization Type
Corporate
Jobseeker Type
Professional
Sr Research Associate I, Biologics Analytical Operations
United States - California - Oceanside

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gileads therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the companys five core values. Thats because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible

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Essential Duties and Job Functions :
  • Under general supervision, develop, optimize and validate potency assays to support biological drug development.
  • The candidate will contribute to developing and validating potency assays, confirming the potency of final drug substance and drug product, participating in structure-function studies as part of a team to characterize the molecule, degradation pathways and define critical quality attributes in a phase appropriate context.
  • The candidate will be responsible for production and maintenance of all critical reagents, cell lines, and cell banks used in potency assays
  • The candidate will contribute to developing and validating potency assays, confirming the potency of final drug substance and drug product, participating in structure-function studies as part of a team to characterize the molecule, degradation pathways and define critical quality attributes in a phase appropriate context.
  • Operates scientific equipment, selects appropriate methods and techniques to perform experiments, and prepare related reports. Plan and organize 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.


Required Education, Experience and Skills:
  • B.S degree with 2+ years of experience OR an M.Sc. with 0+ years of experience 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.
  • A good understanding of bioassay method development (ELISA, Receptor Binding, Flow Cytometry, and Cell-based assays) 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 development and optimization, and define GMP potency platforms.
  • 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 be an exceptional problem-solver.
  • Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining results. Demonstrates 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.

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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 careers@gilead.com for assistance.

Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Gilead has made the decision to require all U.S. employees and contractors to receive the COVID-19 vaccines as a condition of employment. Full vaccination is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation.\u200b

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

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

PAY TRANSPARENCY NONDISCRIMINATION PROVISION

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Gilead Employees and Contractors:

Please log onto your Internal Career Site to apply for this job.
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To apply, visit https://gilead.wd1.myworkdayjobs.com/en-US/gileadcareers/job/United-States---California---Oceanside/Sr-Research-Associate-II--Biologics-Analytical-Operations_R0018267-1

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