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Sr. Research Associate II - Protein Purification Process Development - $8,000* Sign On

Company: Gilead Sciences
Location: Oceanside
Posted on: November 22, 2021

Job Description:

Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensure the health and safety of our teams.

For Current Gilead Employees and Contractors:
Please log onto your Internal Career Site to apply for this job.

Job Description

Sr. Research Associate II - Protein Purification Process Development - $8,000 Sign On

Gilead Sciences, Inc. is a research-based biopharmaceutical company founded in 1987. Together we deliver life-saving therapies to patients in need. With the commitment and drive you bring to the workplace every day, you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives. Our worldwide staff is a close community where you can see the tangible results of your contributions, where every individual matters, and everyone has a chance to enhance their skills through ongoing development. Our scientific focus has resulted in marketed products that are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available to those who could otherwise not afford them. By joining Gilead, you will further our mission to address unmet medical needs and improve life by advancing the care of patients with life-threatening diseases.
Gilead Sciences is seeking a Sr Research Associate I with experience in protein purification process development to support operations at our biologics development and manufacturing site in Oceanside California.

Essential Duties and Job Functions:

  • Plan and execute assigned experiments that support Process Development activities and project goals.
  • Select appropriate methods and techniques for performing experiments.
  • Develop skills in data analysis and interpreting experiment outcomes including the ability to evaluate data quality and recognize anomalous results.
  • Recommend alternatives, research new methods and techniques and proactively seek out senior personnel to discuss potential solutions to problems.
  • Participate in group meetings and present results, data interpretation and conclusions.
  • Demonstrate strong verbal communication and interpersonal skills including the ability to explain processes used to achieve results of assigned tasks.
  • Work with team oriented, collaborative and problem-solving mindset.
  • Always work with safety in mind.
    Knowledge, Experience and Skills:
    • Preferred degree in Chemical/Biochemical Engineering, Biochemistry, Chemistry or a related scientific discipline.
    • Prior experience in biologics purification, with an emphasis on affinity, IEX, and HIC.
    • Prior experience in analytical operations: SEC/HPLC, CE (R/NR), HCP testing is beneficial, but not required.
    • Knowledge of cGMPs, technology transfer, and scaling up bioprocesses.
    • Must be able to work effectively in cross-functional teams.
    • Must demonstrate excellent technical writing skills.
    • Working understanding of downstream process development including centrifugation, normal and tangential flow filtration, chromatography operations, and virus clearance. The ability to demonstrate hands on experience in several of these areas is expected. Experience with multiple modalities (mAbs, bispecifics, fusion and antibody drug conjugates, virus particles) produced in microbial and mammalian expression systems is a plus.
    • Ability to work effectively within the purification team to help design and execute experiments supporting process definition, optimization, and characterization with an increasing level of independence.
    • Ability to collaborate with Technical Operations during technology transfer from process development to GMP manufacturing, including serving as a process development representative during purification operations, providing technical troubleshooting and identifying opportunities for future process and equipment improvements. The candidate will also contribute to the preparation of regulatory filings and process validation and characterization reports.
    • Ability to effectively communicate ideas, project goals and results and should have the ability to proactively identify issues and suggest 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 teams is essential.
    • Self-motivated, organized, and enjoy scientific investigation and thinking. The candidate will monitor and contribute to external literature and scientific conferences.
      Basic Qualifications:
      • BS degree in a relevant scientific discipline and 5+ years of relevant experience; OR
      • MS degree in a relevant scientific discipline and 3+ years of relevant experience
        * This Position qualifies for a $8,000 Sign-on Bonus, $4,000 payable within 30 days of start date and $4,000 payable following 6 months of continuous employment. Payments are subject to a 1-year repayment agreement from date of payment issue.

        Gilead is an equal opportunity employer.

        For jobs in the United States:
        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 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.

        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.

Keywords: Gilead Sciences, Oceanside , Sr. Research Associate II - Protein Purification Process Development - $8,000* Sign On, Other , Oceanside, California

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