Assistant Scientist I (onsite)

Posted 21 Days Ago
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Concord, CA
Senior level
Healthtech
The Role
The Assistant Scientist I supports research and development by executing experiments, analyzing data, and developing new methods for assays. Responsibilities include writing documentation, conducting routine testing in coagulation studies, and ensuring laboratory maintenance while presenting results and contributing to scientific publications.
Summary Generated by Built In

About Cerus:

Cerus aims to be the global leader and trusted partner of blood centers and hospitals whose technology, services, and commitment are the lifeblood of safe and accessible blood for patients around the world.

                             

Summary & Scope of Position:

Support research and/or development activities by performing studies to support development, validation and conduct of assays for multiple projects. 

Primary Responsibilities:

  • Execute experiments, analyze data and interpret results either independently or as a team member.
  • Develop, implement, and validate new methods and technologies for project advancement.
  • Assist with the design and execution of studies, analysis of data, and making recommendations.
  • Write study plans, final reports, notebook entries and other required documentation of work.
  • Conduct routine testing in support of coagulation studies and other research initiatives.
  • Assist in the maintenance of general laboratory function through monitoring of consumables inventory, laboratory waste management, QC of equipment and chemical inventory.
  • Maintain a high level of professional expertise through familiarity with scientific literature.
  • Presents results of data at departmental or project meetings.
  • Contribute to scientific publications.
  • May determine methods and procedures on new assignments.
  • May supervise, mentor or provide guidance to other personnel.
  • Perform other related duties as required.

Qualifications/Requirements/Skills

  • Bachelor’s degree in a scientific discipline with a minimum of 5 years’ experience or Master’s degree in a scientific discipline with a minimum of 2 years’ experience.
  • Some assay development is preferred.
  • Sharp analytical skills, problem solving, troubleshooting, innovative.
  • Proficient with word processing, spreadsheet, scientific and graphics applications. 
  • Strong attention to detail and accuracy.
  • Familiarity with GLP/GMP regulations.
  • Experience working with human blood products preferred.
  • Flexible; ability to adapt to changing priorities.
  • Good communication skills (verbal, written, interpersonal, listening).
  • Ability to work independently.
  • Time management (schedules, timelines, task prioritization).
  • Excellent problem-solving skills; solution oriented.
  • Team oriented.


We understand that our people are essential to our success.  This philosophy is revealed in our competitive benefits package, designed to improve employees’ lives both on and off the job.

Benefits plans: medical, dental, vision, domestic partner benefits, paid maternity and paternity leaves, healthcare and dependent care flexible spending, life and accidental death insurance, long-term and short-term disability insurance, matching 401(k), ESPP, RSUs

Work and family: EAP, legal and financial services, health club membership discounts, tuition reimbursement

Compensation: The base salary range for this position in the selected city is $101,223-113,000 annually.  Compensation may vary outside of this range depending on various factors, including a candidate’s qualifications, skills, competencies, experience, and location. Base pay is one part of the total package to compensate and recognize employees for their work.


All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.  

The Company
HQ: Concord, California
361 Employees
On-site Workplace
Year Founded: 1992

What We Do

Cerus Corporation is dedicated solely to safeguarding the world’s blood supply and aims to become the preeminent global blood products company. Headquartered in Concord, California, the company develops and supplies vital technologies and pathogen-protected blood components to blood centers, hospitals, and ultimately patients who rely on safe blood. The INTERCEPT Blood System for platelets and plasma is available globally and remains the only pathogen reduction system with both CE mark and FDA approval for these two blood components. The INTERCEPT red blood cell system is under regulatory review in Europe, and in late-stage clinical development in the US. Also in the US, the INTERCEPT Blood System for Cryoprecipitation is approved for production of INTERCEPT Fibrinogen Complex, a therapeutic product for the treatment and control of bleeding, including massive hemorrhage, associated with fibrinogen deficiency. For more information about Cerus, visit www.cerus.com and follow us on LinkedIn.

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