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Associate Scientist-Vaccines
Job in
Pearl River, Rockland County, New York, 10965, USA
Listed on 2026-10-14
Listing for:
Pfizer
Full Time
position Listed on 2026-10-14
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Research Scientist, Medical Science
Job Description & How to Apply Below
United States
- New York
- Pearl River:
Full time:
Posted Today:
4964439
** Use Your Power for Purpose
** At Pfizer, our purpose is to deliver breakthroughs that transform patients' lives. Central to this mission is our Research and Development team, which strives to convert advanced science and cutting-edge technologies into impactful therapies and vaccines. Whether you are engaged in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, your role is crucial. You will leverage innovative design and process development capabilities to expedite the delivery of top tier medicines to patients globally.
By integrating advanced scientific knowledge with practical applications, we aim to bring the most effective treatments to those in need, fulfilling our commitment to improving health outcomes worldwide.
** What You Will Achieve
** As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality data in a regulated Good Clinical Laboratory Practices (GCLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures.
The incumbent is responsible for supporting immunoassays in BSL2 conditions within the Clinical Immunology and Diagnostics (CID) group within Pfizer Vaccine. In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs.
Your strong foundation in general scientific practice, principles, and concepts will help in meeting critical deadlines. You will be relied upon as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge.
It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.
** How You Will Achieve It
*** Execute immunological assays to support vaccine clinical programs in a high throughput setting in a timely and efficient manner.
* Conduct immunological clinical assays in accordance with Good Clinical Laboratory Practice (GCLP) requirements.
* Present experimental results at group and project meetings. Write progress reports, as necessary.
* Collect and analyze data on a per project basis to support troubleshooting, qualification, and other lab projects.
* May be asked to learn and perform other assays or tasks within the high-throughput area, as needed.
* Complete required documentation for laboratory work. This includes information and data organization/review.
* Build team skills and collaborate effectively within the work group.
* Stay current on all departmental and corporate training.
* Organize work to meet deadlines and apply technical skills.
* Follow procedures for assigned tasks and seek guidance when necessary.
* Participate in laboratory management by stocking supplies and reagents needed for daily laboratory operation.
* Where applicable, satisfactorily completes all GCLP and safety training in conformance with Departmental requirements.
** Qualifications*
* ** Must-Have
*** BS in a relevant field of science (biology, immunology, microbiology, etc)
* A good foundation in general scientific practice and in the principles and concepts of a relevant scientific discipline.
* Strong attention to detail
* Ability to collaborate and work effectively in a team environment
* Proficiency in the use of Word, Excel, PowerPoint, and relevant scientific software is desirable.
* Good verbal and written communication skills are desirable.
** Nice-to-Have
*** Experience in developing and troubleshooting bioassays designed to assess antibody…
Position Requirements
10+ Years
work experience
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