Associate Scientist - Clinical Immunoassays and Diagnostics
- Pfizer
- Pearl River, New York
- Full Time
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 youll 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 Pfizers 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), with 0-2 years of experience.
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 functionality
Strong problem-solving skills
Excellent communication skills
Ability to work independently and as part of a team
Strong organizational skills
Ability to manage multiple tasks and projects simultaneously
PHYSICAL/MENTAL REQUIREMENTS
- Extended periods of sitting at Bio Safety Cabinet
- Light lifting, standing, walking, bending
- Ability to perform mathematical calculations and ability to perform complex data analysis
Other Job Details:
Last Date to Apply: July 30, 2025.
Work Location Assignment: On Premise
No relocation Support Available
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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