Why Patients Need You
Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. In this role, you will support vaccine clinical trials by applying cutting edge technology to bring the best in class medicines to patients around the world.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 immunoassay data within the Ligand-Binding Immunoassay team in a regulated Good Laboratory Practices (GLP) setting to support Pfizer's vaccine programs. You will perform Luminex assays to support toxicology and clinical studies across multiple programs.
In addition, you will also support throughput activities and provide testing support for clinical and non-clinical research programs through responsibilities such as reagent preparation, equipment maintenance, inventory, assay troubleshooting/QC activities and data review.
The incumbent uses Good Documentation Practices (GDP), follows established safety policies and procedures and performs all work in a compliant manner according to relevant Standard Operating Procedure (SOP) guidelines and cGLP guidelines. How You Will Achieve It
- Perform clinical assays in accordance with cGLP requirements according to SOPs.
- Perform assays to support critical assay reagent testing and qualification, assay development and troubleshooting.
- Perform various duties to assist in assay throughput to complete the testing of human and animal samples from clinical and toxicology studies, including supply management, reagent preparation, data review, equipment maintenance, and inventory, when required.
- Assist in maintaining the laboratory, including ordering/restocking supplies and ensuring cleanliness/compliance.
- Perform job responsibilities in compliance with cGLP and all other regulatory agency requirements.
- Document all aspects of assay throughput to keep accurate, clear and complete records according to current cGDP requirements.
- Assist in managing records and documents associated with ligand-binding immunoassays, including information/data archiving, SOPs and reports.
- Exercise and build basic team effectiveness skills (e.g., communication, collaboration, commitment, feedback, consensus management) within the immediate work group.
- Presents experimental/project results at group meetings, when required. Provides progress updates to the group, when required.
- Complete all cGLP, safety, and site training in conformance with departmental requirements.
- Bachelor's or master's degree in biology, microbiology, molecular biology, chemistry, or relevant field of science. This is a non-PhD position.
- 0-3 years of experience in a relevant field
- Ability to work in a matrixed, collaborative environment with shared resources and effectively communicate within and across teams
- Ability to work independently, manage individual responsibilities, and prioritize work assignments
- Strong attention to detail
- Excellent record-keeping abilities
- Hands-on experience in a laboratory setting
- Experience pipetting
- Proficient in Microsoft Office (Excel, Word, Outlook, etc.)
OTHER JOB DETAILS
- Basic knowledge of/experience with cGLP/GDP
- Basic knowledge of/experience with Luminex technology
- Experience working in a regulated laboratory environment
Eligible for Relocation Package
Eligible for Employee Referral Bonus
Lifting, reaching, bending, ability to perform mathematical calculations and ability to perform complex data analysis.
\nRelocation support available\n
Work Location Assignment: On Premise
Relocation assistance may be available based on business needs and/or eligibility.Pfizer requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, Pfizer will consider requests for Reasonable Accommodations.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 provider's 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.
Research and Development