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. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and 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 in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support virus production and characterization. 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, its principles and concepts will help in meeting critical deadlines. You will be relied on 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. The incumbent will be responsible for supporting viral production under BSL-2 and BSL-3 conditions in support of the Influenza and SARS-CoV-2 strain change program.

How You Will Achieve It
Exercise and build basic team effectiveness skills {e.g., commitment, feedback, consensus management} within the immediate work group.

Perform job responsibilities in compliance with current Good Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements.

Assist in cell culture, virus infection, media preparation, and the CRIIS inventory control system

Perform virus characterization assays (titrations, HAI, TCID50)

Perform the bio-functional immunological assays to support vaccine clinical development (ELISA, ELISPOT, Flow Cytometry, neutralization assays) and virus sequencing support

Conduct clinical assays in accordance with Good Clinical Laboratory Practice (GCLP) requirements.

Present progress on assay development and sample analysis to colleagues and senior management.

Collect and analyze data on a per project basis to support troubleshooting, qualification and other lab projects.

Provide critical data review of clinical and non-clinical data.

Execute sample testing and analysis for toxicology and clinical trials.

Stay current on all departmental and corporate training.

Qualifications
Must-Have
Bachelor's Degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering or relevant field of science

Strong attention to detail and ability to collaborate and work in team environment

Good Computer skills including word processing, Excel, PowerPoint and relevant scientific software

Nice-to-Have
Pharmaceutical and biotech drug discovery experience

Virus infection and virus characterization assays

Knowledge of mammalian cell culture, molecular biology and aseptic techniques

Flow Cytometry, qPCR, ELISA assay expertise

Experience in developing and troubleshooting bioassays designed to assess antibody functionality



Work Location Assignment: On Premise

Other Job Details:

Eligible for relocation package

Eligible for employee referral bonus