Vaccine Bioanalytical Scientist – ELISA & GLP QC

Pfizer; Pearl River (NY); On-site; USD 60,000 - 100,000; Full time

Benefits offered by this job

401(k) with Pfizer matching

Paid vacation

Health benefits

Job summary

Pfizer is seeking a laboratory-based role in Vaccine Research and Development, EBPD – Analytical GLP laboratory group, on premise in the United States. The position involves routine sample testing, assay verification and qualification studies, with emphasis on ELISAs, HPLC, UV-Vis and endotoxin testing.

You will contribute to fast-moving GLP projects and ensure compliance within a regulated environment. Under supervision, you will support toxicology studies, document results, and assist in

Qualifications

• BS or BA degree in biology or related discipline with 0-2 years relevant experience.
• Basic knowledge of bioassay analytical techniques.
• Strong verbal and written communication skills.
• Proficiency with personal computers including word processing, spreadsheets, PowerPoint and relevant scientific software is required.
• Prior experience with plate-based immune methods and automation (Hamilton STAR) is preferred.

Responsibilities

• Under direct supervision, perform sample testing in support of toxicology studies, including release, stability, and assay qualification.
• Document experiments and analyze data from sample testing and method qualification experiments using an electronic laboratory notebook and LIMS with guidance.
• Contribute to the authoring of technical documents including assay qualification reports, analytical test methods, stability protocols/reports.
• Assure safety and compliance.
• Provide daily laboratory operations support.

Skills

Bioassays

Data analysis

Communication

Computing skills

Education

BS or BA in biology

Tools

ELISA

LIMS

Hamilton STAR

HPLC

UV-Vis

Job description

Pfizer is seeking a laboratory-based role in Vaccine Research and Development, EBPD – Analytical GLP laboratory group, on premise in the United States. The position involves routine sample testing, assay verification and qualification studies, with emphasis on ELISAs, HPLC, UV-Vis and endotoxin testing.

You will contribute to fast-moving GLP projects and ensure compliance within a regulated environment. Under supervision, you will support toxicology studies, document results, and assist in