Location: Kenilworth, NJ
Type: Contract
Job #35067

Qualifications: Basic Minimum Qualifications:
Education: *

B.S./B.A. in Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry, Biology, or related biological science discipline. The ideal candidate would possess:
At least 1 year related laboratory experience
Working experience in a regulated environment (GxP, preferably GLP)
Experience with cell culture and cell based assays such as nAb assays, PBMC isolation, or ELISPOT assay.
Experience with immunogenicity assays such as ELISA, Luminex, or MSD.
Familiarity with Laboratory Information Management System (LIMS)
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Ability to manage multiple projects under tight timeline and problem-solving skills
High sense of responsibility, accountability, and professional integrity

ABOUT YOU: You have applicable, hands-on academic or industry experience within a lab assistant position, performing research thesis work, or similar. You have performed actual lab work involving mammalian cell culture (primary cells or cell lines) and/or work with microtiter plate assays, preferably ELISA/ligand binding-type.

Responsibilities: Bioanalytical Scientist responsibilities include, but are not limited to, the following:

Develop and qualify cell-based or ligand-binding based bioanalytical assays to support high priority biological and vaccine programs.
Analyze samples using multiple platforms such as ELISA, ELISPOT, Neutralization assays or flow cytometry
Isolate PBMCs from donors.
Assess analytical result data on acceptability using LIMS or other computer software
Maintain documentation according to guidelines similar to GxP
Work according to established Standard Operating Procedures (SOPs) and regulatory guidance
Maintain accurate records of ongoing projects in adherence with documentation standards
Assist in generation and review of reports and contribute to trouble shooting efforts
Collaborate and communicate within and across the work group
Work in a structured environment under direct to moderate supervision
Adhere to GLP regulations and safety requirements in BSL-2

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Equal Employment Opportunity (EEO) Information

While the position you're applying for may not be for a government role, Astrix is a governmental contractor and, as such, is required to collect certain information in its applicants. Astrix is an Equal Opportunity Employer and does not discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status. Completion of these fields will not affect your opportunity for employment or the terms or conditions of your employment.

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Scientist – I (Assistant) – PA/NJ Only