Senior Research Associate 1, Product Development

The Senior Research Associate 1, PD is responsible for executing experiments, immunoassays, and technical procedures. Working under the supervision of the Manager, this role involves leading the preparation of antigen, vaccine and/or adjuvant formulations, and leading and performing the development, optimization, and qualification of analytical assays. The Senior Research Associate 1, PD will lead research projects, document and interpret research data, write research protocols, SOPs, GR and related documentation and ensure accurate records and reporting of experimental data.

Responsibilities:

· Lead the preparation of antigen, vaccine and/or adjuvant formulations according to project requirements as needed.

· Lead and perform the development, optimization, and/or qualification of analytical assays.

· Lead and perform routine laboratory assays, including ELISAs, cell-based assays, serological assays, and bioassays according to established protocols.

• Write and document research protocols, SOPs, GR and other related documentation.

• Lead the preparation of antigen, vaccine and/or adjuvant formulations according to project requirements as needed.

• Collect, evaluate, interpret, and document research data, maintaining Electronic Lab Notebook in accordance with scientific objectives and company principles.

• Responsible for the proper logging, storing, and maintenance of research samples and materials, ensuring accurate records in Electronic Lab Notebook and databases.

· Manage general laboratory operations, including ordering supplies and equipment maintenance.

Requirements:

· M.S. in a relevant field with 0-2 years of experience or a Bachelor's degree with 5+ years of experience in life sciences related field.

· Strong written and verbal communication skills. Writing skills include routine communications and technical reports detailing procedures, outcomes, and observations. Ability to effectively present information in one-on-one, small groups and lab meetings

· Demonstrated proficiency using Microsoft Office applications (Word, Excel, PPT) as well as job related electronic systems/applications.

· Proficient in applying established mathematical and scientific techniques to compile and analyze data.

· Knowledge of laboratory techniques and protocol development, with adherence to Good Laboratory Practice (GLP) standards.

Physical Demands:

While performing the duties of this job, the employee is regularly required to walk, stand and sit. The employee will be able to use the pipettes for long periods at any given time. The employee must regularly lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus.

Working Environment and Travel: Normal laboratory working conditions. Business travel is not typical for this position.

ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

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