Associate Scientist I: GLP Lab & Regulatory Data

Abbott; North Chicago (IL); Sur place; USD 65 000 - 75 000; Plein temps

Avantages offerts par ce poste

Medical plan

Dental plan

Vision plan

Health Savings Account (HSA)

Flexible Spending Accounts (FSA)

Life Insurance

Disability Insurance

401(k)

Résumé du poste

Abbott Park in Illinois is seeking an Associate Scientist I to support testing and evaluation of new Transfusion Medicine products in a laboratory setting. This role contributes data for regulatory submissions and FDA approval processes.

Responsibilities include executing tests, maintaining records, and assisting with data collection for submissions. Requires a Bachelor’s degree in a scientific discipline and GLP understanding. Two shifts and weekend coverage may apply.

Qualifications

• Bachelor's degree in a scientific discipline required.
• 1–2 years of laboratory experience preferred; strong entry-level candidates will also be considered.
• Understanding of Good Laboratory Practice (GLP).
• Ability to follow protocols and maintain accurate records.
• Adaptable, flexible, and able to learn quickly in a fast-paced laboratory environment.

Responsabilités

• Perform laboratory testing of new products, assays, and instrumentation.
• Execute studies according to established protocols and GLP requirements.
• Generate, document, and maintain accurate study data and records.
• Support data collection for FDA regulatory submissions.
• Complete laboratory documentation and reporting with accuracy and attention to detail.
• 75% laboratory work and 25% documentation/administrative tasks.

Connaissances

GLP

Lab Testing

Documentation

Data Collection

Protocol Execution

Attention to Detail

Quality Awareness

Adaptability

Formation

Bachelor's degree in a scientific discipline

Outils

Abbott instruments

Description du poste

Abbott Park in Illinois is seeking an Associate Scientist I to support testing and evaluation of new Transfusion Medicine products in a laboratory setting. This role contributes data for regulatory submissions and FDA approval processes.

Responsibilities include executing tests, maintaining records, and assisting with data collection for submissions. Requires a Bachelor’s degree in a scientific discipline and GLP understanding. Two shifts and weekend coverage may apply.