Quality Laboratory Analyst I

AbbVie•North Chicago, IL

6d•$21 - $38

About The Position

Understands, implements, and maintains a safe work environment and good manufacturing practices with respect to procedural requirements and laboratory records and requirements. Maintains training certificates as needed for assigned job tasks. Performs product complaint documentation, investigation, and review of all non-medical complaint content. Analyze and test routine to medium complexity products, and evaluate results. Performs test methods as written to support product complaint investigation activities with minimal error. Interprets experimental data for conformance with product and material specifications. Initiates appropriate exception documents in accordance with procedural requirements. Accepts responsibility for acquiring knowledge and experience to support continual personal development. Can work in multiple laboratory functional areas as assigned and can effectively perform a multitude of laboratory techniques for which they are trained on with minimal error and the ability to adjust to unforeseen obstacles to accomplish assignments. Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making. Makes suggestions for improvement based upon scientific and good manufacturing practices understanding. Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GLP. This requires good analytical skills, technical writing, and good documentation. Maintains lab for safety and compliance. Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization.

Requirements

Bachelor’s Degree minimally required, Associate’s Degree with at least 2 years of lab experience, High School Diploma with at least 5 years of directly related lab experience.
Ability to effectively manage their own time to multi-task based upon their completed training matrix.
Accountable to supervisor and assigned teams to meet broader business objectives.
Good analytical skills
Technical writing
Good documentation

Responsibilities

Maintains training certificates as needed for assigned job tasks.
Performs product complaint documentation, investigation, and review of all non-medical complaint content.
Analyze and test routine to medium complexity products, and evaluate results.
Performs test methods as written to support product complaint investigation activities with minimal error.
Interprets experimental data for conformance with product and material specifications.
Initiates appropriate exception documents in accordance with procedural requirements.
Accepts responsibility for acquiring knowledge and experience to support continual personal development.
Can work in multiple laboratory functional areas as assigned and can effectively perform a multitude of laboratory techniques for which they are trained on with minimal error and the ability to adjust to unforeseen obstacles to accomplish assignments.
Budget time effectively to carry out assigned tasks and takes initiative to be involved in team activities and decision making.
Makes suggestions for improvement based upon scientific and good manufacturing practices understanding.
Ensures that complaint documentation meets Good Documentation Practices as well as GMP and GLP.
Maintains lab for safety and compliance.
Works with others to maintain a positive atmosphere to accomplish business objectives and is an active participant in the work structure and fosters positive working relationships with all levels of the organization.