Production and Industrial – Quality Control

Job Description

Job Summary: 

• Client invites you to be part of our team and participate in impactful projects. Collaborate with dedicated colleagues and benefit from opportunities available within our respected organization.
• Using standard operating procedures (SOP) and good manufacturing practices (GMP), the Engineer/Scientist II will perform testing of Raw Material, Semi-finished, and Finished goods including data generation, product stability verification, data analysis and summarization, and other supporting activities.

Duties and Responsibilities:

• Ensure completion and maintenance of applicable testing log and accuracy of product and lab related quality control records.
• Build and maintain database of critical product performance measures for trend analysis.
• Perform routine QC functions such as material testing, equipment calibrations, managing lab supplies, and maintain a clean and orderly laboratory area.
• Process and coordinate testing and disposition of product returns. Review and approve QC test data.
• Assist with laboratory investigations of Out of Specification results and Non-Conformance reports.
• Perform product evaluation tests or special test requests to assist product technical teams with process improvements, corrective and preventative actions.
• Participate in team meetings to tackle product performance and/or process issues.
• Assist with new analytical method validations, stability testing, and method integration of new products into the QC laboratory.
• Assist with training courses for QC Associates in product line testing and various QC departmental functions.
• Assist in the collaboration and editing of departmental standard operation procedures.
• Assist with other QC department functions as needed.

Requirements:

• Bachelor’s degree in a biological or related science from an accredited college or university plus two (2) years of laboratory/relevant experience; OR a High School Diploma and a minimum of 7-10 years of laboratory/relevant experience.
• MS Office digital literacy required for record and analysis reporting – i.e. Word, Excel, etc.
• Knowledge of Basic Good Laboratory Practices (GLP) and GMP requirements.
• Proficiency with the English language.