Overview
Sr. Associate, Quality Engineer – Data Analyst Jobs in Camden, AR at L3Harris Technologies
SUMMARY
The general responsibility of this position is to manage activities within the QC Testing Laboratory at Nomax, Inc. The laboratory is responsible for all testing to support the manufacture of drug, device, supplement, and food products. The scope includes raw materials, finished product testing and stability studies. The manager is responsible for ensuring compliance to regulatory and Nomax, Inc. requirements in our GMP laboratory.
ESSENTIAL DUTIES AND RESPONSIBILITIES
· Perform final review of laboratory data and prepare Certificate of Analysis to support lot release. This includes review of Quality Control results and/or results from 3rd party testing laboratories.
· Lead and/or participate in the investigations for Deviations and Out of Specification events in the lab.
· Coordinate, implement, and review all data for the product stability program including all products manufactured at Nomax, Inc.
· Direct and/or Participate in Method Validation.
· Manage and organize testing schedules to ensure product and material availability.
· Identify and resolve OOS and other Root Cause investigations within timelines to ensure Laboratory compliance.
· Responsible for the full employee life cycle including hiring, providing guidance and direction to subordinates, setting performance standards, and monitoring performance.
· Develop methods for new products as they are introduced.
· Update laboratory documentation to ensure compliance.
· Ensure compliance with safety requirements within the labs.
· Ability to lift up to 20lbs on occasion (retain samples, lab reagents, documents for filing).
· Implement Corrective and Preventative Actions(CAPA) and Change Control actions.
· Manage QC Metrics including coming due and overdue action items.
QUALIFICATIONS
· Experience in a GMP environment with processing of raw materials, production procedures, and quality control.
· High level of critical thinking by using logic and reasoning to identify the strengths and weaknesses of alternative solutions or approaches to problems.
· Exceptional level of attention to detail.
· Initiative to take on responsibilities and challenges without a high level of oversight.
· Effective, clear written and oral communication at all levels of the organization.
· Ability to motivate, develop, coach, coordinate, and direct people to work together and accomplish tasks.
· Proficient in Microsoft Excel, Word, PowerPoint, Outlook
· Working knowledge of HPLC, ICP, IR, UV-Vis and USP test methods
EDUCATION AND/OR EXPERIENCE
· Minimum Required: B.S. or B.A. in Chemistry or related field.
· Minimum Required: 7+ years related progressive laboratory experience with supervisory responsibilities.
Job Type: Full-time
Pay: $85,000.00 – $100,000.00 per year
Benefits:
401(k)
401(k) matching
Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Parental leave
Referral program
Tuition reimbursement
Vision insurance
Schedule:
8 hour shift
Day shift
No weekends
Education:
Bachelor’s (Required)
Experience:
Progressive laboratory experience with supervisory duty.: 7 years (Preferred)
Ability to Commute:
St. Louis, MO 63123 (Required)
Work Location: In person
Title: Sr. Associate, Quality Engineer – Data Analyst
Company: L3Harris Technologies
Location: Camden, AR
