Quality Control Technician II

Takeda•Round Lake, IL

15h•$19 - $30•Onsite

About The Position

As a Quality Control Technician II, your primary responsibility is to ensure compliance with procedures and regulatory requirements in the manufacturing facility. The incumbent is responsible for quality support and oversight of manufacturing operations, which includes presence on the floor and for performing Acceptable Quality Limit (AQL) sampling of finished product. Additional responsibilities include triage for potential issues on the floor, raw material investigations, Quality on the Shop Floor (QOTSF), online batch documentation review, sample management, kitting of batches, and raw materials release. This role is a day shift, 6:00am – 6:30pm in a 2-2-3 work schedule.

Requirements

High School Diploma or GED with 2+ years of related work experience or Associates degree or higher and 1+ years related work experience.
Solid interpersonal skills and great attention to detail.
Team player with good problem solving, and good verbal and written communication skills.
Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
Proficient in Microsoft Word, Excel, Outlook, and SharePoint.
Able to work with JDE, EBM, TW workflows, Systech and other Learning Management and Document Management systems.

Responsibilities

Performs Acceptable Quality Limit (AQL) sampling of finished product.
Identifies and assesses quality risk in production operations daily.
Executes Quality on the Shop Floor (QOTSF) and reviews checklists.
Programs are part of manufacturing support and compliance enforcement.
Initiation of JDE (inventory management system and preventive maintenance system) work orders if required to address issues in a timely manner.
Performs sample management (Sterility, stability, etc.) to appropriate facilities and is responsible for the appropriate storage and disposal of retention samples.
Performs triage with manufacturing, engineering, and maintenance to resolve potential issues on the floor and escalate if needed.
Solid interpersonal skills and great attention to detail.
Team player with good problem-solving and good verbal and written communication skills.
Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP)
Proficient in Microsoft Word, Excel, Outlook, and SharePoint.
Able to learn and work with JDE, EBM, TW workflows, Systech, and other Learning Management and Document Management systems.
Facilitates kitting operations for packaging – issue and return of preprinted materials physically and electronically.
Handles movement of materials/products physically and electronically for quarantine and reject areas.
Review Lead Manufacturing support activities, including batch record documentation review.
Perform review and approval of batch documentation and consult with manufacturing to address any required corrections.
Subject Matter Expert (SME) and provides training to other employees as required.
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, and cGMP regulations.
Monitor product quality through the performance of required visual testing follow-ups.
Actively contributes to a team setting within quality operations and potentially with other work teams to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.
Support regulatory audits as required.

Benefits

U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others.
U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation.

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