Description

We are currently seeking a 3rd Shift Quality Monitor to join our team at Essentra Packaging. In this role, you will be responsible for auditing, inspecting, and testing in-process products to ensure compliance with customer specifications. The primary focus will be to adhere to CGMP, ISO 9001, and standard operating procedures set forth by Essentra Packaging. This full-time, direct hire position offers significant opportunities for growth and career advancement within a strong, growing company.

Company Culture and Environment

Essentra Packaging fosters a culture of diversity and inclusion, where every team member feels safe, respected, valued, and can thrive. We emphasize teamwork and collaboration to achieve our goals.

Career Growth and Development Opportunities

At Essentra Packaging, you will have the opportunity for significant career advancement and professional development as you contribute to our mission in the international pharmaceutical industry.

Detailed Benefits and Perks

• Comprehensive health, dental, and vision plans
• 401k retirement plan with company match
• Company-provided life insurance
• Short-term and long-term disability coverage
• Flexible healthcare spending accounts
• Vacation, Paid Time Off, and holiday pay with competitive compensation
• Bonus eligibility

Compensation and Benefits

• Competitive salary based on experience

Why you should apply for this position today

This is a unique opportunity to join a dedicated team in the pharmaceutical packaging industry where your contributions directly impact product quality and customer satisfaction. Join us and help make a difference while advancing your career.

Skills

• High school graduate or equivalent required
• Previous experience with quality inspection in a manufacturing environment preferred
• Strong computer skills
• Excellent communication skills, both orally and in writing; must be able to read, write, and speak English
• Team player with the ability to work productively with others
• Ability to work well under pressure
• Excellent attention to detail
• Dependable, flexible, and approachable
• Knowledge of CGMP and SOP procedures is desirable
• Availability to work overtime as needed

Responsibilities

• Audit, inspect, and test in-process products for compliance with customer specifications
• Conduct random sampling of products based on company/customer requirements for evaluation
• Perform visual comparator analysis checks
• Input information into batch records to document defects for customer review
• Reconcile final inspection documentation for shipping
• Assist with training as needed
• Complete general ad-hoc duties as directed by management

Qualifications

• Minimum of two years of Quality Monitor experience required
• Minimum of one year of packaging experience in a manufacturing environment needed
• Knowledge of ISO 9000 procedures is a plus

Education Requirements

• High school diploma or equivalent required

Education Requirements Credential Category

• High School Diploma

Experience Requirements

• At least two years of experience as a Quality Monitor
• At least one year of experience in a packaging manufacturing environment

Why work in Charlotte, NC

Charlotte offers a diverse and vibrant community with a thriving job market, particularly in the manufacturing and pharmaceutical sectors. The city’s rich cultural scene, outdoor recreational opportunities, and family-friendly atmosphere make it an appealing place to live and work.