In-Process Quality Supervisor

NEVEON Executive Committee; Monroe (NC); On-site; USD 80,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated In-Process Quality Supervisor to lead a team in a dynamic manufacturing environment. This role involves active leadership, ensuring quality compliance, and overseeing critical inspection processes for semi-finished and finished goods. The ideal candidate will have a strong background in quality control within regulated settings and possess the ability to mentor and guide a team effectively. Join a forward-thinking company that values diversity and inclusion, and make a significant impact on product quality and team performance.

Qualifications

• 7 years of experience in a regulated manufacturing environment.
• 5 years of direct Quality Control work experience.

Responsibilities

• Lead and mentor direct reports while ensuring compliance with safety and quality standards.
• Oversee IPQ inspections and manage non-conforming products.

Skills

Leadership

Quality Control

Laboratory Testing

Statistical Analysis

Problem Solving

Education

Associate’s Degree in Science

Bachelor’s Degree in Science

Tools

SAP

Babtec

MS Office

Job description

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In-Process Quality Supervisor

Location: Monroe, US, 28110

Employment Type: Permanent

Responsibilities:

1. Active leadership, supervision, and mentoring of direct reports. Tasks include goal setting and regular performance review for direct reports.
2. Coordinating daily operational activities to meet departmental Safety, People, Quality, Responsiveness, and Cost KPI’s.
3. Coordinating and performing IPQ inspection and release for semi-finished and finished goods inspections according to valid procedure(s). This includes injection molding and final assembly departments.
4. Providing direct oversight for the identification and handling of nonconforming product according to valid procedure(s).
5. Performing timely compliance review and closure of production batch records.
6. Establishing clear procedures and documents compliant to Good Manufacturing Practice.
7. Supporting timely execution of Quality Assurance and Engineering validation activities including IQ, OQ, PQ, Product Verifications, Engineering Studies, Measurement Requests, etc.
8. Supporting Regulatory Affairs by performing customer complaint investigations, change control, internal/external audits, and corrective actions.
9. Supporting maintenance of testing equipment including troubleshooting, scheduling, and/or the performance of internal/external calibrations as required.
10. Performing periodic cycle counting and ordering of IPQ supplies as needed.
11. Performing other administrative duties to ensure IPQ operational readiness as required.

Authority includes:

1. The recruiting, hiring, training and retraining for IPQ Leads and Inspectors.
2. The direct monitoring and management of employee compliance in accordance to GBO NA Safety, Quality, HR, and payroll policies.
3. The evaluation of products, control of non-conforming products, and IPQ release according to valid procedures.
4. Responsible for ERP transactions such as stock transfers, quality hold and releases (SAP).
5. Responsible for the creation, revision, and distribution of IPQ documents.
6. Responsible for the creation, revision, and distribution of testing plans in the IPQ Laboratory Information Management System (Babtec).

Your Profile

1. Associate’s Degree in Science, life sciences, or related field; Bachelor’s Degree is preferred.
2. 7 years of experience in an ISO 9001, ISO 13485, or similar regulated manufacturing environment; relevant leadership experience preferred.
3. 5 years of direct Quality Control work experience.
4. Intermediate-level experience with laboratory testing equipment, instrumentation, and analysis, as well as laboratory data processing and review.
5. Intermediate-level MS office skills.
6. Intermediate-level knowledge of statistics, calculations, and reporting.

Physical Requirements:

1. Must be able to stand and walk for up to 8-12 hours.
2. Must be able to lift up to 50 lbs.
3. Must have appropriate vision to perform detailed quality inspections as outlined in SOP’s or TP’s.

We provide equal opportunities for everyone and see diversity as our strength. Therefore, we welcome all applicants – regardless of identifying characteristics such as gender, age, background, social status, veteran status, sexual orientation, religion, or mental and physical abilities. We have additionally set the goal of empowering women and increasing female leader representation. We foster an inclusive work environment and encourage all individuals to apply.

Job ID: 2683