QC Supervisor
Nordson Corporation

Job Info

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Collaboration drives Nordson's success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find Nordson employees sharing our success by giving back in the communities around the world where we live and work.

Job Summary

Supervise quality control personnel, scheduling, attendance, training, IMT applications including maintaining site level calibration program. Will assist maintaining site QMS compliance to ISO 13485 (current revision) requirements and corporate QMS, scheduling, hosting and follow up all internal and external audits. Actively participate in lean and continuous improvement projects.

Essential Job Duties and Responsibilities

• Assure compliance with ISO Standards and SOP's as defined by Nordson MEDICAL (PA), (Fluortek LLC) policies, practices and procedures.
• Maintain daily and weekly assignments and priorities for QC inspectors/Leads.
• Review, complete and approve QC Inspectors/Lead timecards, also assist with scheduling and approving PTO requests.
• Assist address day to day challenges for QC team, especially for ones don't have email
• Maintain site program for equipment calibration.
• Interface with gage / tools suppliers and external calibration providers.
• Approve and qualify new suppliers with supplier audits as required.
• Support and actively participate in the implementation of Lean/Cost Saving Initiatives and CI projects.

• Support in the proper documentation and disposition of non-conforming product.

• Train Quality Control Inspectors in understanding specifications, new product, procedures and measurement techniques.

• Lead or participate in internal/external Quality System audits.
• Maintain effective working relations, communications, and feedback with all other departments.
• Other duties as assigned

Education and Experience Requirements

• Education Bachelor's Degree preferred or 5 years of experience in Medical Device Manufacturing Environment.
• 3-5 years of experience in ISO certified QMS compliance & audits.

Skills and Abilities

• MS Office suite
• ISO Internal Auditor Certification
• Lean & Six sigma tools such as DMAIC
• Blueprint reading and/or GD&T (Basic)

Working Conditions and Physical Demands

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Travel Required

Minimal

Nordson Corporation provides equal employment opportunity to all applicants and employees. No person is to be discriminated against in any aspect of the employment relationship due to race, religion, color, sex, age, national origin, ancestry, disability, sexual orientation, gender identity, genetic information, citizenship status, marital status, pregnancy, veteran status or any other status protected by applicable federal, state, or local law. All employment offers are contingent upon successful completion of our pre-employment drug screening and background/criminal check, consistent with applicable laws.

This job has expired.