QHSE Coordinator

Over onze klant

Our client is a leading manufacturer and provider of thermal packaging solutions to the pharmaceutical, biotech, health care and medical device industries. We are a technically advanced, financially secure company with more than 50 years of experience and a history of vigorous growth.

The cpmpany is ISO 9001 registered and is headquartered in Franklin, MA with a global manufacturing and distribution network including facilities in The Netherlands, MA, TN, NV, PA, IL, and a larger global footprint in EMEA and LATAM. Our affiliated design and testing laboratories are highly recognized throughout the industry as world-class.

Functie

Overall responsibilities include maintenance of the quality system documentation, in-process and final inspections, supplier quality assurance, incoming material inspection, internal audits, trend analysis reporting, and special projects. The position requires knowledge of commonly used concepts, practices and procedures within the field and relies on a certain degree of experience and judgement to plan and accomplish tasks.

• Carry out quality audits of the production areas as required to ensure procedural compliance and continuously improve quality performance.
• Support 3rd party and customer audits for the site.
• Perform incoming inspections to ensure defect-free material flow.
• Prepare Certificates of Compliance (COCs)
• Conduct internal audits of the quality management system when assigned.
• Prepare trend charts for key quality metrics and assist in responding to negative trends.
• Conduct First Article Inspections
• Interface with external customers and suppliers on quality-related issues.
• Identify supplier quality non-conformances, issue, and track Supplier Corrective Action Requests(SCARs).
• Manage supplier performance through DMR.
• Provide input to customer complaint investigations.
• Support problem solving and continuous improvement projects utilizing Lean/Six Sigma tools and methodologies.
• Evaluate the effectiveness of implemented corrective action plans.
• Ensure full compliance with all documentation related to the quality management system and define opportunities to simplify and standardize across multiple sites.
• Actively support EH&S Rules and regulations.
• Other duties and responsibilities as assigned

• At least 5 years of experience in a manufacturing environment.
• Working knowledge of Quality Management System standards (i.e., ISO 9001:2015, AS9100, IATF 16949).
• Experience in QA/QHSE.
• Must be fluent in English both orally and in writing.
• Must have previous experience working in a quality role in the European Union.
• Experience in a cGMP environment
• Ability to accurately measure materials using standard metrology equipment.
• Problem solving experience
• Proficient with Microsoft Word, Excel, Access
• Experience working with a manufacturing ERP SW application.
• Proven experience working remote from corporate function.
• Skilled problem solver, specifically related to customer and 3rd party audit findings.
• Ability to quicky adapt to changing priorities and customer requirements
• Ability to multitask and work with associates at all levels of the organization (up, down and across the organization).
• Excellent verbal and written communication skills.
• Proficiency or fluency in another European language would be an advantage, e.g Spanish

• Direct a permanent contract
• Gross annual salary: between 64,800 and 90,000
• A Bonus opportunity to all employee based on 10% ebidta
• Pension scheme: 1 third/2 third employer
• Sickness costs fully paid by our client