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Quality Manager

Job Overview
Job Order:JO00018302
Date Posted:Jul 10
Salary:
Category:2 - Engineering & Manufacturing
Metro Area:

Our client in Vandalia, Ohio is in need of a Quality Manager

The Quality Manager is a manufacturing quality specialist responsible for developing and managing the Quality Management System; oversees Quality inspection of processes and products; assures and certifies product compliance. Maintains quality system conformance, quality data collection/reporting, Field Return system/analysis, and Corrective and Preventive Action system. A key part of the role is to ensure 100% quality product is manufactured on a first time basis through process control and effective production techniques. This requires a highly integrated and hands on approach with engineering and production operations.

Responsibilities:

Establishes quality standards and metrics for new processes with Engineering and Operations, defining methods & standards to improve product quality and productivity. Active in Genba Kaizan activities company wide.

Coordinates/manages the scheduling and control of inspection activities and enforcement requirements for raw materials, components, product and package specifications and regulatory agencies.

Determines overall plant product quality by coordinating the implementation of methods and procedures for inspecting, testing and evaluation of products and production equipment.

Maintains compliance with all documented Quality Policies and Objectives; assists in obtaining and maintaining required Quality certifications.

Assists in resolving quality problems by driving efforts of quality, engineering, and operations personnel to identify root causes of problems and appropriate corrective and preventive action.

Coordinates field return/ failure analysis system, calibration, change control and material review board.

Act as front line for customer concerns on quality issues or related technical questions.

Establishes and maintains effective inspection and tests to ensure product quality/reliability.

Ensure compliance with all corporate directives or initiatives for quality, control processes etc. Achieve compliance.

Act as instructor, facilitator, coordinator and auditor to ensure implementation is effective.

Requirements

Basic Qualifications:

3+ Years of FDA and Medical Device Experience (ISO 13485)

Bachelor’s degree in Engineering or Science based discipline

6+ Years of experience working in Quality

Eligible to work in the United States without sponsorship

Preferred Qualifications:

Solid knowledge of Design Controls, Quality Control and assurance practices.

Internal Audit experience

Change Control and Supplier Management experience

Knowledge and Practical implementation of ISO 9001 and ISO 13485

Prior practical experience with 6 Sigma, SPC, Cpk, AQPQ, PPAP

RoHS/REACH/SVHC/IMDS reporting is desired

If you are a high performer and would like to work for an equally high performing company and you think the above opportunity is appropriate for you, we invite you to submit your resume in Microsoft Word format to abarry@venteon.us.com.

We treat all resumes with strict confidentiality. We will always contact you first before submitting your resume to our client(s) for review. If you do not receive correspondence, you are not a fit for this position.

At Venteon our talent acquisition team is proud to provide our clients with the most qualified Accounting & Finance, Engineering, IT and Administrative talent in the industry today.