Quality Systems Specialist at Vonco Products LLC

Indianapolis, Indiana, United States -

Full Time

Start Date

Immediate

Expiry Date

30 Jul, 26

Salary

0.0

Posted On

01 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management Systems, Document Control, Change Control, CAPA, Internal Auditing, Complaint Handling, Standard Operating Procedures, Root Cause Analysis, Nonconformance Process, ISO 13485, FDA Regulations, Microsoft Word, Microsoft Excel, Microsoft Outlook, Data Entry, Technical Writing

Industry

Packaging and Containers Manufacturing

Description

Description Basic Purpose and Function: Independently perform quality-related functions within the Quality Department. Maintain and monitor quality systems, including document control, change control, CAPA (Corrective and Preventive Actions), internal audits, and complaint handling. Job Responsibilities: · Manages the review cycle of customer complaints and CAPA’s · Lead internal audit program · Assist in the development, revision, and control of Standard Operating Procedures (SOPs) and other controlled documents. · Identify training needs and conduct Quality Assurance-related training to associates in tandem with the Quality Manager · Facilitate the nonconformance process and ensure timely investigation, root cause analysis, and resolution. · Supports the maintenance and upkeep of the Quality Management System · Support performance metrics system for continual improvement · Assist with inspections, document reviews, and data entry when additional support is required to maintain production or quality timelines Other Responsibilities: · Responsible for adhering to the quality system and good manufacturing procedures · Must be able to communicate effectively with the supervisor and co-workers to provide and receive directions · Demonstrate good time management skills independent of supervision · Maintain timely and regular attendance per company policy · Performs other duties as assigned Requirements Qualifications: · Associates degree or equivalent; or 3-5 years related experience and or training; or equivalent combination of education and experience in medical device manufacturing · Proficient in applicable regulations/standards (ISO 13485, FDA, etc.) · Ability to read, analyze, and interpret general business periodicals, professional journals, or governmental regulations. · Ability to write reports, business correspondence, and procedure manuals · Ability to effectively present information and respond to questions from employees, supervisors, managers, executive staff, customers, and suppliers · Reaching, standing, walking, pushing, pulling, lifting, typing, grasping, feeling, talking, hearing, seeing and repetitive motions · Proficiency in Microsoft Word, Excel, and Outlook or similar e-mail programs · Responsible for adhering to the quality system and good manufacturing procedures · Must be able to communicate effectively with the manager and co-workers to provide and receive direction · Demonstrate good time management skills independent of supervision · Maintain timely and regular attendance per company policy Physical Requirements: · Reaching, standing, walking, pushing, pulling, lifting, typing, grasping, feeling, talking, hearing, seeing and repetitive motions · The associate must occasionally lift and/or move up to 40 pounds · Specific vision abilities required by this job include close vision and the ability to adjust focus

Responsibilities

The Quality Systems Specialist manages customer complaints, CAPA processes, and internal audits while maintaining the Quality Management System. They also assist in the development of SOPs and provide quality assurance training to associates.