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Form of workAlltrista Plastics LLC, is a subsidiary of Jadex Inc., and is a leading manufacturer in high-volume, precision injection molded parts. The company designs and manufactures with proprietary engineering processes and extensive manufacturing capabilities, from five (5) locations worldwide. From the first spark of an idea, through the design of the mold to the actual manufactured product, Alltrista Plastics focuses all efforts on delivering innovative plastic solutions. The company's core markets include Consumer Products, Medical/Healthcare, Personal Care, Health & Beauty, Caps & Closures, and Packaging.
Quality Systems Administrator - Springfield, MO
Assist the Quality Manager in maintaining all Quality Systems at the Alltrista, Springfield facility will help to monitor and improve quality recordkeeping, batch record systems, ISO documents, and internal/external audits.
Primary Functions- Oversees and administers the Alltrista Springfield Quality systems including all internal and external audits.
- Maintains internal and external customers current specification revision and communicates to other plant personnel.
- Maintains internal and external document control logs.
- Approves each batch record in a timely manner to ensure all components are complete and accurate.
- Recommends changes and implements changes to batch record review.
- Identify any necessary deviations for corrective action.
- Ensures that project books and protocols are complete, accurate, and controlled in a central location by quality assurance.
- Maintains records and files for Good Manufacturing Practices.
- Writes, reviews, and implements new documents under the direction of the Quality Manager.
- Performs revision changes to current documents and disposes of expired documents.
- Works closely with other departments to facilitate the total quality function by completing, assisting in directing, and participating in internal audits.
- Identifies any deviations for corrective action and follows up for closure.
- Assists in the necessary activities relative to internal and external customer complaints, audit and disposition of goods, corrective action, and documentation.
- Assists in training all new and existing quality personnel on new and revised documents.
- Assists with training all new and existing plant personnel on current Good Manufacturing Practices.
- Assists in developing and maintaining label control procedures and identifies deviations for corrective actions and follow up.
- Reviews new and revised customer specifications and product drawings for identifying any necessary additions or alterations to existing tooling, techniques, procedures, or other normal operating procedures.
- Assures all non-conforming materials are properly dispositioned and that the necessary corrective actions are effective and implemented in a timely manner.
Key Qualifications
- Certified Quality Auditor and Lead Auditor certification preferred.
- Minimum two to five years of experience in a document control position with demonstrated successful performance.
- Minimum two to five years metrology/precision measurement experience.
- Minimum two years of experience in an injection molding and quality assurance environment.
- Working knowledge of SPC/SQC, statistical sampling, and auditing principles.
- Familiarity with 21 CFR 820 medical device regulations, Good Manufacturing Practices, ISO 9001 or similar Quality Systems.
- Familiarity with reviewing and executing validation protocols and validations or use of electronic document control systems.
- Working knowledge of computer applications.
Specifics:
- Competitive salary and bonus structure
- Full benefits package
- 401K with match
- Strong vacation and corporate holiday policy
- Job Family Operations
- Pay Type Salary
