Petoskey Plastics aspires to stand out as an industry leader in sustainability, using advanced recycling technology to manufacture high-quality films, bags, and resins from post-consumer materials. Our commitment to eco-friendly innovation sets us apart, as we strive to earn the appreciation and respect of our customers, associates, and communities. If you are seeking a family-oriented company that values career growth and provides robust paid training, explore the comprehensive benefits listed below to see how Petoskey Plastics can support your professional journey.
We’re headquartered in Petoskey where our Lake Michigan shores are clasped by rhythmic waves of seafoam and cobalt. We’re honored to have roots in Texas, Tennessee, and Indiana as our production has expanded over the years. Our custom-engineered solutions tackle a variety of industries, including automotive, industrial, institutional, retail, construction, home improvement, medical, and more.
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Coordinate and prepare PPAP documentation in accordance with AIAG standards and customer-specific requirements
Support new product launches and engineering changes by managing PPAP timelines and deliverables
Ensure timely submission PPAP packages to customers and track approvals
Communicate with customers and internal team regarding PPAP status, feedback, and required revisions
Interface with engineering, manufacturing, and quality teams to gather necessary data and documentation
Ensure compliance with ISO 9001, GMP, ISO 13485, FDA SQR and other applicable quality standards
Ensure medical device documentation record and submission records, including CoAs
Ensure material compliance reporting through IMDS or other required system reporting
Monitor and maintain customer portals to ensure APQP & PPAP deliverables
Maintain PPAP records and documentation in an organized and accessible format
Monitor and maintain customer scorecards
Assist in root cause analysis and corrective actions related to PPAP rejections or quality concerns
Support generation of customer requested CoA’s
Perform other duties as assigned by management
Strong knowledge of AIAG Core Tools
Proficient in the development and authoring of Quality Control Documents (PFlow, FMEA, Control Plan, Inspection Documents)
Familiarity with IATF 16949 and ISO 9001 Standards
Familiarity with ISO 13485:2016 and FDA QSR (21 CFR 820)
Familiarity with GMP
Ability to read blueprints and specifications
Strong attention to detail and ability to organize and manage multiple project PPAP’s simultaneously
Excellent communication and interpersonal skills
Strong verbal and written communication skills
Proficient in Microsoft Office Suite and quality management systems
Data entry accuracy and keyboarding skills
