What are the responsibilities and job description for the QUALITY ASSURANCE SUPERVISOR position at Berry Global, Inc?
Overview
About BerryAt Berry Global Group, Inc. (NYSE: BERY), we create innovative packaging and engineered products that we believe make life better for people and the planet. We do this every day by leveraging our unmatched global capabilities, sustainability leadership, and deep innovation expertise to serve customers of all sizes around the world. Harnessing the strength in our diversity and industry-leading talent of over 40,000 global employees across more than 250 locations, we partner with customers to develop, design, and manufacture innovative products with an eye toward the circular economy. The challenges we solve and the innovations we pioneer benefit our customers at every stage of their journey. For more information, visit our website, or connect with us on LinkedIn or Twitter.Responsibilities
Seeking a Quality Supervisor who will supervise the quality department for a high volume plastics manufacturing plant with a mostly pharmaceutical customer base. Supervise personnel and systems to ensure quality products and records.
Essential Responsibilities and Duties:
- Schedule employees for work including call offs and vacations.
- Translate the daily plant needs into tasks and projects to ensure they are accomplished.
- Review daily non-conforming products, disposition, tagging, and accounting for inventory.
- Apply quality systems to daily inspector tasks.
- Participate in continuous improvement activities.
- Oversee batch record review and scanning.
- Assist with training of employees on defect recognition and cGMP.
- Participate in customer audits.
- Manager vendor complaint program.
- Performs internal audits.
- Do weekly walks on the production floor to conduct quality checks.
- Assist with custom certificates of conformance as needed. Reviews and signs certificates.
- Works with department managers and others on CAPA events, and develops plant wide quality systems.
- Back up Quality Manager, Quality Engineer, and Document control coordinator, as required.
- Accepts responsibility to comply with all safety, quality, customer, ISO, and any other regulatory requirements. Has the authority to report any concerns that could impact these requirements or suggest areas for improvement.
- Performs other duties as assigned.
Qualifications
Education/Experience:
- High school diploma or general education degree (GED) required.
- BA or BS degree preferred.
- Must possess a working knowledge regarding ISO quality standards and Quality Systems.
- Experience with pharma, medical devices, FDA, or packaging are highly desirable.
- Trained internal auditor preferred. .
- Two to five years related experience.
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