Hello Everyone,
This is Vydehi from Intellectt Inc. We currently have an opening for a QA Specialist I with one of our medical device clients. If you or anyone you know is interested in this opportunity, please feel free to send your updated resume to vydehi@intellectt.com or reach out to me directly at +1 732 355 7412
Role: QA Specialist I
Location: Abbott Park, IL
Duration: 08 Months
Job Description:
An QA Specialist I is responsible for supporting the quality assurance processes within a manufacturing environment. They work closely with production teams to ensure that products are manufactured to the highest standards of quality and safety through review and verification of batch records.
Day-to-Day Responsibilities:
Quality Inspections: Conduct regular batch record inspections on products to ensure they meet specified quality standards.
Standard Operating Procedures (SOPs): Follow and enforce SOPs to maintain consistency and quality in production.
Non-Conformance Management: Identify, evaluate, and manage non-conformances in products, ensuring they are addressed promptly.
Documentation: Maintain accurate records of inspections and other quality-related activities.
Support Production Teams: Assist production teams by providing guidance on quality standards and helping to resolve any quality-related issues.
Support File Room: Assist with maintaining the file room by filing/scanning/ and fulfilling customer requests.
Continuous Improvement: Participate in continuous improvement initiatives to enhance product quality and manufacturing processes.
Health and Safety Compliance: Ensure compliance with health, safety, and environmental regulations.
Training: Train on quality assurance processes and standards.
5S Activities: Engage in 5S activities to maintain a clean, organized, and efficient work environment.
These responsibilities ensure that the QA Specialist I play a vital role in maintaining the quality and reliability of products, contributing to the overall success of the manufacturing process.
Education/ Experience:
- H.S diploma, with at least 2 years of experience working in a
- relevant device/pharma/food facility where following procedures and following good
- documentation practices is required.
Top 5 skills/requirements
- Manufacturing/quality experience, good documentation practices,
attention to detail, SAP experience, following Standard operating procedures.
