QA Tech I - Rotating Day Shift
Rockline Industries, people who make it right · Sheboygan, Wisconsin, United States · $53K/yr
Manufacturing · 1,001-5,000 employees
About the role
Provide quality assurance support for production and product development by reviewing test data and production records. Conduct non-conforming material investigations and write reports to ensure compliance with customer and regulatory requirements.
What they look for
Requirements
Requires 0 to 3 years of related experience and strong Microsoft Office skills. An associate degree in a related field and knowledge of FDA regulations are considered pluses.
Benefits
Full description
POSITION SUMMARY:
Provide Quality Assurance support for production, purchasing, product development, project managers, and customers. Assist various groups to interpret and ensure product regulations and customer requirements are met. Quality Technicians review test data results, CoAs, and production records for both raw material and finished product releases. Duties may also involve working directly with the customer’s Quality Assurance group or internal product development teams. Compose investigation reports to be submitted to the Quality Assurance Manager for approval of product disposition. Investigation reports are investigated by the technician to gather factual information to provide a bracketing rationale. Technicians are also relied upon for writing procedures and work instructions. Technicians may also be relied upon to provide information to the Quality Operations Manager or QA Manager to assist in quality decisions.
SHIFT:
- Rotating Day Shift: 5:30AM - 5:30PM
- Week 1: Mon, Tues, Fri, Sat, Sun
- Week 2: Wed, Thurs
COMPENSATION:
- Minimum starting pay: $25.65 per hour!
- Quarterly check-ins with the ability to increase your wage with yearly merit reviews!
- Voluntary overtime available.
- Eligible for quarterly bonus program.
• FLSA Status: Non-exempt.
QUALIFICATION REQUIREMENTS:
- 0 to 3 years of related experience required.
- Strong Microsoft Office skills required.
- Associates degree in related field a plus.
- Previous audit experience a plus
- Working knowledge of FDA regulations from 21 CFR a plus
- Experience with document control – report writing and creating procedures a plus
- ASQ certificate a plus.
WORK ENVIRONMENT:
- 80% Inside work
- 18% Noise
- 2% Travel
ESSENTIAL ACCOUNTABILITIES:
- Device History Record and test data review and release of Finished Goods.
- Provide daily support to all manufacturing cells and other internal customers for Quality related issues and concerns.
- Non-conforming material investigations. Write investigation reports. Update NCM raw materials and finished product disposition.
- Customer support via emails, conference calls and production line tours.
- Work on special projects as assigned by the QA Manager or QA Supervisor.
- Training and development of production floor associates in the area of quality, procedures, and production records.
- Provide data as needed on request for Quality and Operational issues.
- Provide external customers with required finished good samples.
- Provide external customers with Certificates of Analysis or Certificates of Manufacture for products produced by Rockline.
- Demonstrate commitment to Rockline/Iatric’s RRITE Values of Renew, Respect, Integrity, Teamwork, and Excellence.
- Associates have a direct and important role in ensuring that all work is performed in a safe manner. Effectiveness in carrying out this responsibility is part of each associate’s essential accountabilities.
- Contribute to a cooperative working effort by demonstrating a willingness to perform other job-related work, as needed, or requested
FLSA Status: Non-exempt.
