Quality Technician (2nd Shift)

Talent Acquisition TeamCaledonia, MI
Onsite

About The Position

This position offers the opportunity to support validation and risk build activities with the manufacturing and engineering group. The role involves performing customer complaint investigations, including product dispositions and serving as the point of contact for quality-related customer communications. You will conduct root cause analysis, identify solutions, and implement corrective actions for internal nonconformances, customer complaints, and CAPAs. Responsibilities include initiating non-conforming dispositions, CRs, and COs, as well as writing, training, and ensuring the implementation of Quality Alerts, rework instructions, and planned deviations. The role also requires maintaining, reviewing, and updating manufacturing and purchasing Control Plans in IFS, fostering supplier relationships, and driving continuous improvement. You will participate in supplier selection and cost reduction initiatives with Supply Chain, perform First Article Inspections (FAI) for new products and changes, and maintain supplier quality files with necessary audits. A key aspect is continuously identifying areas for improvement in manufacturing processes to ensure compliance and enhance product quality, partnering with manufacturing for implementation. Analysis of improvement opportunities through MRB monitoring and developing training to build quality awareness are also part of the role. Additionally, you will support manufacturing and engineering in resolving technical issues.

Requirements

  • High School Diploma or equivalent
  • 3+ years of experience responsible for Quality improvement projects preferred
  • 3+ years of experience in a regulated industry experience that includes FDA and ISO requirements preferred
  • Communication – displays developed interpersonal skills: leadership, team orientation, ability to communicate at all levels
  • Flexibility and Adaptability – make effective decisions and maintain effectiveness under changing circumstances and priorities
  • Teamwork, communication, positive attitude required to support the manufacturing environment
  • Ability to read and analyze technical prints and drawings
  • Problem Solving – able to perform root cause analysis and implement effective corrective actions
  • Project Management – able to effectively manage and complete multiple projects simultaneously.
  • Computer Skills – Excellent computer skills including but not limited to Microsoft Office Suite, IFS, EtQ
  • Knowledge of quality system including the quality manual, quality policy and applicable procedures and work instructions
  • Establish, implement, and maintain the quality system in accordance with FDA Quality System Regulation, ISO 13485, European Union Medical Device Regulations, and MDSAP participating countries regulations

Responsibilities

  • Support validation and risk build activities with manufacturing and engineering group
  • Perform Customer Complaint Investigations, including customer complaint product dispositions and being the point of contact for quality related customer communications
  • Perform root cause analysis, identify solutions and implement effective corrective action for internal nonconformances, customer complaints and CAPAs
  • Initiate non-conforming dispositions
  • Initiate CR’s and CO’s
  • Write, train and ensure the proper implementation of Quality Alerts, rework instructions and planned deviations.
  • Maintain, review, and make updates to manufacturing and purchasing Control Plans in IFS
  • Maintain relationships with suppliers and actively drives continuous improvement
  • Participate with Supply Chain in supplier selection process and purchased materials cost reduction
  • Perform FAI for new product and product changes
  • Maintain supplier quality files and performs audits as necessary per the QMS
  • Continuously identify areas of improvement in the manufacturing processes to ensure compliance or that would enhance product quality and partner with manufacturing to implement the improvements
  • Analyze improvement opportunities through MRB monitoring
  • Develop trainings to build quality awareness
  • Support manufacturing and engineering to resolve technical issues
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