Quality/Process Engineer at Illinois Tool Works
Solon, OH 44139, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Oct, 25

Salary

0.0

Posted On

13 Jul, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Peer Leadership, Data Analysis, Reporting, Organization Skills, Communication Skills, It, Interpersonal Skills

Industry

Pharmaceuticals

Description

QUALIFICATIONS

  • Bachelor’s Degree in Engineering, technology, or related area.
  • 4-7 years of work experience in QC/QA and Continuous Improvements Roles; 2-3 years in chemical field.
  • Demonstrated ability to work efficiently with minimal supervision.
  • Self-starter with initiative and follow through.
  • Demonstrated peer leadership.
  • Experience with data analysis and reporting.
  • Results driven. Desire to show improvement and impact.
  • Team player willing to do what it takes to get the job done and pitch in where needed.
  • Strong interpersonal skills and ability to work well with others. This person will partner with many departments and functional areas and will need to develop effective relationships.
  • Excellent communication skills with all levels of an organization. Clear communication and follow through are important for success.
  • Curiosity and ability to trouble shoot.
  • Computer literate and strong organization skills.
Responsibilities
  • Promotes and follows all safety guidelines and procedures. Recommend safety improvements as needed.
  • Overall product quality. From raw materials to WIP to finished goods, the Quality/Process Engineer is responsible for reviewing, analyzing, and addressing quality complaints and compliance.
  • Identify opportunities to improve and streamline process efficiency and effectiveness to continuously improve OEE.
  • Measure and continuously eliminate waste from the manufacturing process by implementing ITW Tool Box (Lean Practices).
  • Training in Quality and Operational Activities and Front to Back Toolbox.
  • Define Quality controls for the Manufacturing Processes and maintain registers of quality controls for audit processes
  • Implement Standard Operating Procedures, training material, and visual support for Manufacturing Processes to facilitate operations
  • Issue non-conformances (SCAR – CAR) – both internally and with outside vendors. Place materials on hold as needed.
  • Conduct root cause analyses for quality and operational issues, implementing corrective actions.
  • Develop and implement corrective actions. Follow up to determine if corrective actions have been effective.
  • Track quality complaints and non-conformances. Identify trends and opportunities. Generate monthly reports to share with management.
  • Show improvement in overall quality through reduction in complaints, non-conformances, improvement in customer satisfaction, etc.
  • Conduct internal audits to ensure compliance with work instructions, quality specifications, and SOPs.
  • Identify opportunities and solutions for process improvements resulting in higher OEE.
  • Support vendor audit program, attending and conducting regular audits with our top suppliers when required.
  • Contribute to ISO 9001:2015 efforts across the organization. This includes semi-annual ISO audits, annual QMS audits, and management review meetings.
  • Develop a robust understanding of our products and manufacturing processes.
  • Manage/Operate process equipment and device calibration program.
  • Backup and support others operational roles
  • Additional duties as assigned
Loading...