QA Clerk

Join Frencken's IMS Division: Innovating for the Future

At Frencken, our Integrated Manufacturing Services (IMS) division is at the forefront of delivering high-quality, end-to-end manufacturing solutions to leading global industries. From precision engineering to complex assembly, IMS excels in integrating cutting-edge technology with world-class processes to meet the diverse needs of our clients.

By joining the IMS team, you'll be part of a dynamic division that thrives on innovation, collaboration, and the pursuit of excellence. Whether you're an engineer, technician, or operations specialist, you'll find endless opportunities to grow and make an impact in industries such as automotive, medical and consumer electronics.

Explore career opportunities with IMS at Frencken and be part of a team shaping the future of manufacturing. Ready to take the next step in your career?

a. Documentation & Record Management
Maintain accurate and up-to-date quality records including Incoming Quality Control (IQC), In-Process Quality Control (IPQC), Outgoing Quality Control (OQC), and First Article (FA) inspection reports.

Update and maintain the Quality Inspection Plan (QIP), filing systems, and all quality-related documentation. Ensure all documents and master lists are properly controlled and aligned with the Document Control Register (DCR).

b. Data Entry & Quality Reporting
Record and update inspection results into Statistical Process Control (SPC) charts and quality databases.

Prepare and generate OQC reports, Certificates of Conformance (COC), and Certificates of Analysis (COA) for shipment purposes.

c. Issue Tracking & Corrective Action Follow-Up
Generate Corrective and Preventive Action (CAPA) requests to internal departments or suppliers for any quality-related incidents.

Monitor and ensure timely submission of CAPA responses within the stipulated timeline.

Track Non-Conformance Reports (NCR) and follow up on corrective and preventive actions until closure.

d. Quality Documentation Preparation
Prepare, update, and maintain QC reports, Standard Operating Procedures (SOPs), quality alerts, inspection checklists, and other quality-related documents as required.

e. Document Revision Control
Monitor and control document revisions to ensure only the latest approved versions are used and distributed within the organization.

What Do We Offer at Frencken IMS?

At Frencken IMS, we believe that our people are our greatest asset. We are committed to providing a dynamic and supportive environment where talent thrives, and careers flourish. Here's what you can expect when you join our team:

• Career Growth and Development
  We invest in your future. With opportunities for continuous learning, skill development, and cross-functional experiences, we help you achieve your career goals through tailored growth plans.

• Innovative Work Environment
  Join a division where technology meets ingenuity. You'll work alongside industry experts on cutting-edge projects that push the boundaries of modern manufacturing and engineering.

• Global Opportunities
  As part of a global organization, we offer the chance to work with international teams and expand your horizons. Whether you're looking to take on new challenges locally or globally, the possibilities are limitless.

• Inclusive Culture
  At Frencken IMS, we foster a culture of collaboration and inclusion, where diverse perspectives drive innovation. We believe that every individual plays a crucial role in our success.

• Work-Life Balance
  We understand the importance of balance and offer flexibility and support to help you thrive both professionally and personally.

Discover your potential and make a difference at Frencken IMS. Join us, and let’s shape the future of manufacturing together.