ASSOCIATE QUALITY ENGINEER

GENERAL DESCRIPTION

The Associate Quality Engineer plays a vital role within the Quality Assurance Department, contributing to the consistent delivery of high-quality products and processes. This multifaceted position encompasses a wide range of responsibilities, including inspection and testing activities, internal audits, documentation control, and cross-functional collaboration to ensure compliance with established quality standards.

The ideal candidate will possess a keen eye for detail, exceptional organizational abilities, and a proactive mindset geared toward continuous improvement. Success in this role requires the ability to work effectively in a fast-paced, team-oriented environment, applying analytical thinking and problem-solving skills to uphold and advance quality excellence across the organization.

ESSENTIAL FUNCTIONS & RESPONSIBILITIES

Inspection & Verification

• Develop and maintain receiving inspection criteria for electronic/electrical components, including First Article Inspections (FAI).
• Perform audits of in-process and final products, including operation and interpretation of Automated Optical Inspection (AOI) results.
• Ensure inspection records are complete, accurate, and compliant with established procedures.
• Provide process training and verification support to Department personnel.
• Maintain DITEK part number data in inspection databases.

Supplier & Compliance Management

• Manage the intake and documentation of Supplier Certificates of Conformance.
• Collect and manage environmental compliance documentation (RoHS, REACH, Prop 65).•
• Assist with generating Product Compliance Certificates upon request.•
• Assist in the preparation of Supplier Quality Reports and performance evaluations.

Returns & Non Conformance Handling

• Process customer returns in SAP, including evaluation, disposition coordination, and repackaging.
• Participate in Material Review Board (MRB) meetings and recommend disposition actions.
• Support root cause investigations and corrective action planning.

Audits & Documentation Control

• Participate in internal audits of the Quality Management System (QMS).
• Complete audit checklists and prepare supporting documentation.
• Review, release, and manage process documentation in Factory Logix and DOCSVAULT.
• Recommend and implement process improvements to enhance quality and efficiency.

Cross-Functional Collaboration

• Interface with departments including Receiving, Purchasing, and Engineering to support safety and continuous improvement initiatives.
• Actively participate in the development and maintenance of product Failure Modes and Effects Analyses (FMEAs), ensuring risk mitigation strategies are integrated into design and production processes.

QUALIFICATIONS

• Associate’s Degree or Technical Certificate required
• 2–3 years of experience in Quality Assurance or Quality Engineering within electronics manufacturing.
• Familiarity with electronic/electrical components and inspection tools (e.g., calipers, multimeters, AOI).
• Understanding of environmental regulations (RoHS, REACH, Prop 65).
• Experience with ISO 9001 or similar quality systems.

KNOWLEDGE, SKILLS, AND ABILITIES

• Strong work ethic and professional relationship-building skills.
• Self-motivated and capable of working independently after training.
• Flexible and willing to cross-train across QA functions.
• Analytical mindset with a focus on process improvement.
• Ability to interpret technical documentation and visual aids.
• Competent in computer navigation and data entry.
• Team-oriented with a track record of success in fast-paced environments.
• Able to perform job functions without posing a safety risk to others.
• Experience with IPC-A-610 and J-STD-001 Standards.
• Experience with SAP or similar ERP systems.
• Skilled in maintaining accurate inspection records.
• Proficient in Microsoft Office; experience with Access, SPC, or quality software is a plus.
• Strong communication skills and ability to work in cross-functional teams.
• Proficient in reading technical drawings and specifications (GD&T).

PHYSICAL ABILITIES

The physical demands described here are representative of those that must be met by an employee to successfully
perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with
disabilities to perform the essential functions.

• Sit for 2-4 hours a day.
• Walk for up to 2 hours per day.
• Stand for up to 6 hours per day.
• Occasionally lift up to 30 pounds.
• Occasionally bend, squat, climb, reach, kneel, and/or twist.

LOGS AND RECORDS

A master (electronic media or hardcopy) of this document is retained in the Quality Assurance Department. Any
revisions to this document must be forwarded to Quality Assurance for maintaining in an appropriate filing system.

ABOUT US

DITEK, a leader in surge protection solutions, is proud to have been voted one of Tampa Bay's Top Workplaces for 15 years in a row. We are dedicated to fostering a positive and dynamic work environment where employees can thrive and contribute to our ongoing success. Join us and be part of a team that values innovation, excellence, and employee satisfaction. 

 DITEK is a drug-free workplace and participates in E-Verify. DITEK provides equal employment opportunities (EE0) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics.