Quality control operator job description

Company Information

DAK Americas is a globally competitive supplier of Terephthalic acid (TPA) - Monomers, Polyethylene Terephthalate Resins (PET) and Polyester Staple Fibers (PSF) for the western hemisphere. The company is headquartered in Charlotte, NC with manufacturing facilities in the Carolinas. This opening is located at our Moncks Corner, SC facility. DAK Americas is a division of Alpek, the petrochemicals and synthetic fibers business group of Alfa, S.A.B. de C.V., one of Mexico's largest corporations.

POSITION SUMMARY:

* Perform routine analytical quality testing in QC/QA lab for Resins manufacturing.
* Ensure proper operation of lab equipment through routine standard checks and maintenance.
* Maintain a clean and orderly laboratory working environment.
* Effectively communicate with staff, and ensure that lab results are delivered in a clear and timely manner.
* Adhere to all applicable laboratory safety and documentation guidelines.
* Preferred knowledge in the following analytical instruments and techniques: AA, GC, LC, FTIR, titration, extraction, gravimetric analysis, and preparation of standards.
* Work schedule is 12hr shifts (36/48), rotating shifts.

DAK Americas LLC is subject to US Department of Commerce export regulations and thus must hire individuals who meet national security requirements. Interested applicants (or temporary employees) must meet eligibility requirements. DAK Americas LLC is an Equal Opportunity Employer.

Job Requirements:

* Good organizational skills and ability to manage time / multi-task.
* Excellent command of written and spoken English is required. Ability to read and interpret safety rules, operation instructions, and procedures. Strong written and verbal skills required to effectively communicate with operations.
* Proven command of math and computer literacy (Microsoft Office suite).
* Ability to work independently & safely.
* Preferred experience in ISO 9001 / 14001, LIMS and SAP experience but not required.
* Teamwork philosophy.
* Manufacturing background preferred with at least 2 years laboratory experience
* 4 year degree preferred, but will consider years of experience and background

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• High school education or equivalent; Degree is preferred with at least 1 year of relevant work experience.

• Experience in Medical Device, Pharmaceutical, and/or regulated industry is preferred

• Must have sufficient communication and writing skills.

• Must have been QC trainee for a period of 3 months.

• Must pass pre-employment test.

• Basic computer knowledge and MS Office skills.

• Operational knowledge of Computer Aided Quality (CAQ) inspection data base (i.e. BABTEC)

• Must be able to stand and walk for up to 8 to12 hours.

• Must be able to lift up to 70 lbs.

• Must have appropriate vision to perform detailed quality inspection as outlined in SOPs and TPs.

Physical Requirements:

• Must be able to stand and walk for up to 8/12 hours.

• Must be able to lift up to 70 lbs.

• Must have appropriate vision to perform detailed quality inspection as outlined in SOPs and TPs.

Company DescriptionCuriosity is in our genes. Greiner Bio-One employs visionaries who, rather than just waiting, help to shape the future of biotechnology with their drive and forward-thinking. We are team players who share our knowledge and entertain new ideas. We work in a future-oriented environment. What’s more, we value individuality, stability and purpose, since these are the qualities that make us strong. Greiner Bio-One employs people who are able to laugh at themselves and are proud of achieving something worthwhile through their efforts. Future in our Blood.

Greiner Bio-One feels like home.

For visionaries with drive and ideas;
For team players who share their knowledge and entertain new ways of thinking;
For people who are able to laugh at themselves and are proud to make a difference through their work.

Our door is always open to achievers, doers and hidden talents and we want to show you what it means to be part of our team.

Position Title : Quality Control Operator Level 3

Reports To: QC Production Manager

Department Name: Mfg – Quality Control

Location: Milpitas

FLSA Status: Non-Exempt

Swing shift: Monday-Friday 2:30pm-11:00pm

POSITION SUMMARY

Perform visual inspection of integrated circuit units of dies and assembled units by using a microscope to ensure compliance.

KEY RESPONSIBILITIES/ESSENTIAL FUNCTIONS INCLUDE

Must be proficient in 2 or more of the following functions:

• IQA Using microscope for 90% of the time, and may use other equipment: -
  1. (IQA) Incoming and Outgoing Wafer and Dies
  2. (IQA) Incoming and Outgoing Materials and Substrate
  3. Measuring Accept and Reject Defects

• 2nd Op
  1. Ability to select a random sample using a 0.65% AQL and visually inspect each die under a microscope.
  2. Compare the number of rejects to the accept/reject criteria of the AQL table.
  3. Accept lots and proceed to the next operation shown on the traveler.
  4. Record inspection result on the traveler and 2nd Optical Summary Report.
  5. Performs 100% Die Orientation Monitor.
  6. Transferring Inspected dice from the mother traveler to individual job travelers for Assembly.
  7. Review paperwork entries on Traveler and Reject Summaries.
• 3rd Optical
  1. Familiar with High-Power and Low Power microscope.
  2. Familiar with Condition A for QML Class S (V) and Condition B for QML Class B Q) Devices.
  3. Familiar with Visual examination of the die, Solder bump and die sidewall inspection.
  4. Able to Record all Third Optical rejects and after sign-off traveler.
• 4th Optical
  1. PACKAGES: ability to identified all the packages defects.
  2. LEADS/SOLDER BALL: ability to identified all the Leads and Solder ball defects.
  3. SEAL/FILL: ability to identified all the Seal/Fill defects Mark: ability to identified all the Mark defects and all other specifies defects.
• QFN/DFN
  1. Inspect All QFN/DFN Lead Frames purchased by Integra Technologies. Review the Co C as part of the IQA inspection
  2. Read and understand the Lead Frame Drawing.
  3. Document the IQA inspection results.
  4. Check First Article lead frame shipments.
• Final QA
  1. Ensure that the products shipped meet customer specification.
  2. Completely and accurately fill out all respective documentations incl. travelers, process control data, or logs.
  3. Verify the correct quantity needed to be shipped, ensures that all excess materials are returned to customer if specified.
• Communicate any repeatable QC findings to QC Manager
• Willing to work overtime as needed
• Flexibility to perform other duties as assigned

JOB REQUIREMENTS INCLUDE

Education: High school diploma or equivalent required

Experience:

• Minimum of 3-5 years of experience in semiconductor industry.
• Minimum of 3-5 years of experience using a microscope.

Knowledge/Skills:

• Effectively communicate with internal and external customers, both verbally and in writing.
• Self-motivated with excellent customer service, teambuilding, and interpersonal skills with the ability to defuse any situation.
• Must possess the ability to:
  1. Adapt to changes in the work environment, delays or unexpected events; manage competing demands; change approach or method to best fit the situation.
  2. Remain flexible, dependent on the needs of the customer, in order to meet deadlines as well as customer expectations.
  3. Interact effectively with other internal departments.
  4. Recognize and adhere to specific customer requirements for ESD.
  5. Lead and train others.
  6. Perform 100% Die Inspection in Wafers or Dice
• Proficiency with Microsoft Office Suite.

SUPERVISORY RESPONSIBILITIES

Total Number of Employees Directly Supervising: _0_

Number of Subordinate Supervisors Reporting to Position: _0_

This job description is intended to describe the general nature and level of work being performed. This is not intended to be an all-inclusive list of responsibilities, duties, skills required of employees so classified.

In addition, this is not an employment contract and should not be construed or interpreted as creating an implied or expressed guarantee of continued employment. The employment relationship at Integra Technologies Inc is by mutual consent (Employment at Will).