6Q02 - Quality - QCTC - QC TECHNICIAN C (2nd Shift)

Medegen Medical Products/Medira; Gallaway (TN); On-site; USD 42,000 - 54,000; Full time

Job summary

Inteplast Group in Tennessee is seeking a QC Technician C (2nd Shift) to perform routine to complex QA tasks, measure and test parts to specifications, and log data electronically. The role requires handling NCMR, DHR, and pre-production protocols, with attention to startup procedures and customer specs.

The candidate should have a minimum 1 year in manufacturing, a preferred Certified Quality Auditor, and experience with plastic injection or blow molding.

Qualifications

• 1+ year experience in production/manufacturing
• Certified Quality Auditor certificate preferred
• Experience in plastic injection/blow molding desired
• High school diploma or equivalent; related college preferred

Responsibilities

• Completes operational lot control procedures and forms
• Archives quality records and logs procedures
• Perform in-process product audits in a manufacturing environment, according to product specifications and procedures
• Create and complete 1st article inspection reports
• Conduct periodic process audits as requested and completes necessary documentation
• Assist shift personnel with quality issues and/or measurement techniques
• Assist in problem resolution with customers as requested
• Must be knowledgeable with startup procedures, customer specifications, cosmetics criteria, rejection report procedures, and end of run procedures
• Must be able to complete and close a NCMR request, the DHR procedure, the deviation procedure, how to write and stag a customer return, and how to complete pre-production approval protocols
• Responsible for accurate data input into databases
• Must have knowledge of blueprints applications and the use of measurement equipment

Skills

Quality assurance

Reading basics

Attention to detail

Communication

Problem solving

Education

High school diploma

Tools

Microsoft Office

Database systems

Job description

TITLE: QC Technician C (2nd Shift)

POSITION OBJECTIVE:

Quality Assurance Auditor will be capable of doing routine to complex quality assurance tasks. Must have excellent ability to measure and test parts to specifications, electronically record data, and initiate corrective actions as applicable.

QUALIFICATIONS:

• A minimum of one year experience in a production/manufacturing environment is required and a Certified Quality Auditor certificate is preferred. Experience in plastic injection and/or blow molding is desired.
• High school graduate or equivalent, some related college preferred.
• Ability to read a limited number of two-and three-syllable words and to recognize similarities and differences between words and between series of numbers. Ability to print and speak simple sentences.
• Ability to add and subtract two-digit numbers and to multiply and divide with 10's and 100's. Ability to perform these operations using units of American money and weight measurement, volume, and distance
• Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions, Ability to deal with problems involving a few concrete variables in standardized situations.
• Computer literate in Microsoft Office and experience with imputing data into dbases systems is a must
• Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary.
• Capable of effectively managing job-related stress and fostering productive workplace interactions.

JOB RESPONSIBILITIES:

• Completes operational lot control procedures and forms
• Archives quality records and logs procedures
• Perform in-process product audits in a manufacturing environment, according to product specifications and procedures
• Create and complete 1st article inspection reports
• Conduct periodic process audits as requested and completes necessary documentation
• Assist shift personnel with quality issues and/or measurement techniques.
• Assist in problem resolution with customers as requested.
• Must be knowledgeable with startup procedures, customer specifications, cosmetics criteria, rejection report procedures, and end of run procedures
• Must be able to complete and close a NCMR request, the DHR procedure, the deviation procedure, how to write and stag a customer return, and how to complete pre-production approval protocols.
• Responsible for accurate data input into databases.
• Must have knowledge of blueprints applications and the use of measurement equipment.

WORK ENVIRONMENT CONDITIONS SUBJECTED TO IN THIS POSITION:

• While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is very loud and requires hearing protection.

Inteplast Group is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

If you need a reasonable accommodation for any part of the employment process, please contact us by email at [e-mail] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.

For more information, about our commitment to equal employment opportunity, view the EEO - Know Your Rights and Pay Transparency Statement.