Quality Technician I - 2nd Shift

Comar; Vineland (NJ); On-site; USD 42,000 - 54,000; Full time

Job summary

Comar on the 2nd shift (3:00pm-11:30pm) seeks a Quality Technician I in Vineland, NJ, to ensure products meet ISO 9001 and ISO 13485 standards. You will perform first piece, daily visual and dimensional analyses, and verify product conformance.

This role emphasizes attention to detail, reading procedures, and collaboration to complete quality checks and audits, with accurate documentation of results.

Qualifications

• High School Diploma or GED required.
• 0-1 year of Quality Control or GMP manufacturing experience preferred.
• Proficiency with computers and basic software.
• Familiarity with Statistical Process Control (SPC) tools and techniques.
• Understanding of Gauge Repeatability and Reproducibility (Gauge R&R).

Responsibilities

• Perform first piece and daily visual and dimensional inspections of finished products per inspection plans.
• Conduct first article inspections to verify product conformity.
• Perform floor audits of paperwork, materials, finished products, and control plans.
• Inspect non-conforming products and initiate containment actions; document results.
• Collaborate with team to complete all required quality checks daily.
• Escalate non-conformances to Lead Quality Inspector for resolution.
• Maintain accurate records of inspections and non-conformances per ISO standards.

Skills

Reading & interpreting documents

Teamwork & communication

Dimensional analysis

Attention to detail

Math basics

Education

High School Diploma / GED

Bachelor's in Science/Engineering (preferred)

Job description

Description

Quality Technician I - 2nd Shift 3:00pm-11:30pm

We are seeking a detail-oriented and diligent Quality Technician to join our team on the 2nd Shift , ensuring our products meet the highest standards of quality and compliance with ISO 9001 and ISO 13485 standards. This role offers an excellent opportunity to contribute to a quality-driven organization committed to continuous improvement and excellence in manufacturing.

Key Responsibilities:

• Perform first piece and daily visual and dimensional analysis of finished products at specified intervals according to inspection plans.
• Conduct first article inspections and evaluations to verify product conformity.
• Perform floor audits of paperwork, materials, finished products, and control plans as outlined in inspection schedules.
• Inspect non-conforming products, initiate containment activities, and execute control procedures for non-conforming items, documenting results accurately.
• Collaborate with team members to ensure all required quality checks and tasks are completed daily.
• Escalate issues or non-conformances promptly to the Lead Quality Inspector for resolution.
• Maintain accurate records of inspections, audits, and non-conformance reports in compliance with ISO standards.

Skills and Abilities:

• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure materials
• Ability to work independently and in a team environment
• Skilled at learning the use of equipment for dimensional analysis
• Detailed-oriented/capability of discovering nonconformances in both paperwork and materials
• Ability to apply basic math skills: add, subtract, multiply, divide. Compute rate, ratio, percent.
• Ability to carry out instructions provided in written, oral, or visual/diagram format.
• Ability to communicate their job related functions with other employees, cross-department, with customers and auditors as needed.
• Ability to interact with manufacturing associates in a meaningful way to ensure collaboration

Physical Demands

• Stand and walk for the most of the work shift
• Use hands and fingers to handle or feel; reach with hands and arms; crouch, stoop, kneel, and only occasionally sit
• Lift/move up to 25 pounds. Heavier items can be moved with assistance of equipment
• Use close, color and peripheral vision, depth perception, and adjust focus.

Work Environment

• The noise level in the work environment is usually loud
• Employee with regularly operate in an ISO environment

Requirements

Basic Qualifications

• High School Diploma or General Education Degree (GED)
• Have 0-1 Years Experience in Quality Control or in a GMP Manufacturing Environment
• Understanding of computers and software
• Understanding of Statistical Process Control (SPC) tools and techniques.
• Understanding of Gauge Repeatability and Reproducibility (Gauge R&R)

Preferred Qualifications

• Bachelor's Degree for Science, Technology, Engineering or significant applicable experience, training, and certifications
• Experience working in medical device, pharmaceutical, or food manufacturing environments
• Experience with visual inspection standards and processes
• Experience working in an ISO or regulated environment
• Experience working in a cleanroom environment