Quality Inspector I-A1/B1 (SLC)

eTeam; Salt Lake City (UT); On-site; USD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Quality Inspector I to join their team in Salt Lake City. This entry-level position involves performing visual inspections and functional testing to ensure product compliance with specifications. The ideal candidate will possess a high school diploma or GED, with a preference for those with an AA or technical degree. You'll be part of a dedicated team, ensuring quality standards are met while gaining valuable experience in a dynamic environment. If you're detail-oriented and eager to contribute to quality assurance, this role offers a great opportunity for growth.

Qualifications

• Entry-level inspection experience preferred.
• Understanding of FDA standards is a plus.

Responsibilities

• Conduct mechanical, physical, and visual inspections of materials.
• Initiate Non-Conformance reports when necessary.

Skills

Basic computer skills

Good written and oral communication skills

Knowledge of medical device regulations

Education

High school diploma or GED

AA or technical degree

Tools

Microscopes

Calipers

Micrometers

Agile software

Job description

Job Title: Quality Inspector I

Location: 4455 Atherton Drive, Salt Lake City, UT 84123

Duration: 12 Months

Shift: (12 hr) Rotating Shift | 6:30 AM - 6:30 PM

Pay Range: $18.00 to $19.00

Position Summary:

Perform entry-level inspection, including repetitive visual inspections and basic functional testing. Ensure products comply with internal and external specifications through routine and non-routine inspections. Use microscopes, calipers, and micrometers to perform inspections, completing 10-15 different types.

Essential Duties & Responsibilities:

1. Conduct accurate mechanical, physical, and visual inspections of raw materials, components, and sub-assemblies according to inspection plans and specifications.
2. Perform PCI activities for NA Notifications at the US Regional Service Center as needed.
3. Follow procedural requirements to maintain compliance with Quality System Regulations (e.g., cGMP).
4. Support document archival, including preparing pallets for shipment and scanning documents into Agile.
5. Initiate Non-Conformance reports when necessary.
6. Support NC and CAPA activities as required.
7. Participate in special projects as they arise.

Knowledge, Skills & Qualifications:

• High school diploma or GED; AA or technical degree preferred.
• Basic computer skills for documentation and data entry.
• Good written and oral communication skills.
• Knowledge of medical device regulations and FDA standards is preferred.

Travel Requirements:

Less than 5% travel expected.

Physical Requirements and Work Environment:

• Work primarily in an office environment.
• Long periods of sitting; manual dexterity for operating office equipment.
• Occasional lifting up to 25 lbs.