General Assembler

MillenniumSoft Inc; Tempe (AZ); On-site; USD 22,000 - 28,000; Full time

Benefits offered by this job

Potential temp to hire

Safety shoes provided

Job summary

MillenniumSoft Inc is seeking a General Assembler for a 12-month contract in Tempe, AZ. 2nd shift from 1:15PM to 9:45PM, 40 hours per week, on W2. The role involves small part assembly, use of a microscope and tweezers in a clean room environment, with PPE provided.

Potential temp-to-hire; good attendance required. Responsibilities include completing device history records, data entry, and performing inspections.

Qualifications

• High school diploma or equivalent.
• Manufacturing experience preferred, but not required, Small part Assembly, use of tweezers.

Responsibilities

• Accurately complete Device History Records and associated paperwork.
• Assist with projects and qualifications concerning the process when needed.
• Communicate effectively with co-workers.
• Enter batch information into database.
• Utilize small hand tools and/or precision devices to aid in the manufacturing process.
• Perform inspection of own work of prior manufacturing operations.

Skills

Attention to detail

Good attendance

Effective communication

Education

High school diploma or equivalent

Tools

Microscope

Tweezers

Small hand tools

Job description

Level Of Experience: Entry Level

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)

Assembly

2nd shift

1:15PM - 9:45PM

Position : General Assembler

Location : Tempe, AZ

Duration : 12 Months

Total Hours/week : 40.00

pay range -$16-20/hr

Client: Medical Device Company

Job Category: Industrial

Level Of Experience: Entry Level

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)

Description

Assembly

2nd shift

1:15PM - 9:45PM

Potential temp to hire

Must have good attendance- reliable!

Safety shoes required.

Small part assembly, use of a higher powered microscope, tweezers.

Candidates with sewing exp, workng with small delicate parts are ideal candidates.

Summary Of Position With General Responsibilities

Perform various processes for PTFE manufacturing which is primarily done in a clean room environment.

This requires following the SOPs and GMPs.

Essential Job Functions

• Accurately complete Device History Records and associated paperwork
• Assist with projects and qualifications concerning the process when needed
• Communicate effectively with co-workers
• Enter batch information into database
• Utilize small hand tools and/or precision devices to aid in the manufacturing process
• Perform inspection of own work of prior manufacturing operations

Basic Qualifications

• Accurately complete Device History Records and associated paperwork
• Assist with projects and qualifications concerning the process when needed
• Communicate effectively with co-workers
• Enter batch information into database
• Utilize small hand tools and/or precision devices to aid in the manufacturing process
• Perform inspection of own work of prior manufacturing operations

Education And/or Experience

• High school diploma or equivalent.
• Manufacturing experience preferred, but not required, Small part Assembly, use of tweezers.

Full suit, clean room regulated controlled temperature environment.

May be use small blades. Protection, PPE and training provided.

Must have good communication skills

Physical Demands

While performing the duties of this job, the employee is regularly required to stand, walk, sit and use hands to manipulate, handle or feel objects, tools, controls and office equipment. The employee frequently is required to talk and hear. The employee is occasionally required to reach with hands and arms and stoop, kneel or crouch. Performs any combination of tasks involved in the fabrication, manufacture, assembly, testing and packaging of medical devices as well as setting up, operating, performing maintenance on and troubleshooting equipment. May conduct quality inspections on processing line in accordance with quality specifications. Works within clearly defined SOPs and / or scientific methods and adheres to quality guidelines.