at Adecco US, Inc. in Wheeling, Illinois, United States
Job Description
Operates department machine and equipment according to Standard Operating Procedures (SOPs), Machine Setup (MS), Manufacturing Procedure (MP) instructions, job orders, specifications, engineering drawings, and job order special instructions. Maintains quality system requirements for medical device manufacturer according to ISO 13485 and FDA 21 CFR 820.
Essential functions
- Adheres to Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP).
- Reads work order and/or engineering drawings and manufacturing specifications to produce product as required.
- Communicates with co-workers and supervisors to receive instructions and coordinate activities along with job order performance.
- Visually inspects or measures in-process and finished product for specified quality attributes.
- Completes work orders and other related Device History Record (DHR) paperwork as required.
- Supports 55, Lean Six Sigma, and continuous improvement projects within the department and facility to support quality objectives, along with customer and business needs.
- Other duties may be assigned
Competencies
- Great Attention to detail
- Must speak/read/write English.
- Must be organized, have initiative, and ability to work well and cooperate with all levels of the department.
Required education and experience
- Minimum High School Diploma or GED.
- One (1) to three (3) years related experience and/or training or equivalent combination of education and experience.
- Must be familiar with Good Manufacturing Practices (GMP)/Quality System Regulations (QSR)/Good Documentation Practices (GDP).
Preferred Education and experience
- Previous experience in the medical device industry
CAQ
Operates department machine and equipment according to Standard Operating Procedures (SOPs), Machine Setup (MS), Manufacturing Procedure (MP) instructions, job orders, specifications, engineering drawings, and job order special instructions. Maintains quality system requirements for medical device manufacturer according to ISO 13485 and FDA 21 CFR 820.
Essential functions
- Adheres to Good Manufacturing Practices (GMPs) and Good Documentation Practices (GDP).
- Reads work order and/or engineering drawings and manufacturing specifications to produce product as required.
- Communicates with co-workers and supervisors to receive instructions and coordinate activities along with job order performance.
- Visually inspects or measures in-process and finished product for specified quality attributes.
- Completes work orders and other related Device History Record (DHR) paperwork as required.
- Supports 55, Lean Six Sigma, and continuous improvement projects within the department and facility to support quality objectives, along with customer and business needs.
- Other duties may be assigned
Competencies
- Great Attention to detail
- Must speak/read/write English.
- Must be organized, have initiative, and ability to work well and cooperate with all levels of the department.
Required education and experience
- Minimum High School Diploma or GED.
- One (1) to three (3) years related experience and/or training or equivalent combination of education and experience.
- Must be familiar with Good Manufacturing Practices (GMP)/Quality System Regulations (QSR)/Good Documentation Practices (GDP).
Preferred Education and experience
- Previous experience in the medical device industry
CAQ
Pay Details: $19.50 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.
