Manufacturing Quality Technician

Integrated Resources Inc.; Columbia Heights (MN); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Referral bonus of $500

Job summary

A premier staffing firm seeks a Quality Assurance Technician in Minnesota. The role involves supporting manufacturing quality processes, ensuring compliance with regulatory standards, and documenting quality data. Candidates with experience in medical devices or pharmaceuticals are preferred, alongside strong communication skills. A referral bonus is available for qualified candidates.

Qualifications

• Two years of experience in pharmaceuticals or medical devices.
• Knowledge of inspection techniques with minimal supervision.
• Experience with process documentation and regulations.

Responsibilities

• Support Manufacturing Quality Engineers in reviewing device history records.
• Act as liaison between manufacturing and quality teams.
• Ensure deviations are addressed before product release.

Skills

Communication

Interpersonal skills

Technical writing

Tools

Microsoft Office

FACTORYworks

Job description

Integrated Resources, Inc. is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since 1996. Our mission centers on delivering top-quality talent, the first time and every time. We provide resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.

Job Description

Position Summary: Perform various technical quality duties in Incoming Quality Assurance, Production, Secondary Packaging, and general Quality Systems, following industry standards, company procedures, and regulatory policies. Possess some knowledge of quality terms, investigative and data analysis tools. Work under limited supervision, following general instructions for daily activities and minor projects. Eager to learn and implement quality processes and improvements. Experience in medical devices or regulated industries is preferred.

Responsibilities

• Support Manufacturing Quality Engineers in reviewing device history records for conformity and releasing products upon acceptance.
• Resolve production and process issues to meet manufacturing schedules, especially on the drug kitting line.
• Act as liaison between manufacturing and quality teams, communicating regularly.
• Ensure deviations and non-conformances are addressed before product release.
• Suggest and communicate procedure improvements to engineering.
• Disposit non-conforming components and perform inspections.
• Participate in audits and self-assessments of production and Quality Assurance.
• Support production activities, including manufacturing execution systems.
• Document quality and manufacturing data accurately.
• Perform other related duties as assigned.
• Attend meetings as required.
• Spend extended periods working on computers.

Preferred Qualifications

• Two years of experience in pharmaceutical or medical device production.
• Proficiency in MS Office and FACTORYworks.
• Strong communication, interpersonal, and technical writing skills.
• Ability to work as part of a team and support multiple projects.
• Knowledge of inspection techniques with minimal supervision.
• Availability for shift work if needed.
• Knowledge of 21 CFR 820, 210/211 regulations.

Qualifications

• Minimum two years of experience in pharmaceuticals or medical devices.
• Experience with process documentation and regulations.
• Proficiency in Microsoft Office applications.

Additional Information

Referral bonus of $500 available for referring qualified candidates.

Thanks & Regards,
Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences & Allied Healthcare CRO
Certified MBE | GSA Schedule 66 & 621I
Direct: 732-844-8724

LinkedIn: https://in.linkedin.com/in/seemachawhan

Gold Seal JCAHO Certified for Healthcare Staffing

"INC 5000’s Fastest Growing, Privately Held Companies" (8th Year in a Row)