Manufacturing Quality Technician

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.

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.

• 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.

• Two years of experience in pharmaceutical or medical device production.
• Proficiency in MS Office and FACTORY works.
• 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.

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

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:

Linked In:

Gold Seal JCAHO Certified for Healthcare Staffing

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