Quality Control Technician

Integrated Resources, Inc

North Haven, Connecticut

Apply

JOB DETAILS

JOB TYPE

Temporary

SKILLS

Code of Federal Regulations, Discrepancy Report, Employee Retention, Environmental Health, Establish Priorities, Healthcare, Laboratory Equipment, Manufacturing, Medical Equipment, Microsoft Excel, Microsoft Office, Microsoft Word, OSHA, Organizational Skills, Pathogens, Presentation/Verbal Skills, Process Flow, Process Management, Product Testing, Quality Control, Reconciliation, Root Cause Analysis, Safety/Work Safety, Scientific Research, Secondary School, Staff Requirements, Talent Management, Testing, Time Management, Time Tracking, Training/Teaching Curriculum, Writing Skills

LOCATION

North Haven, Connecticut

POSTED

3 days ago

Quality Control TechnicianIntegrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.Job DescriptionJob Title: Quality Control TechnicianLocation: North Haven, CT Duration: 7+ months (possibility of extension)Job Roles & ResponsibilityThe candidate will support the Post Market Vigilance Investigations team's activities for the Surgical Solutions Division.These activities include; assist in managing the receipt of incoming physical complaint product, conducting follow ups with accounts and/or International Subsidiaries to rectify discrepancies with product receipt, assisting in managing the process flow of complaint investigations, performing Device History Record Reviews, and performing root cause analysis on product customer returns to ensure high levels of quality, reliability, safety, and efficacy.Additional responsibilities include management of clinically applied medical device retains and associated paper records in accordance with Healthcare Record Retention Policies and support staffing needs.Essential FunctionsAssist PMV Investigations Coordinator with managing receipt of physical complaint product samples, in addition to corresponding with domestic and international accounts to rectify discrepancies in product receipt.Assist in the prioritization of complaint investigations.Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Client Manufacturing facilities, as well as coordinating the investigation process with internal Engineering and Quality groups.Test and thoroughly evaluate rudimentary products to determine root cause analysis within a closely monitored time frame.Certification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030 and adherence to Corporate and Local Environmental Health and Safety Policies.Minimum Requirements:Education Required: High School DiplomaEducation Preferred: BS Degree in a Technical curriculum preferred or equivalent industry experience.Minimum ExperienceExperience in a laboratory environment and with laboratory equipment or academic knowledge in scientific research methods.Experience with medical devices preferred but not required.Skills/Qualifications:Must be proficient with MS Office (with emphasis on Excel and Word).Time management skills.Critical independent thinking and timely follow up.Excellent written and verbal skills necessary.Quality AssuranceManufacturingEngineeringResearch and DevelopmentRegulatory AffairsLegalMarketing/SalesAdditional InformationWe do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.

About the Company

Integrated Resources, Inc

Resume Resources

Free Resume Templates Free Resume Builder