Lab Technician II

Integrated Resources, Inc

Boulder, Colorado

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Adverse Events, Auditory, C++ Programming Language, Centers for Disease Control and Prevention (CDC), Clinical Research, Code of Federal Regulations, Communication Skills, Continuous Improvement, Corrective Action, Customer Response, Electricity, FDA (Food and Drug Administration), Failure Analysis, Functional Testing, Healthcare, High School Diploma, In Vivo Testing, Information Technology & Information Systems, Interpersonal Skills, Investigative Reports, Laboratory, Laboratory Equipment, Lean Six Sigma, Manufacturing, Market Analysis, Medical Equipment, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, OSHA, Pathogens, Presentation/Verbal Skills, Product Testing, Quality Assurance Methodology, Quality Control, Regulations, Rehabilitation Nursing, Root Cause Analysis, Safety/Work Safety, Scientific Research, Staff Requirements, Standard Operating Procedures (SOP), Surgical Supplies, Testing, Time Management, Training/Teaching Curriculum, Writing Skills

LOCATION

Boulder, Colorado

POSTED

1 day ago

Lab Technician IIIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: Lab Technician IILocation: Boulder, CO Duration: 12+months (Possibility of extension)Job Role:The candidate will support the Post Market Vigilance Analytics and Investigations team's activities for the Surgical Solutions Division.These activities include; performing failure analysis on clinically applied medical device customer returns to ensure high levels of quality, reliability, safety, and efficacy, MDR (Medical Device Reporting) /AE (Adverse Event) reporting, a review of the FDA MAUDE database for complaints involving Healthcare Surgical Solutions products, and assisting in implementing Continuous Improvements identified through Lean/Six Sigma tools.Continuous Improvement projects will entail Standard Work Instructions, and Gauge Repeatability & Reproducibility studies.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 Functions:Test and thoroughly evaluate rudimentary surgical devices to determine root cause analysis Identifying the appropriate visual and functional test method/regiment from existing Standard Operating Procedures for complaint product evaluation, execute the method, and interpret the data (technical) for definitive root cause analysis determination.Test methods may include dimensional and/or tensile testing and interpretation of the technical data yielded in accordance with USP/EP/ASTM standardsReplicate reported failure mode with bench top or in vivo test methods and document observations accordinglyInitiate and distribute Corrective Action Requests to Manufacturing or Engineering Departments as neededPrepare technical investigation reports based on results of evaluation and/or review of the manufacturing plant reports to be documented in the complaint database and incorporated into customer response lettersAssist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Healthcare Manufacturing facilitiesCertification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030Maintain the highest level of compliance to the Code of Federal Regulations, Medical Device Directive (European Union), Canadian Medical Device Regulations, Japan MHLW, China SFDA and Australian RegulationsRequirements:Must be available to work at least 40 hours a weekExperience in a laboratory environment and with laboratory equipment orAcademic knowledge in scientific research methodsExperience with medical devices preferred but not requiredKnowledge of quality control concepts desirableMust be proficient with MS Office (with emphasis on Excel and PowerPoint)Experience writing and reading code (C++) preferred but not requiredMust have knowledge in using electronic/electrical toolsTime management skillsCritical independent thinking and timely follow upExcellent written and verbal skills necessary to include technical writingEducation:High School Diploma requiredBS Degree in a technical curriculum or equivalent industry experience preferredWorking Conditions/Physical Activities:Time will be spent equally in an office setting and a Biohazardous laboratory environment requiring use of personal protective equipment in accordance with CDC and OSHA regulationsLab Environment: Required to perform laboratory activities within a biohazard laboratory setting requiring the use of personal protective equipment.Frequent sitting, walking, standing and occasional kneeling, crouching, crawling, balancing, stooping climbing required.Frequent use of eye, hand and finger coordination in laboratory investigations and use of equipment will be necessary.Oral and auditory capacity enabling interpersonal communication as well as communication through automated devices such as the telephone is required.Physical effort required by handling objects up to 20 pounds

Lab Technician II

Integrated Resources, Inc

Boulder, Colorado

About the Company

Integrated Resources, Inc

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