Lab Technician II

Integrated Resources Inc.; Boulder (CO); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading staffing firm is seeking a Lab Technician II in Boulder, CO. The role involves supporting Quality Assurance through analyzing medical device returns and executing continuous improvement projects. Candidates need a High School diploma, lab experience, and proficiency in MS Office. A strong understanding of quality control principles and excellent communication skills are essential for success.

Benefits

Referral bonus of $500 per candidate

Qualifications

• Experience with medical devices preferred but not required.
• Experience writing and reading code (C++) preferred but not required.
• Academic knowledge in scientific research methods.

Responsibilities

• Perform failure analysis on medical device customer returns.
• Test and evaluate surgical devices for root cause analysis.
• Prepare technical investigation reports based on lab evaluations.

Skills

Experience in a laboratory environment

Knowledge of quality control concepts

Proficient with MS Office

Critical independent thinking

Excellent written and verbal skills

Education

High School Diploma

BS Degree in technical curriculum

Tools

Laboratory equipment

Electronic/electrical tools

Job description

Integrated 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 Description

Job Title: Lab Technician II

Location: 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
The following functions will be performed under direct supervision;

· 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 standards

· Replicate reported failure mode with bench top or in vivo test methods and document observations accordingly

· Initiate and distribute Corrective Action Requests to Manufacturing or Engineering Departments as needed

· Prepare 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 letters

· Assist in the coordination of sanitization of clinically applied medical device returns and shipment to respective Healthcare Manufacturing facilities

· Certification with OSHA's BloodBorne Pathogens Standard 29 CFR 1910.1030

· Maintain 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 Regulations

REQUIREMENTS:

· Must be available to work at least 40 hours a week

· Experience in a laboratory environment and with laboratory equipment or

· Academic knowledge in scientific research methods

· Experience with medical devices preferred but not required

· Knowledge of quality control concepts desirable

· Must be proficient with MS Office (with emphasis on Excel and PowerPoint)

· Experience writing and reading code (C++) preferred but not required

· Must have knowledge in using electronic/electrical tools

· Critical independent thinking and timely follow up

· Excellent written and verbal skills necessary to include technical writing

EDUCATION
• High School Diploma required
• BS Degree in a technical curriculum or equivalent industry experience preferred
WORKING 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 regulations

· Lab 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

Additional Information

we 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.

Thanks & Regards,

Seema Chawhan Clinical Recruiter Integrated Resources , Inc. IT Life Sciences Allied Healthcare CRO Certified MBE | GSA - Schedule 66 I GSA - Schedule 621I

DIRECT # - 732-844-8724 |

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

Gold Seal JCAHO Certified for Health Care Staffing “INC 5 0 0 0 ’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)