Clinical and Health - QC Technologist

Job Description
Pay#####-22.00 an hour
Monday - Thursday 0700- 1730 p.m.
Interview required.

PLEASE NOTE

THE ROLE BELOW REQUIRES ADDITIONAL TESTING BEFORE THE CANDIDATE CAN BEGIN WORK. A candidate issued an offer must also take and CLEAR a TB Blood Test and Ichihara Vision test before they can work in the lab.

Company Information
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity. Our four premier brands - Life Technologies, Thermo Scientific, Fisher Scientific and Unity Lab Services - offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive support.

For more information, please visit

Job Title:

Quality Control Technologist

Reports To:

Quality Control Team Lead
Group/Division: SDG/MBD
Career Band:
Band 4
Job Track:
Professional

Position Location:

Lenexa Kansas
Number of Direct Reports: none
Day/Shift: Monday - Thursday 0700- 1730 p.m
FLSA Status (Exempt/Non-Exempt):
Non-Exempt
Pay #####-22 an hour/hr

Position Summary:

Responsible for all quality control aspects of finished product testing. Ensure that performance of finished product is in compliance with testing standards per IFU and SOP's in addition to customer requirements and regulating agencies' guidelines. Documentation control duties per Quality Assurance compliance requirements.

Key Responsibilities:

• Review and maintain product compliance specifications, documentation control.

• Gain proficiency on all testing areas.

• Documentation of testing results and determining disposition.

• Maintain consistency in training in Master Control.

• Establish and maintain SOP criteria for inspection/testing.

• Responsible for maintaining department equipment and requesting consumables as needed.

• Exercise and monitor GMP compliance in work environment.

• Work closely with Quality Assurance department as a quality team.

• Execute Stability Study testing in accordance with QA requirements.

• Work in conjunction with Customer Service Representatives to achieve on time product releases for standing orders and special products.

• Work with the continuous improvement program within the department.

• Work closely with a team in a fast paced laboratory setting.

• Understand and exercise all safety requirements and procedures.

• Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.

• Participate in achieving department goals.

• Support all company policies.

• Performs other duties as assigned.

Minimum Requirements /

Qualifications:

• Possess at least a 4-year degree in the biological sciences. Must have course work in microbiology with a laboratory or a 4-year degree with 5+ years of microbiology lab experience.

• Familiarity with virology or cell line preferred.

• Familiarity with FDA regulations for medical devices.

• Possess the ability to manage many tasks and in an organized fashion.

• Able to communicate effectively with a variety of departments regarding quality testing parameters.

• Possess intermediate computer skills, preferably with experience in Microsoft word to include Word, Excel and PowerPoint programs. Experience working in SAP is a plus.

• Listen to, and follow, written and verbal instructions in English.

• Able to adapt and to learn new procedures and to maintain a scientific and objective approach.

• Must be available to work weekend shifts when needed.

• Self-motivated, highly responsible and possess a good teamwork spirit.

• Excellent verbal and written skills in English.
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