Hybrid QC Technician II bei Thermo Fisher

Work Schedule

Environmental Conditions

Job Description

Job Title:  Quality Control Technician I

Reports To:  Quality Control Supervisor

Group/Division:  SDG/MBD

Career Band:  Band 1

Job Track: Associate

Position Location:  Lenexa Kansas

Number of Direct Reports none

Day/Shift (if applicable):  Monday - Thursday Schedule may be flexed to a Tuesday – Friday, 7am – 5:30pm based on Laboratory needs.

FLSA Status (Exempt/Non-Exempt):  Non-Exempt

Position Summary:

Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, control of documents, and maintaining good general laboratory practices.

Key Responsibilities:  

• Review and maintain product compliance specifications, documentation control.
• Gain proficiency on all testing areas.
• Documentation of testing results and determination of aesthetic quality on finished product.
• Maintain consistency for training tasks in Master Control.
• Maintain SOP criteria for inspection/testing.
• Responsible for maintaining department equipment and ordering consumable stock supplies when necessary.
• Exercise GMP and GLP compliance in work environment.
• Work well in a high volume fast paced environment.
• Work closely with Quality Assurance department as a quality team.
• Work with the continuous improvement program within the department.
• Understand and exercise all safety requirements and procedures.
• Assists in maintaining standards in accordance with GMP's/SOP's and ISO regulations.
• Accomplish department goals.
• Support all company policies.
• Performs other duties as assigned.

Minimum Requirements/Qualifications:

• Possess a high school diploma or equivalent.
• Some laboratory experience in a biological sciences laboratory is preferred.
• A minimum combined 1-2 years of experience of in related QC/QA, microbiology laboratory work in a laboratory setting, or an equivalent combination of education and experience is a plus.
• Some familiarity with FDA regulations for medical devices.
• Possess the ability to manage many tasks and in an organized fashion.
• 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 alternate shifts when needed.
• Must maintain a professional workplace attitude.
• Self-motivated, highly responsible and possess a good teamwork spirit.