Qc Technician I Jobs

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Location/Division Specific Information

Lenexa, KS

Specialty Diagnostics Group

Shift: Monday-Thursday 7:00am-5:30pm

Discover Impactful Work:

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.

A Day in the Life:

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

Minimum Requirements/Qualifications:

• Possess a high school diploma or equivalent.
• Able to adapt and to learn new procedures and to maintain a scientific and objective approach.
• 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.
• Must maintain a professional workplace attitude.
• Must be available to work alternate shifts when needed.
• 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.
• Self-motivated, highly responsible and possess a good teamwork spirit.
• Some laboratory experience in a biological sciences laboratory is preferred.
• Listen to, and follow, written and verbal instructions in English.
• Some familiarity with FDA regulations for medical devices.