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Job Requirements of QC Technician I:
-
Employment Type:
Contractor
-
Location:
Lenexa, KS (Onsite)
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QC Technician I
Careers Integrated Resources Inc
Lenexa, KS (Onsite)
Contractor
Job Description: Job Title: Quality Control Technician I
Position Location: Lenexa Kansas
Day/Shift (if applicable): Friday to Monday 7am to 5:30 PM (Weekend).
Position Summary:
Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, documenting results, and maintaining good general laboratory practices.
Key Responsibilities:
Perform tasks following all work instructions and established procedures.
Perform microbiological tasks including inoculations, maintain stock, dilutions, gram stains and physical assessment of finished and intermediate samples.
Product proficiency on all technician testing areas.
Document inspection results accurately and consistently.
Maintain consistency in training tasks within Master Control.
Responsible daily calibrations of measuring equipment within the QC laboratory.
Order consumable stock supplies when necessary.
Exercise Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) compliance in the work environment.
Work effectively in a high-volume, fast-paced environment.
Collaborate closely with the Quality Assurance department as part of the quality team.
Participate in the continuous improvement program within the department.
Understand and adhere to all safety requirements and procedures.
Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations.
Support department and company goals.
Adhere to and support all company policies.
Perform other duties as assigned.
Minimum Requirements/Qualifications:
Possess at least an Associates degree in Biology.
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.
Previous experience working in an FDA regulated environment preferred.
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.
Comments for Suppliers:
Position Location: Lenexa Kansas
Day/Shift (if applicable): Friday to Monday 7am to 5:30 PM (Weekend).
Position Summary:
Responsible for the evaluation of quality control samples through physical evaluation and microbial load testing of plated and non-plated media, documenting results, and maintaining good general laboratory practices.
Key Responsibilities:
Perform tasks following all work instructions and established procedures.
Perform microbiological tasks including inoculations, maintain stock, dilutions, gram stains and physical assessment of finished and intermediate samples.
Product proficiency on all technician testing areas.
Document inspection results accurately and consistently.
Maintain consistency in training tasks within Master Control.
Responsible daily calibrations of measuring equipment within the QC laboratory.
Order consumable stock supplies when necessary.
Exercise Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) compliance in the work environment.
Work effectively in a high-volume, fast-paced environment.
Collaborate closely with the Quality Assurance department as part of the quality team.
Participate in the continuous improvement program within the department.
Understand and adhere to all safety requirements and procedures.
Assist in maintaining standards in accordance with GMPs, SOPs, and ISO regulations.
Support department and company goals.
Adhere to and support all company policies.
Perform other duties as assigned.
Minimum Requirements/Qualifications:
Possess at least an Associates degree in Biology.
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.
Previous experience working in an FDA regulated environment preferred.
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.
Comments for Suppliers:
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