Quality Control Specialist 2 job

Organization
GE Healthcare
Job Location
Logan, UT
Job Description

The Quality Control Specialist 2 performs incoming product inspection of production processes, finished products, assemblies and compounds for good manufacturing/laboratory practices (GMP/GLP) to verify product meets specifications and are free of damage or defects. Essential Responsibilities Key Responsibilities Include (but are not limited to): 
• Perform in-process, finished product, and raw material testing of cell culture products 
• Discard or reject products, material and equipment not meeting specifications 
• Inspect, test, or measure materials, products, installations and work for conformance to specifications 
• Maintain and operate laboratory equipment 
• Verify conformance to specifications and protocols and report outcomes 
• Maintain supportive relationship with customers 
• Trains team members when required 
• Comply with EHS regulations & policies 

Quality Specific Goals: 
1. Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure that a device conforms to it's specification and out of specification items are properly handled. 
2. Knowledge and understanding of Stop Orders, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, as associated with this job type/position 
3. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 
4. Complete all planned Quality & Compliance training within the defined deadlines 
5. Identify and report any quality or compliance concerns and take immediate corrective action as required 
6. Training: Aware of and comply with GEHC training requirements

Requirements: 

1. Bachelor's degree in biology, chemistry, or related field 
2. One year of experience in a lab setting 
3. Knowledge of aseptic procedures and techniques 
4. Strong communication skills 
5. Detail-oriented and focus on accuracy 
6. Ability to follow complex instructions in written or oral form 
7. Proficient with software applications applicable to the job 
8. Ability to work effectively with little or no supervision 
9. Ability to lift 40-50 pounds Additional Eligibility Qualifications GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. Desired Characteristics 1. Knowledge of cGMP requirements and a wide range of testing procedures 
2. Attention to detail 
3. Technical / Associate Degree 
4. Three years relevant experience in quality and/or inspection 
5. Six Sigma Green Belt certified 
6. Cell Culture Experience/Aseptic technique

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