Abbott
The Opportunity
This position works out of our Liberty, SC location. This is an onsite role. What You’ll Work On
Interfaces with Safety Regulatory Agencies as required ensuring compliant product is released (i.e. Provides quality engineering support to the site to ensure manufacturing/quality requirements are met. Understands and elevate issues related quality validations. Implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members. Implements Process Monitoring Systems by identifying critical process steps which could culminate in possible sources of manufacturing defects and devising methods to reduce process variation in order to reduce/eliminate the cause of defects. Contribute to the development of appropriate reliability program for the division/site. Lead/Assist in writing, executing, and analyzing various types of protocols (i.e. engineering studies, verification protocols, validation, etc.). Provides assistance or lead projects as assigned. Reduces and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by assisting efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. Helps assure that Division projects meet scheduled dates and are compliant with the regulations. May be involved in all levels of projects from simple design changes to total design changes. Education and Experience You’ll Bring
Required Experience: Bachelors Degree in Engineering or Related Field 2 years’ Quality Assurance, Manufacturing or Engineering experience and demonstrated use of Quality tools/methodologies. Working Knowledge of applicable regulations, compliance requirements, quality systems, and engineering / quality principles as relates to applicable manufacturing environment, preferably consumable goods. Preferred Experience: Experience with Process Improvement Experience with GLP Improvements Experience with Inspections and Validations Experience with Scrap Reduction Six Sigma, a plus Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is
$60,000.00 – $120,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY:
Operations Quality
DIVISION:
CRM Cardiac Rhythm Management
LOCATION:
United States > Liberty : 253 Financial Blvd.
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law: English and Spanish versions available.
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This position works out of our Liberty, SC location. This is an onsite role. What You’ll Work On
Interfaces with Safety Regulatory Agencies as required ensuring compliant product is released (i.e. Provides quality engineering support to the site to ensure manufacturing/quality requirements are met. Understands and elevate issues related quality validations. Implements product quality plans, documents and systems by creating product specifications, quality specifications, quality plans, risk analyses, FMEAs in conjunction with other product development team members. Implements Process Monitoring Systems by identifying critical process steps which could culminate in possible sources of manufacturing defects and devising methods to reduce process variation in order to reduce/eliminate the cause of defects. Contribute to the development of appropriate reliability program for the division/site. Lead/Assist in writing, executing, and analyzing various types of protocols (i.e. engineering studies, verification protocols, validation, etc.). Provides assistance or lead projects as assigned. Reduces and controls manufacturing process defects (scrap, nonconforming material, customer complaints) by assisting efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. Helps assure that Division projects meet scheduled dates and are compliant with the regulations. May be involved in all levels of projects from simple design changes to total design changes. Education and Experience You’ll Bring
Required Experience: Bachelors Degree in Engineering or Related Field 2 years’ Quality Assurance, Manufacturing or Engineering experience and demonstrated use of Quality tools/methodologies. Working Knowledge of applicable regulations, compliance requirements, quality systems, and engineering / quality principles as relates to applicable manufacturing environment, preferably consumable goods. Preferred Experience: Experience with Process Improvement Experience with GLP Improvements Experience with Inspections and Validations Experience with Scrap Reduction Six Sigma, a plus Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:
www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is
$60,000.00 – $120,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY:
Operations Quality
DIVISION:
CRM Cardiac Rhythm Management
LOCATION:
United States > Liberty : 253 Financial Blvd.
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law: English and Spanish versions available.
#J-18808-Ljbffr