Abbott
Abbott – Quality Engineer I
Abbott is a global healthcare leader that develops life‑changing technologies in diagnostics, medical devices, nutritionals and branded generic medicines. With more than 114,000 colleagues in more than 160 countries, Abbott is committed to improving people’s health at all stages of life.
Working at Abbott
Career development within an international company where you can grow the career you dream of.
Employees are eligible for free medical coverage in our Health Investment Plan (HIP) PPO plan in the next calendar year.
High‑contribution retirement savings plan.
Tuition reimbursement and student debt programs support affordable education.
Named one of the most admired companies worldwide by Fortune.
The Opportunity As a global leader in Cardiac Rhythm Technologies, we focus on innovations that improve how doctors treat heart arrhythmias. The Quality Engineer I performs administrative and tactical activities that support the efficient functioning of Quality Assurance and the Quality System.
What You’ll Work On
Implement effective process control systems to support development, qualification and ongoing manufacturing.
Assist in implementing assurances, process controls and CAPA systems that meet internal and external requirements.
Develop and execute streamlined business systems to identify and resolve quality issues.
Apply systematic problem‑solving methodologies to identify, prioritize, communicate and resolve quality issues.
Design and conduct experiments for process optimization and improvement.
Document experiment plans and results, including protocol writing and reports.
Lead process control and monitoring of CTQ parameters and specifications.
Lead and implement Six Sigma and Lean Manufacturing improvement methodologies.
Investigate, resolve and prevent product and process nonconformances.
Support quality disciplines, decisions and practices as a Core Team Member.
Maintain risk analysis and product verification and validation.
Collaborate with design engineering, microbiology and other cross‑functional teams.
Support company initiatives and regulatory requirements under FDA, ISO 13485 and company policies.
Assist in personnel training as directed by management.
Education and Experience
Bachelor’s degree or equivalent combination of education and work experience; entry level with 0–2 years of experience.
Engineering degree preferred.
Knowledge of FDA Quality System requirements and applicable U.S. Code of Federal Regulations for devices.
Knowledge of ISO 13485, quality management techniques and application.
Strong communication, interpersonal, organizational and problem‑solving skills.
Ability to work independently and cross‑functionally.
Critical‑thinking and database/software usage skills.
Prioritization, multitasking and contingency planning skills.
Equal Opportunity Abbott is an Equal Opportunity Employer, committed to employee diversity.
Location and Compensation Base pay for this position is $72,100.00 – $114,700.00. In specific locations, the pay range may vary from the range posted.
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Working at Abbott
Career development within an international company where you can grow the career you dream of.
Employees are eligible for free medical coverage in our Health Investment Plan (HIP) PPO plan in the next calendar year.
High‑contribution retirement savings plan.
Tuition reimbursement and student debt programs support affordable education.
Named one of the most admired companies worldwide by Fortune.
The Opportunity As a global leader in Cardiac Rhythm Technologies, we focus on innovations that improve how doctors treat heart arrhythmias. The Quality Engineer I performs administrative and tactical activities that support the efficient functioning of Quality Assurance and the Quality System.
What You’ll Work On
Implement effective process control systems to support development, qualification and ongoing manufacturing.
Assist in implementing assurances, process controls and CAPA systems that meet internal and external requirements.
Develop and execute streamlined business systems to identify and resolve quality issues.
Apply systematic problem‑solving methodologies to identify, prioritize, communicate and resolve quality issues.
Design and conduct experiments for process optimization and improvement.
Document experiment plans and results, including protocol writing and reports.
Lead process control and monitoring of CTQ parameters and specifications.
Lead and implement Six Sigma and Lean Manufacturing improvement methodologies.
Investigate, resolve and prevent product and process nonconformances.
Support quality disciplines, decisions and practices as a Core Team Member.
Maintain risk analysis and product verification and validation.
Collaborate with design engineering, microbiology and other cross‑functional teams.
Support company initiatives and regulatory requirements under FDA, ISO 13485 and company policies.
Assist in personnel training as directed by management.
Education and Experience
Bachelor’s degree or equivalent combination of education and work experience; entry level with 0–2 years of experience.
Engineering degree preferred.
Knowledge of FDA Quality System requirements and applicable U.S. Code of Federal Regulations for devices.
Knowledge of ISO 13485, quality management techniques and application.
Strong communication, interpersonal, organizational and problem‑solving skills.
Ability to work independently and cross‑functionally.
Critical‑thinking and database/software usage skills.
Prioritization, multitasking and contingency planning skills.
Equal Opportunity Abbott is an Equal Opportunity Employer, committed to employee diversity.
Location and Compensation Base pay for this position is $72,100.00 – $114,700.00. In specific locations, the pay range may vary from the range posted.
#J-18808-Ljbffr