Quality Engineer - Sturgis, MI Plant

Abbott (abbottcareers2 board); United States; Vor Ort; USD 75.000 - 110.000; Vollzeit

Benefits dieser Stelle

Health benefits start day 1

Tuition assistance

Vacation 120 hours + 3 personal days +

401(k) retirement plan with companyit

Zusammenfassung

Abbott Nutrition in Sturgis, MI is seeking a Quality Engineer to develop and sustain quality engineering methods across new product development and manufacturing. You will apply Six Sigma and Lean principles to improve processes and ensure compliance with FDA and GMP standards.

You will collaborate with design, manufacturing, and microbiology teams to verify products, control CTQ parameters, and lead investigation of nonconformances while coaching junior staff to ensure robust and compliant

Qualifikationen

• Bachelor's degree plus 2–5 years in Quality Assurance, Manufacturing or Engineering
• Demonstrated use of quality tools; knowledge of FDA, GMP
• Strong project management and data analysis skills

Aufgaben

• Develop and maintain quality engineering methods for new products and manufacturing
• Lead the development and execution of process controls to meet requirements
• Coach and mentor non-exempt and entry-level staff
• Document experiments, protocols and results with reports
• Lead risk analysis and product verification activities with cross-functional teams
• Investigate, resolve and prevent quality issues and nonconformances

Kenntnisse

Quality Assurance

GMP knowledge

Statistical analysis

Project leadership

Ausbildung

Bachelor's Degree in Engineering

Tools

Minitab

Jobbeschreibung

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

Job Title: Quality Engineer

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

• Production areas that are clean, well-lit and temperature-controlled
• Training and career development , with onboarding programs for new employees and tuition assistance
• Financial security through competitive compensation, incentives and retirement plan
• Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1
• Vacation - 120 hours of accrued vacation (1st yr is prorated) + vacation buy program + 3 personal days + 10 paid holidays
• Retiree Healthcare program
• Robust 401(k) retirement savings with a generous company match
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A stable company with a record of strong financial performance and history of being actively involved in local communities
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Sturgis, MI location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® - to help them get the nutrients they need to live their healthiest lives.

For over 70 years, Abbott's Sturgis, Mich. , has been impacting its community while producing products that provide essential nutrition to millions of families around the world. Working here, you'll feel part of a family that is dedicated to making a difference and helping others.

What You'll Work On

• The Quality Engineer is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support.
• Identify and implement effective process control systems to support the development, qualification, and on-going manufacturing of products to meet or exceed internal and external requirements
• Lead, coach, and mentor non-exempt and entry level exempt personnel
• Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues
• Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
• Design and conduct experiments for process optimization and/or improvement
• Appropriately document experiment plans and results, including protocol writing and reports
• Lead process control and monitoring of CTQ parameters and specifications
• Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)
• Lead the investigation, resolution and prevention of product and process nonconformances
• Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member)
• Lead in the completion and maintenance of risk analysis
• Work with design engineering in the completion of product verification and validation
• Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities
• Support all Divisional initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements

You’ll be accountable for meeting our compliance standards including FDA, OSHA and Abbott policies and procedures.

Required Qualifications

• Bachelor's Degree plus 2-5 years of relevant experience in Quality Assurance, Manufacturing or Engineering experience OR Master's Degree plus 1-3 years of relevant experience in Quality Assurance, Manufacturing or Engineering
• Demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP
• Strong project management and leadership skills
• Advanced computer skills, including statistical/data analysis and report writing skills.