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Quality Engineer II (2nd Shift)

Abbott Laboratories

This is a Full-time position in Atlanta, GA posted November 24, 2021.

Location United States
– Georgia
– Atlanta Category Quality

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 109,000 colleagues serve people in more than 160 countries.

Leading an active lifestyle is important to the many people we serve.

In Abbott’s Heart Failure division, we’re advancing the treatment of heart and vascular disease through breakthrough medical technologies in electrophysiology and heart failure (EPHF) , allowing people to restore their health and get on with their lives.

For years, Abbott’s MEDICAL DEVICES businesses have offered technologies that are faster, more effective, and less invasive.

Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier.

Every day, our technologies help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine finger sticks.

Our Quality Engineer II is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support.

2nd Shift Hours: 2:30pm to 11pm

WHAT YOU’LL DO

  • 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 in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements
  • 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 non-conformances
  • 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 Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
  • Complies with U.S.

    Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.

    Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

EDUCATION AND EXPERIENCE YOU’LL BRING

  • Bachelors Degree –
    – Engineering or Technical Field or equivalent experience
  • 2-5 years Engineering experience and demonstrated use of Quality tools/methodologies.

    Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971

  • Solid communication and interpersonal skills.

    Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner.

    Advanced computer skills, including statistical/data analysis and report writing skills

  • Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing).

    ASQ CQE or other certifications preferred.

  • Experience working in a broader enterprise/cross-division business unit model preferred.

    Ability to work in a highly matrixed and geographically diverse business environment.

    Ability to work within a team and as an individual contributor in a fast-paced, changing environment.

    Ability to leverage and/or engage others to accomplish projects.

    Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.

    Multitasks, prioritizes and meets deadlines in timely manner.

    Strong organizational and follow-up skills, as well as attention to detail.

WHAT WE OFFER

At Abbott, you can have a good job that can grow into a great career.

We offer:

· A fast-paced work environment where your safety is our priority

· 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 plans

· Health care and well-being programs including medical, dental, vision, wellness and occupational health programs

· Paid time off

· 401(k) retirement savings with a generous company match

· The stability of a company with a record of strong financial performance and history of being actively involved in local communities

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future.

Abbott is an Equal Opportunity Employer, committed to employee diversity.

Job Id 30999744 Location United States
– Georgia
– Atlanta Medical surveillance No Division EPHF Electrophysiology & Heart Failure Travel Yes, 5 % of the Time Additional Location 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)

PLAN FOR SUCCESS

CAREER OPPORTUNITIES

Our business encompasses many different functions and capabilities, which allows you to explore careers in various fields.

GROWTH PLANNING

Growth Planning and Performance Excellence is an annual process through which you’ll be able to have open career discussions with your manager to help you determine your own career path and future.

TRAINING & NETWORKS

We provide a wide range of classroom and e-learning courses to help you develop new skills and enhance your career.

WE’RE RECOGNIZED AROUND THE WORLD

DOW JONES SUSTAINABILITY INDEX

BEST CORPORATE CITIZENS

FORTUNE CHANGE
THE WORLD

FORTUNE’S MOST ADMIRED COMPANIES

JOIN OUR TALENT COMMUNITY

We will notify you about relevant positions, and keep you in mind when we have interesting opportunities.

Abbott welcomes and encourages diversity in our workforce including Minorities, Women, Individuals with Disabilities and Protected Veterans.

We provide reasonable accommodation to qualified individuals with disabilities.

Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates.

No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company.