Quality Engineer I at Abbott Laboratories
Minnetonka, Minnesota, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

50000.0

Posted On

09 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Manufacturing Analysis, Post Market Surveillance, Iso, Gmp

Industry

Pharmaceuticals

Description

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 114,000 colleagues serve people in more than 160 countries.

REQUIRED QUALIFICATIONS

  • Bachelor’s degree in engineering or Technical Field or an equivalent combination of education and work experience
  • 0-2 years Engineering experience
  • 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
  • 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

PREFERRED QUALIFICATIONS

  • Prior medical device experience preferred
  • Experience working in a broader enterprise/cross-division business unit model preferred
  • CAPA owner or a key cross-functional team member leading a CAPA project
  • Use of quality tools/methodologies. Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971
  • Risk management, post market surveillance, and manufacturing analysis

How To Apply:

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Responsibilities

Please refer the Job description for details

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