Job Details
Abbott
Inspector 1
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 113,000 colleagues serve people in more than 160 countries.
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
Career development with an international company where you can grow the career you dream of .
Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the [Register to View] student debt program and [Register to View] 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.
The Opportunity
This position works out of our Liberty, SC location in the Cardiac Rhythm Management division.
As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.
We are looking for an Inspector I for 2nd shift, M-Th 5:30pm-03:30am.
The inspector will perform inspection and testing of purchased materials, components and products in accordance with policy and procedures.
What You’ll Work On
Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
Records inspection and test data as prescribed by written instructions and procedures.
Recommends changes to policies and procedures.
Documents non-conformances in Non-Conforming Material Review system.
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.
Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
Performs other related duties and responsibilities, on occasion, as assigned.
Required Qualifications
High School Diploma / GED
0-2 year’s experience.
Good communication and computer skills, including Microsoft Word and Excel.
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.
Willing to work overtime as required.
Ability to maintain regular and predictable attendance.
Preferred Qualifications
Prior medical device component inspection experience.
Experience with optical measurement equipment, hand tools, gages, pressure and force gage testing.
Training in blueprint reading and experience with inspection sampling techniques.
Knowledge of FDA, GMP, ISO 13485.
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