Technician I, Manufacturing at Abbott Laboratories
Atlanta, GA 30383
About the Job
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.
MAIN PURPOSE OF ROLE
Summarize the main purpose of the role.
Responsible for the production of high quality medical device hardware and systems. Includes detailed assembly and testing of various electronic components and finished devices in a controlled manufacturing environment.
MAIN RESPONSIBILITIES
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Perform mechanical assembly of electromechanical subassemblies and devices.
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Ability to handle and maneuver small components and parts.
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Perform testing of electronic components and assemblies using automated test equipment.
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Follow safety guidelines and utilize appropriate safety devices when performing all operations.
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Participate in continuous improvement/quality initiatives in order to enhance production processes to achieve quality and profitability metrics.
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Maintain accurate records to ensure DHR and quality documents are accurate, all parts are traceable and quality issues can be addressed to assure the quality of all products.
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Ability to read, comprehend, and follow written procedures; understand and follow verbal instructions.
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Understanding of and ability to utilize electronic data collection systems and computer software packages.
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Ability to prioritize work by determining the sequencing and timing of different jobs based on precedence and importance.
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Positively represent the company during tours by demonstrating techniques and sharing appropriate information.
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Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
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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.
QUALIFICATIONS
Education
Education Level
Major/Field of Study
Or
Education Level
High School Diploma / GED
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an equivalent combination of education and work experience
Technical Diploma (± 12 years)
Technical degree/certificate in electronics preferred.
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Experience/Background
Experience
Experience Details
Some
0-2 years experience with electronic assembly and test, preferably in medical device industry.
Demonstrated experience in troubleshooting equipment, building and or testing of electronic assemblies.
Experience in GMP, ISO, and FDA controlled environments preferred.
Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
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.
Ability to leverage and/or engage others to accomplish tasks.
Ability to maintain regular and predictable attendance.
Ability to work scheduled overtime as required is preferred.
The base pay for this position is $17.80 – $35.60 per hour. In specific locations, the pay range may vary from the range posted.
