How much does a Quality Technician make at companies like ABBOTT LABORATORIES in the United States? The average salary for Quality Technician at companies like ABBOTT LABORATORIES in the United States is $52,064 as of October 25, 2023, but the range typically falls between $45,525 and $58,603. Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target. View the Cost of Living in Major Cities2
About ABBOTT LABORATORIES
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View abbott laboratories Salary
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 115,000 colleagues serve people in more than 160 countries.
MAIN RESPONSIBILITIES
-Quality/Compliance -Support manufacturing and testing operations as required; adhering to Good Manufacturing Practices and Good Laboratory Practices.
-Demonstrate strong knowledge of all technical processes/procedures within area of responsibility.
-Conduct business in a manner that will protect human health; safety and the environment by complying with all applicable EHS laws; as well at the Abbott Global and Technical standards.
-Comply with Abbott Quality System (QS) requirements. Share Quality -Knowledge liaising with colleagues within team.
-Train others in multiple key processes within work area. Assists with the collation of information requested during audits.
-Complete Quality testing as appropriate for products per procedures and review all data to determine conformance with specifications. b. Ensure that plant Environmental Monitoring program if applicable is executed per procedural requirements and schedule; and that environmental data is tracked and trended. Conduct Inspections of incoming items per standard requirements. b. Ensure storage of samples and documents in the appropriate filling systems.
-Initiates site Change Plan and Document Change Request activities for changes Co-ordinate and manage Change Plan and Document Change requests through to closure. Including tracking of identified deliverables and action items.
-Work in conjunction with relevant Document/ Process owners to identify and organize CFTs.
-Complete required document authoring and approval tasks as required for QSR and DMR documents.
QUALIFICATIONS
Education
-High School graduated or equivalent plus a certificate in relevant Science Area.
-0 -2 years work experience
Preferred
-Ideally a bachelor’s degree in a science or closely related discipline or equivalent relevant experience to demonstrate equivalence to a Degree.
-Minimum 2 years
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Includes base and annual incentives
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