Supplier Quality Engineer

Supplier Quality Engineer


Supplier Quality Engineer

Details of the offer

At Abbott, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.
We have an exciting opportunity for a Supplier Quality Engineer within our Abbott Rapid Diagnostics business located at Richmond, VA or Portsmouth, VA. In this role, you will responsible for third party manufacturer (TPM) and other supplier master data and specifications, managing qualification and surveillance audits of TPM suppliers and other suppliers as assigned, managing lifecycle of supplier nonconformances and the Supplier Corrective Action (SCAR) process, and collecting, assessing, and reporting on supplier quality data.
Abbott Rapid Diagnostics (formerly Alere) is part of Abbott?s Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
Manages several projects independently, maintain timelines, priorities and executes tasks in a manner that supports the organization?s top-level project goals.
Evaluates vendors and products according to supplier qualification and management processes.
Maintains up-to-date records of approved suppliers, materials, contracts, and audit schedules.
Leads manage and collaborate on Third Party Manufacturer (TPM) supplier quality audits.
Manages nonconformity and Supplier Corrective Action (CAPA) lifecycle for suppliers.

Manages quality agreement lifecycle with TPM and other suppliers and maintains up to date status on corresponding commercial agreement status.
Identifies and manages the collection, assessment, and reporting of supplier quality data as required by company processes.
May support multiple sites within Toxicology Business Unit.
Communicates quality issues with suppliers and works proactively to deliver acceptable quality solutions.

Bachelor's degree in Biology, Manufacturing, Engineering or other related technical/scientific discipline or the equivalent combination of education and experience.
3+ yrs. of participating in internal or external audits

Experience participating in supplier quality audits of manufacturers in the medical device or pharmaceutical industry.

1+ yr of leading internal or external audits

3+ years of experience in a GMP or FDA regulated manufacturing environment
2+ years of experience in a quality assurance or supplier quality/engineering role
Experience participating in laboratory GxP audits with a focus on ISO 17025, GLP, CLIA, CAP, NLCP, or similar regulatory schemes.
ASQ certification as Quality or Biomedical Auditor (CQA or CBA) or equivalent certification
Documented training as an auditor or lead auditor to ISO 13485:2016, ISO 17025:2017, and/or ISO 9001:2015.

About Abbott
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, nutritional, and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries.
Connect with us at , on LinkedIn at , on Facebook at and on Twitter @AbbottNews and @AbbottGlobal.
An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities. To request an accommodation, please send an email to **********.
#LI-JR1JobQualityOther LocationsNA-USA-Virginia-PortsmouthOrganizationOperations/COSScheduleFull-time

Source: Jobsxl


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