Principal Operations Quality Engineer jobs in United States
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Guerbet · 6 hours ago

Principal Operations Quality Engineer

Guerbet is a global leader in medical imaging, offering a portfolio of pharmaceuticals, medical devices, and AI solutions. The Principal Operations Quality Engineer will ensure compliance levels are maintained, lead audits, and oversee the quality assurance processes within the organization.

Health CareMedicalPharmaceutical

Responsibilities

Lead position in the site execution of external audits from regulatory agencies (i.e SME, Inspection Room Representative). Position will take a lead role in the formulation of inspection responses and commitment completion follow-up
Assist in the department completion of trending and metrics (i.e Cost of Poor Quality, Key Performance Indicators, Quality Management Reviews, & Data Trend Analysis)
Complete department requirements for site Annual Product Quality Reviews (APQRs). Must have the ability to assess shifts and trends, as well as associate CAPA response as it relates to data obtained
Ability to write, review and final approve site related complaints, exceptions, and CAPA RCA investigations within a timely manner. When needed, may also perform investigations within each of the compliance quality systems
Possess process technical knowledge and writing capabilities
Ability to lead site Kaizens or brainstorming initiatives
Ability to support site annual or non-routine GMP training
Primary designee for Quality Operations Manager in his/her absence
Proactively manage and maintain regulatory compliance (US/EU/WHO/Brazilian/Korean standards)
Providing day to day supervision and oversight of Operations QEs
Performs other duties as assigned by management
Work safely in accordance with regulations, standards, and procedures and in a manner that eliminates unreasonable risk to health and the environment. Notify management of unsafe conditions or practices, unlawful activities and activities which present unreasonable health and/or environmental risk. Report all safety and/or environmental incidents to management immediately
Support various information requests from Corporate and other departments. Interact with corporate support groups to drive global continuous improvement validation and supplier management programs
Assist QA Compliance Manager with special assignments or projects as directed
Seek out and apply best quality assurance methods and practices in support of Quality objectives
Performs other duties as assigned by management

Qualification

Regulatory complianceQuality Management ReviewsCAPA investigationsASQ certificationAnalytical knowledgeMulti-taskingTechnical writingDocumentation skillsOrganizational skillsInterpersonal skills

Required

Minimum BS/BA degree in Life Sciences or Business
Minimum 8-12 years' experience in a pharmaceutical setting
Ability to lead site Kaizens or brainstorming initiatives
Ability to support site annual or non-routine GMP training
Proactively manage and maintain regulatory compliance (US/EU/WHO/Brazilian/Korean standards)
Providing day to day supervision and oversight of Operations QEs
Good documentation skills with eye for details and ability to identify hidden problems within processes and systems
Ability to work in a fast-paced environment; Proficient in multi-tasking; Well organized and reliable for consistent decision making
Strong Technical Writing Skills
Competent with MS Office software environment
Ability to interact with all levels of the organization

Preferred

MS preferred
ASQ certified inspector/auditor preferred
Analytical knowledge of Microbiology and Chemistry is preferred

Company

Guebert is a pharmaceutical company based in France and is mainly focused on research.

Funding

Current Stage
Public Company
Total Funding
$0.96M
2022-09-26Post Ipo Equity· $0.96M
1999-04-01IPO

Leadership Team

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François Convenant
Senior Vice President of Interventional Radiology
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