132 QA Engineering Jobs in Raleigh, NC, United States

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• Position Summary The Quality Assurance (QA) Engineer is responsible for ensuring that agrochemical products are manufactured, tested, packa…
• Quality & Compliance Quality Management Systems (QMS) GMP, GLP, & ISO 9001, compliance Regulatory compliance (EPA, FIFRA, and industry stan…

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• Technical Skills: Proficiency in quality assurance methodologies, regulatory compliance, and risk management.
• This involves auditing established programs for regulatory, customer, and Flowserve compliance, implementing quality assurance programs ali…

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• Job Description The role provides support for the various elements of the Quality System, including but not limited to the…
• The Quality Engineer applies the appropriate statistical tools to analyze data, identify root cause and develop corrective actions for effe…

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• Experience in product quality, reliability, or product engineering for PCB, PCBA and Electronic assembly & Servers.
• Develop and implement supplier quality management strategies that drive manufacturing excellence, product reliability, and compliance with…

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• Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going b…
• Quality oversight of new product introduction activities covering facilities, utilities, equipment, systems and process with alignment into…

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• Experience using Quality Management Systems (i.e. Track Wise or Veeva) for Deviation investigations and CAPAs Demonstrated project manageme…
• This individual contributor position reports into the Senior Manager of the MFG Technical Training team and interacts broadly across the…

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• Proficient in Quality Management System(s).
• The Opportunity We're seeking a highly skilled Maintenance Specialist with direct Pharmaceutical Packaging Equipment experience who will be…

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• Preferred Qualifications Current ASCP (or equivalent) certification; ASCP Specialist in Molecular Biology (SM/MB) Additional Job Standards…
• Knowledge of preclinical/clinical assays and companion diagnostics (CDx) development.

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• The Quality Assurance Specialist 2 plays a key role in the day ‑ to ‑ day execution and maintenance of…
• This position supports QMS process management by performing system administration and data entry activities, monitoring timelines and perfo…

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• Minimum of 10+ years of laboratory experience to include at least 5+ years of experience in managing an anatomic and…
• Current ASCP certification as a Medical Technologist, Laboratory Scientist, Cytotechnologist, Histotechnologist or equivalent.

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• Essential Functions: Performs detailed QC review of clinical and regulatory documents, tables, publications, annual reports, literature sum…
• Works on special QC projects and initiatives to help drive consistency and performance of the QC team regarding best processes/practices,…

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• Working closely with multiple subject areas, including manufacturing, process engineering, process development, utility operations, mainten…
• Provide engineering support for design, construction, startup, commissioning and qualification of new or modified systems.

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• Working closely with multiple subject areas, including manufacturing, process engineering, process development, utility operations, mainten…
• Provide engineering support for design, construction, startup, commissioning and qualification of new or modified systems.

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• The Technical Certification Engineer (Compliance) will be responsible for driving product certification and regulatory compliance initiativ…
• Strong technical writing skills with experience creating compliance documentation and engineering reports.

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• The Quality Assurance Specialist 2 plays a key role in the day ‑ to ‑ day execution and maintenance of…
• This position supports QMS process management by performing system administration and data entry activities, monitoring timelines and perfo…

Role highlights

• Serve as a technical subject matter expert within an area of regulatory compliance, to include EMC, RF or other applicable…
• Basic Qualifications Bachelor’s Degree in Electrical Engineering, Computer Engineering, RF Engineering, or related field AND a minimum of 5…

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• Key responsibilities include: Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics…
• Strong understanding of regulatory requirements and guidelines for clinical trials, including ICH-GCP and local regulatory requirements.

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• Validation Engineer with 7–11 years of experience to lead validation activities across equipment, utilities, facilities, computerized syste…
• Lead the generation and execution of validation lifecycle documentation (FAT, SAT, IOQ, PQ) for equipment, utilities, facilities, cleaning…

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• POSITION OVERVIEW The Manufacturing Quality Assurance (MQA) Specialist – 3rd shift is responsible for providing quality oversight to all ma…
• HOW YOU’LL MAKE AN IMPACT The responsibilities of this job include, but are not limited to, the following: Required to…

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• Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipmen…
• As a Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and…

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• About the Role The Senior Clinical Project Manager, Clinical Development is responsible for leading the planning, execution, oversight, and…
• Preferred Qualifications 5+ years’ experience of clinical trial management for late phase studies Experience with IMP/clinical drug supply…

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• The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed.
• These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and…

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• Support sustaining engineering efforts for the manufacturing plants as applicable.
• Serve as a participant in integrated core teams as the Sustaining Engineering representative and/or technical lead.

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• This position is a senior individual contributor and cross-functional leader responsible for driving complex, high-impact programs across p…
• Key Responsibilities Lead end-to-end program management for complex technical operations initiatives including new product introductions, t…

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• What You'll Do Serving as a subject matter expert in nonclinical safety (toxicology and safety pharmacology) and regulatory strategy, you…
• Experience monitoring outsourced nonclinical toxicology and safety pharmacology at CROs Demonstrated ability to communicate complex scienti…