- Arthrex (Pendleton, SC)
- …Cause Analysis Investigations and assist or lead ( Sr . & Principal ) Corrective/Preventive Action Plans ( CAPA 's) investigations. Facilitate completion of ... activities in accordance with Quality System requirements. Support, initiate or lead ( Sr . & Principal ) Continuous Improvement projects. Responsible for reviewing… more
- DivIHN Integration Inc (Medina, NY)
- …Specialists Sivanesan at 224 369 0756 Infant at 224 507 1261 Title: Principal Validation Engineer Location: Medina, NY Duration: 3 Months Description: Top Skills: ... the employment prerequisites and job responsibilities for the position of Principal Engineer, Quality Validation. II. ESSENTIAL FUNCTIONS: The person in this… more
- Medtronic (Los Angeles, CA)
- …SharePoint Online, Excel, etc.). Deliver ongoing reporting & analytics of KPIs to the SR Leadership Team and for CAPA Board meetings. **Must Have: Minimum ... compassionate world. **A Day in the Life** In this exciting role as a Principal Quality Engineer, you will have responsibility for supporting the CAPA process,… more
- West Pharmaceutical Services (Scottsdale, AZ)
- …or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening. Sr Principal Quality Engineer ... strategies for various projects. + May review and approve Complaint, CAPA , Audit Findings, Issue Reviews, Non-conformances investigations to provide guidance to… more
- Lilly (Indianapolis, IN)
- …entering manufacturing and laboratory areas which require wearing appropriate PPE. + Sr . Principal /Advisor level is considered equivalent to QA Associate ... potential improvement opportunities: + Deviation Cycle Time + Event Root Causes + Overdue CAPA items **Basic Requirements:** + 5 plus years of work experience in a… more
- Lilly (Indianapolis, IN)
- …supporting our mission to deliver life-saving medications to patients worldwide. As a Sr . Principal Engineer, you will provide technical oversight and will work ... and production issues and work on the identification and implementation of CAPA plans to address such events and prevent recurrence. **Regulatory Compliance:** +… more
- Boehringer Ingelheim (St. Joseph, MO)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Principal Specialist, Production Execution Systems will be the project ... activities to meet requirements and timelines. + Responsible for leading/managing CAPA implementation, auditing, and revision of standard operating procedures for… more
- Lilly (Indianapolis, IN)
- …required): + Provide guidance and support for deviations, change controls, CAPA identification, technical report writing, as needed. + Review/approve major ... deviations and change controls, technical reports, and any other analytical document, as needed. + Lead critical/complex deviations (as required). + Provide laboratory accreditation support. Perform the annual laboratory accreditation plan to ensure compliance… more
- West Pharmaceutical Services (Exton, PA)
- Sr Quality Engineer, Integrated Systems Requisition ID: 66823 Date: Sep 10, 2024 Location: Exton, Pennsylvania, US Department: Quality Description: At West, we're a ... through our sustainability efforts. **Job Summary:** In this role, the Senior Quality Engineer provides quality direction, governance, and Quality Management System… more
- BioFire Diagnostics, LLC. (Hazelwood, MO)
- …required (QSMR, weekly and quarterly trending, monthly site metrics). + Act as principal Quality contact for department risk management activities. + Act as a ... First Article Inspection of components as needed. + Participate in site CAPA activities, including analysis of data and trends, nonconforming material, complaints,… more
- Teleflex (Chelmsford, MA)
- …to ensure that product quality and services are achieved and maintained. ** Principal Responsibilities** * Nonconformance (NC) and CAPA processing - lead ... in 5 main areas of the Quality Management System including CAPA & Nonconformance (NC) Processes; Incoming Inspection Improvements; Perpetual Audit readiness;… more
- Medtronic (Mounds View, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Principal Electrical Engineer for Medtronic CRM RPE will be responsible for device electrical ... (CA) to modify maintain design documentation (BOM's, Specs, drawings) *Supports CAPA 's (Corrective & Preventive Actions) and RPI's (Released Product Investigations)… more
- Verista (Las Vegas, NV)
- …skills and learn from our experiences to enhance our collective expertise Principal Quality/GxP Auditor Responsibilities: + Develop and present Compliance plans and ... Quality Lead level requirements. + Demonstrated capability to deliver on the Senior Quality Lead Responsibilities. + Demonstrated expert knowledge of GxP regulatory… more
- Medtronic (Mounds View, MN)
- …in a more connected, compassionate world. **A Day in the Life** As a Senior Test Engineer within the Mechanical Produce Engineering Team, you will be part of ... procedures, manufacturing processes, or new testing requirements. + Supports CAPA 's (Corrective & Preventive Actions) & RPI's (Released Product Investigations).… more
- UT Health (Houston, TX)
- Senior Manager Clinical Trial Program (Stroke Institute) **Location:** Texas Medical Center-Houston, Texas **Category:** Research McGovern Medical School at UTHealth ... and is capable of leading internal audits on the studies.** **Experience with CAPA (Corrective and Preventative Action) plans and being able to oversee 8 research… more
- West Pharmaceutical Services (Scottsdale, AZ)
- Senior Validation Engineer Requisition ID: 65729 Date: Sep 18, 2024 Location: Scottsdale, Arizona, US Department: Engineering Description: **Who We Are:** Working at ... and ensure the process Quality + Initiate, support, execute CAPA and other quality initiatives + Ensure compliance with...reflect the general details considered necessary to describe the principal functions of the job identified and shall not… more
- Cirtec Medical (Lowell, MA)
- …7 years of experience in a regulated medical device environment, preferably as a Sr or Principal Quality Engineer or Quality Manager, with supervisory and ... manufacturing practices, supplier auditing & management, quality control (GD&T, MRB, etc.), CAPA and customer complaints. + Experience with Class II and Class III… more
- Motion Recruitment Partners (Boston, MA)
- …and ensure seamless operations. We seek a highly experienced and detail-oriented Senior / Principal Manufacturing Engineer with a strong focus on Quality ... Engineering to join our esteemed team. As a Senior / Principal Manufacturing Engineer focusing on Quality Engineering,...+ Demonstrated expertise in root cause analysis, problem-solving, and CAPA processes at a senior level. +… more
- University of Michigan (Ann Arbor, MI)
- …skills to join our growing research team. This position will work with principal investigators and other research team members to accurately and efficiently carry ... review of study processes and documents. **CHARACTERISTIC DUTIES AND RESPONSIBILITIES: CRC- Senior ** 20% - Clinical Coordinator Responsibilities + Contributes to the… more
