| Distance: | Resume alert | Resumes 391 - 400 of 25477 |
Senior Field Engineer, Process, Quality Project Manager
Spain
... Highly skilled in mechatronics, mechanical troubleshooting, line modifications, DeltaV, Symcade, CIP/SIP, UF/DF systems, CMMS, MES, SOPs, IQ/OQ/PQ, GMP, xGMP, and regulatory compliance (FDA 21 CFR, ISO 9001, 14001, 27701). Key Responsibilities & ... - 2025 Sep 09
... Highly skilled in mechatronics, mechanical troubleshooting, line modifications, DeltaV, Symcade, CIP/SIP, UF/DF systems, CMMS, MES, SOPs, IQ/OQ/PQ, GMP, xGMP, and regulatory compliance (FDA 21 CFR, ISO 9001, 14001, 27701). Key Responsibilities & ... - 2025 Sep 09
Automation Testing Test Engineer
New Berlin, WI
... Contributed to FDA submission documents with validated test evidence and traceability for software verification. Prepared comprehensive test plans and created and executed functional tests for web services. Performed Functional, E2E, UAT, Regression ... - 2025 Sep 09
... Contributed to FDA submission documents with validated test evidence and traceability for software verification. Prepared comprehensive test plans and created and executed functional tests for web services. Performed Functional, E2E, UAT, Regression ... - 2025 Sep 09
Clinical Research Coordinator
St. Louis, MO
... Trials •GCP •Laboratory Experience •Medical Office Experience •FDA Regulations •Epic •REDCap •OnCore •Medidata Rave •OpenClinica •IRT •myIRB Certifications and Licenses Good Clinical Practice Necessary Elements in the Fundamentals of Human Research - 2025 Sep 09
... Trials •GCP •Laboratory Experience •Medical Office Experience •FDA Regulations •Epic •REDCap •OnCore •Medidata Rave •OpenClinica •IRT •myIRB Certifications and Licenses Good Clinical Practice Necessary Elements in the Fundamentals of Human Research - 2025 Sep 09
Quality Control Chemist
Kingston, PA
... • Calibrated instruments and maintained FDA compliance. • Investigated quality incidents and supported audits. Wren Kitchens – Sugar Notch, PA Quality Control Technician Nov 2022 – Aug 2023 • Inspected raw materials, components, and finished ... - 2025 Sep 09
... • Calibrated instruments and maintained FDA compliance. • Investigated quality incidents and supported audits. Wren Kitchens – Sugar Notch, PA Quality Control Technician Nov 2022 – Aug 2023 • Inspected raw materials, components, and finished ... - 2025 Sep 09
Clinical Research Regulatory Compliance
Parkville, MD, 21234
... In-House Clinical Research Associate April-2021 – June-2025 Processed and reviewed essential regulatory documents according to FDA, ICH, and sponsor guidelines. Supported Phase I-IV clinical trials across 60+ sites, facilitated SMT meetings and ... - 2025 Sep 09
... In-House Clinical Research Associate April-2021 – June-2025 Processed and reviewed essential regulatory documents according to FDA, ICH, and sponsor guidelines. Supported Phase I-IV clinical trials across 60+ sites, facilitated SMT meetings and ... - 2025 Sep 09
Manual Testing Clinical Trials
Hyderabad, Telangana, India
... Ensure compliance with GxP/FDA guidelines in clinical domain projects. Professional Experience Signant Health Pvt. Ltd – Hyderabad QA Lead Dec 2022 – Present Led QA activities for multiple pharma clients: AstraZeneca, Roche, Pfizer, GSK, Janssen, ... - 2025 Sep 09
... Ensure compliance with GxP/FDA guidelines in clinical domain projects. Professional Experience Signant Health Pvt. Ltd – Hyderabad QA Lead Dec 2022 – Present Led QA activities for multiple pharma clients: AstraZeneca, Roche, Pfizer, GSK, Janssen, ... - 2025 Sep 09
Supply Chain Assistant Manager
Mumbai, Maharashtra, India
... 2015 FDA Approval in Liquid oral. WORK EXPERIENCE: Total Work Experience: 18+ years 7. Livealth biopharma pvt. ltd, Mahape Assistant manager- Production planning. From (may.2020 to till date) 1.Searching suitable manufacturing sites for export ... - 2025 Sep 09
... 2015 FDA Approval in Liquid oral. WORK EXPERIENCE: Total Work Experience: 18+ years 7. Livealth biopharma pvt. ltd, Mahape Assistant manager- Production planning. From (may.2020 to till date) 1.Searching suitable manufacturing sites for export ... - 2025 Sep 09
Nurse Practitioner Registered
Studio City, CA
... Presided over development and implementation of clinical resources and tools in accordance with industry best practices and FDA guidelines. Significantly contributed towards FDA and HRSA submissions by formulating detailed reports outlining adverse ... - 2025 Sep 09
... Presided over development and implementation of clinical resources and tools in accordance with industry best practices and FDA guidelines. Significantly contributed towards FDA and HRSA submissions by formulating detailed reports outlining adverse ... - 2025 Sep 09
Clinical Research Start Up
Sandviken, Gavleborg, 811 33, Sweden
... Louis, MO 63110 Clinical Research Specialist (hybrid) Jan 2020 – Nov 2021 Subject matter expert in regulatory submissions and project management (Single patient compassionate treatment submission to FDA, industry sponsored studies, secondary ... - 2025 Sep 08
... Louis, MO 63110 Clinical Research Specialist (hybrid) Jan 2020 – Nov 2021 Subject matter expert in regulatory submissions and project management (Single patient compassionate treatment submission to FDA, industry sponsored studies, secondary ... - 2025 Sep 08
Supply Chain Project Management
Mukwonago, WI
... Responsible for the successful turnarounds to improve profit margins in supply chain, purchasing and project management in the supply base in multiple OEM and Tier 1 settings as well as FDA requirements and processes. Extensive experience with low ... - 2025 Sep 08
... Responsible for the successful turnarounds to improve profit margins in supply chain, purchasing and project management in the supply base in multiple OEM and Tier 1 settings as well as FDA requirements and processes. Extensive experience with low ... - 2025 Sep 08