- Eurofins (King Of Prussia, PA)
- …Testing. + GMP review of Qualification and Media Release testing. + GMP review of facility cleaning data and in-processing testing, including but not ... stocks in Europe over the past 20 years. + Water Systems + GMP review of microbiological testing of the facility and/or laboratory water purification system… more
- Eurofins (King Of Prussia, PA)
- …performing stocks in Europe over the past 20 years. Water Systems + Perform GMP reviews of microbiological testing data for facility and laboratory water ... purification systems, including LAL and bioburden results. + Review analytical testing data for water systems,...completion of quarterly trend reports. Raw Materials + Conduct GMP reviews of raw material test data ,… more
- Sanofi Group (Swiftwater, PA)
- …CAPA to prevent reoccurrence. + Conducts real time reviews to assess aseptic performance, GMP data entries, and all metrics are accurately updated + Understands ... works with them to maintain a positive rapport. **Delivery:** + Perform data review and analysis to identify and drive initiatives and projects to continuously… more
- Eurofins (King Of Prussia, PA)
- …+ Microbiological testing of the facility and/or laboratory water purification system samples. + GMP review of data + Qualification and Release of Media ... water system monitoring, microbiological testing, and environmental monitoring in a GMP -regulated setting. The analyst will be responsible for collecting and testing… more
- Fujifilm (Warminster, PA)
- …+ Support scale-up of formulation and lyophilization processes for pilot and GMP manufacturing. + Present formulation data to cross-functional teams and ... + Able to troubleshoot equipment and experimental problems independently. + Perform advanced data analysis, use of statistical software and generate summary data … more
- Eurofins (Lancaster, PA)
- …data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. + Review simple and complex routine and non-routine ... laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations + Review simple and complex routine and non-routine data (for… more
- Eurofins (Lancaster, PA)
- …confidence + Demonstrate motivation and take initiative + Follow through on assignments + Process/ review data , generate/ review reports, and evaluate data ... client received quality data by reviewing laboratory data for accuracy, clarity and adherence to GMP...technique, and high degree of accuracy and precision + Perform/ review preparations of reagents, samples, and standards according to… more
- Eurofins (Lancaster, PA)
- …confidence + Demonstrate motivation and take initiative + Follow through on assignments + Process/ review data , generate/ review reports, and evaluate data ... client received quality data by reviewing laboratory data for accuracy, clarity and adherence to GMP...technique, and high degree of accuracy and precision + Perform/ review preparations of reagents, samples, and standards according to… more
- Eurofins (Lancaster, PA)
- … data as required, as well as understand data patterns + Identify and report data patterns found during data review + Document data following SOPs ... entire network of Eurofins companies. Essential Duties and Responsibilities: + Applies GMP /GLP in all areas of responsibility, as appropriate + Demonstrates and… more
- Eurofins (Lancaster, PA)
- … data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations + Review simple and complex routine and non-routine ... This individual will work in a duel analyst and data reviewer role. The Scientist will be...analytical procedures; ensure all work is performed according to GLP/ GMP requirements and apply GLP/ GMP in all… more
- Sanofi Group (Swiftwater, PA)
- …(eg, environmental monitoring system [EMS], batch record management systems [MES], Data Historian, Process Control Systems (eg, distributed control system [DCS], ... standards, and industry practices. + Function as a key quality reviewer and approver of CSV lifecycle documents, including user requirements/functional… more
- NTT DATA North America (Pittsburgh, PA)
- …GMP / Qualified Platform (Non-Validated) DEV/ STAGE/ TRAIN * New Aws/ RHOS GMP / Qualified Platform (Validated) TEST/PROD/GOLD * Data Integrity Assessment * CIS ... **Req ID:** 329139 NTT DATA strives to hire exceptional, innovative and passionate...MES Interface Validation SDLC Documentation * New AWS/ RHOS GMP / Qualified Platform (Non-Validated) DEV/ STAGE/ TRAIN planning for… more
- Meta (Harrisburg, PA)
- …(DEC) organization to direct contracting across the full E2E project lifecycle of data center campuses in North America. There has never been a more exciting ... team of industry leaders! **Required Skills:** Lead Contracts Manager - Data Center Design, Engineering & Construction Responsibilities: 1. Direct the overall… more
- WuXi AppTec (Philadelphia, PA)
- …The **Technical Operations Specialist I** is responsible for generating and/or review manufacturing related technical documents and manage timely closure of these ... of technical transfer activities + Understands the application of GMP concepts and is able to recommend and identify...analysis, interprets, and draws conclusion of scientific and process data per good document practices + Follows compliance and… more
- Teva Pharmaceuticals (West Chester, PA)
- …your main responsibilities will be scheduling and supporting microbiological laboratory testing, data review , analysis of endotoxin and bioburden samples, and ... clinical development and commercial production for biological products manufactured in a GMP production facility. **How you'll spend your day** Position Summary: *… more
- West Pharmaceutical Services (Radnor, PA)
- …integrity (CCI) assessments in compliance with Good Manufacturing Practice ( GMP ) regulations. This role involves method execution, documentation, and collaboration ... strong analytical skills, and a thorough hands-on understanding of GMP requirements. **Essential Duties and Responsibilities** + Conduct performance and… more
- ThermoFisher Scientific (Collegeville, PA)
- …documentation to support sterile manufacturing. + Coordinate the preparation of GMP /GLP documents such as Standard Operating Procedures, Production Forms, batch ... needs. + Report and maintain metrics as appropriate. **Technical Writing and Review :** + Prepare, revise, and archive technical documents such as area rationales,… more
- Charles River Laboratories (Malvern, PA)
- …quality systems and processes specific to the testing platforms supporting GMP activities while ensuring compliance with all appropriate worldwide governmental ... meetings. ⦁ Provide assistance with the development and implementation of global GMP training programs to provide compliance managers and staff in designated staff… more
- Eurofins (Lancaster, PA)
- …other written material. Technical Writer Essential Duties and Responsibilities: + Applies GMP /GLP in all areas of responsibility, as appropriate + Applies the ... and any other documents + With support, Interact with Group Leaders, Data Reviewers and Scientists to gather the information necessary to the generation… more
- Eurofins (Lancaster, PA)
- …efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations ... Essential Duties and Responsibilities: + Applies GMP /GLP in all areas of responsibility, as appropriate +...technique, and high degree of accuracy and precision + Perform/ Review preparations of reagents, samples, and standards according to… more