- Cambrex High Point (High Point, NC)
- …filings. + Provide regulatory feedback on new and existing raw material, in- process and product specifications and test methods. + Provide feedback and/or lead ... resolve them. + Manage and carry out product quality review and continued process verification programs. Compile data from paper and electronic sources to complete… more
- Takeda Pharmaceuticals (Social Circle, GA)
- By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... laboratory operations with a focus on microbiological testing, compliance, and process excellence. You will help ensure product integrity through method execution,… more
- West Pharmaceutical Services (Cidra, PR)
- …a prevention base based on quality initiatives including: finished product process inspections, raw material inspections, active participation in work teams to ... of manufacturing records. **Essential Duties and Responsibilities** * Inspects work-in- process components to ensure compliance with customer specifications, ensuring… more
- Nitto Denko Corp. (Cincinnati, OH)
- …implementing/enforcing ICH Q guidelines, and regulatory guidance documents related to process and computerized system validation . + Strong critical thinking ... and effective CAPA, implementation of timely and effective changes, on-time material/in- process control/product testing, and lot disposition. + Develop and present… more
- Quality Consulting Group (Juncos, PR)
- QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... and repair equipment/system failures + Interpret and review utility, process system/ equipment, plumbing, ductwork plans, architectural, and HVAC P&ID's.… more
- Merck (Wilson, NC)
- …+ Provides guidance to engineering support teams (Automation/Reliability/Maintenance/Cleaning Validation )for site high risk work and contractor management ... A minimum of three years working within a cGDP environment for pharmaceutical and/or vaccine manufacturing. + Experience managing small capital projects (ie… more
- Abbott (Alameda, CA)
- …product design projects to ensure compliance with the internal design control process and external standards and regulations. + Contributes to the planning and ... and other release documentation for products used in design verification/ validation testing, clinical investigations, research use and demonstration purposes. +… more
- Bristol Myers Squibb (Seattle, WA)
- …+ Development and implementation of scalable AI solutions to address complex pharmaceutical business challenges. + Develop new AI/Gen AI tools aligned with business ... requirements into technical specifications and solutions. + Conduct thorough testing and validation of AI models to ensure accuracy and reliability. + Develop… more
- Quality Consulting Group (Humacao, PR)
- …Electrical Engineering + 2 to 5 years of relevant experience + Knowledge in Process Validation and Computerized System Validations + CAD Design proficiency + ... QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is...+ Develops manufacturing processes that are applicable to statistical process control and may develop those techniques. + Provides… more
- Lilly (Indianapolis, IN)
- …including due diligence reviews. + Specification development, engineering studies, qualification/ validation testing and support. + Printed packaging materials plan ... includes accountability for materials selection, design, technical transfer, and packaging process consulting to the Project Team. + Field Study packaging support… more