- Bristol Myers Squibb (Devens, MA)
- …maintaining material inventory accuracy using required systems and equipment. + Support process investigations & CAPAs. + Provide support and suggestions on special ... projects such as validation of Material Operations areas. Document & Work Review...logbooks & worksheets. + Review work throughout the work process and at completion, in order to ensure that… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …to maintain robust processes and high functioning teams + Partner with Validation and Engineering to identify, implement and effectively use Packaging Equipment and ... + Three years of Supervisory and/or management experience required + Pharmaceutical Packaging and Manufacturing experience required + Detailed knowledge of the… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- 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 ... and maintenance of computerized systems utilized in the manufacturing process . Automation engineers solve automation system and manufacturing equipment issues… more
- Bristol Myers Squibb (Devens, MA)
- …Leadership Team. **Key Responsibilities** + Establishes and oversees a unified, process -centric Quality Management System (QMS) that spans the entire product ... performance and sustain improvement. + Builds and develops a cross-divisional Global Process Owner Network that will develop and sustain the QMS working… more
- BD (Becton, Dickinson and Company) (El Paso, TX)
- …and leadership direction within the Production QA function to include In- Process Inspection, Finished Goods Inspection, Final Product Release, Quality Engineering, ... for strategic oversight and leadership direction of In-Coming Inspection, In- Process Inspection, Finished Goods Inspection, Final Product Release, Quality… more
- Bayer (Saxonburg, PA)
- …device or pharmaceutical manufacturing experience including: ISO13485 requirements, process and product validation , change management, QA/RA; + Manufacturing ... implemented into manufacturing through design transfer activities; + Implement process and product changes including: creation of material masters, manufacturing… more
- Lilly (Indianapolis, IN)
- …including risk assessments and documenting and maintaining the state of process /sterility assurance/cleaning validation . **Key Objectives / Deliverables:** + ... governance to the technical/scientific agenda for the site via the Science Lead Team ( process monitoring) + Represent the TS/MS organization at the Site Lead Team +… more
- Genentech (Los Angeles, CA)
- …support for newly built facilities with respect to the Infrastructure for process , utility and building systems. Lead Infrastructure impacting projects with large ... standards and best practices across all Site OT and Process Automation platforms, working with other process ...configuration, and upgrade of platform. + Execute computer system validation and control system lifecycle management. + Produce and… more
- Bristol Myers Squibb (Summit, NJ)
- …cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements, and good documentation practices. + Advanced understanding of ... pharmaceutical , manufacturing, and laboratory systems and equipment. + Strong...office-based, but will require entry into laboratory or GMP process areas with proper gowning, lab coats, PPE (safety… more
- Fujifilm (Research Triangle Park, NC)
- …+ Executes, documents, and leads manufacturing processing steps or support activities, process monitoring and control within at least one functional area (eg, ... Filtration, Homogenization/ Centrifugation, Fermentation, Chromatography, Cell Culture) + Performs in- process testing (eg, pH, conductivity, visual inspection) + Executes… more
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