Sap Manufacturing Jobs in Salinas Vc

The QA Documentation Specialist process edit verify and custody documents on the documentation system such as: procedures specifications test methods production control records (PCRs) and support documentation systems and SAP. Verify changes are aligned with operating system such as S More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

The Biologics Support Operator I  perform cleaning sterilization weighing and dispensing of materials. Monitor alarm systems. Assemble and inspect equipment in the manufacturing area to confirm operational status. Work is performed in aseptic or nonaseptic environments. Perf More...

The Technician QA I primary purpose of this position is to ensure the quality of raw materials commodities and durable & consumable received are acceptable per the appropriate quality attributes.primary purpose of this position is to ensure the quality of raw materials comm More...

The Parenteral Support Operator I perform different equipment in one of the functional areas assigned. Perform inspection and pack syringes. Assemble and inspect equipment in the manufacturing area to confirm operational status. Perform cleaning and sterilization procedures. Work is p More...

Provides technical and sustaining engineering support in a manufacturing area. Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies manufacturing techniques as well as production yields for existing products. Integ More...

PurposeThe Digital Technology Senior Analyst reports to the Site BTS Lead and be responsible for championing the sites Technology Agenda through the implementation of Digital and Emerging Technology Solutions that meet the business needs in line with the corporate IT strategy and will More...

Sr Validation Scientist with experience in:URS DS and Equipment Risk AssessmentsCharacterization and Validation experienceDevelopment of Characterization and Validation protocolsExecution of Characterization and Validation protocolsDevelop Characterization and Validation reportsDevice More...

Project Manager with experience managing change control as Owner in Trackwise. RequirementsDoctorate degree or Masters degree and 2 years of Project Management experience or Bachelors degree and 4 years of Project Management experience or Associate s degree and 10 years of Project M More...

Process Development Principal Scientist with experience in combinations products or Medical Devices. Skills:Characterization and ValidationDevelopment of Characterization and Validation ProtocolsDevices assembly equipment and packaging equipment validation RequirementsDoctorate degree More...

Sr Engineer with experience in regulated industry performing Characterization and Validation.Tasks:URS DS and Equipment Risk AssessmentsDevelopment of Characterization and Validation protocolsExecution of Characterization and Validation protocolsDevelop Characterization and Validation More...

The Pharmaceutical Operator I is responsible to properly execute the Manufacturing processes and equipment Operation according to process order. The execution should be always according the Manufacturing instructions following the Good Manufacturing Practices (cGMP) and Safe More...

The Associate Technician Electronic Instrument provide preventive maintenance calibration programming configuration and repair services to instruments systems or equipment that measure and control different variables in industrial manufacturing processes primarily supporting instrumen More...

Regulatory Consultant will provide expert guidance and support in navigating the regulatory landscape specifically in aseptic production environments. Responsibilities: Provide expert regulatory advice for aseptic manufacturing processes ensuring compliance with FDA and global regulat More...

Validation Specialist to provide support in validation of biochemical processes. Must have experience and knowledge in validation of laboratory and manufacturing equipment and validation life cycle. To perform: Method Transfer in Biotechnology Process Test Methods ValidationEquipment More...

MS&T Validation Specialist with experience in regulated industry.Duties:Lead projects focused on technology transfer process optimization and scaleup activities to support manufacturing operations.Oversee activities related to process validation troubleshooting and the introductio More...

Your responsibilities will include: Execution of component qualifications for manufacturing lines. Foster open and transparent communication with suppliers to ensure mutual understanding of expectations and objectives. Collaborate with crossfunctional teams including Quali More...

The Quality Manager provides leadership and direction to the quality function they are responsible for within Operations. Role is responsible for the effective implementation of AbbVie Quality System for which they are responsible for. This could include be two or more of the followin More...