Experience Design Jobs in Puerto Rico

Sr Engineer with experience in the Medical Device or Pharma industries. Knowledge and experience working with Change Controls on Trackwise.Knowledge in: Packaging equipmentDesign of new equipment processEngineering ProjectValidations and CommissioningCAPA and ComplianceRequirementsDoc More...

Specialist QA with knowledge of and experience with processes involved in manufacturing and distribution QA QAL validation and process development.Skills:Review and approve MPsEnvironmental characterization reportsInvestigations Risk assessmentsCAPAChange ControlRequirementsDoctorate 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...

Engineer with previous experiences in any regulated environment (Biotechnology Pharmaceutical Medical Devices etc.) experience in drug substance /API operations. Preferred experience in equipment start up troubleshooting PLC. Resource should understand control systems (input output c 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...

Sr. Validation Scientist with experience working with Analytical Instruments and knowledge in validation equipment qualification cleaning and sterilization. RequirementsDoctorate degree or Masters degree and 3 years of directly related experience or Bachelors degree and 5 years of dir More...

Project Manager with experience in:Change Control Deviations (as owner)Managing/leading New Product Introduction (Product Transfer)Product lifecycle managementProcess Improvements ProjectsRequirementsDoctorate degree or Masters degree and 2 years of Project Management experience or Ba More...

Sr. Validation Scientist with experience in Validation with preference in Process Validation in a regulated environment. To provide technical validation engineering support of process and/or equipment upgrades replacements and modifications in the laboratory manufacturing or manufactu More...

Process Development Scientist with experience in: Process Validation Formulation Process Mixing Studies Technical Writing RequirementsDoctorate or Masters degree and 5 years of Scientific experienceor Bachelors degree and 6 years of Scientific experience. Bilingual (Spanish/English) 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...

Investigations Specialist with experience in regulated industries. Strong knowledge of complaints and processes deviations. Will be responsible for performing through detailed and timely investigations and generation of high quality and timely investigation reports.Responsibilities:Un More...

Process Safety Specialist with experience in established and implement a governance process. Manages and monitors safety metrics process documentation policies and procedures that meet OSHA and other applicable requirements. Responsible for collecting data documentation and reports on 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...

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...

The CSV Specialist will be responsible for:Development of custom field formula and system report SOPs and validation documents and summary report. Chromatohraphic Software and server qualification. Assure project work & deliverables are provided in a timely and efficient manner.Re More...

Head of Customer Support SaaS Leadership RemoteJoin RoverPass a leading online booking platform for RV parks and campgrounds across the United States as our Head of Customer Support. This pivotal role combines team leadership operational excellence and strategic collaboration to en 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...

About Us:We are CodeGalaxy a leading U.S.based EdTech company specializing in delivering advanced engaging technology and coding education programs to children aged 515. We aim to bridge the gap in tech education by equipping students with a deep understanding of computer science and More...

Engineer with previous experiences in any regulated environment (Biotechnology Pharmaceutical Medical Devices etc.) New Products Introductions optimization and commercial manufacturing. Experience in Validation with preference in Process Validation.RequirementsMasters or Bachelors de More...

Coder / Configurator/ ProgrammerSummary:Responsible for configuration and simulation on Checklist Manager application (prototypes and reports). Must have knowledge of databases and the SQL language (for reports that s critical) and experience in the pharmaceutical industry.Requireme More...