Engineering Supports Jobs in Puerto Rico

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...

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...

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...

Manufacturing Systems Engineer with:Ability to read and update electrical design packages including User Requirements (URS) Functional Specifications (FS) Design Specifications (DS) wiring diagrams and P&ID.Proficient in PLC Controller and HMI programming skills.Qualifications: Ba 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...

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...

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...

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...

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...

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...

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...

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...

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...