Pharmaceutical Manufacturing Jobs in Puerto Rico

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...

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...

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...

Occupational Nurse to promote preservation of worker health prevention and care of work accidents occupational diseases and rehabilitation of the disabled through programs that not only reach the workers but also the circulated population.Duties: Provide plant employees with daily med 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...

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...

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...

Sr. Engineer with expertise in aseptic processing FDA product submissions and validation activities within a regulated pharmaceutical environment.Responsibilities:Lead efforts in the design implementation and improvement of aseptic processes and systems to ensure highquality productio 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...

QA Project Manager with experience in regulated industry.Duties:Oversee projects focused on implementation of digital and AI solutions that drive process performance and enhance operational excellence.Lead initiatives related to data integrity compliance ensuring compliance with regul 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...

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 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...

The Maintenance Engineer is responsible for planning coordinating and executing activities related to preventive corrective and predictive maintenance of equipment and systems used in the manufacture of parenteral products. This role includes implementing technical improvements ensuri More...

Responsible for the calibration of instrumentation loops controllers recorders transmitters balances and other devices used in pharmaceutical production. Parameters include but are not limited to temperature pressure weight force and humidity.Willing to work on the USEast CoastUsual a 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...

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...