Technical Writing Jobs in Arecibo

SUMMARYUnder general supervision provides characterization of process optimization strategies and/or troubleshooting of operational issues in the operations manufacturing pilot plant or capital projects environment.Applies basic engineering principles to the design and implementation of system modif...

We are seeking a highly skilled and detail-oriented CSV Validation Specialist to lead validation activities for computerized systems related to labeling inspection and vision technologies in a regulated pharmaceutical environment. This role ensures that all systems meet compliance requirements and o...

 Sr Engineer with experience in Parenteral products automatic and manual product inspection vision system device assembly and packaging.Qualifications : Doctorate or Masters 2 years of Engineering experienceBachelors in Engineering 4 years of Engineering experienceBilingual (Spanish/English)(Writ...

 We are seeking a skilled and innovative Engineer to join our dynamic team. The ideal candidate will have a background in engineering principles and practices with experience in the purification process of protein working with investigations troubleshooting process improvements and technical writing...

Validation Specialist with a strong knowledge of injection molding processes to support the development execution and documentation of validation activities (Protocols Tests Reports). Familiarized with IQ OQ and PQ validation phases for molds and equipment.IQ: Confirmation of Drawings (including mol...

CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to:Encapsulator CheckweigherCompression machineHardness testerEncapsulation machineAuxiliary equipmentMain activities should include:Verification of the equipment installed and configur...

Investigation Specialist for Parenteral industry will be responsible for performing thorough detailed and timely investigations and generation of high quality and timely investigation reports. Responsibilities: Understanding of the investigation process as it applies to manufacturing issues in th...

Quality Engineer with experience in the Medical Devices industry focused on CAPA management investigations quality assurance and ensuring compliance with quality and regulatory requirements.Duties:Revision and approvals of technical documents like URS Design Report of technical data.Auditing Equipme...

Process Development Scientist with knowledge in:Fluid DynamicsThermodynamicsInspection SystemsVisual InspectionMachine VisionStatistical AnalysisProcess CharacterizationRequirementsDoctorate or Masters 2 years of Scientific experience orBachelors 4 years of Scientific experience. Education in Engi...

Specialist QA with experience in the Medical Devices industry:Duties:Revision and approvals of technical documents like URS Design Report of technical data.Auditing Equipment/Facilities/Utilities of Qualification Protocols and execution.Commissioning and Qualification of Equipment/Systems/Facilities...