وظيفة في بورتوريكو

Process Development Scientist with experience in Vision files, Inspection equipment, Inspection processes and document management.Develops and implements new and novel protocols to address specific issues.Conceives and designs, executes or evaluates, and interprets experimental strate المزيد...

Assures the quality of manufactured products and processes per standard operating processes (SOPS) and GMP (Good Manufacturing Practices).This position is for a Non-Standard Shift.RequirementsHigh School diploma and 1 year of previous experience in similar role/industryGood communicat المزيد...

Assures the quality of manufactured products and processes per standard operating processes (SOPS) and GMP (Good Manufacturing Practices).This position is for a Non-Standard Shift.RequirementsHigh School diploma and 1 year of previous experience in similar role/industryGood communicat المزيد...

Assures the quality of manufactured products and processes per standard operating processes (SOPS) and GMP (Good Manufacturing Practices).Second ShiftRequirementsHigh School diploma and 1 year of previous experience in similar role/industryGood communications skills in English and Spa المزيد...

Manufacturing Engineerwith experience in medical devices industry.Project managementExercise knowledge of technical skills and understanding of the business objectives.Review of verification validation activities.CAPA and GMP Process.FDA regulations.RequirementsBS Engineering with 2 y المزيد...

Care Technician I with experience in customer service, product support, IT, and telecommunications in medical device industry tomonitoring inquiries and complaints from health care professionals, field personnel, patients, and various internal departments.Answer inquiries regarding te المزيد...

Lead new and existing products change implementation review, from process evaluation through FDA approval and products launch. Execute all related activities to new products introduction andproduct changes and Change Control procedures. Assures that the Company complies with allintern المزيد...

Description Leads the integration of the Sarbanes and Oxley Law efforts implementation to assure compliance with all legal aspects on company policies procedures and acceptable accounting legal practices. Examines financial statements and documents for conformance with accounting/fin المزيد...

Assures the quality of manufactured products and processes per Standard Operating Processes(SOPS) andGood Manufacturing Practices(GMP).Availability to work at 2nd. & 3rd. shift.RequirementsAssociate Degree in Science + 1 year of previous experience in similar role/industry. Profic المزيد...

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 المزيد...

Specialist Quality Control with experience in medical device or pharmaceutical industry. Responsibilities: Providing technical support to the quality control laboratory.Qualification/validation of HPLC methods and routine/non-routine testing lifecycle at the QC laboratories.Method tre المزيد...

To provide support on ongoing construction projects for a medical devices industry. Will coordinate constructions projects and will serve as liaison between project team and department management.RequirementsBachelors Degree in EngineeringExperience coordinating constructions projects المزيد...

Project Engineer with experience in process validations, equipment qualification, engineering projects, preferably in medical device industry. Verify manufacturing process documentation and quality documentation or regulations to make changes or modify the product labels as needed. C المزيد...

Sr. Engineer with experience in medical device or pharmaceutical industry. Knowledge in:Packaging equipmentDesign of new equipment processEngineering ProjectCAPA and ComplianceValidations and CommissioningRequirementsDoctorate degree or Master s degree and 3 years of Engineering exp المزيد...

Validation Consultant to provide qualification support for NIKON OPTICAL COMPARATORS.Development and approval of Qualification documents,Installation Qualification, Operational Qualification, and Performance Qualification.Execution of Qualification Protocols; development and approval المزيد...

Experience as Specialist QA in Pharmaceutical GMP regulated manufacturing.Responsibilities:Review and approve product MPs.Approve process validation protocols and reports for manufacturing processes. - Request Quality on incident triage team.Approve Environmental Characterization repo المزيد...

Provides overall quality assurance leadership in the management and qualification of suppliers. Establishes and maintains quality assurance programs, procedures, and controls, ensuring that performance metrics of both the supplier quality systems and suppliers are continually measured المزيد...

Quality Assurance professional with validations and commissioning & qualifications (manufacturing process, equipment and Critical Utilities) experience, technical writing, Quality Systems (Deviations, Change Control), Maintenance (PM, Work Orders, Job Plans review and approval) an المزيد...

Validation Specialist to perform activities related to qualification of laboratory and manufacturing equipment in the Medical Devices industry.RequirementsBachelor Degree3-5 years of experienceKnowledge and experience in a GMP regulated environmentBilingual: English and Spanish; writt المزيد...

Quality Assurance Specialist to provides support to complaint product return, investigation, and resolutions and conduct quality-related activities to deliver consistent, high-quality documents, services, products, and processes.Responsibilities:Completes compliant documentation and p المزيد...